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    • 专利摘要:
    Disclosed are compounds that have excellent insecticidal activity and are usable as agricultural and horticultural insecticides. Compounds represented by formula (I) or agriculturally and horticulturally acceptable acid addition salts thereof have excellent insecticidal activity and are usable as agricultural and horticultural insecticides.
    公开号:EP1780202A1
    申请号:EP05768511
    申请日:2005-08-03
    公开日:2007-05-02
    发明作者:Kazumi Meiji Seika Kaisha Ltd. YAMAMOTO；Ryo Meiji Seika Kaisha Ltd. HORIKOSHI；Kazuhiko Meiji Seika Kaisha Ltd. OYAMA；Hiroshi Meiji Seika Kaisha Ltd. KURIHARA；Shizuo Shimano；Takaaki Miyake；Hiroki Hotta；Jun Iwabuchi
    申请人:Meiji Seika Kaisha Ltd；Nippon Kayaku Co Ltd；
    IPC主号:C07D215-00
    专利说明:
    [0001] This patent application is an application claiming priority based on an early filed Japanese patent application, Japanese Patent Application No. 228337/2004 (filing date: August 4, 2004 ). The whole disclosure of Japanese Patent Application No. 228337/2004 is incorporated herein by reference. BACKGROUND OF THE INVENTIONField of the Invention
    [0002] The present invention relates to quinoline derivatives and agricultural and horticultural insecticides comprising the same as an active ingredient. Background Art
    [0003] Various compounds having control effect have hitherto been developed. For example, WO 98/055460 discloses quinoline derivatives having fungicidal activity, but on the other hand, it does not disclose the insecticidal activity of these derivatives. Japanese Patent No. 2633377 and U.S. Patent No. 4168311 disclose quinoline derivatives having insecticidal activity. The compounds described in these publications are different from quinoline derivatives represented by formula (I) which will be described below in the structure of the substituent at the 6-position of quinoline. Regarding agricultural and horticultural insecticides, it can be said that, due to problems associated with, for example, the presence of insect species which have low sensitivity to these compounds or are difficult to be controlled, the development of novel agricultural and horticultural insecticides having excellent insecticidal activity are still desired. SUMMARY OF THE INVENTION
    [0004] The present inventors have now found that novel quinoline derivatives represented by formula (I) have significant insecticidal activity. The present invention has been made based on such finding.
    [0005] Accordingly, an object of the present invention is to provide novel quinoline derivatives having significant insecticidal activity and to provide agricultural and horticultural insecticides comprising the same as an active ingredient which have reliable effect and can be safely used.
    [0006] According to the first aspect of the present invention, there is provided a quinoline derivative. This derivative is a compound represented by formula (I) or an agriculturally and horticulturally acceptable acid addition salt thereof:
    [0007] According to the second aspect of the present invention, there is provided an agricultural and horticultural insecticide. This insecticide comprises as an active ingredient a quinoline derivative represented by formula (I) or an agriculturally and horticulturally acceptable acid addition salt thereof.
    [0008] According to the third aspect of the present invention, there is provided an agricultural and horticultural insecticide. This insecticide comprises as an active ingredient a compound represented by formula (Ia) or an agriculturally and horticulturally acceptable acid addition salt thereof:
    [0009] The quinoline derivative according to the present invention has exellent control effect against agricultural and horticultural insect pests and thus are useful as agricultural and horticultural insecticides. DETAILED DESCRIPTION OF THE INVENTION Compounds represented by formula (I) and formula (Ia)
    [0010] The term "halogen" as used herein means a fluorine, chlorine, bromine, or iodine atom, preferably a fluorine or chlorine atom."Alkali metal" represented by R1 includes sodium or potassium."Alkaline earth metal" represented by R1 includes calcium or magnesium.
    [0011] C1-18 alkyl represented by R1, R3, R4, R5, R6, R7, or R8 may be either a straight-chain or branched-chain configuration, preferably C1-10 alkyl, more preferably C1-4 alkyl. The C1-18 alkyl group may be substituted. Substituents in this case include a halogen atom, C1-4 alkyloxy, C1-4 alkyloxy-C1-4 alkyloxy, C1-4 alkyloxycarbonyl, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom. Preferred examples thereof include a halogen atom, C1-4 alkyloxy, C1-4 alkyloxy-C1-4 alkyloxy, C1-4 alkyloxycarbonyl, cyano, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom. The substituent in R1 is more preferably C1-4 alkyloxy-C1-4 alkyloxy or C1-4 alkyloxycarbonyl. The substituent in R3 is more preferably a halogen atom or acetyloxy. The substituent in R4 is more preferably C1-4 alkyloxy or acetyloxy. The substituent in R5 is more preferably a halogen atom or C1-4 alkyloxy. The substituent in R6, R7, or R8 is more preferably a halogen atom, C1-4 alkyloxy, or acetyloxy.
    [0012] Specific examples of C1-18 alkyl represented by R1, R3, R4, R5, R6, R7, or R8 include methyl, ethyl, propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, (2- or 3-methyl)butyl, 2,3-dimethylpropyl, n-hexyl, (2,3- or 4-methyl)pentyl, (2,3-, 2,4-or 3,4-dimethyl)butyl, 2,3,4-trimethylpropyl, n-heptyl, n-octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, chloromethyl, trichloromethyl, trifluoromethyl, (1- or 2-)chloroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, 2-cyanoethyl, cyclopropylmethyl, cyclopropylethyl, cyclopropylpropyl, 1-methylcyclopropylmethyl, 2-(1-methylcyclopropyl)ethyl, 3-(1-methylcyclopropyl)propyl, 2,2-dimethylcyclopropylmethyl, 2-(2,2-dimethylcyclopropyl)ethyl, 3-(2,2-dimethylcyclopropyl)propyl, 2,2-dichlorocyclopropylmethyl, 2-(2,2-dichlorocyclopropyl)ethyl, 3-(2,2-dichlorocyclopropyl)propyl, 2,2-difluorocyclopropylmethyl, 2-(2,2-difluorocyclopropyl)ethyl, or 3-(2,2-difluorocyclopropyl)propyl.
    [0013] C1-4 alkyl represented by R2 may be in either a straight-chain or branched-chain configuration. The C1-4 alkyl group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom, preferably a halogen atom or cyano.
    [0014] Specific examples of C1-4 alkyl represented by R2 include methyl, ethyl, propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, chloromethyl, trichloromethyl, trifluoromethyl, (1- or 2-)chloroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 2-trifluoromethoxyethyl,cyanomethyl, or 2-cyanoethyl.
    [0015] C2-18 alkenyl represented by R1, R4, R5, or R8 may be in either a straight-chain or branched-chain configuration, preferably C2-10 alkenyl, more preferably C2-4 alkenyl. The C2-18 alkenyl group may be substituted, and examples of substituent include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom. The substituent in R4 or R5 is preferably a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, or acetyloxy. The substituent in R1, R4, R5, or R8 is more preferably a halogen atom.
    [0016] Specific examples of C2-18 alkenyl represented by R1, R4, R5, or R8 include vinyl, (1- or 2-)propenyl, (1-, 2- or 3-)butenyl, (1-, 2-, 3- or 4-)pentenyl, (1-, 2-, 3-, 4- or 5-)hexenyl, (1-, 2-, 3-, 4-, 5- or 6-)heptenyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)octenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)nonenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-)decenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9- or 10-)undecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10- or 11-)dodecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11- or 12-)tridecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12- or 13-)tetradecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13- or 14-)pentadecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14- or 15-)hexadecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15- or 16-)heptadecenyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, 16- or 17-)octadecenyl, 1-methyl vinyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1,2-dimethyl-1-propenyl, 1-methyl-1-butenyl, 1-methyl-2-butenyl, 2-fluoro vinyl, 2-chloro vinyl, 2,2-difluoro vinyl, 2,2-dichloro vinyl, or 2-trifluoromethoxy vinyl.
    [0017] C2-4 alkenyl represented by R3 may be in either a straight-chain or branched-chain configuration. The C2-4 alkenyl group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom, preferably a halogen atom.
    [0018] C2-18 alkynyl represented by R1, R4, R5, or R8 may be in either a straight-chain or branched-chain configuration, preferably C2-10 alkynyl, more preferably C2-4 alkynyl. The C2-18 alkynyl group may be substituted, and examples of substituent include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom.
    [0019] Specific examples of C2-18 alkynyl represented by R1, R4, R5 or R8 include ethynyl, (1- or 2-)propynyl, (1-, 2- or 3-)butynyl, (1-, 2-, 3- or 4-)pentynyl, (1-, 2-, 3-, 4- or 5-)hexynyl, (1-, 2-, 3-, 4-, 5- or 6-)heptynyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)octynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)nonynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-)decynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9- or 10-)undecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10- or 11-)dodecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11- or 12-)tridecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12- or 13-)tetradecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13- or 14-)pentadecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14- or 15-)hexadecynyl, (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15- or 16-)heptadecynyl, or (1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, 16- or 17-)octadecynyl.
    [0020] C3-10 cycloalkyl repersented by R1, R4, R5 or R8 is preferably C3-6 cycloalkyl. The C3-10 cycloalkyl group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethyl, trifluoromethoxy, acetyl, acetyloxy, C1-4 alkyl, or C3-6 cycloalkyl optionally substituted by halogen atom, preferably a halogen atom or C1-4 alkyl.
    [0021] Specific examples of C3-10 cycloalkyl represented by R1, R4, R5 or R8 include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 1-methyl-2-ethylcyclopropyl, 2-chlorocyclopropyl, 2-fluorocyclopropyl, 2,2-dimethylcyclopropyl, 2,2-dichlorocyclopropyl, 2,2-difluorocyclopropyl, 1-methyl-2-chlorocyclopropyl, 1-methyl-2-fluorocyclopropyl, 1-methyl-2,2-dimethylcyclopropyl, 1-methyl-2,2-dichlorocyclopropyl, 1-methyl-2,2-difluorocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 2-chlorocyclobutyl, 2-fluorocyclobutyl, 2,2-dimethylcyclobutyl, 2,2-dichlorocyclobutyl, 2,2-difluorocyclobutyl, 1-methylcyclopentyl, 2-methylcyclopentyl, 3-methylcyclopentyl, 3-chlorocyclopentyl, 3-fluorocyclopentyl, 3,3-dimethylcyclopentyl, 3,3-dichlorocyclopentyl, 3,3-difluorocyclopentyl, 1-methylcyclohexyl, or 2,2-dimethylcyclohexyl.
    [0022] Preferably, phenyl lower alkyl represented by R1, R4, R5 or R8 is C1-4 alkyl containing phenyl. The phenyl group in the phenyl lower alkyl group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyl, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom.
    [0023] Specific examples of phenyl lower alkyl represented by R1, R4, R5 or R8 include benzyl, (1- or 2-)phenylethyl, (1-, 2- or 3-)phenylpropyl, (1-, 2-, 3- or 4-)phenylbutyl.
    [0024] Preferably, phenoxy lower alkyl represented by R1, R4, R5 or R8 is phenoxy-containing C1-4 alkyl. In this case, the phenyl grop in the phenoxy lower alkyl group may be substituted, and examples of substituents include halogen atom, C1-4 alkyl, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom.
    [0025] Specific examples of phenoxy lower alkyl represented by R1, R4, R5 or R8 include phenoxymethyl, (1- or 2-)phenoxyethyl, (1-, 2- or 3-)phenoxypropyl, or (1-, 2-, 3- or 4-)phenoxybutyl. The phenyl group may be substituted, and preferred substituents include a halogen atom, C1-4 alkyl, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, or acetyloxy.
    [0026] Phenyl represented by R1, R4, R5, R6, R7 or R8 may be substituted, and preferred substituents include a halogen atom, C1-4 alkyl, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom.
    [0027] The heterocyclic group represented by R1, R4, R5 or R8 is preferably a five- or six-membered saturated heterocyclic or aromatic ring containing one S, O, or N as a heteroatom, a five- or six-membered saturated heterocyclic or aromatic ring containing two N as a heteroatom, a five- or six-membered saturated heterocyclic or aromatic ring containing O or S and one N as heteroatoms, more preferably a cyclic group selected from the group consisting of thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolyl, thiazolyl, oxazolyl, pyridyl, and pyrimidinyl. The heterocyclic group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyl, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom.
    [0028] Specific examples of the heterocyclic group represented by R1, R4, R5 or R8 include (2- or 3-)thienyl, (2- or 3-)furyl, (1-, 2- or 3-)pyrrolyl, (1- or 2-)imidazolyl, (1-, 3-, 4- or 5-)pyrazolyl, (3-, 4- or 5-)isothiazolyl, (3-, 4- or 5-)isoxazolyl, (2-, 4- or 5-)thiazolyl, (2-, 4- or 5-)oxazolyl, (2-, 3- or 4-)pyridyl, or (2-, 4-, 5- or 6-)pyrimidinyl.
    [0029] C1-4 alkylthio represented by R4 may be in either a straight-chain or branched-chain configuration. The C1-4 alkylthio group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom, preferably a halogen atom.
    [0030] C1-4 alkoxy represented by R3 may be in either a straight-chain or branched-chain configuration. The C1-4 alkoxy group may be substituted, and examples of substituents include a halogen atom, C1-4 alkyloxy, nitro, cyano, formyl, trifluoromethoxy, acetyl, acetyloxy, or C3-6 cycloalkyl optionally substituted by halogen atom, preferably a halogen atom.
    [0031] Specific examples of C1-4 alkyl optionally substituted by halogen atom represented by X1, X2, and X3 include methyl, ethyl, n-propyl, n-butyl, iso-propyl, iso-butyl, s-butyl, t-butyl, trifluoromethyl, trichloromethyl, difluoromethyl, dichloromethyl, trifluoroethyl, trichloroethyl, tetrafluoroethyl, or tetrachloroethyl, preferably methyl, ethyl, trifluoromethyl, trichloromethyl, difluoromethyl, dichloromethyl, trifluoroethyl, trichloroethyl, pentafluoroethyl, or pentachloroethyl, more preferably methyl, ethyl, trifluoromethyl, or difluoromethyl.
    [0032] Specific examples of C1-4 alkyloxy optionally substituted by halogen atom represented by X1, X2, and X3 include methoxy, ethoxy, n-propyloxy, n-butyloxy, iso-propyloxy, iso-butyloxy, s-butyloxy, t-butyloxy, trifluoromethoxy, trichloromethoxy, difluoromethoxy, dichloromethoxy, trifluoroethoxy, trichloroethoxy, pentafluoroethoxy, or pentachloroethoxy, preferably methoxy, ethoxy, trifluoromethoxy, trichloromethoxy, difluoromethoxy, dichloromethoxy, trifluoroethoxy, trichloroethoxy, pentafluoroethoxy, or pentachloroethoxy, more preferably methoxy, ethoxy, trifluoromethoxy, or difluoromethoxy.
    [0033] Specific examples of C1-4 alkylthio optionally substituted by halogen atom represented by X1, X2, and X3 include methylthio, ethylthio, n-propylthio, n-butylthio, iso-propylthio, iso-butylthio, s-butylthio, t-butylthio, trifluoromethylthio, trichloromethylthio, difluoromethylthio, dichloromethylthio, trifluoroethylthio, trichloroethylthio, pentafluoroethylthio, or pentachloroethylthio, preferably methylthio, ethylthio, trifluoromethylthio, trichloromethylthio, difluoromethylthio, dichloromethylthio, trifluoroethylthio, trichloroethylthio, tetrafluoroethylthio, or tetrachloroethylthio, more preferably methylthio, ethylthio, trifluoromethylthio, or difluoromethylthio.
    [0034] Specific examples of C1-4 alkyloxycarbonyl optionally substituted by halogen atom represented by X1, X2, and X3 include methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, n-butyloxycarbonyl, iso-propyloxycarbonyl, iso-butyloxycarbonyl, s-butyloxycarbonyl, t-butyloxycarbonyl, trifluoromethoxycarbonyl, trichloromethoxycarbonyl, difluoromethoxycarbonyl, dichloromethoxycarbonyl, trifluoroethoxycarbonyl, trichloroethoxycarbonyl, tetrafluoroethoxycarbonyl, tetrachloroethoxycarbonyl, pentafluoro ethoxycarbonyl, or pentachloroethoxycarbonyl, preferably methoxycarbonyl, ethoxycarbonyl, trifluoromethoxycarbonyl, trichloromethoxycarbonyl, difluoromethoxycarbonyl, dichloromethoxycarbonyl, trifluoroethoxycarbonyl, trichloroethoxycarbonyl, pentafluoroethoxycarbonyl, or pentachloroethoxycarbonyl, more preferably methoxycarbonyl, ethoxycarbonyl, trifluoromethoxycarbonyl, or difluoromethoxycarbonyl.
    [0035] Preferably, W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, and, preferably, W11, W12, and W13 represent C-Y11, C-Y12, and C-Y13, respectively.
    [0036] C1-8 alkyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more groups selected from one or more halogen atoms which may be the same or different, C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different, and C2-4 alkenyloxy substituted by one or more halogen atoms which may be the same or different. The C1-8 alkyl group is preferably substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different, more preferably by one or more halogen atoms which may be the same or different. Specific examples of C1-8 alkyl include chloromethyl, (1- or 2-)chloroethyl, (1-, 2- or 3-)chloro-n-propyl, (1-, 2-, 3- or 4-)chloro-n-butyl, (1-, 2-, 3-, 4- or 5-)chloro-n-pentyl, (1-, 2-, 3-, 4-, 5- or 6-)chloro-n-hexyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)chloro-n-heptyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)chloro-n-octyl, fluoromethyl, (1- or 2-)fluoroethyl, (1-, 2- or 3-)fluoro-n-propyl, (1-, 2-, 3- or 4-)fluoro-n-butyl, (1-, 2-, 3-, 4- or 5-)fluoro-n-pentyl, (1-, 2-, 3-, 4-, 5- or 6-)fluoro-n-hexyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)fluoro-n-heptyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)fluoro-n-octyl, dichloromethyl, difluoromethyl, trichloromethyl, trifluoromethyl, trichloroethyl, trifluoroethyl, pentachloroethyl, pentafluoroethyl, 3,3,3-trichloropropyl, 3,3,3-trifluoropropyl, 2,2,3,3-tetrachloropropyl, 2,2,3,3-tetrafluoropropyl, ditrifluoromethylmethyl, 2,2-ditrifluoromethylethyl, heptafluoro-iso-propyl, nonafluoro-iso-butyl, chloromethoxymethyl, (1- or 2-)chloromethoxyethyl, (1-, 2- or 3-)chloromethoxy-n-propyl, (1-, 2-, 3- or 4-)chloromethoxy-n-butyl, (1-, 2-, 3-, 4- or 5-)chloromethoxy-n-pentyl, (1-, 2-, 3-, 4-, 5- or 6-)chloromethoxy-n-hexyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)chloromethoxy-n-heptyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)chloromethoxy-n-octyl, fluoromethoxymethyl, (1-or 2-)fluoromethoxyethyl, (1-, 2- or 3-)fluoromethoxy-n-propyl, (1-, 2-, 3- or 4-)fluoromethoxy-n-butyl, (1-, 2-, 3-, 4- or 5-)fluoromethoxy-n-pentyl, (1-, 2-, 3-, 4-, 5- or 6-)fluoromethoxy-n-hexyl, (1-, 2-, 3-, 4-, 5-, 6- or 7-)fluoromethoxy-n-heptyl, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)fluoromethoxy-n-octyl, dichloromethoxymethyl, difluoromethoxymethyl, trichloromethoxymethyl, trifluoromethoxymethyl, trichloromethoxyethyl, trifluoromethoxyethyl, pentachloroethoxymethyl, pentafluoroethoxymethyl, pentachloroethoxyethyl, pentafluoroethoxyethyl, 3,3,3-trichloropropyloxymethyl, 3,3,3-trifluoropropyloxymethyl, 3,3,3-trichloropropyloxyethyl, 3,3,3-trifluoropropyloxyethyl, 2,2,3,3-tetrachloropropyloxymethyl, 2,2,3,3-tetrafluoropropyloxymethyl, or trifluoromethoxy-1,1,2-trifluoroethyl, preferably chloromethyl, (1- or 2-)chloroethyl, (1-, 2- or 3-)chloro-n-propyl, fluoromethyl, (1- or 2-)fluoroethyl, (1-, 2- or 3-)fluoro-n-propyl, dichloromethyl, difluoromethyl, trichloromethyl, trifluoromethyl, trichloroethyl, trifluoroethyl, pentachloroethyl, pentafluoroethyl, 3,3,3-trichloropropyl, 3,3,3-trifluoropropyl, 2,2,3,3-tetrachloropropyl, 2,2,3,3-tetrafluoropropyl, ditrifluoromethylmethyl, 2,2-ditrifluoromethylethyl, heptafluoro-iso-propyl, chloromethoxymethyl, (1- or 2-)chloromethoxyethyl, (1-, 2- or 3-)-chloromethoxy-n-propyl, (1-, 2-, 3- or 4-)chloromethoxy-n-butyl, fluoromethoxymethyl, (1- or 2-)fluoromethoxyethyl, (1-, 2- or 3-)-fluoromethoxy-n-propyl, (1-, 2-, 3- or 4-)fluoromethoxy-n-butyl, dichloromethoxymethyl, difluoromethoxymethyl, trichloromethoxymethyl, trifluoromethoxymethyl, trichloromethoxyethyl, trifluoromethoxyethyl, pentachloroethoxymethyl, pentafluoroethoxymethyl, pentachloroethoxyethyl, pentafluoroethoxyethyl, 3,3,3-trichloropropyloxymethyl, 3,3,3-trifluoropropyloxymethyl, 3,3,3-trichloropropyloxyethyl, 3,3,3-trifluoropropyloxyethyl, 2,2,3,3-tetrachloropropyloxymethyl, 2,2,3,3-tetrafluoropropyloxymethyl, or trifluoromethoxy-1,1,2-trifluoroethyl, more preferably trifluoromethyl, trifluoroethyl, tetrafluoroethyl, 3,3,3-trifluoropropyl, 2,2,3,3-tetrafluoropropyl, difluoromethoxymethyl, trifluoromethoxymethyl, trifluoromethoxyethyl, pentafluoroethoxymethyl, pentafluoroethoxyethyl, 3,3,3-trifluoropropyloxymethyl, 3,3,3-trifluoropropyloxyethyl, 2,2,3,3-tetrafluoropropyloxymethyl, or trifluoromethoxy-1,1,2-trifluoroethyl.
    [0037] C2-8 alkenyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more groups selected from one or more halogen atoms which may be the same or different, C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different, and C2-4 alkenyloxy substituted by one or more halogen atoms which may be the same or different, preferably substituted by one or more halogen atoms which may be the same or different. Specific examples of C2-8 alkenyl include 2-chloro-3,3,3-trifluoro-1-propenyl.
    [0038] C1-8 alkyloxy represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more groups selected from one or more halogen atoms which may be the same or different, C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different, and C2-4 alkenyloxy substituted by one or more halogen atoms which may be the same or different. This C1-8 alkyloxy group is preferably substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. In one embodiment, this C1-8 alkyloxy group is substituted by one or more halogen atoms which may be the same or different. Specific examples of C1-8 alkyloxy include chloromethyloxy, (1- or 2-)chloroethyloxy, (1-, 2- or 3-)chloro-n-propyloxy, (1-, 2-, 3- or 4-)chloro-n-butyloxy, (1-, 2-, 3-, 4-or 5-)chloro-n-pentyloxy, (1-, 2-, 3-, 4-, 5- or 6-)chloro-n-hexyloxy, (1-, 2-, 3-, 4-, 5-, 6- or 7-)chloro-n-heptyloxy, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)-chloro-n-octyloxy, fluoromethyloxy, (1-or 2-)fluoroethyloxy, (1-, 2- or 3-)-fluoro-n-propyloxy, (1-, 2-, 3- or 4-)fluoro-n-butyloxy, (1-, 2-, 3-, 4- or 5-)fluoro-n-pentyloxy, (1-, 2-, 3-, 4-, 5- or 6-)fluoro-n-hexyloxy, (1-, 2-, 3-, 4-, 5-, 6- or 7-)fluoro-n-heptyloxy, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)fluoro-n-octyloxy, dichloromethyloxy, difluoromethyloxy, trichloromethyloxy, trifluoromethyloxy, trichloroethyloxy, trifluoroethyloxy, pentachloroethyloxy, pentafluoroethyloxy, 3,3,3-trichloropropyloxy, 3,3,3-trifluoropropyloxy, 2,2,3,3-tetrachloropropyloxy, 2,2,3,3-tetrafluoropropyloxy, ditrifluoromethylmethyloxy, 2,2-ditrifluoromethylethyloxy, heptafluoro-iso-propyloxy, nonafluoro-iso-butyloxy, chloromethoxymethoxy, (1- or 2-)chloromethoxymethoxy, (1-, 2- or 3-)chloromethoxy-n-propyloxy, (1-, 2-, 3- or 4-)chloromethoxy-n-butyloxy, (1-, 2-, 3-, 4- or 5-)chloromethoxy-n-pentyloxy, (1-, 2-, 3-, 4-, 5- or 6-)chloromethoxy-n-hexyloxy, (1-, 2-, 3-, 4-, 5-, 6- or 7-)-chloromethoxy-n-heptyloxy, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)-chloromethoxy-n-octyloxy, fluoromethoxymethoxy, (1- or 2-)-fluoromethoxyethoxy, (1-, 2-or 3-)fluoromethoxy-n-propyloxy, (1-, 2-, 3- or 4-)fluoromethoxy-n-butyloxy, (1-, 2-, 3-, 4- or 5-)fluoromethoxy-n-pentyloxy, (1-, 2-, 3-, 4-, 5- or 6-)fluoromethoxy-n-hexyloxy, (1-, 2-, 3-, 4-, 5-, 6- or 7-)fluoromethoxy-n-heptyloxy, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)-fluoromethoxy-n-octyloxy, dichloromethoxymethoxy, difluoromethoxymethoxy, trichloromethoxymethoxy, trifluoromethoxymethoxy, trichloromethoxyethoxy, trifluoromethoxyethoxy, pentachloroethoxymethoxy, pentafluoroethoxymethoxy, pentachloroethoxyethoxy, pentafluoroethoxyethoxy, 3,3,3-trichloropropyloxymethoxy, 3,3,3-trifluoropropyloxymethoxy, 3,3,3-trichloropropyloxyethoxy, 3,3,3-trifluoropropyloxyethoxy, 2,2,3,3-tetrachloropropyloxymethoxy, 2,2,3,3-tetrafluoropropyloxymethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,2,2-trifluoroethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,1,2-trifluoroethoxy, or trifluoromethoxy-1,1,2-trifluoroethoxy, preferably chloromethyloxy, (1- or 2-)chloroethyloxy, (1-, 2- or 3-)chloro-n-propyloxy, fluoromethyloxy, (1- or 2-)fluoroethyloxy, (1-, 2- or 3-)fluoro-n-propyloxy, dichloromethyloxy, difluoromethyloxy, trichloromethyloxy, trifluoromethyloxy, trichloroethyloxy, trifluoroethyloxy, pentachloroethyloxy, pentafluoroethyloxy, 3,3,3-trichloropropyloxy, 3,3,3-trifluoropropyloxy, 2,2,3,3-tetrachloropropyloxy, 2,2,3,3-tetrafluoropropyloxy, ditrifluoromethylmethyloxy, 2,2-ditrifluoromethylethyloxy, heptafluoro-iso-propyloxy, chloromethoxymethoxy, (1- or 2-)chloromethoxyethoxy, (1-, 2- or 3-)-chloromethoxy-n-propyloxy, (1-, 2-, 3- or 4-)chloromethoxy-n-butyloxy, fluoromethoxymethoxy, (1- or 2-)fluoromethoxyethoxy, (1-, 2-or 3-)-fluoromethoxy-n-propyloxy, (1-, 2-, 3- or 4-)fluoromethoxy-n-butyloxy, dichloromethoxymethoxy, difluoromethoxymethoxy, trichloromethoxymethoxy, trifluoromethoxymethoxy, trichloromethoxyethoxy, trifluoromethoxyethoxy, pentachloroethoxymethoxy, pentafluoroethoxymethoxy, pentachloroethoxyethoxy, pentafluoroethoxyethoxy, 3,3,3-trichloropropyloxymethoxy, 3,3,3-trifluoropropyloxymethoxy, 3,3,3-trichloropropyloxyethoxy, 3,3,3-trifluoropropyloxyethoxy, 2,2,3,3-tetrachloropropyloxymethoxy, 2,2,3,3-tetrafluoropropyloxymethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,2,2-trifluoroethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,1,2-trifluoroethoxy, or trifluoromethoxy-1,1,2-trifluoroethoxy, more preferably trifluoromethyloxy, trifluoroethyloxy, pentafluoroethyloxy, 3,3,3-trifluoropropyloxy, 2,2,3,3-tetrafluoropropyloxy, difluoromethoxymethoxy, trifluoromethoxymethoxy, trifluoromethoxyethoxy, pentafluoroethoxymethoxy, pentafluoroethoxyethoxy, 3,3,3-trifluoropropyloxymethoxy, 3,3,3-trifluoropropyloxyethoxy, 2,2,3,3-tetrafluoropropyloxymethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,2,2-trifluoroethoxy, 1,1,2,2,3,3,3-heptafluoropropyloxy-1,1,2-trifluoroethoxy, or trifluoromethoxy-1,1,2-trifluoroethoxy.
    [0039] C2-8 alkenyloxy represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more groups selected from one or more halogen atoms which may be the same or different, C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different, and C2-4 alkenyloxy substituted by one or more halogen atoms which may be the same or different. Specific examples of C2-8 alkenyloxy include 3,3-dichloro-2-propenyloxy or 3-chloro-4,4,4-trifluoro-2-butenyloxy.
    [0040] C1-8 alkyloxycarbonyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. Specific examples of C1-8 alkyloxycarbonyl include ethyloxycarbonyl.
    [0041] C1-8 alkylthio represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally sbustituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. This C1-8 alkylthio group is preferably C1-8 alkylthio substituted by one or more halogen atoms which may be the same or different. Specific examples of C1-8 alkylthio include methylthio, ethylthio, n-propylthio, n-butylthio, iso-propylthio, iso-butylthio, s-butylthio, t-butylthio, n-pentylthio, (2- or 3-methyl)butylthio, 2,3-dimethylpropylthio, n-hexylthio, (2 or 3 or 4-methyl)pentylthio, (2,3- or 2,4- or 3,4-dimethyl)butylthio, 2,3,4-trimethylpropylthio, n-heptylthio, n-octylthio, trifluoromethylthio, trichloromethylthio, difluoromethylthio, dichloromethylthio, trifluoroethylthio, trichloroethylthio, pentafluoroethylthio, pentachloroethylthio, chloromethoxymethylthio, (1- or 2-)-chloromethoxyethylthio, (1-, 2- or 3-)chloromethoxy-n-propylthio, (1-, 2-, 3- or 4-)chloromethoxy-n-butylthio, (1-, 2-, 3-, 4- or 5-)chloromethoxy-n-pentylthio, (1-, 2-, 3-, 4-, 5- or 6-)chloromethoxy-n-hexylthio, (1-, 2-, 3-, 4-, 5-, 6- or 7-)chloromethoxy-n-heptylthio, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)-chloromethoxy-n-octylthio, fluoromethoxymethylthio, (1- or 2-)-fluoromethoxyethylthio, (1-, 2- or 3-)fluoromethoxy-n-propylthio, (1-, 2-, 3- or 4-)fluoromethoxy-n-butylthio, (1-, 2-, 3-, 4- or 5-)fluoromethoxy-n-pentylthio, (1-, 2-, 3-, 4-, 5- or 6-)fluoromethoxy-n-hexylthio, (1-, 2-, 3-, 4-, 5-, 6- or 7-)fluoromethoxy-n-heptylthio, (1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-)-fluoromethoxy-n-octylthio, dichloromethoxymethylthio, difluoromethoxymethylthio, trichloromethoxymethylthio, trifluoromethoxymethylthio, trichloromethoxyethylthio, trifl uoromethoxyethylth io, pentach loroethoxymethylth io, pentafluoroethoxymethylthio, pentachloroethoxyethylthio, pentafluoroethoxyethylthio, 3,3,3-trichloropropyloxymethylthio, 3,3,3-trifluoropropyloxymethylthio, 3,3,3-trichloropropyloxyethylthio, 3,3,3-trifluoropropyloxyethylthio, 2,2,3,3-tetrachloropropyloxymethylthio, 2,2,3,3-tetrafluoropropyloxymethylthio, or trifluoromethoxy-1,1,2-trifluoroethylthio, preferably methylthio, ethylthio, trifluoromethylthio, trichloromethylthio, difluoromethylthio, dichloromethylthio, trifluoroethylthio, trichloroethylthio, tetrafl uoroethylth io, tetrach loroethylth io, chloromethoxymethylthio, (1- or 2-)chloromethoxyethylthio, (1-, 2- or 3-)chloromethoxy-n-propylthio, (1-, 2-, 3- or 4-)chloromethoxy-n-butylthio, fluoromethoxymethylthio, (1- or 2-)-fluoromethoxyethylthio, (1-, 2- or 3-)fluoromethoxy-n-propylthio, (1-, 2-, 3- or 4-)fluoromethoxy-n-butylthio, dichloromethoxymethylthio, difluoromethoxymethylthio, trichloromethoxymethylthio, trifluoromethoxymethylthio, trichloromethoxyethylthio, trifluoromethoxyethylthio, pentachloroethoxymethylthio, pentafluoroethoxymethylthio, pentachloroethoxyethylthio, pentafluoroethoxyethylthio, 3,3,3-trichloropropyloxymethylthio, 3,3,3-trifluoropropyloxymethylthio, 3,3,3-trichloropropyloxyethylthio, 3,3,3-trifluoropropyloxyethylthio, 2,2,3,3-tetrachloropropyloxymethylthio, 2,2,3,3-tetrafluoropropyloxymethylthio, or trifluoromethoxy-1,1,2-trifluoroethylthio, more preferably methylthio, ethylthio, trifluoromethylthio, difluoromethylthio, difluoromethoxymethylthio, trifluoromethoxymethylthio, trifluoromethoxyethylthio, pentafluoroethoxymethylthio, pentafluoroethoxyethylthio, 3,3,3-trifluoropropyloxymethylthio, 3,3,3-trifluoropropyloxyethylthio, 2,2,3,3-tetrafluoropropyloxymethylthio, or trifluoromethoxy-1,1,2-trifluoroethylthio.
    [0042] C2-8 alkenylthio represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. Specific examples of C2-8 alkenylthio include 3,4,4-fluoro-3-butenylthio and 3,3-dichloro-2-propenylthio.
    [0043] C1-8 alkylsulfinyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different.
    [0044] C2-8 alkenylsulfinyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different.
    [0045] C1-8 alkylsulfonyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. This C1-8 alkylsulfonyl group is preferably substituted by one or more halogen atoms which may be the same or different. Specific examples of C1-8 alkylsulfonyl include trifluoromethylsulfonyl.
    [0046] C2-8 alkenylsulfonyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is optionally substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different.
    [0047] Phenyl represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more halogen atoms which may be the same or different, C1-4 alkyl substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. This phenyl group is preferably substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different. Specific examples of phenyl include 4-trifluoromethyl-phenyl.
    [0048] Phenoxy represented by Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 is substituted by one or more halogen atoms which may be the same or different, C1-4 alkyl substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different. This phenoxy group is preferably substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different. Specific examples of phenoxy include 4-trifluoromethyl-phenoxy.
    [0049] Two of Y1, Y2, Y3, Y4, and Y5 adjoining each other, or two of Y11, Y12, Y13, Y14, and Y15 adjoining each other together may represent -O-(CH2)n-O- optionally substituted by halogen atom, -(CH2)n-O- optionally substituted by halogen atom, -S-(CH2)n-S-optionally substituted by halogen atom, -(CH2)n-S- optionally substituted by halogen atom, or -(CH2)n- optionally substituted by halogen atom, preferably -O-(CH2)n-O- optionally substitutied by halogen atom. In this case, n is 1, 2, or 3, preferably 1 or 2. Specific examples of such groups include -O-(CF2)2-O-, -O-(CH2)2-O-, -(CF2)2-O-, -O-(CF2)2-(CH2)-, -S-(CF2)2-S-, -(CF2)2-S-, and -(CF2)3-, preferably -O-(CF2)2-O-.
    [0050] Z represents a bond (a single bond), an oxygen atom, a sulfur atom, SO, SO2, -Q-, -O-Q-, -O-Q-O-, or CO. In this case, Q represents C1-4 alkylene optionally substituted by halogen atom, cyano, or C1-4 alky optionally substituted by halogen atom; -(CH2)p-CR10R11-(CH2)q- wherein R10 and R11 together combine with the carbon atom to which they are attached to represent C3-6 cycloalkyl optionally substituted by halogen atom or C1-4 alkyl optionally substituted by halogen atom, p and q are each independently an integer of 0 to 3; or C2-4 alkenylene optionally substituted by halogen atom, cyano, or C1-4 alkyl optionally substituted by halogen atom. Preferably, Q represents C1-4 alkylene optionally substituted by halogen atom, cyano, or C1-4 alkyl optionally substituted by halogen atom. Specific examples of Q include methylene, ethylene, propylene, and 2,2-dimethylpropylene. When Z represents a bond (a single bond), in formula (I) or formula (Ia), two ring parts are attached directry (without through any atom). Z preferably represents a bond (a single bond), an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO, more preferably an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, or CO, more preferably an oxygen atom, OCH2, or O(CH2)3O, still more preferably an oxygen atom.
    [0051] In a preferred embodiment of the present invention, R1 represents a hydrogen atom; an alkali metal; an alkaline earth metal; optionally substituted C1-18 alkyl; COR4 wherein R4 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, optionally substituted C3-10 cycloalkyl, optionally substituted C1-4 alkylthio, OR5 wherein R5 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom, or optionally substituted C1-18 alkyl, or SO2R8 wherein R8 represents optionally substituted C1-18 alkyl. More preferably, R1 represents a hydrogen atom; an alkali metal; an alkaline earth metal; C1-18 alkyl optionally substituted by C1-4 alkyloxycarbonyl or C1-4 alkyloxy-C1-4 alkyloxy; COR4 wherein R4 represents C1-18 alkyl optionally substituted by C1-4 alkyloxy or acetyloxy, C2-18 alkenyl, C3-10 cycloalkyl, C1-4 alkylthio, OR5 wherein R5 represents C1-18 alkyl optionally substituted by halogen atom or C1-4 alkyloxy, C2-18 alkenyl, or phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl; or SO2R8 wherein R8 represents C1-18 alkyl. Still more preferably, R1 represents a hydrogen atom, COR4 wherein R4 represents C1-4 alkyl, OR5 wherein R5 represents C1-4 alkyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl. Particularly preferably, R1 represents COR4' or COOR5 wherein R4' and R5 represent C1-4 alkyl.
    [0052] In another preferred embodiment, R1 represents a hydrogen atom; an alkali metal; an alkaline earth metal; or COR4 wherein R4 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, C1-4 alkylthio, or OR5 wherein R5 represents optionally substituted C1-18 alkyl, or optionally substituted C2-18 alkenyl, optionally substituted phenyl. More preferably R1 represents a hydrogen atom; an alkali metal; an alkaline earth metal; or COR4 wherein R4 represents C1-18 alkyl, C2-18 alkenyl, C1-4 alkylthio, or OR5 wherein R5 represents C1-18 alkyl optionally substituted by halogen atom or C1-4 alkyloxy, C2-18 alkenyl, or phenyl. Still more preferably, R1 represents a hydrogen atom or COR4 wherein R4 represents C1-4 alkyl or OR5 wherein R5 represents C1-4 alkyl.
    [0053] In a preferred embodiment of the present invention, R2 represents a hydrogen atom or optionally substituted C1-4 alkyl, more preferably a hydrogen atom or C1-4 alkyl, still more preferably C1-4 alkyl.
    [0054] In a preferred embodiment of the present invention, R3 represents optionally substituted C1-18 alkyl, or R2 and R3 together represent -(CH2)m- wherein m is 3 or 4. More preferably, R3 represents C1-18 alkyl optionally substituted by halogen atom or acetyloxy, or R2 and R3 together form -(CH2)m-wherein m is 3 or 4. More preferably, R3 represents C1-4 alkyl, or R2 and R3 together represent -(CH2)m- wherein m is 3 or 4, more preferably C1-4 alkyl.
    [0055] In a preferred embodiment of the present invention, X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, C1-4 alkyloxycarbonyl optionally substituted by halogen atom, nitro, or cyano, provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom. More preferably, X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, C1-4 alkyloxycarbonyl, nitro, or cyano, provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom. Still more preferably, X1 and X2 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, or C1-4 alkyloxycarbonyl, provided that X1 and X2 do not simultaneously represent a hydrogen atom, and X3 represents a hydrogen atom. Particularly preferably, X1 and X2 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom, provided that X1 and X2 do not simultaneously represent a hydrogen atom, and X3 represents a hydrogen atom.
    [0056] In another preferred embodiment, X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, nitro, or cyano, provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom. More preferably, X1 and X2 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom, and X3 represents a hydrogen atom.
    [0057] In a preferred embodiment of the present invention, Z represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO, more preferably an oxygen atom, OCH2, or O(CH2)3O. More preferably, Z represents an oxygen atom.
    [0058] In a preferred embodiment of the present invention, when W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, or when W11, W12, and W13 represent C-Y11, C-Y12, and C-Y13, respectively, Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 each independently represent a hydrogen atom, the following A' or B', provided that, when Z represents a bond, methylene optionally substituted by one or two methyl, or an oxygen atom, at least one of Y1, Y2, Y3, Y4, and Y5 represents a group selected from A', or adjacent two of Y1, Y2, Y3, Y4, and Y5, or adjacent two of Y11, Y12, Y13, Y14, and Y15 may together represent -O-(CH2)n-O-, wherein n is 1 or 2, substituted by halogen atom.
    [0059] Here, wherein A' represents a group selected from the group consisting of: C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxycarbonyl; C1-8 alkylthio substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl substituted by one or more halogen atoms which may be the same or different; phenyl substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; and phenoxy substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different. In one embodiment, A' represents a group selected from the group consisting of: C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl subsituted by one or more halogen atoms which may be the same or different; phenyl substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; and phenoxy substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different. B' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano.
    [0060] In a further preferred embodiment of the present invention, when W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, or when W11, W12, and W13 represent C-Y11, C-Y12, and C-Y13, respectively, Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 each independently represent a hydrogen atom; C1-8 alkyl substituted by one or more halogen atoms which may be the same or different, C1-8 alkyloxy substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio substituted by one or more halogen atoms which may be the same or different; or a halogen atom, provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents a group other than a hydrogen atom and a halogen atom. Alternatively, two of Y1, Y2, Y3, Y4, and Y5, or two of Y11, Y12, Y13, Y14, and Y15 adjoining each other together represent -O-(CH2)n-O-, wherein n is 1 or 2, substituted by one or more halogen atoms. In one embodiment, Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 each independently represent a hydrogen atom; C1-8 alkyloxy substituted by one or more halogen atoms which may be the same or different; or a halogen atom, provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyloxy substituted by halogen atom, or two of Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 adjoining each other together represent -O-(CH2)n-O-, wherein n is 1 or 2, substituted by one or more halogen atoms.
    [0061] In a preferred embodiment of the present invention, when any one of W1, W2, and W3 represents a nitrogen atom and the remaining two groups represent the corresponding C-Y1, C-Y2, or C-Y3, or when any one of W11, W12, and W13 represents a nitrogen atom and the remaining two groups represent the corresponding C-Y11, C-Y12, or C-Y13, Y1, Y2, Y3, Y4, and Y5, or Y11, Y12, Y13, Y14, and Y15 each independently represent a hydrogen atom; C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; or a halogen atom.
    [0062] In a preferred embodiment of the present invention, when W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, and Z represents a sulfur atom, at least one of Y1, Y2, Y3, Y4, and Y5 represents A. When W11, W12 and W13 represent C-Y11, C-Y12, and C-Y13 and Z represents an oxygen atom or a sulfur atom, preferably at least one of Y11, Y12, Y13, Y14, and Y15 represent A.
    [0063] In a preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,optionally substituted C1-18 alkyl,COR4 wherein R4 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; optionally substituted C3-10 cycloalkyl; optionally substituted C1-4 alkylthio; OR5 wherein R5 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or optionally substituted C1-18 alkyl, orSO2R8 wherein R8 represents optionally substituted C1-18 alkyl,R2 represents a hydrogen atom or optionally substituted C1-4 alkyl,R3 represents optionally substituted C1-18 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, C1-4 alkyloxycarbonyl optionally substituted by halogen atom, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0064] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,C1-18 alkyl optionally substituted by C1-4 alkyloxycarbonyl or C1-4 alkyloxy-C1-4 alkyloxy,COR4 wherein R4 represents C1-18 alkyl optionally substituted by C1-4 alkyloxy or acetyloxy; C2-18 alkenyl; C3-10 cycloalkyl; C1-4 alkylthio; OR5 wherein R5 represents C1-18 alkyl optionally substituted by halogen atom or C1-4 alkyloxy, C2-18 alkenyl, or phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl, orSO2R8 wherein R8 represents C1-18 alkyl,R2 represents a hydrogen atom or C1-4 alkyl,R3 represents C1-18 alkyl optionally substituted by halogen atom or acetyloxy,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, C1-4 alkyloxycarbonyl, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0065] In still another preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinW1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom, A', or B',provided that, when Z represents a bond, methylene optionally substituted by one or two methyl, or an oxygen atom, at least one of Y1, Y2, Y3, Y4, and Y5 represents A',wherein A' represents a group selected from the group consisting of: C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxycarbonyl; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl which is subsituted by one or more halogen atoms which may be the same or different;phenyl which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; andphenoxy which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different,B' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0066] In a further preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include thosewhereinany one of W1, W2, and W3 represents a nitrogen atom, and the other two groups represent the corresponding C-Y1, C-Y2, or C-Y3, andY1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; or a halogen atom.
    [0067] In a still further preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 represents a hydrogen atom; or COR4 wherein R4 represents C1-4 alkyl, OR5 wherein R5 represents C1-4 alkyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1 and X2 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, or C1-4 alkyloxycarbonyl,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom, andZ represents an oxygen atom, OCH2, or O(CH2)3O.
    [0068] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinW1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, and Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0069] In still another preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,optionally substituted C1-18 alkyl,COR4 wherein R4 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; optionally substituted C3-10 cycloalkyl; optionally substituted C1-4 alkylthio; OR5 wherein R5 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or optionally substituted C1-18 alkyl, orSO2R8 wherein R8 represents optionally substituted C1-18 alkyl,R2 represents a hydrogen atom or optionally substituted C1-4 alkyl,R3 represents optionally substituted C1-18 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, C1-4 alkyloxycarbonyl optionally substituted by halogen atom, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andW1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom, A', or B',provided that, when Z represents a bond, methylene optionally substituted by one or two methyl, or an oxygen atom, at least one of Y1, Y2, Y3, Y4, and Y5 represents A',wherein A' represents a group selected from the group consisting of: C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxycarbonyl; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl which is subsituted by one or more halogen atoms which may be the same or different;phenyl which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; andphenoxy which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different,B' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0070] In a further preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,optionally substituted C1-18 alkyl,COR4 wherein R4 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; optionally substituted C3-10 cycloalkyl; optionally substituted C1-4 alkylthio; OR5 wherein R5 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or optionally substituted C1-18 alkyl, orSO2R8 wherein R8 represents optionally substituted C1-18 alkyl,R2 represents a hydrogen atom or optionally substituted C1-4 alkyl,R3 represents optionally substituted C1-18 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, C1-4 alkyloxycarbonyl optionally substituted by halogen atom, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andany one of W1, W2, and W3 represents a nitrogen atom, and the other two groups represent the corresponding C-Y1, C-Y2, or C-Y3, andY1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; or a halogen atom, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0071] In a still further preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 represents a hydrogen atom; or COR4 wherein R4 represents C1-4 alkyl, OR5 wherein R5 represents C1-4 alkyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1 and X2 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, or C1-4 alkyloxycarbonyl,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom,W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2, andZ represents an oxygen atom, OCH2, or O(CH2)3O.
    [0072] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (I) include those whereinR1 represents COR4' or COOR5 wherein R4' and R5 represent C1-4 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,X1 and X2 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom,W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2, andZ represents an oxygen atom.
    [0073] Further, in a preferred embodiment of the present invention, a group of compounds of formula (I) wherein W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, include compounds of formula (II) or agriculturally and horticulturally acceptable acid addition salts thereof:
    [0074] In a preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinR101 representsa hydrogen atom,an alkali metal,an alkaline earth metal, orCOR104 wherein R104 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; C1-4 alkylthio; or OR105 in which R105 is optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl,R102 represents a hydrogen atom or optionally substituted C1-4 alkyl,R103 represents optionally substituted C1-18 alkyl,alternatively R102 and R103 together represent -(CH2)m- wherein m is 3 or 4, andX101, X102, and X103 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, nitro, or cyano,provided that X101, X102, and X103 do not simultaneously represent a hydrogen atom.
    [0075] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinR101 representsa hydrogen atom,an alkali metal,an alkaline earth metal, orCOR104 wherein R104 represents C1-18 alkyl; C2-18 alkenyl; C1-4 alkylthio; or OR105 in which R105 represents C1-18 alkyl optionally substituted by halogen atom or C1-4 alkyloxy; C2-18 alkenyl; or phenyl,R102 represents a hydrogen atom or C1-4 alkyl,R103 represents C1-18 alkyl optionally substituted by halogen atom or acetyloxy,alternatively R102 and R103 together represent -(CH2)m- wherein m is 3 or 4,X101, X102, and X103 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, nitro, or cyano,provided that X101, X102, and X103 do not simultaneously represent a hydrogen atom.
    [0076] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinY101, Y102, Y103, Y104, and Y105 each independently represent a hydrogen atom, A100' or B100',provided that, when Z100 represents an oxygen atom, at least one of Y101, Y102, Y103, Y104, and Y105 represents A100',wherein A100' represents a group selected from the group consisting of: C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl which is substituted by one or more halogen atoms which may be the same or different;phenyl which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; andphenoxy which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different,B100' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano,alternatively adjacent two of Y101, Y102, Y103, Y104, and Y105 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0077] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinR101 represents a hydrogen atom; or COR104 wherein R104 represents C1-4 alkyl or OR105 wherein R105 represents C1-4 alkyl, R102 represents C1-4 alkyl,R103 represents C1-4 alkyl,alternatively R102 and R103 together represents -(CH2)m- wherein m is 3 or 4,X101 and X102 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom, provided that they do not simultaneously represent a hydrogen atom,X103 represents a hydrogen atom, andZ100 represents an oxygen atom.
    [0078] In another preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinY101, Y102, Y103, Y104, and Y105 each independently represent a hydrogen atom; or C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, or a halogen atom,provided that at least one of Y101, Y102, Y103, Y104, and Y105 represents C1-4 alkyloxy in which the C1-8 alkyloxy group is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y101, Y102, Y103, Y104, and Y105 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0079] In a further preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinR101 representsa hydrogen atom,an alkali metal,an alkaline earth metal, orCOR104 wherein R104 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; C1-4 alkylthio; or OR105 wherein R105 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl,R102 represents a hydrogen atom or optionally substituted C1-4 alkyl, andR103 represents optionally substituted C1-18 alkyl,alternatively R102 and R103 together represent -(CH2)m- wherein m is 3 or 4,X101, X102, and X103 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, nitro, or cyano,provided that X101, X102, and X103 do not simultaneously represent a hydrogen atom,Y101, Y102, Y103, Y104, and Y105 each independently represent a hydrogen atom, A100', or B100',provided that, when Z100 represents an oxygen atom, at least one of Y101, Y102, Y103, Y104, and Y105 represents A100',wherein A100' represents a group selected from the group consisting of: C1-8 alkyl which is optionally substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is optionally substituted by one or more halogen atoms which may be the same or different; C1-8 alkylsulfonyl which is substituted by one or more halogen atoms which may be the same or different;phenyl which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; andphenoxy which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different,B100' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano,alternatively adjacent two of Y101, Y102, Y103, Y104, and Y105 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0080] Further, in a still further preferred embodiment of the present invention, a group of preferred compounds represented by formula (II) include those whereinR101 represents a hydrogen atom; or COR104 wherein R104 represents C1-4 alkyl, or OR105 wherein R105 represents C1-4 alkyl, R102 represents C1-4 alkyl,R103 represents C1-4 alkyl,alternatively R102 and R103 together represent -(CH2)m- wherein m is 3 or 4,X101 and X102 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom, provided that they do not simultaneously represent a hydrogen atom,X103 represents a hydrogen atom,Z100 represents an oxygen atom, andY101, Y102, Y103, Y104, and Y105 each independently represent a hydrogen atom; C1-8 alkyloxy substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y101, Y102, Y103, Y104, and Y105 represents C1-4 alkyloxy in which the C1-8 alkyloxy is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y101, Y102, Y103, Y104, and Y105 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0081] Further, in a preferred embodiment of the present invention, a group of compounds represented by formula (Ia)wherein W11, W12, and W13 represent C-Y11, C-Y12, and C-Y13, respectively, include compounds represented by formula (IIa) or agriculturally and horticulturally acceptable acid addition salt thereof:
    [0082] Further, specific examples of compounds of formula (I) or formula (Ia) include compounds shown in Tables 1 to 14 below. Table 1 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 1 H Me Me Cl H H O C H C H C Cl H H 2 Ac Me Me Cl H H O C H C H C Cl H H 3 COOMe Me Me Cl H H O C H C H C Cl H H 4 CO Bu Me Me Cl H H O C H C H C Cl H H 5 Ac Et Me Cl H H O C H C H C Cl H H 6 Ac Bu Me Cl H H O C H C H C Cl H H 7 Ac H Me Cl H H O C H C H C Cl H H 8 Ac Me Et Cl H H O C H C H C Cl H H 9 COOMe Me Et Cl H H O C H C H C Cl H H 10 Ac H I-Pr Cl H H O C H C H C Cl H H 11 Ac Me Bu Cl H H O C H C H C Cl H H 12 Ac H CF3 Cl H H O C H C H C Cl H H 13 Ac Me CH2-OAc Cl H H O C H C H C Cl H H 14 Ac Me Me CN H H O C H C H C Cl H H 15 Ac Me Me F H H O C H C H C Cl H H 16 Ac Me Me Me H H O C H C H C Cl H H 17 COOMe Me Et Me H H O C H C H C Cl H H 18 H Me Me CF3 H H O C H C H C Cl H H 19 Ac Me Me CF3 H H O C H C H C Cl H H 20 COOMe Me Et CF3 H H O C H C H C Cl H H 21 Ac Me Me H CF3 H O C H C H C Cl H H 22 Ac Me Me H C1 H O C H C H C Cl H H 23 COOMe Me Me H C1 H O C H C H C Cl H H 24 CO Bu Me Me H C1 H O C H C H C Cl H H 25 Ac Et Me H C1 H O C H C H C Cl H H 26 Ac Bu Me H C1 H O C H C H C Cl H H 27 Ac H Me H C1 H O C H C H C Cl H H 28 Ac Me Et H C1 H O C H C H C Cl H H 29 Ac H I-Pr H C1 H O C H C H C Cl H H 30 Ac Me Bu H C1 H O C H C H C Cl H H 31 Ac Me Me H F H O C H C H C Cl H H 32 Ac Me Me H Me H O C H C H C Cl H H 33 COOMe Me Et H Me H O C H C H C Cl H H 34 Ac Me Me H OMe H O C H C H C Cl H H 35 Ac Me Me H H CF3 O C H C H C Cl H H 36 Ac Me Me Me Me H O C H C H C Cl H H 37 COOMe Me Et Me Me H O C H C H C Cl H H 38 Ac Me IPr Cl H H O C H C H C Cl H H 39 Ac Me Me NO2 H H O C H C H C Cl H H 40 Ac Me Me Cl H H O C H C Cl C H H H 41 Ac Me Me H Cl H O C H C Cl C H H H 42 Ac Me Me C1 H H O C Cl C H C H H H 43 Ac Me Me H Cl H O C Cl C H C H H H 44 Ac Me Me Cl H H O C H C H C CN H H 45 Ac Me Me H Cl H O C H C H C CN H H 46 Ac Me Me Cl H H O C H C H C F H H 47 Ac Me Me H Cl H O C H C H C F H H 48 Ac Me Me Cl H H O C H C H C Me H H 49 Ac Me Me H Cl H O C H C H C Me H H 50 Ac Me Me Cl H H O C H C H C OMe H H 51 Ac Me Me H Cl H O C H C H C OMe H H Table 2 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 52 Ac Me Me Cl H H O C H C OMe C H H H 53 Ac Me Me H Cl H O C H C OMe C H H H 54 Ac Me Me Cl H H O C 0Me C H C H H H 55 Ac Me Me H Cl H O C OMe C H C H H H 56 Ac Me Me Cl H H O C H C H C CF3 H H 57 C00Me Me Et Cl H H O C H C H C CF3 H H 58 Ac Me Me Me H H O C H C H C CF3 H H 59 Ac Me Et Me H H O C H C H C CF3 H H 60 COOMe Me Et Me H H O C H C H C CF3 H H 61 Ac Me Me CF3 H H O C H C H C CF3 H H 62 Ac Me Et CF3 H H O C H C H C CF3 H H 63 COOMe Me Et CF3 H H O C H C H C CF3 H H 64 Ac Me Me H Cl H O C H C H C CF3 H H 65 Ac Me Me H Me H O C H C H C CF3 H H 66 Ac Me Et H Me H O C H C H C CF3 H H 67 COOMe Me Et H Me H O C H C H C CF3 H H 68 Ac Me Me H CF3 H O C H C H C CF3 H H 69 Ac Me Me Me Me H O C H C H C CF3 H H 70 Ac Me Et Me Me H O C H C H C CF3 H H 71 COOMe Me Et Me Me H O C H C H C CF3 H H 72 Ac Me Me Cl H H O C H C CF3 C H H H 73 COOMe Me Et Cl H H O C H C CF3 C H H H 74 Ac Me Me Me H H O C H C CF3 C H H H 75 COOMe Me Et Me H H O C H C CF3 C H H H 76 Ac Me Me CF3 H H O C H C CF3 C H H H 77 COOMe Me Et CF3 H H O C H C CF3 C H H H 78 Ac Me Me H Me H O C H C CF3 C H H H 79 COOMe Me Et H Me H O C H C CF3 C H H H 80 Ac Me Me H CF3 H O C H C CF3 C H H H 81 Ac Me Me Me Me H O C H C CF3 C H H H 82 COOMe Me Et Me Me H O C H C CF3 C H H H 83 Ac Me Me Cl H H O C H C H C OCF3 H H 84 COOCH3 Me Et Cl H H O C H C H C OCF3 H H 85 H Me Me Me H H O C H C H C OCF3 H H 86 Ac Me Me Me H H O C H C H C OCF3 H H 87 COOCH3 Me Et Me H H O C H C H C OCF3 H H 88 Ac Me Et Me H H O C H C H C OCF3 H H 89 H Me Me CF3 H H O C H C H C OCF3 H H 90 Ac Me Me CF3 H H O C H C H C OCF3 H H 91 COEt Me Me CF3 H H O C H C H C OCF3 H H 92 CO-nBu Me Me CF3 H H O C H C H C OCF3 H H 93 CO-n-Oc Me Me CF3 H H O C H C H C OCF3 H H 94 CO-Pr Me Me CF3 H H O C H C H C OCF3 H H 95 CO-iBu Me Me CF3 H H O C H C H C OCF3 H H 96 CO-cPr Me Me CF3 H H O C H C H C OCF3 H H 97 CO-cBu Me Me CF3 H H O C H C H C OCF3 H H 98 CO-CH=CH2 Me Me CF3 H H O C H C H C OCF3 H H 99 CO-C(CH3)=CH2 Me Me CF3 H H O C H C H C OCF3 H H 100 CO-C (CH3)=CH (CH3 Me Me CF3 H H O C H C H C OCF3 H H 101 COOCH3 Me Me CF3 H H O C H C H C OCF3 H H 102 COOEt Me Me CF3 H H O C H C H C OCF3 H H 103 COO-nBu Me Me CF3 H H O C H C H C OCF3 H H Table 3 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 104 COO-nOc Me Me CF3 H H O C H C H C OCF3 H H 105 COOPh Me Me CF3 H H O C H C H C OCF3 H H 106 COO-iBu Me Me CF3 H H O C H C H C OCF3 H H 107 COO-CH2CH=CH2 Me Me CF3 H H O C H C H C OCF3 H H 108 COO-CH2CCl3 Me Me CF3 H H O C H C H C OCF3 H H 109 COO-(CH2)2OCH3 Me Me CF3 H H O C H C H C OCF3 H H 110 COSCH3 Me Me CF3 H H O C H C H C OCF3 H H 111 H Me Et CF3 H H O C H C H C OCF3 H H 112 COOMe Me Et CF3 H H O C H C H C OCF3 H H 113 Ac Me Et CF3 H H O C H C H C OCF3 H H 114 Ac -(CH2)3- CF3 H H O C H C H C OCF3 H H 115 Ac -(CH2)4- CF3 H H O C H C H C OCF3 H H 116 Ac Me Me H Cl H O C H C H C OCF3 H H 117 H Me Me H Me H O C H C H C OCF3 H H 118 Ac Me Me H Me H O C H C H C OCF3 H H 119 H Me Et H Me H O C H C H C OCF3 H H 120 COOCH3 Me Et H Me H O C H C H C OCF3 H H 121 Ac Me Et H Me H O C H C H C OCF3 H H 122 Ac Me Me H CF3 H O C H C H C OCF3 H H 123 COOMe Me Et H CF3 H O C H C H C OCF3 H H 124 Ac Me CF3 H CF3 H O C H C H C OCF3 H H 125 Ac -(CH2)3- H CF3 H O C H C H C OCF3 H H 126 Ac -(CH2)4- H CF3 H O C H C H C OCF3 H H 127 Ac Me Me Cl Cl H O C H C H C OCF3 H H 128 COOMe Me Me Cl Cl H O C H C H C OCF3 H H 129 Ac Me Et Cl Cl H O C H C H C OCF3 H H 130 COOMe Me Et Cl Cl H O C H C H C OCF3 H H 131 H Me Me Me Me H O C H C H C OCF3 H H 132 Ac Me Me Me Me H O C H C H C OCF3 H H 133 COOMe Me Me Me Me H O C H C H C OCF3 H H 134 Ac Me Et Me Me H O C H C H C OCF3 H H 135 COOMe Me Et Me Me H O C H C H C OCF3 H H 136 Ac Me Me CF3 Cl H O C H C H C OCF3 H H 137 Ac Me Me CF3 H Me O C H C H C OCF3 H H 138 Ac Me Me Cl CF3 H O C H C H C OCF3 H H 139 Ac Me Me Cl H H O C H C OCF3 C H H H 140 COOMe Me Et Cl H H O C H C OCF3 C H H H 141 Ac Me Me Me H H O C H C OCF3 C H H H 142 COOMe Me Et Me H H O C H C OCF3 C H H H 143 Ac Me Me CF3 H H O C H C OCF3 C H H H 144 COOMe Me Et CF3 H H O C H C OCF3 C H H H 145 Ac Me Me H Me H O C H C OCF3 C H H H 146 COOMe Me Et H Me H O C H C OCF3 C H H H 147 Ac Me Me H CF3 H O C H C OCF3 C H H H 148 H Me Me Me Me H O C H C OCF3 C H H H 149 Ac Me Me Me Me H O C H C 0CF3 C H H H 150 COOMe Me Et Me Me H O C H C OCF3 C H H H 151 Ac Me Me Cl H H O C H C H C SCF3 H H 152 COOCH3 Me Et Cl H H O C H C H C SCF3 H H 153 Ac Me Me Me H H O C H C H C SCF3 H H 154 COOCH3 Me Et Me H H O C H C H C SCF3 H H 155 Ac Me Et Me H H O C H C H C SCF3 H H Table 4 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 156 Ac Me Me CF3 H H O C H C H C SCF3 H H 157 COOCH3 Me Et CF3 H H O C H C H C SCF3 H H 158 Ac Me Et CF3 H H O C H C H C SCF3 H H 159 Ac Me Me H Cl H O C H C H C SCF3 H H 160 Ac Me Me H Me H O C H C H C SCF3 H H 161 COOCH3 Me Et H Me H O C H C H C SCF3 H H 162 Ac Me Et H Me H O C H C H C SCF3 H H 163 Ac Me Me H CF3 H O C H C H C SCF3 H H 164 Ac Me Me Me Me H O C H C H C SCF3 H H 165 COOCH3 Me Et Me Me H O C H C H C SCF3 H H 166 Ac Me Et Me Me H O C H C H C SCF3 H H 167 Ac Me Me CF3 H H O C H C H C SO2CF3 H H 168 Ac Me Me H CF3 H O C H C H C SO2CF3 H H 169 Ac Me Me Cl H H O C H C SCF3 C H H H 170 COOCH3 Me Et Cl H H O C H C SCF3 C H H H 171 Ac Me Me Me H H O C H C SCF3 C H H H 172 COOCH3 Me Et Me H H O C H C SCF3 C H H H 173 Ac Me Me CF3 H H O C H C SCF3 C H H H 174 COOCH3 Me Et CF3 H H O C H C SCF3 C H H H 175 Ac Me Me H Me H O C H C SCF3 C H H H 176 COOCH3 Me Et H Me H O C H C SCF3 C H H H 177 Ac Me Me Me Me H O C H C SCF3 C H H H 178 COOCH3 Me Et Me Me H O C H C SCF3 C H H H 179 Ac Me Me Cl H H O C H C H C OCF2CHF2 H H 180 COOCH3 Me Et Cl H H O C H C H C OCF2CHF2 H H 181 H Me Me Me H H O C H C H C OCF2CHF2 H H 182 Ac Me Me Me H H O C H C H C OCF2CHF2 H H 183 COOCH3 Me Et Me H H O C H C H C OCF2CHF2 H H 184 Ac Me Et Me H H O C H C H C OCF2CHF2 H H 185 Ac Me Me CF3 H H O C H C H C OCF2CHF2 H H 186 COOCH3 Me Et CF3 H H O C H C H C OCF2CHF2 H H 187 Ac Me Et CF3 H H O C H C H C OCF2CHF2 H H 188 H Me Me H Me H O C H C H C OCF2CHF2 H H 189 Ac Me Me H Me H O C H C H C OCF2CHF2 H H 190 COOCH3 Me Et H Me H O C H C H C OCF2CHF2 H H 191 Ac Me Et H Me H O C H C H C OCF2CHF2 H H 192 Ac Me Me H CF3 H O C H C H C OCF2CHF2 H H 193 COOCH3 Me Et H CF3 H O C H C H C OCF2CHF2 H H 194 H Me Me Me Me H O C H C H C OCF2CHF2 H H 195 Ac Me Me Me Me H O C H C H C OCF2CHF2 H H 196 H Me Et Me Me H O C H C H C OCF2CHF2 H H 197 COOCH3 Me Et Me Me H O C H C H C OCF2CHF2 H H 198 Ac Me Et Me Me H O C H C H C OCF2CHF2 H H 199 Ac Me Me Cl H H O C H C OCF2CHF2 C H H H 200 COOCH3 Me Et Cl H H O C H C OCF2CHF2 C H H H 201 Ac Me Me Me H H O C H C OCF2CHF2 C H H H 202 COOCH3 Me Et Me H H O C H C OCF2CHF2 C H H H 203 Ac Me Me CF3 H H O C H C OCF2CHF2 C H H H 204 COOCH3 Me Et CF3 H H O C H C OCF2CHF2 C H H H 205 Ac Me Me H Me H O C H C OCF2CHF2 C H H H 206 COOCH3 Me Et H Me H O C H C OCF2CHF2 C H H H 207 Ac Me Me Me Me H O C H C OCF2CHF2 C H H H Table 5 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 208 COOCH3 Me Et Me Me H O C H C OCF2CHF2 C H H H 209 Ac Me Me CF3 H H O C H C H C OCH2CF3 H H 210 Ac Me Et CF3 H H O C H C H C OCH2CF3 H H 211 COOMe Me Et CF3 H H O C H C H C OCH2CF3 H H 212 Ac Me Me H CF3 H O C H C H C OCH2CF3 H H 213 Ac Me Me CF3 H H O C H C H C O-iPr H H 214 Ac Me Me H CF3 H O C H C H C O-iPr H H 215 Ac Me Me CF3 H H O C Cl C H C C1 H H 216 Ac Me Me H CF3 H O C Cl C H C C1 H H 217 Ac Me Me CF3 H H O C H C CF3 C H CF3 H 218 Ac Me Me H CF3 H O C H C CF3 C H CF3 H 219 Ac Me Me Me H H O C Cl C H C CF3 H H 220 COOCH3 Me Et Me H H O C Cl C H C CF3 H H 221 Ac Me Et Me H H O C Cl C H C CF3 H H 222 Ac Me Me CF3 H H O C Cl C H C CF3 H H 223 COOCH3 Me Et CF3 H H O C Cl C H C CF3 H H 224 Ac Me Et CF3 H H O C Cl C H C CF3 H H 225 Ac Me Me H Me H O C Cl C H C CF3 H H 226 COOCH3 Me Et H Me H O C Cl C H C CF3 H H 227 Ac Me Et H Me H O C Cl C H C CF3 H H 228 Ac Me Me H CF3 H O C Cl C H C CF3 H H 229 Ac Me Me Me Me H O C Cl C H C CF3 H H 230 COOCH3 Me Et Me Me H O C Cl C H C CF3 H H 231 Ac Me Et Me Me H O C Cl C H C CF3 H H 232 Ac Me Me Cl H H O C H C Cl C CF3 H H 233 COOCH3 Me Et Cl H H O C H C Cl C CF3 H H 234 Ac Me Me Me H H O C H C Cl C CF3 H H 235 COOCH3 Me Et Me H H O C H C Cl C CF3 H H 236 Ac Me Et Me H H O C H C Cl C CF3 H H 237 Ac Me Me CF3 H H O C H C Cl C CF3 H H 238 COOCH3 Me Et CF3 H H O C H C Cl C CF3 H H 239 Ac Me Et CF3 H H O C H C Cl C CF3 H H 240 Ac Me Me H Me H O C H C Cl C CF3 H H 241 COOCH3 Me Et H Me H O C H C Cl C CF3 H H 242 Ac Me Et H Me H O C H C Cl C CF3 H H 243 Ac Me Me H CF3 H O C H C Cl C CF3 H H 244 Ac Me Me Me Me H O C H C Cl C CF3 H H 245 COOCH3 Me Et Me Me H O C H C Cl C CF3 H H 246 Ac Me Et Me Me H O C H C Cl C CF3 H H 247 Ac Me Me CF3 H H O C H C-O-CF2-CF2-O-C H H 248 Ac Me Me H CF3 H O C H C-O-CF2-CF2-O-C H H 249 Ac Me Me Me H H O C Cl C H C OCF3 H H 250 COOCH3 Me Et Me H H O C Cl C H C OCF3 H H 251 Ac Me Et Me H H O C Cl C H C OCF3 H H 252 H Me Me CF3 H H O C Cl C H C OCF3 H H 253 Ac Me Me CF3 H H O C Cl C H C OCF3 H H 254 COOCH3 Me Et CF3 H H O C Cl C H C OCF3 H H 255 Ac Me Et CF3 H H O C Cl C H C OCF3 H H 256 Ac Me Me H Me H O C Cl C H C OCF3 H H 257 COOCH3 Me Et H Me H O C Cl C H C OCF3 H H 258 Ac Me Et H Me H O C Cl C H C OCF3 H H 259 Ac Me Me H CF3 H O C Cl C H C OCF3 H H Table 6 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 260 COOCH3 Me Et H CF3 H O C Cl C H C OCF3 H H 261 Ac Me Me Me Me H O C Cl C H C OCF3 H H 262 COOCH3 Me Et Me Me H O C Cl C H C OCF3 H H 263 Ac Me Et Me Me H O C Cl C H C OCF3 H H 264 Ac Me Me Cl H H O C H C Cl C OCF3 H H 265 COOCH3 Me Et Cl H H O C H C Cl C OCF3 H H 266 Ac Me Me Me H H O C H C Cl C OCF3 H H 267 COOCH3 Me Et Me H H O C H C Cl C OCF3 H H 268 Ac Me Et Me H H O C H C Cl C OCF3 H H 269 Ac Me Me CF3 H H O C H C Cl C OCF3 H H 270 COOCH3 Me Et CF3 H H O C H C Cl C OCF3 H H 271 Ac Me Et CF3 H H O C H C Cl C OCF3 H H 272 Ac Me Me H Me H O C H C Cl C OCF3 H H 273 COOCH3 Me Et H Me H O C H C Cl C OCF3 H H 274 Ac Me Et H Me H O C H C Cl C OCF3 H H 275 Ac Me Me H CF3 H O C H C Cl C OCF3 H H 276 Ac Me Me Me Me H O C H C Cl C OCF3 H H 277 COOCH3 Me Et Me Me H O C H C Cl C OCF3 H H 278 Ac Me Et Me Me H O C H C Cl C OCF3 H H 279 Ac Me Me CF3 H H O C F C H C OCF3 H H 280 Ac Me Me H CF3 H O C F C H C OCF3 H H 281 Ac Me Me CF3 H H O C Br C H C CF3 H H 282 Ac Me Me H CF3 H O C Br C H C CF3 H H 283 Ac Me Me Me H H O C Me C H C CF3 H H 284 COOCH3 Me Et Me H H O C Me C H C CF3 H H 285 Ac Me Et Me H H O C Me C H C CF3 H H 286 Ac Me Me CF3 H H O C Me C H C CF3 H H 287 COOCH3 Me Et CF3 H H O C Me C H C CF3 H H 288 Ac Me Et CF3 H H O C Me C H C CF3 H H 289 Ac Me Me H Me H O C Me C H C CF3 H H 290 COOCH3 Me Et H Me H O C Me C H C CF3 H H 291 Ac Me Et H Me H O C Me C H C CF3 H H 292 Ac Me Me H CF3 H O C Me C H C CF3 H H 293 Ac Me Me Me Me H O C Me C H C CF3 H H 294 COOCH3 Me Et Me Me H O C Me C H C CF3 H H 295 Ac Me Et Me Me H O C Me C H C CF3 H H 296 Ac Me Me Me H H O C H C Me C CF3 H H 297 COOCH3 Me Et Me H H O C H C Me C CF3 H H 298 Ac Me Me CF3 H H O C H C Me C CF3 H H 299 COOCH3 Me Et CF3 H H O C H C Me C CF3 H H 300 Ac Me Me H Me H O C H C Me C CF3 H H 301 COOCH3 Me Et H Me H O C H C Me C CF3 H H 302 Ac Me Me Me Me H O C H C Me C CF3 H H 303 COOCH3 Me Et Me Me H O C H C Me C CF3 H H 304 Ac Me Me Cl H H O C Me C H C OCF3 H H 305 COOCH3 Me Et Cl H H O C Me C H C OCF3 H H 306 Ac Me Me Me H H O C Me C H C OCF3 H H 307 COOCH3 Me Et Me H H O C Me C H C OCF3 H H 308 Ac Me Me CF3 H H O C Me C H C OCF3 H H 309 COOCH3 Me Et CF3 H H O C Me C H C OCF3 H H 310 Ac Me Me H Me H O C Me C H C OCF3 H H 311 COOCH3 Me Et H Me H 0 C Me C H C OCF3 H H Table 7 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 312 Ac Me Me H CF3 H O C Me C H C OCF3 H H 313 Ac Me Me Me Me H O C Me C H C OCF3 H H 314 COOCH3 Me Et Me Me H O C Me C H C OCF3 H H 315 Ac Me Me Me H H O C H C Me C OCF3 H H 316 COOCH3 Me Et Me H H O C H C Me C OCF3 H H 317 Ac Me Me CF3 H H O C H C Me C OCF3 H H 318 COOCH3 Me Et CF3 H H O C H C Me C OCF3 H H 319 Ac Me Me H Me H O C H C Me C OCF3 H H 320 COOCH3 Me Et H Me H O C H C Me C OCF3 H H 321 Ac Me Me Me Me H O C H C Me C OCF3 H H 322 COOCH3 Me Et Me Me H O C H C Me C OCF3 H H 323 Ac Me Me Me H H O C Cl C H C OCF2CHF2 H H 324 C00CH3 Me Et Me H H O C Cl C H C OCF2CHF2 H H 325 Ac Me Et Me H H O C Cl C H C OCF2CHF2 H H 326 Ac Me Me CF3 H H O C Cl C H C OCF2CHF2 H H 327 COOCH3 Me Et CF3 H H O C Cl C H C OCF2CHF2 H H 328 Ac Me Et CF3 H H O C Cl C H C OCF2CHF2 H H 329 H Me Me H Me H O C Cl C H C OCF2CHF2 H H 330 Ac Me Me H Me H O C Cl C H C OCF2CHF2 H H 331 H Me Et H Me H O C Cl C H C OCF2CHF2 H H 332 COOCH3 Me Et H Me H O C Cl C H C OCF2CHF2 H H 333 Ac Me Et H Me H O C Cl C H C OCF2CHF2 H H 334 H Me Me Me Me H O C Cl C H C OCF2CHF2 H H 335 Ac Me Me Me Me H O C Cl C H C OCF2CHF2 H H 336 H Me Et Me Me H O C Cl C H C OCF2CHF2 H H 337 COOCH3 Me Et Me Me H O C Cl C H C OCF2CHF2 H H 338 Ac Me Et Me Me H O C Cl C H C OCF2CHF2 H H 339 Ac Me Me Me H H O C H C Cl C OCF2CHF2 H H 340 COOCH3 Me Et Me H H O C H C Cl C OCF2CHF2 H H 341 Ac Me Et Me H H O C H C Cl C OCF2CHF2 H H 342 Ac Me Me CF3 H H O C H C Cl C OCF2CHF2 H H 343 COOCH3 Me Et CF3 H H O C H C Cl C OCF2CHF2 H H 344 Ac Me Et CF3 H H O C H C Cl C OCF2CHF2 H H 345 Ac Me Me H Me H O C H C Cl C OCF2CHF2 H H 346 COOCH3 Me Et H Me H O C H C Cl C OCF2CHF2 H H 347 Ac Me Et H Me H O C H C Cl C OCF2CHF2 H H 348 Ac Me Me Me Me H O C H C Cl C OCF2CHF2 H H 349 COOCH3 Me Et Me Me H O C H C Cl C OCF2CHF2 H H 350 Ac Me Et Me Me H O C H C Cl C OCF2CHF2 H H 351 Ac Me Me CF3 H H O C Cl C H C CF3 H Cl 352 Ac Me Me H CF3 H O C Cl C H C CF3 H Cl 353 Ac Me Me CF3 H H O C Cl C H C OCF3 H Cl 354 Ac Me Me H CF3 H O C Cl C H C OCF3 H Cl 355 Ac Me Me Me H H O C Me C H C OCF2CHF2 H H 356 COOCH3 Me Et Me H H O C Me C H C OCF2CHF2 H H 357 Ac Me Me CF3 H H O C Me C H C OCF2CHF2 H H 358 COOCH3 Me Et CF3 H H O C Me C H C OCF2CHF2 H H 359 Ac Me Me H Me H O C Me C H C OCF2CHF2 H H 360 COOCH3 Me Et H Me H O C Me C H C OCF2CHF2 H H 361 Ac Me Me Me Me H O C Me C H C OCF2CHF2 H H 362 COOCH3 Me Et Me Me H O C Me C H C OCF2CHF2 H H 363 Ac Me Me CF3 H H O C H C H C (4"-CF3-Ph)-O H H Table 8 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 364 Ac Me Me H CF3 H O C H C H C (4"-CF3-Ph)-O H H 365 Ac Me Me CF3 H H O C H C H C 4"-CF3-Ph h H H 366 Ac Me Me H CF3 H O C H C H C 4"-CF3-Ph H H 367 Ac Me Me Cl H H OCH2 C H C H C Cl H H 368 Ac Me Me H Cl H OCH2 C H C H C Cl H H 369 Ac Me Me Cl H H CO C H C H C Cl H H 370 Ac Me Me H Cl H CO C H C H C Cl H H 371 Ac Me Me Cl H H S C H C H C Cl H H 372 Ac Me Me H Cl H S C H C H C Cl H H 373 Ac Me Me Cl H H SO C H C H C Cl H H 374 Ac Me Me Cl H H SO2 C H C H C Cl H H 375 Ac Me CH2-OAc Cl H H SO2 C H C H C Cl H H 376 Ac Me Me H Cl H SO2 C H C H C Cl H H 377 Ac Me Me Cl H H CH2 C H C H C Cl H H 378 Ac Me Me H Cl H CH2 C H C H C Cl H H 379 Ac Me Me H Et H O C H C Cl C CF3 H H 380 COOCH3 Me Et H Et H O C H C Cl C CF3 H H 381 COOCH3 Me Me H F H O C H C Cl C CF3 H H 382 COOCH3 Me Me COOMe H H O C H C Cl C CF3 H H 383 Ac Me Me H OMe H O C H C Cl C CF3 H H 384 COOCH3 Me Et H OMe H O C H C Cl C CF3 H H 385 Ac Me Me H Et H O C Cl C H C CF3 H H 386 COOCH3 Me Et H Et H O C Cl C H C CF3 H H 387 COOCH3 Me Me H F H O C Cl C H C CF3 H H 388 COOCH3 Me Me COOMe H H O C Cl C H C CF3 H H 389 Ac Me Me H OMe H O C Cl C H C CF3 H H 390 COOCH3 Me Et H OMe H O C Cl C H C CF3 H H 391 Ac Me Me H Et H O C H C H C CF3 H H 392 COOCH3 Me Et H Et H O C H C H C CF3 H H 393 COOCH3 Me Me F F H O C H C H C CF3 H H 394 COOCH3 Me Me H F H O C H C H C CF3 H H 395 COOCH3 Me Me COOMe H H O C H C H C CF3 H H 396 Ac Me Me F H H O C H C H C CF3 H H 397 COOCH3 Me Et Me Me H O(CH2)30 C H C H C CF3 H H 398 COOCH3 Me Et Me Me H O-CH2-C(CH3)2-CH2-O C H C H C CF3 H H 399 COOCH3 Me Et Me Me H O(CH2)20 C H C H C CF3 H H 400 Ac Me Me H OMe H O C H C H C CF3 H H 401 COOCH3 Me Et H OMe H O C H C H C CF3 H H 402 Ac Me Me H Et H O C Me C H C CF3 H H 403 COOCH3 Me Et H Et H O C Me C H C CF3 H H 404 COOCH3 Me Me H F H O C Me C H C CF3 H H 405 COOCH3 Me Me COOMe H H O C Me C H C CF3 H H 406 Ac Me Me H OMe H O C Me C H C CF3 H H 407 COOCH3 Me Et H OMe H O C Me C H C CF3 H H 408 Ac Me Me H Et H O C H C Me C CF3 H H 409 COOCH3 Me Et H Et H O C H C Me C CF3 H H 410 COOCH3 Me Me H F H O C H C Me C CF3 H H 411 COOCH3 Me Me COOMe H H O C H C Me C CF3 H H 412 Ac Me Me H OMe H O C H C Me C CF3 H H 413 COOCH3 Me Et H OMe H O C H C Me C CF3 H H 414 Ac Me Me H Me H O C CF3 C H C CF3 H H 415 COOCH3 Me Et H Me H O C CF3 C H C CF3 H H Table 9 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 416 Ac Me Me H Me H O C H C CF3 C CF3 H H 417 COOCH3 Me Et H Me H O C H C CF3 C CF3 H H 418 COOCH3 Me Et H Me H O C H C H C CF2CHFCF3 H H 419 COOCH3 Me Et Me Me H O C H C H C CF2CHFCF3 H H 420 Ac Me Me H F H O C H C H C CF2CHFCF3 H H 421 COOCH3 Me Et H Et H O C H C H C CF2CHFCF3 H H 422 Ac Me Me H Et H O C H C Cl C OCF3 H H 423 COOCH3 Me Et H Et H O C H C Cl C OCF3 H H 424 COOCH3 Me Me H F H O C H C Cl C OCF3 H H 425 Ac Me Me H F H O C H C Cl C OCF3 H H 426 COOCH3 Me Me COOMe H H O C H C Cl C OCF3 H H 427 Ac Me Me H OMe H O C H C Cl C OCF3 H H 428 COOCH3 Me Et H OMe H O C H C Cl C OCF3 H H 429 Ac Me Me H Et H O C Cl C H C OCF3 H H 430 COOCH3 Me Et H Et H O C Cl C H C OCF3 H H 431 COOCH3 Me Me H F H O C Cl C H C OCF3 H H 432 COOCH3 Me Me COOMe H H O C Cl C H C OCF3 H H 433 COOCH3 Me Et H OMe H O C Cl C H C OCF3 H H 434 Ac Me Me H OMe H O C Cl C H C OCF3 H H 435 Ac Me Me H CF3 H S C H C H C OCF3 H H 436 Ac Me Me H CF3 H - C H C H C OCF3 H H 437 Ac Me Me H CF3 H SO2 C H C H C OCF3 H H 438 CON (CH3)2 Me Me H CF3 H O C H C H C OCF3 H H 439 SO2CH3 Me Me H CF3 H O C H C H C OCF3 H H 440 Ac Me Me H CF3 H OCH2 C H C H C OCF3 H H 441 CH3 Me Me H CF3 H O C H C H C OCF3 H H 442 Ac Me Me H CHF2 H O C H C H C OCF3 H H 443 COOCH3 Me Et H CHF2 H O C H C H C OCF3 H H 444 Ac Me Me H COOMe H O C H C H C OCF3 H H 445 Ac Me Me H Et H O C H C H C OCF3 H H 446 COOCH3 Me Et H Et H O C H C H C OCF3 H H 447 Ac Me Me H F H O C H C H C OCF3 H H 448 H Me Me H F H O C H C H C OCF3 H H 449 COOCH3 Me Me H F H O C H C H C OCF3 H H 450 COOCH3 Me Me F F H O C H C H C OCF3 H H 451 Ac Me Me F F H O C H C H C OCF3 H H 452 Ac Me Me CF3 H Cl O C H C H C OCF3 H H 453 Ac Me Me CF3 H H S C H C H C OCF3 H H 454 Ac Me Me CF3 H H - C H C H C OCF3 H H 455 Ac Me Me CF3 H H SO2 C H C H C OCF3 H H 456 CON (CH3)2 Me Me CF3 H H O C H C H C OCF3 H H 457 SO2CH3 Me Me CF3 H H O C H C H C OCF3 H H 458 CH3 Me Me CF3 H H O C H C H C OCF3 H H 459 Ac Me Me COOMe H H O C H C H C OCF3 H H 460 Ac Me Me F H H O C H C H C OCF3 H H 461 COCH2OMe Me Me CF3 H H O C H C H C OCF3 H H 462 COCH2OCOMe Me Me CF3 H H O C H C H C 0CF3 H H 463 COOCH3 Me Me COOMe H H O C H C H C OCF3 H H 464 COOCH3 Me Et Me Me H OCH2 C H C H C 0CF3 H H 465 CO (CH2)7CH3 Me Et H Me H O C H C H C 0CF3 H H 466 COCH2OMe Me Et H Me H O C H C H C 0CF3 H H 467 COCH20COMe Me Et H Me H O C H C H C 0CF3 H H Table 10 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 468 CH2COOMe Me Et H Me H O C H C H C OCF3 H H 469 CO-cPr Me Et H Me H O C H C H C OCF3 H H 470 4-OMe Me Et H Me H O C H C H C OCF3 H H 471 CH2-O-CH2CH2-O-CH3 Me Et H Me H O C H C H C OCF3 H H 472 Ac Me Me H OMe H O C H C H C OCF3 H H 473 COOCH3 Me Et H OMe H O C H C H C OCF3 H H 474 Ac Me Me H Et H O C Me C H C OCF3 H H 475 COOCH3 Me Et H Et H O C Me C H C OCF3 H H 476 COOCH3 Me Me H F H O C Me C H C OCF3 H H 477 COOCH3 Me Me COOMe H H O C Me C H C OCF3 H H 478 Ac Me Me H OMe H O C Me C H C OCF3 H H 479 COOCH3 Me Et H OMe H O C Me C H C OCF3 H H 480 Ac Me Me H Et H O C H C Me C OCF3 H H 481 COOCH3 Me Et H Et H O C H C Me C OCF3 H H 482 COOCH3 Me Me H F H O C H C Me C OCF3 H H 483 COOCH3 Me Me COOMe H H O C H C Me C OCF3 H H 484 Ac Me Me H OMe H O C H C Me C OCF3 H H 485 COOCH3 Me Et H OMe H O C H C Me C OCF3 H H 486 Ac Me Me H Me H O C 0CF3 C H C OCF3 H H 487 COOCH3 Me Et H Me H O C 0CF3 C H C OCF3 H H 488 Ac Me Me H Me H O C H C OCF3 C OCF3 H H 489 COOCH3 Me Et H Me H O C H C OCF3 C OCF3 H H 490 Ac Me Me H OMe H O C H C Cl C OCF2CHF2 H H 491 COOCH3 Me Et H OMe H O C H C Cl C OCF2CHF2 H H 492 COOCH3 Me Me COOMe H H O C H C Cl C OCF2CHF2 H H 493 COOCH3 Me Me H F H O C H C Cl C OCF2CHF2 H H 494 Ac Me Me H Et H O C H C Cl C OCF2CHF2 H H 495 COOCH3 Me Et H Et H O C H C Cl C OCF2CHF2 H H 496 Ac Me Et H CF3 H O C Cl C H C OCF2CHF2 H H 497 COOCH3 Me Et H OMe H O C H C H C OCF2CHF2 H H 498 Ac Me Me H OMe H O C H C H C OCF2CHF2 H H 499 COOCH3 Me Me COOMe H H O C H C H C OCF2CHF2 H H 500 Ac Me Me F H H O C H C H C OCF2CHF2 H H 501 COOCH3 Me Me H F H O C H C H C OCF2CHF2 H H 502 COOCH3 Me Me F F H O C H C H C OCF2CHF2 H H 503 Ac Me Me H Et H O C H C H C OCF2CHF2 H H 504 COOCH3 Me Et H Et H O C H C H C OCF2CHF2 H H 505 Ac Me Me H OMe H O C Cl C H C OCF2CHF2 H H 506 COOCH3 Me Et H OMe H O C Cl C H C OCF2CHF2 H H 507 COOCH3 Me Me COOMe H H O C Cl C H C OCF2CHF2 H H 508 COOCH3 Me Me H F H O C Cl C H C OCF2CHF2 H H 509 Ac Me Me H Et H O C Cl C H C OCF2CHF2 H H 510 COOCH3 Me Et H Et H O C Cl C H C OCF2CHF2 H H 511 Ac Me Me H OMe H O C Me C H C OCF2CHF2 H H 512 COOCH3 Me Et H OMe H O C Me C H C OCF2CHF2 H H 513 COOCH3 Me Me COOMe H H O C Me C H C OCF2CHF2 H H 514 COOCH3 Me Me H F H O C Me C H C OCF2CHF2 H H 515 Ac Me Me H Et H O C Me C H C OCF2CHF2 H H 516 COOCH3 Me Et H Et H O C Me C H C OCF2CHF2 H H 517 Ac Me Me H OMe H O C H C Me C OCF2CHF2 H H 518 COOCH3 Me Et H OMe H O C H C Me C OCF2CHF2 H H 519 COOCH3 Me Me COOMe H H O C H C Me C OCF2CHF2 H H Table 11 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 520 COOCH3 Me Me H F H O C H C Me C OCF2CHF2 H H 521 Ac Me Me H Et H O C H C Me C OCF2CHF2 H H 522 COOCH3 Me Et H Et H O C H C Me C OCF2CHF2 H H 523 Ac Me Me H Me H O C OMe C H C OCF2CHF2 H H 524 COOCH3 Me Et H Me H O C OMe C H C OCF2CHF2 H H 525 Ac Me Me H Me H O C Cl C Cl C OCF2CHF2 H H 526 COOCH3 Me Et H Me H O C Cl C Cl C OCF2CHF2 H H 527 Ac Me Me H Me H O C Cl C H C OCF2CHF2 Cl H 528 COOCH3 Me Et H Me H O C Cl C H C OCF2CHF2 Cl H 529 COOCH3 Me Et H Me H O C H C H C OCF2CHFCF3 H H 530 COOCH3 Me Et Me Me H O C H C H C OCF2CHFCF3 H H 531 COOCH3 Me Et H Me H O C H C H C OCF2CF2CF3 H H 532 COOCH3 Me Et Me Me H O C H C H C OCF2CF2CF3 H H 533 COOCH3 Me Et H Me H O C H C H C OCF2CHFCF2CF3 H H 534 COOCH3 Me Et Me Me H O C H C H C OCF2CHFCF2CF3 H H 535 COOCH3 Me Et H Me H O C H C H C OCF2CHFOCF3 H H 536 COOCH3 Me Et Me Me H O C H C H C OCF2CHFOCF3 H H 537 COOCH3 Me Et H Me H O C H C H C OCF2CHFOCF2CF3 H H 538 COOCH3 Me Et Me Me H O C H C H C OCF2CHFOCF2CF3 H H 539 COOCH3 Me Et Me H H O C H C H C OCF2CHFOCF2CF2CF3 H H 540 COOCH3 Me Et H Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 541 COOCH3 Me Et Me Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 542 Ac Me Et H Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 543 Ac Me Me H Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 544 Ac Me Et Me Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 545 Ac Me Me Me Me H O C H C H C OCF2CHFOCF2CF2CF3 H H 546 Ac Me Me H M e0 H O C H C H C OCF2CHFOCF2CF2CF3 H H 547 COOCH3 Me Et H M e0 H O C H C H C OCF2CHFOCF2CF2CF3 H H 548 Ac Me Me H F H O C H C H C OCF2CHFOCF2CF2CF3 H H 549 COOCH3 Me Me H F H O C H C H C OCF2CHFOCF2CF2CF3 H H 550 COOCH3 Me Et H F H O C H C H C OCF2CHFOCF2CF2CF3 H H 551 Ac Me Me F F H O C H C H C OCF2CHFOCF2CF2CF3 H H 552 COOCH3 Me Et H Et H O C H C H C OCF2CHFOCF2CF2CF3 H H 553 COOCH3 Me Et H Me H OCH2 C H C H C OCF2CHFOCF2CF2CF3 H H 554 Ac Me Me H Me H OCH2 C H C H C OCF2CHFOCF2CF2CF3 H H 555 COOCH3 Me Et H Me H O(CH2)3O C H C H C OCF2CHFOCF2CF2CF3 H H 556 Ac Me Me H Me H O(CH2)3O C H C H C OCF2CHFOCF2CF2CF3 H H 557 COOCH3 Me Et Me Me H O C H C H C OCH2CH=CC 12 H H 558 COOCH3 Me Et H Me H O C H C H C OCH2CH=CC 12 H H 559 COOCH3 Me Et Me Me H O C H C H C OCH2CH=C(CF3)Cl H H 560 COOCH3 Me Et H Me H O C H C H C OCH2CH=C(CF3)Cl H H 561 COOCH3 Me Et Me Me H O C H C H C CH=C(CF3)Cl H H 562 COOCH3 Me Et H Me H O C H C H C CH=C(CF3)Cl H H 563 COOCH3 Me Et Me Me H O C H C H C CH=C(CF3)2 H H 564 COOCH3 Me Et H Me H O C H C H C CH=C(CF3)2 H H 565 COOCH3 Me Et H Me H O C H C H C OCF(CF3)2 H H 566 COOCH3 Me Et Me Me H O C H C H C OCF(CF3)2 H H 567 COOCH3 Me Et H Me H O C H C H C OCH (CF3)CH3 H H 568 COOCH3 Me Et Me Me H O C H C H C OCH (CF3)CH3 H H 569 COOCH3 Me Me H F H O C H C Cl C C1 H H 570 COOCH3 Me Me COOMe H H O C H C H C C1 H H 571 COOCH3 Me Me F F H O C H C H C C1 H H Table 12 Compound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 572 Ac Me Me H F H O C H C H C COOEt H H 573 Ac Me Me F H H O C H C H C COOEt H H 574 Ac Me Me Me H H O C H C H C Me H H 575 Ac Me Me H Me H O C H C H C Me H H 576 COOCH3 Me Me H F H O C H C Me C Me H H 577 Ac Me Me H F H O C H C H C Et H H 578 COOCH3 Me Me H F H O C H C H C SCF3 H H 579 COOCH3 Me Me F F H O C H C H C SCF3 H H 580 Ac Me Me F F H O C H C H C SCF3 H H 581 Ac Me Me H F H O C H C H C SCF3 H H 582 COOCH3 Me Me F H H O C H C H C SCF3 H H 583 Ac Me Me H 0Me H O C H C H C SCF3 H H 584 COOCH3 Me Et H 0Me H O C H C H C SCF3 H H 585 COOCH3 Me Me COOMe H H O C H C H C SCF3 H H 586 Ac Me Me F H H O C H C H C SCF3 H H 587 Ac Me Me H Et H O C H C H C SCF3 H H 588 COOCH3 Me Et H Et H O C H C H C SCF3 H H 589 COOCH3 Me Et Me Me H O C H C H C SCH2CH=CCl2 H H 590 COOCH3 Me Et H Me H O C H C H C SCH2CH=CCl2 H H 591 COOCH3 Me Et Me Me H O C H C H C SCH2CH2CF=CF2 H H 592 COOCH3 Me Et Me Me H O C H C H C SO2CF3 H H 593 COOCH3 Me Et Me Me H O C Cl C H C SO2CF3 H H 594 COOCH3 Me Et H Me H O C H C H C SO2CF3 H H 595 Ac Me Et H Me H O C H C H C SO2CF3 H H 596 Ac Me Me H Me H O C H C H C SO2CF3 H H 597 Ac Me Et Me Me H O C H C H C SO2CF3 H H 598 Ac Me Me Me Me H O C H C H C SO2CF3 H H 599 Ac Me Me H MeO H O C H C H C SO2CF3 H H 600 COOCH3 Me Et H MeO H O C H C H C SO2CF3 H H 601 Ac Me Me H F H O C H C H C SO2CF3 H H 602 COOCH3 Me Me H F H O C H C H C SO2CF3 H H 603 COOCH3 Me Et H F H O C H C H C SO2CF3 H H 604 Ac Me Me F F H O C H C H C SO2CF3 H H 605 COOCH3 Me Et H Et H O C H C H C SO2CF3 H H 606 COOCH3 Me Et H Me H O C Cl C H C SO2CF3 H H 607 Ac Me Et H Me H O C Cl C H C SO2CF3 H H 608 Ac Me Me H Me H O C Cl C H C SO2CF3 H H 609 Ac Me Et Me Me H O C Cl C H C SO2CF3 H H 610 Ac Me Me Me Me H O C Cl C H C SO2CF3 H H 611 Ac Me Me H OMe H O C H C CF3 C H H H 612 COOCH3 Me Et H OMe H O C H C CF3 C H H H 613 COOCH3 Me Me COOMe H H O C H C CF3 C H H H 614 Ac Me Me F H H O C H C CF3 C H H H 615 COOCH3 Me Me H F H O C H C CF3 C H H H 616 COOCH3 Me Me F F H O C H C CF3 C H H H 617 COOCH3 Me Me H F H O C H C OCF3 C H H H 618 COOCH3 Me Me F H H O C H C OCF3 C H H H 619 Ac Me Me H OMe H O C H C OCF3 C H H H 620 COOCH3 Me Et H OMe H O C H C OCF3 C H H H 621 COOCH3 Me Me COOMe H H O C H C OCF3 C H H H 622 Ac Me Me F H H O C H C OCF3 C H H H 623 COOCH3 Me Me F F H O C H C OCF3 C H H H Table 13 Com pound No R1 R2 R3 X1 X2 X3 z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 624 Ac Me Me H Et H O C H C OCF3 C H H H 625 COOCH3 Me Et H Et H O C H C OCF3 C H H H 626 Ac Me Me H OMe H O C H C OCF2CHF2 C H H H 627 COOCH3 Me Et H OMe H O C H C OCF2CHF2 C H H H 628 COOCH3 Me Me COOMe H H O C H C OCF2CHF2 C H H H 629 Ac Me Me F H H O C H C OCF2CHF2 C H H H 630 COOCH3 Me Me H F H O C H C OCF2CHF2 C H H H 631 COOCH3 Me Me F F H O C H C OCF2CHF2 C H H H 632 Ac Me Me H Et H O C H C OCF2CHF2 C H H H 633 COOCH3 Me Et H Et H O C H C OCF2CHF2 C H H H 634 COOCH3 Me Me H F H O C H C SCF3 C H H H 635 Ac Me Me H F H O C H C SCF3 C H H H 636 COOCH3 Me Me F H H O C H C SCF3 C H H H 637 Ac Me Me H OMe H O C H C SCF3 C H H H 638 COOCH3 Me Et H OMe H O C H C SCF3 C H H H 639 COOCH3 Me Me COOMe H H O C H C SCF3 C H H H 640 Ac Me Me F H H O C H C SCF3 C H H H 641 COOCH3 Me Me F F H O C H C SCF3 C H H H 642 Ac Me Me H Et H O C H C SCF3 C H H H 643 COOCH3 Me Et H Et H O C H C SCF3 C H H H 644 Ac Me Me Me H H O C OCF3 C H C H H H 645 Ac Me Me H Me H O C OCF3 C H C H H H 646 Ac Me Me CF3 H H O C OCF3 C H C H H H 647 Ac Me Me H CF3 H O C OCF3 C H C H H H 648 COOCH3 Me Et H Me H O C H C-O-CF2-CF2-O-C H H 649 COOCH3 Me Et Me H H O C H C-O-CF2-CF2-O-C H H 650 COOCH3 Me Me H F H O C H C-O-CF2-CF2-O-C H H 651 Ac Me Me H F H O C H C-O-CF2-CF2-O-C H H 652 COOCH3 Me Me F H H O C H C-O-CF2-CF2-O-C H H 653 COOCH3 Me Et Me Me H O C H C-O-CF2-CF2-O-C H H 654 H Me Et H Me H O C H C-O-CF2-CF2-O-C H H 655 Ac Me Et H Me H O C H C-O-CF2-CF2-O-C H H 656 Ac Me Me H Me H O C H C-O-CF2-CF2-O-C H H 657 Ac Me Et Me Me H O C H C-O-CF2-CF2-O-C H H 658 Ac Me Me Me Me H O C H C-O-CF2-CF2-O-C H H 659 Ac Me Me H M e0 H O C H C-O-CF2-CF2-O-C H H 660 C00CH3 Me Et H M e0 H O C H C-O-CF2-CF2-O-C H H 661 COOCH3 Me Et H Et H O C H C-O-CF2-CF2-O-C H H 662 COOCH3 Me Et H Me H OCH2 C H C-O-CF2-CF2-O-C H H 663 Ac Me Me H Me H OCH2 C H C-O-CF2-CF2-O-C H H 664 C00CH3 Me Et H Me H O(CH2)30 C H C-O-CF2-CF2-O-C H H 665 Ac Me Me H Me H O(CH2)30 C H C-O-CF2-CF2-O-C H H 666 COOCH3 Me Me H Me H O C H C-CF2-CF2-O-C H H 667 COOCH3 Me Et H Me H O C H C-CF2-CF2-O-C H H 668 COOCH3 Me Et Me Me H O C H C-CF2-CF2-O-C H H 669 Ac Me Me H Me H O C H C-O-CF2-CF2-CH2-C H H 670 COOCH3 Me Et H Me H O C H C-O-CF2-CF2-CH2-C H H 671 Ac Me Me H Me H O C H C-CH2-CF2-CF2-O-C H H 672 COOCH3 Me Et H Me H O C H C-CH2-CF2-CF2-O-C H H 673 Ac Me Me H Me H O C H C-S-CF2-CF2-S-C H H 674 COOCH3 Me Et H Me H O C H C-S-CF2-CF2-S-C H H 675 Ac Me Me H Me H O C H C-CF2-CF2-S-C H H Table 14 Com pound No. R1 R2 R3 X1 X2 X3 Z W1 W2 W3 Y4 Y5 Y1 Y2 Y3 676 COOCH3 Me Et H Me H O C H C-CF2-CF2-S-C H H 677 Ac Me Me H Me H O C H C-CF2-CF2-CF2-C H H 678 COOCH3 Me Et H Me H O C H C-CF2-CF2-CF2-C H H 679 Ac Me Me Cl H H O N C H C Cl H H 680 Ac Me Me H Cl H O N C H c Cl H H 681 Ac Me Me CF3 H H O N C H c CF3 H Cl 682 Ac Me Me H CF3 H O N C H c CF3 H Cl 683 COOCH3 Me Et Me Me H O(CH2)30 N C H c CF3 H H 684 Ac Me Me Me Me H O N C H c CF3 H Cl 685 COOCH3 Me Et Me Me H O N C H c CF3 H Cl 686 Ac Me Me H Me H O N C H c CF3 H H 687 COOCH3 Me Me H Me H O N C H c CF3 H H 688 Ac Me Me Me Me H O N C H c CF3 H H 689 COOCH3 Me Et Me Me H O N C H c CF3 H H 690 Ac Me Me H MeO H O N C H c CF3 H H 691 COOCH3 Me Et H MeO H O N C H c CF3 H H 692 Ac Me Me H F H O N C H c CF3 H H 694 COOCH3 Me Et H Me H O C H N c CF3 H H 695 Ac Me Me Me Me H O C H N c CF3 H H 696 COOCH3 Me Et Me Me H O C H N c CF3 H H 697 Ac Me Me H MeO H O C H N c CF3 H H 698 COOCH3 Me Et H MeO H O C H N c CF3 H H 699 Ac Me Me H F H O C H N c CF3 H H 700 C00CH3 Me Me H F H O N C H c CF3 H Cl
    [0083] Agriculturally and horticulturally acceptable acid addition salts in the compounds of formula (I) or formula (Ia) include, for example, hydrochlorides, nitrates, sulfates, phosphates, or acetates.
    [0084] Compounds represented by formula (I) or formula (Ia) may be produced by the process shown in the following scheme. Specifically, compounds represented by formula (1b), which are compounds represented by formula (I) or formula (Ia) wherein R1 represents COR4, may be provided by the process described in Japanese Patent No. 2633377 . In the following scheme, R2, R3, and R4, X1, X2, and X3, Y1, Y2, Y3, Y4, and Y5, and Z are as defined above, Y1, Y2, Y3, Y4, and Y5 may be Y11, Y12, Y13, Y14, and Y15 in compound represented by formula (Ia).
    [0085] Compounds represented by formula (1b) may be synthesized by reacting a compound represented by formula (2) with a reagent represented by formula (3a) or formula (3b) in the presence or absence of a base and optionally subjecting the reaction product to a substituent exchange.
    [0086]
    [0087] Compounds represented by formula (1c), which are compounds represented by formula (I) or formula (Ia) wherein R1 represents R1' which represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, optionally substituted C2-18 alkynyl, optionally substituted C3-10 cycloalkyl, optionally substituted phenyl lower alkyl, optionally substituted phenoxy lower alkyl, optionally substituted phenyl, optionally substituted hetero ring, may be synthesized by reacting a compound represented by formula (2) wherein R1 represents a hydrogen atom with a compound represented by formula (3c), or reacting a compound represented by formula (4) wherein R1 represents a chlorine atom with a compound represented by formula (3d), in an organic solvent, for example, methanol, ethanol, acetone, ethyl acetate, benzene, chloroform, dichloromethane, tetrahydrofuran, or dimethylformamide in the presence or absence of a base and optionally subjecting the reaction product to a substituent exchange. The compound represented by formula (4) wherein R1 represents a chlorine atom may be prepared by reacting the compound represented by formula (2) with a halogenating agent such as thionyl choride, oxalyl chloride, or phosphorus oxychloride, in an organic solvent or in the absence of a solvent.
    [0088]
    [0089] Here bases include, for example, organic amines such as triethylamine or pyridine, and inorganic alkalis such as sodium carbonate, potassium carbonate, and sodium hydride.
    [0090] Compounds represented by formula (I) or formula (Ia)wherein R1 represents an alkali metal or an alkaline earth metal may be produced by mixing and reacting a compound represented by formula (I) or formula (Ia) wherein R1 represents a hydrogen atom or COR4 with a base such as a hydroxide, hydride, alkylate or the like of an alkali metal or alkaline earth metal, for example, sodium hydroxide, potassium hydroxide, sodium hydride, or butyllithium, in an organic solvent, for example, methanol, ethanol, acetone, ethyl acetate, benzene, chloroform, dichloromethane, or tetrahydrofuran.
    [0091] The compound represented by formula (2) as a starting compound may be produced by a conventional method, J. Am. Chem. Soc. 70, 2402 (1948) or Tetrahedron Lett. 27, 5323 (1986). In the following scheme, R9 represents C1-4 lower alkyl.
    [0092]
    [0093] The compound represented by formula (2) is a tautomer of a compound represented by formula (I) or formula (Ia) wherein R1 represents a hydrogen atom. That is, the compound represented by formula (I) or formula (Ia) wherein R1 represents a hydrogen atom may be produced according to the above scheme.
    [0094] Further, compounds represented by formula (5) may be produced by reducing a nitro group in a compound represented by formula (7) according to the following scheme.
    [0095]
    [0096] Compounds represented by formula (7a) which are compounds represented by formula (7) wherein Z represents an oxygen atom may be produced from a compound represented by formula (8a) and a compound represented by formula (9a), from a compound represented by formula (8b) and a compound represented by formula (9b), or from a compound represented by formula (8c) and a compound represented by formula (9c), by the method shown in the following scheme.
    [0097]
    [0098] Specifically, compounds as phenyl ether derivatives represented by formula (7a) are synthesized by reacting a generally available phenol derivative represented by formula (8a) with a nitrated compound represented by formula (9a), or reacting a generally available nitrophenol derivative represented by formula (9b) with a halogenated aryl compound represented by formula (8b), in the presence or absence of a base, or by reacting a generally available phenol derivative represented by formula (9c) with a halogenated aryl compound represented by formula (8c) in the presence or absence of a base, and nitrating the compound as a phenyl ether derivative represented by formula (7a'). Here X4 represents a halogen atom such as chlorine, bromine, iodine, or fluorine.
    [0099] Compounds represented by formula (7b) which are compounds represented by formula (7) wherein Z represents a sulfur element may be synthesized by reacting a compound represented by formula (10) with a compound represented by formula (9).
    [0100]
    [0101] Compounds represented by formula (7c) which are compounds represented by formula (7) wherein Z represents SO, or compounds represented by formula (7d) which are compounds represented by formula (7) wherein Z represents SO2 may be synthesized by oxidizing a compound represented by formula (7b).
    [0102]
    [0103] Compounds represented by formula (7e) which are compounds represented by formula (7) wherein Z represents OCH2 may be synthesized by reacting a compound represented by formula (11) with a compound represented by formula (9).
    [0104]
    [0105] Compounds represented by formula (7f) which are compounds represented by formula (7) wherein Z represents CO may be synthesized by a Friedel-Crafts reaction using a compound represented by formula (12) and a compound represented by formula (13).
    [0106]
    [0107] Compounds represented by formula (5g) which are compounds represented by formula (5) wherein Z represents CH2 may be synthesized by a route through a compound represented by formula (7g) produced by reducing CO in formula (7f), or by a route through a compound represented by formula (5f) produced by reducing a nitro group in formula (7f).
    [0108]
    [0109] Compounds represented by formula (7h) which are compounds represented by formula (7) wherein Z represents a bond may be synthesized by reacting a compound represented by formula (14) with a compound represented by formula (9).
    [0110]
    [0111] Compounds represented by formula (7i) which are compounds represented by formula (7) wherein Z represents - O-Q-O- may be synthesized by reacting a compound represented by formula (9) with a compound represented by formula (15) to give a compound represented by formula (16) and reacting the compound with a compound represented by formula (8). Here X5 and X6 represent a halogen atom such as chlorine, bromine, iodine, or fluorine.
    [0112]
    [0113] As is apparent from the following Examples, the compounds represented by formula (I) or formula (Ia) have excellent control effect against insect pests. Accordingly, according to the present invention, there is provided an agricultural and horticultural insecticide comprising a compound represented by formula (I) or formula (Ia) as an active ingredient. The agricultural and horticultural insecticide according to the present invention may comprise an agriculturally and horticulturally acceptable acid addition salt of the compound represented by formula (I) or formula (Ia) as an active ingredient.
    [0114] Insect pest species as targets to be controlled in the present invention (insect pest species against which the compounds represented by formula (I) or formula (Ia) have control effect) are not particularly limited, and preferred insect pest species include Lepidopteran insect pests (for example, Noctuidae such as Spodoptera litura, Spodoptera exigua, Pseudaletia separata, Mamestra brassicae, Agrotis ipsilon, Trichoplusia spp., Heliothis spp., and Helicoverpa spp.; Pyralidae such as Chilo suppressalis, Cnaphalocrocis medinalis, Ostrinia nubilalis (European cornborer), Hellula undalis, Parapediasia teterrella, Haritalodes derogatus, and Plodia interpunctella; Pieridae such as Pieris rapae; Tortricidae such as Adoxophyes spp., Grapholita molesta, and Cydia pomonella; Carposinidae such as Carposina niponensis; Lyonetiidae such as Lyonetia spp.; Lymantriidae such as Lymantria spp. and Euproctis spp.; Yponomeutidae such as Plutella xylostella; Gelechiidae such as Pectinophora gossypiella; Arctiidae such as Hyphantria cunea; Tineidae such as Tinea translucens and Tineola bisselliella and the like), Hemipteran insect pests (for example, Aphididae such as Myzus persicae and Aphis gossypii; Delphacidae such as Laodelphax striatellus, Nilaparvata lugens and Sogatella furcifera; Deltocephalidae such as Nephotettix cincticeps; Pentatomidae such as Trigonotylus caelestialium, Plautia crossota stali, Nezara viridula and Riptortus clavatus; Aleyrodidae such as Trialeurodes vaporariorum, and Bemisia argentifolli (silverleaf whitefly); Coccoidea such as Pseudococcus comstocki; Tingidae; Psyllidae and the like), Coleoptera insect pests (for example, Curculionidae such as Sitophilus zeamais (maize weevil), Lissorhoptrus oryzophilus, Callosobruchuys chienensis; Tenebrionidae such as Tenebrio molitor; Scarabaeidae such as Anomala cuprea and Anomala rufocuprea; Chrysomelidae such as Phyllotreta striolata, Aulacophora femoralis, Leptinotarsa decemlineata (Colorado Potato Beetle), Diabrotica virgifera virgifera (Western Corn Rootworm), and Diabrotica undecimpunctata howardi (Southern Corn Rootworm); Epilachna such as Oulema oryzae, Paederus fuscipes, Bostrychidae, and Epilachna vigintioctopunctata; Cerambycidae and the like), Acarina insect pests (for example, Tetranychidae such as Tetranychus urticae, Tetranychus kanzawai, Panonychus citri, Panonychus ulmi, and Oligonychus spp.; Eriophyidae such as Aculops lycopersici, Aculops pelekassi, and Calacarus carinatus; Tarsonemidae such as Polyphagotarsonemus latus; Acaridae and the like), Hymenopteran insect pests (for example, Tenthredinidae such as Athalia rosae ruficornis and the like), Orthopteran insect pests (for example, Acrididae and the like), Dipteran insect pests (for example, Muscidae; Culex; Anopheles; Chironomidae; Calliphoridae; Sarcophagidae; Fannia canicularis; Anthomyiidae; Agromyzidae such as Liriomyza trifolii, Liriomyza sativae, and Liriomyza bryoniae; Tephritidae; Phoridae; Drosophilidae; Psychodidae; Simuliidae; Tabanidae; Stomoxys calcitrans and the like), Thysanopteran insect pests (for example, Thrips palmi, Frankliniella occidentalis, Thrips tabaci, Thrips hawaiiensis, Scirtothrips dorsalis, Frankliniella intonsa, Ponticulothrips diospyrosi and the like), Plant Parasitic Nematodes (for example, Meloidogyne; Pratylenchus; Heterodera; and Aphelenchoides such as Aphelenchoides besseyi; Bursaphelenchus xylophilus and the like), more preferably Lepidopteran insect pests, Hemipteran insect pests, Coleoptera insect pests, Acarina insect pests, Dipteran insect pests, or Thysanopteran insect pests. In an embodiment using the compounds represented by formula (II) or formula (IIa) or agriculturally and horticulturally acceptable acid addition salts thereof, target insect pests are preferably Lepidopteran insect pests, Hemipteran insect pests, Acarina insect pests, or Thysanopteran insect pests.
    [0115] When the compounds represented by formula (I) or formula (Ia) are used as an agricultural and horticultural insecticide, the compounds represented by formula (I) or formula (Ia) as such may be used. Alternatively, the compounds represented by formula (I) or formula (Ia) may be mixed with suitable solid carriers, liquid carriers, gaseous carriers or the like, surfactants, dispersants and other adjuvants for formulations, to prepare any suitable formulation, such as emulsifiable concentrates, EW formulation, liquid formulations, suspension, wettable powder, granular wettable powder, dust, DL (low drift) dust, fine subtilaes, granules, tablets, oil solutions, aerosols, floables, dry floables, and microcapsules.
    [0116] Accordingly, according to another aspect of the present invention, there is provided use of a compound represented by formula (I) or an agriculturally and horticulturally acceptable acid addition salt thereof as an agricultural and horticultural insecticide.According to a further aspect of the present invention, there is provided use of a compound represented by formula (Ia) or an agriculturally and horticulturally acceptable acid addition salt thereof as an agricultural and horticultural insecticide.
    [0117] Solid carriers usable herein include, for example, talc, bentonite, clay, kaolin, diatomaceous earth, vermiculite, white carbon, calcium carbonate, acid clay, silica sand, silica stone, zeolite, pearlite, attapulgite, pumice, ammonium sulfate, sodium sulfate, and urea.
    [0118] Examples of liquid carriers include: alcohols, such as methanol, ethanol, n-hexanol, ethylene glycol, and propylene glycol; ketones, such as acetone, methyl ethyl ketone, and cyclohexanone; aliphatic hydrocarbons, such as n-hexane, kerosine, and kerosene; aromatic hydrocarbons, such as toluene, xylene, and methylnaphthalene; ethers, such as diethyl ether, dioxane, and tetrahydrofuran; esters, such as ethyl acetate; nitriles, such as acetonitrile and isobutyronitrile; acid amides, such as dimethylformamide and dimethylacetamide; vegetable oils, such as soy bean oil and cotton seed oil; dimethylsulfoxide; and water.
    [0119] Gaseous carriers include, for example, LPG, air, nitrogen, carbon dioxide, and dimethyl ether.
    [0120] Surfactants and dispersants include, for example, alkylsulfonic esters, alkyl(aryl)sulfonic acid salts, polyoxyalkylene alkyl(aryl) ethers, polyhydric alcohol esters, lignin sulfonic acid salts, alkylsulfosuccinic acid salts, formalin condensates of alkylnaphthalenesulfonic acid salts, polycarboxylic acid salts, POE polystyryl phenyl ether sulfonic acid salts and POE polystyryl phenyl ether phosphoric acid salts, and POE-POP block polymers.
    [0121] Adjuvants for formulations include, for example, carboxymethylcellulose, hydroxypropylcellulose, polyvinyl alcohol, xanthan gum, pregelatinized starch, gum arabic, polyethylene glycol, liquid paraffin, calcium stearate, and antifoaming agents and preservatives.
    [0122] The above carriers, surfactants, dispersants, and adjuvants may be used either alone or in a combination of two or more according to need.
    [0123] The content of the active ingredient in the formulation is not particularly limited. Preferably, however, the content of the active ingredient in the formulation is 1 to 75% by weight for emulsifiable concentrates; 0.3 to 25% by weight for dust; 1 to 90% by weight for wettable powder; and 0.5 to 10% by weight for granules.
    [0124] The agricultural and horticultural insecticide according to the present invention may be used as such or after dilution. Further, the agricultural and horticultural insecticide according to the present invention may be used as a mixture or in a combination with, for example, other insecticides, fungicides, miticides, herbicides, plant growth-regulating agents, or fertilizers. Agents which may be mixed or used in combination include those described, for example, in The Pesticide Manual, 13th edition, published by The British Crop Protection Council and SHIBUYA INDEX, the 9th edition, 2002, published by SHIBUYA INDEX RESEARCH GROUP; and SHIBUYA INDEX, the 10th edition, 2005, published by SHIBUYA INDEX RESEARCH GROUP.
    [0125] More specifically, insecticides usable herein include, for example, organophosphate compounds such as acephate, dichlorvos, EPN, fenitothion, fenamifos, prothiofos, profenofos, pyraclofos, chlorpyrifos-methyl, and diazinon; carbamate compounds such as methomyl, thiodicarb, aldicarb, oxamyl, propoxur, carbaryl, fenobucarb, ethiofencarb, fenothiocarb, pirimicarb, carbofuran, and benfuracarb; nereistoxin derivatives such as cartap and thiocyclam; organochlorine compounds such as dicofol and tetradifon; pyrethroid compounds such as permethrin, tefluthrin, cypermethrin, deltamethrin, cyhalothrin, fenvalerate, fluvalinate, ethofenprox, and silafluofen; benzoylurea compounds such as diflubenzuron, teflubenzuron, flufenoxuron, and chlorfluazuron; and juvenile hormone-like compounds such as methoprene. Other insecticides include buprofezin, hexythiazox, amitraz, chlordimeform, pyridaben, fenpyroxymate, pyrimidifen, tebufenpyrad, fluacrypyrim, acequinocyl, fipronyl, ethoxazole, imidacloprid, chlothianidin, pymetrozine, bifenazate, spirodiclofen, chlorfenapyr, pyriproxyfene, indoxacarb, pyridalyl, or spinosad, avermectin, milbemycin, organometallic compounds, dinitro compounds, organosulfur compounds, urea compounds, triazine compounds, hydrazine compounds or other compounds. The agricultural and horticultural insecticides according to the present invention may also be used as a mixture or in a combination with microbial pesticides such as BT formulations and insect pathological viral agents.
    [0126] Fungicides usable herein include, for example, strobilrin compounds such as azoxystrobin, kresoxym-methyl, and trifloxystrobin; anilinopyrimidine compounds such as mepanipyrim, pyrimethanil, and cyprodinil; azole compounds such as triadimefon, bitertanol, triflumizole, etaconazole, propiconazole, penconazole, flusilazole, myclobutanil, cyproconazole, tebuconazole, hexaconazole, prochloraz, and simeconazole; quinoxaline compounds such as quinomethionate; dithiocarbamate compounds such as maneb, zineb, mancozeb, polycarbamate, and propineb; phenylcarbamate compounds such as diethofencarb; organochlorine compounds such as chlorothalonil and quintozene; benzimidazole compounds such as benomyl, thiophanate-methyl, and carbendazole; phenylamide compounds such as metalaxyl, oxadixyl, ofurase, benalaxyl, furalaxyl, and cyprofuram; sulfenic acid compounds such as dichlofluanid; copper compounds such as copper hydroxide and oxine-copper; isoxazole compounds such as hydroxyisoxazole; organophosphorus compounds such as fosetyl-aluminium and tolclofos-methyl; N-halogenothioalkyl compounds such as captan, captafol, and folpet; dicarboxyimide compounds such as procymidone, iprodione, and vinchlozolin; benzanilide compounds such as flutolanil and mepronil; morpholine compounds such as fenpropimorph and dimethomorph; organotin compounds such as fenthin hydroxide, and fenthin acetate; and cyanopyrrole compounds such as fludioxonil and fenpiclonil. Other fungicides include fthalide, fluazinam, cymoxanil, triforine, pyrifenox, fenarimol, fenpropidin, pencycuron, cyazofamid, iprovalicarb, and benthiavalicarbisopropyl.
    [0127] According to another aspect of the present invention, there is provided a method for controlling an agricultural and horticultural insect pest, comprising the step of applying an effective amount of a compound represented by formula (I) or an agriculturally and horticulturally acceptable acid addition salt thereof to a plant or soil. According to a further aspect of the present invention, there is provided a method for controlling an agricultural and horticultural insect pest, comprising the step of applying an effective amount of a compound represented by formula (Ia) or an agriculturally and horticulturally acceptable acid addition salt thereof to a plant or soil. The control method according to the present invention includes a method in which the compound represented by formula (I) or (Ia) or an agriculturally and horticulturally acceptable acid addition salt thereof is applied by smoking treatment in a sealed space. EXAMPLES
    [0128] The present invention is further illustrated by the following Examples that are not intended as a limitation of the invention. Synthesis Example 1 4-Acetoxy-5-chloro-6-(4-chlorophenoxy)-2,3-dimethyl-quinoline (compound No. 2) and 4-acetoxy-7-chloro-6-(4-chlorophenoxy)-2,3-dimethyl-quinoline (compound No. 22)
    [0129] A mixture composed of 2.2 g of 3-chloro-4-(4-chlorophenoxy)-aniline, 2.63 g of ethyl 2-methylacetoacetate, and 0.5 mL of ethanol was added dropwise to 3.8 g of polyphosphoric acid heated to 150°C. The mixed solution was stirred at 150 to 160°C while removing ethanol by evaporation for 3 hr. The reaction solution was poured into 175 mL of iced water containing 2 mL of concentrated hydrochloric acid to produce crystals. The crystals were collected by filtration and were recrystallized from water/methanol to give 2.8 g of a mixture of 5-chloro-6-(4-chlorophenoxy)-4-hydroxy-2,3-dimethyl-quinoline with 7-chloro-6-(4-chlorophenoxy)-4-hydroxy-2,3-dimethyl-quinoline (yield 93%). The mixture (2.8 g) was stirred in 42 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated, ethyl acetate was then added to the concentrate, the mixture was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and the solvent was removed under the reduced pressure to give a crude product. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.03 g of 4-acetoxy-5-chloro-6-(4-chlorophenoxy)-2,3-dimethyl-quinoline (yield 32.6%) and 0.68 g of 4-acetoxy-7-chloro-6-(4-chlorophenoxy)-2,3-dimethyl-quinoline (yield 21.0%). Synthesis Example 2 4-Acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline (compound No. 90) and 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline (compound No. 122)
    [0130] A solution of 3.4 g of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethyl-aniline, 2.4 g of ethyl 2-methylacetoacetate, and 0.3 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 36 hr. This reaction solution was cooled, and the precipitated crystals were collected by filtration to give 1.73 g of 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline. The filtrate was concentrated under the reduced pressure to give 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline. Acetic anhydride (40 mL) was added to 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline obtained from the filtrate, and the mixture was heated at 120 to 125°C for one hr. This reaction solution was concentrated under the reduced pressure, ethyl acetate was then added to the concentrate, and the mixture was washed with brine. Thereafter, the solvent was removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.35 g of 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline.
    [0131] Acetic anhydride (40 mL) was added to 1.73 g of 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline obtained as crystals, and the mixture was heated at 120 to 125°C for one hr. This reaction solution was concentrated under the reduced pressure, ethyl acetate was then added to the concentrate, and the mixture was washed with brine. Thereafter, the solvent was removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.82 g of 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline. Synthesis Example 3 5-Trifluoromethyl-6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3-dimethyl-quinoline (compound No. 89)
    [0132] 4-Acetoxy-5-trifluoromethyl-6-(4-trifluoromethoxyphenoxy)-2,3-dimethyl-quinoline (1.5 g) prepared in Synthesis Example 2 was dissolved in 10 mL of ethanol. A 20% sodium hydroxide solution (10 mL) was added to the solution, and the mixture was stirred at 50°C for 3 hr. This reaction mixture was added to 20 mL of water, and the mixture was neutralized with 1 N hydrochloric acid. The precipitated crystals were collected by filtration under the reduced pressure to give 1.34 g of 5-trifluoromethyl-6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3-dimethyl-quinoline (yield 98.0%). Synthesis Example 4 4-Acetoxy-6-(2-chloro-4-trifluoromethylphenoxy)-2,3-dimethyl-5-trifluoromethyl-quinoline (compound No. 222) and 4-acetoxy-6-(2-chloro-4-trifluoromethyl-phenoxy)-2,3-dimethyl-7-trifluoromethyl-quinoline (compound No. 228)
    [0133] A solution of 3.43 g of 4-(2-chloro-4-trifluoromethyl-phenoxy)-3-trifluoromethyl-aniline, 3.1 g of ethyl 2-methylacetoacetate, and 1.83 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 19 hr. The reaction solution was cooled, and the precipitated crystals were collected by filtration to give 4.79 g of a mixture of 6-(2-chloro-4-trifluoromethyl-phenoxy)-2,3-dimethyl-4-hydroxy-5-trifluoromethyl-quinoline with 6-(2-chloro-4-trifluoromethyl-phenoxy)-2,3-dimethyl-4-hydroxy-7-trifluoromethyl-quinoline. Next, 20 mL of acetic anhydride was added to 2.4 g of the crystals, and the mixture was heated at 120 to 125°C for one hr. This reaction solution was concentrated under the reduced pressure. Ethyl acetate was then added to the concentrate, and the mixture was washed with brine. Thereafter, the solvent was removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.45 g of 4-acetoxy-6-(2-chloro-4-trifluoromethyl-phenoxy)-2,3-dimethyl-5-trifluoromethyl-quinoline (yield 19.5%) and 1.02 g of 4-acetoxy-6-(2-chloro-4-trifluoromethyl-phenoxy)-2,3-dimethyl-7-trifluoromethyl-quinoline (yield 44.3%). Synthesis Example 5 4-Methoxycarbonyloxy-2-ethyl-3-methyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline (compound No. 112) and 4-methoxycarbonyloxy-2-ethyl-3-methyl-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline (compound No. 123)
    [0134] A solution of 3.4 g of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethyl-aniline, 3.5 g of ethyl 2-methyl-3-oxopentanoate, and 2.1 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 10 hr. The reaction solution was cooled, and the precipitated crystals were then collected by filtration to give 6.0 g of a mixture of 2-ethyl-3-methyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline with 2-ethyl-3-methyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline. Next, 50 mL of dimethylacetamide was added to 6.0 g of the crystals, and 1.7 g of 60% sodium hydride and 4.6 g of methyl chloroformate were added thereto at 0°C. The mixture was stirred at 4 to 24°C for 1.5 hr, and 100 mL of toluene and 100 mL of distilled water were then added to the reaction solution. The organic layer was washed with water and was then concentrated under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.63 g of 4-methoxycarbonyloxy-2-ethyl-3-methyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline (yield 12.9%) and 2.00 g of 4-methoxycarbonyl-2-ethyl-3-methyl-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline (yield 40.9%). Synthesis Example 6 4-Acetoxy-6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-5-trifluoromethyl-quinoline (compound No. 253) and 4-acetoxy-6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-7-trifluoromethyl-quinoline (compound No. 259)
    [0135] A solution of 3.43 g of 4-(2-chloro-4-trifluoromethoxyphenoxy)-3-trifluoromethyl-aniline, 4.1 g of ethyl 2-methylacetoacetate, and 2.5 g of p-toluenesulfonic acid dissolved in 130 mL of xylene was heated under reflux for 17 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration to give 6.18 g of a mixture of 6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-4-hydroxy-5-trifluoromethyl-quinoline with 6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-4-hydroxy-7-trifluoromethyl-quinoline. Next, 30 mL of acetic anhydride was added to 2.4 g of the crystals, and the mixture was heated at 120 to 125°C for 1.5 hr. This reaction solution was concentrated under the reduced pressure, ethyl acetate was then added to the concentrate, and the mixture was washed with brine. Thereafter, the solvent was removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.33 g of 4-acetoxy-6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-5-trifluoromethyl-quinoline (yield 10.4%) and 1.11 g of 4-acetoxy-6-(2-chloro-4-trifluoromethoxyphenoxy)-2,3-dimethyl-7-trifluoromethyl-quinoline (yield 35.1%). Synthesis Example 7 4-Acetoxy-5-chloro-6-(4-methoxyphenoxy)-2,3-dimethyl-quinoline (compound No. 50) and 4-acetoxy-7-chloro-6-(4-methoxyphenoxy)-2,3-dimethyl-quinoline (compound No. 51)
    [0136] A mixture composed of 2.9 g of 3-chloro-4-(4-methoxyphenoxy)-aniline, 2.9 g of ethyl 2-methylacetoacetate, and 0.5 mL of ethanol was added dropwise to 4.2 g of polyphosphoric acid heated to 150°C. This reaction solution was stirred at 140 to 150°C while removing ethanol by evaporation for 3 hr and was then poured into 195 mL of iced water containing 2 mL of concentrated hydrochloric acid. The crystals were collected by filtration and were washed with n-hexane to give 3.29 g of a mixture of 5-chloro-6-(4-methoxyphenoxy)-4-hydroxy-2,3-dimethyl-quinoline with7-chloro-6-(4-methoxyphenoxy)-4-hydroxy-2,3-dimethyl-quinoline (yield 100%).
    [0137] The crystals of the mixture thus obtained stirred in 50 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated, ethyl acetate and toluene was then added to the concentrate, and the mixture was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine. The solvent was then removed under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.4 g of 4-acetoxy-5-chloro-6-(4-methoxyphenoxy)-2,3-dimethyl-quinoline (yield 37.7%) and 1.07 g of 4-acetoxy-7-chloro-6-(4-methoxyphenoxy)-2,3-dimethyl-quinoline (yield 28.8%). Synthesis Example 8 4-Acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,5-trimethylquinoline (compound No. 86) and 4-acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,7-trimethyl-quinoline (compound No. 118)
    [0138] A solution of 2.2 g of 4-(4-trifluoromethoxyphenoxy)-3-methyl-aniline, 2.6 g of ethyl 2-methylacetoacetate, and 1.52 g of p-toluenesulfonic acid dissolved in 81 mL of xylene was heated under reflux for 12 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration and were washed with distilled water and n-hexane to give 3.88 g of a mixture of 6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3,5-trimethyl-quinoline with 6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3,7-trimethyl-quinoline (yield 100%). The crystals of the mixture (2.9 g) thus obtained were stirred in 30 mL of acetic anhydride with heating at 120 to 125°C for 2 hr. The reaction solution was concentrated, ethyl acetate was then added to the concentrate, and the mixture was washed with saturated brine. The solvent was then removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.4 g of 4-acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,5-trimethyl-quinoline (yield 12.4%) and 0.19 g of 4-acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,7-trimethyl-quinoline (yield 6%). Synthesis Example 9 4-Acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,5,7-tetramethyl-quinoline (compound No. 132)
    [0139] A solution of 1.78 g of 4-(4-trifluoromethoxyphenoxy)-3,5-dimethylaniline, 1.92 g of ethyl 2-methylacetoacetate, and 1.14 g of p-toluenesulfonic acid dissolved in 61 mL of xylene was heated under reflux for 9 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration and were washed with distilled water and n-hexane to give 2.94 g of 6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3,5,7-tetramethyl-quinoline 2.26 g (yield 100%). A 1.14 g portion in the crystals thus obtained was stirred in 15 mL of acetic anhydride with heating at 120 to 125°C for 2 hr. The reaction solution was concentrated, ethyl acetate was then added to the concentrate, the mixture was washed with saturated brine, and the solvent was then concentrated under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.74 g of 4-acetoxy-6-(4-trifluoromethoxyphenoxy)-2,3,5,7-tetramethyl-quinoline (yield 58.4%). Synthesis Example 10 4-Acetoxy-5-chloro-6-(4-chlorophenylthio)-2,3-dimethyl-quinoline (compound No. 371) and 4-acetoxy-7-chloro-6-(4-chlorophenylthio)-2,3-dimethyl-quinoline (compound No. 372)
    [0140] A mixture composed of 2.7 g of 3-chloro-4-(4-chlorophenylthio)-aniline, 3.2 g of ethyl 2-methylacetoacetate, and 0.5 mL of ethanol was added dropwise to 4.2 g of polyphosphoric acid heated to 150°C. This reaction solution was stirred at 130 to 140°C while removing ethanol by evaporation for one hr. The reaction solution was then poured into 195 mL of iced water containing 2 mL of concentrated hydrochloric acid. As a result, crystals were produced. The crystals were collected by filtration and were washed with n-hexane to give 3.61 g of a mixture of 5-chloro-6-(4-chlorophenylthio)-4-hydroxy-2,3-dimethyl-quinoline with 7-chloro-6-(4-chlorophenylthio)-4-hydroxy-2,3-dimethyl-quinoline. The crystal of the mixture (3.5 g) thus obtained were stirred in 50 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated, and the crude product was then purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.95 g of 4-acetoxy-5-chloro-6-(4-chlorophenylthio)-2,3-dimethyl-quinoline (yield 24.2%) and 0.15 g of 4-acetoxy-7-chloro-6-(4-chlorophenylthio)-2,3-dimethyl-quinoline (yield 4%). Synthesis Example 11 4-Acetoxy-5-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (compound No. 369) and 4-acetoxy-7-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (compound No. 370)
    [0141] A solution of 2.7 g of 3-chloro-4-(4-chlorobenzoyl)aniline, 2.4 g of ethyl 2-methylacetoacetate, and 0.3 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 31 hr. This reaction solution was cooled, and the precipitated crystals were collected by filtration and were washed with n-hexane to give 2.68 g of a mixture of 5-chloro-6-(4-chlorobenzoyl)-4-hydroxy-2,3-dimethyl-quinoline with 7-chloro-6-(4-chlorobenzoyl)-4-hydroxy-2,3-dimethyl-quinoline (yield 77%). The crystals of the mixture thus obtained were stirred in 40 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated, and the crude product was then purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.0 g of 4-acetoxy-5-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (yield 32.6%) and 0.47 g of 4-acetoxy-7-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (yield 15.6%). Synthesis Example 12 4-Acetoxy-5-chloro-6-(4-chlorobenzyl)-2,3-dimethylquinoline (compound No. 377) and 4-acetoxy-7-chloro-6-(4-chlorobenzyl)-2,3-dimethyl-quinoline (compound No. 378)
    [0142] A solution of 3.0 g of 3-chloro-4-(4-chlorobenzyl)aniline, 2.9 g of ethyl 2-methylacetoacetate, and 0.4 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 15 hr. This reaction solution was cooled, and the precipitated crystals were collected by filtration and were washed with n-hexane to give 4.06 g of a mixture of 5-chloro-6-(4-chlorobenzyl)-4-hydroxy-2,3-dimethylquinoline with 7-chloro-6-(4-chlorobenzyl)-4-hydroxy-2,3-dimethylquinoline. The crystals of the mixture (3.9 g) thus obtained were stirred in 40 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated, ethyl acetate was then added to the concentrate, and the mixture was washed with saturated brine. The solvent was then removed under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.28 g of 4-acetoxy-5-chloro-6-(4-chlorobenzyl)-2,3-dimethyl-quinoline (yield 28.5%) and 0.56 g of 4-acetoxy-7-chloro-6-(4-chlorobenzyl)-2,3-dimethylquinoline (yield 12.5%). Synthesis Example 13 4-Cyclopropanecarbonyloxy-2,3-di methyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline (compound No. 96)
    [0143] 5-Trifluoromethyl-6-(4-trifluoromethoxyphenoxy)-4-hydroxy-2,3-dimethyl-quinoline (30 mg) prepared in Synthesis Example 3 was dissolved in 1 mL of dimethylformamide. Under ice cooling, 4.3 mg of 60% sodium hydride was added to the solution, and the mixture was stirred for one hr. Thereafter, 10.4 mg of cyclopropanecarbonyl chloride was added thereto, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was added to 5 mL of water, and the mixture was extracted with 5 mL of ethyl acetate. The ethyl acetate layer was washed with a saturated sodium hydrogencarbonate solution and saturated brine, was dried over anhydrous sodium sulfate, and was then concentrated under the reduced pressure. The crude product thus obtained was purified by chromatography on silica gel (Mega Bond Elut SI (Varian) 10 mL, solvent: n-hexane/ethyl acetate) to give 4-Cyclopropanecarbonyloxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline (13.8 mg, yield 39.5%). Synthesis Example 14 4-Acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenyl)-5-trifluoromethyl-quinoline (compound No. 454) and 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenyl)-7-trifluoromethylquinoline (compound No. 436)
    [0144] A solution of 2.97 g of 4-amino-4'-trifluoromethoxy-2-trifluoromethylbiphenyl, 2.97 g of ethyl 2-methylacetoacetate, and 1.76 g of p-toluenesulfonic acid dissolved in 94 mL of xylene was heated under reflux for 11 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration and were washed with n-hexane to give 4.05 g of a mixture of 5-trifluoromethyl-6-(4-trifluoromethoxyphenyl)-4-hydroxy-2,3-dimethylquinoline with 7-trifluoromethyl-6-(4-trifluoromethoxyphenyl)-4-hydroxy-2,3-dimethylquinoline. The crystals of the mixture (3.71 g) thus obtained were stirred in 35 mL of acetic anhydride with heating at 120 to 125°C for 2 hr. The reaction solution was concentrated, ethyl acetate was then added to the concentrate, and the mixture was washed with saturated brine. The solvent was concentrated under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.5 g of 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenyl)-5-trifluoromethylquinoline (yield 12.2%) and 1.07 g of 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenyl)-7-trifluoromethylquinoline (yield 26.1%). Synthesis Example 15 4-Methoxycarbonyloxy-6-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-2-ethyl-3,5,7-trimethylguinoline (compound No. 685)
    [0145] A solution of 1.52 g of 4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-3,5-dimethylaniline, 1.75 g of methyl 2-methyl-3-oxopentanoate, and 0.92 g of p-toluenesulfonic acid dissolved in 49 mL of xylene was heated under reflux for 8 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration and were washed with n-hexane and distilled water and were dried to give 2.56 g of 6-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-2-ethyl-4-hydroxy-3,5,7-trimethyl-quinoline. Dimethylacetamide (30 mL) was then added to 1.97 g of the crystals thus obtained, and 0.38 g of 60% sodium hydride and 0.9 g of methyl chloroformate were added thereto at room temperature. The mixture was stirred at room temperature for 2 hr, and ethyl acetate and distilled water were then added. The organic layer was washed with brine and was then concentrated under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.25 g of 4-methoxycarbonyloxy-6-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-2-ethyl-3,5,7-trimethylquinoline (yield 55.6%). Synthesis Example 16 4-Acetoxy-5-chloro-6-(5-chloropyridin-2-yloxy)-2,3-dimethylquinoline (compound No. 679) and 4-acetoxy-7-chloro-6-(5-chloropyridin-2-yloxy)-2,3-dimethylquinoline (compound No. 680)
    [0146] A solution of 3.16 g of 3-chloro-4-(5-chloropyridin-2-yloxy)aniline, 2.98 g of ethyl 2-methylacetoacetate, and 0.4 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 16 hr. This reaction solution was cooled, and the precipitated crystals were then collected by filtration and was washed with n-hexane to give 3.09 g of a mixture of 5-chloro-6-(5-chloropyridin-2-yloxy)-4-hydroxy-2,3-dimethylquinoline with 7-chloro-6-(5-chloropyridin-2-yloxy)-4-hydroxy-2,3-dimethyl-quinoline. The crystals of the mixture thus obtained were stirred in 40 mL of acetic anhydride with heating at 120 to 125°C for one hr. The reaction solution was concentrated. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) and was further recrystallized from n-hexane/ethyl acetate to give 0.53 g of 4-acetoxy-5-chloro-6-(5-chloropyridin-2-yloxy)-2,3-dimethylquinoline (yield 15.2%) and 0.12 g of 4-acetoxy-7-chloro-6-(5-chloropyridin-2-yloxy)-2,3-dimethylquinoline (yield 3.5%). Synthesis Example 17 4-Methoxycarbonyloxy-2-ethyl-3,5,7-trimethyl-6-(3-(4-trifluoromethyl-phenoxy)propoxy)guinoline (compound No. 397)
    [0147] A solution of 1.18 g of 3,5-dimethyl-4-(3-(4-trifluoromethylphenoxy)propoxy)aniline, 1.35 g of methyl 2-methyl-3-oxopentanoate, and 0.7 g of p-toluenesulfonic acid dissolved in 38 mL of xylene was heated under reflux for 7 hr. This reaction solution was cooled, and ethyl acetate and sodium bicarbonate water were added thereto, followed by separation. The ethyl acetate layer was washed with brine and was further concentrated under the reduced pressure to give 1.38 g of 2-ethyl-4-hydroxy-3,5,7-trimethyl-6-(3-(4-trifluoromethylphenoxy)propoxy)quinoline. Next, 1.38 g of the product thus obtained was added to 15 mL of dimethylacetamide, and 0.26 g of 60% sodium hydride and 0.6 g of methyl chloroformate were added thereto at room temperature. The reaction solution was stirred at room temperature for 2 hr, and ethyl acetate and distilled water were then added thereto. The organic layer was washed with brine and was concentrated under the reduced pressure. The crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) and was then recrystallized from n-hexane/ethyl acetate to give 1.13 g of 4-methoxycarbonyloxy-2-ethyl-3,5,7-trimethyl-6-(3-(4-trifluoromethylphenoxy)propoxy)quinoline (yield 72.2%).
    [0148] 1H-NMR data of the compounds according to the present invention synthesized in the same manner as described above were as summarized in Tables 15 to 25 below.
    [0149] Table 15Compound No.NMR spectral dataSolvent for measurementm.p.27.94(1H,d,J=9.0), 7.32(1H,d,J=9.0), 7.27(2H,d,J=9.0), 6.89(2H,d,J=9.0), 2.71(3H,s), 2.46(3H,s), 2.27(3H,s)CDCl3167~16937.93(1H,d,J=9.5), 7.33(1H,d,J=9.5), 7.27(2H,d,J=8.8), 6.90(2H,d,J=8.8), 3.97(3H,s), 2.72(3H,s), 2.34(3H,s)CDCl389~9147.93(1H,d,J=8.1), 7.32(1H,d,J=8.1), 7.29(2H,d,J=8.6), 6.89(2H,d,J=8.6), 2.71(3H,s), 2.27(3H,s), 1.47(9H,s)CDCl3155~15657.94(1H,d,J=9.0), 7.33(1H,d,J=9.0), 7.29(2H,d,J=7.0), 6.89(2H,d,J=7.0), 2.76(3H,s), 2.69(2H,broad), 2.46(3H,s), 1.21(3H,t,J=7.2)CDCl3123~12467.93(1H,d,J=9.0), 7.33(1H,d,J=9.0), 7.29(2H,d,J=8.8), 6.88(2H,d,J=8.8), 2.75(3H,s), 2.64(2H,broad), 2.45(3H,s), 1.59-1.40(4H,m), 1.00(3H.t.J=7.4)CDCl3122~12377.97(1H,d,J=8.3), 7.38(1H,d,J=8.3),7.29(2H,d,J=7.7), 7.07(1H,s), 6.87(2H,d,J=7.7), 2.73(3H,s), 2.41(3H,s)CDCl3-87.97(1H,d,J=9.0), 7.33(1H,d,J=9.0), 7.29(2H,d,J=9.0), 6.88(2H,d,J=9.0), 3.02(2H,q,J=7.2), 2.46(3H,s), 2.30(3H,s), 1.38(3H,t,J=7.2)CDCl3136~137108.01(1H,d,J=9.5), 7.38(1H,d,9.5), 7.28(2H,d,J=8.3), 6.88(2H,d,J=8.3), 3.23(1H,m,J=6.5), 2.44(3H,s), 1.40(6H,d,6.5)CDCl3-117.96(1H,d,J=9.6), 7.32(1H,d,J=9.6), 7.28(2H,d,J=8.9), 6.88(2H,d,J=8.9), 2.98(2H,t,J=7.8), 2.46(3H,s), 2.29(3H,s), 1.77(2H,m), 1.50(2H,s), 0.99(3H,t,J=7.1)CDCl3153~155128.18(1H,d,J=8.9), 7.54(1H,s), 7.50(1H,d,J=8.9), 7.37(2H,d,J=8.6), 6.96(2H,d,J=8.6), 2.48(3H,s)CDCl3-138.01(1H,d,J=9.0),7.35(1H,d,J=9.0), 7.31(2H,d,J=8.8), 6.90(2H,d,J=8.8), 5.39(2H,s), 2.48(3H,s), 2.31(3H,s), 2.18(3H,s)CDCl3186~187148.12(1H,d,J=9.0), 7.39(2H,d,J=8.8), 7.20(1H,d,J=9.0), 7.07(2H,d,J=8.8), 2.72(3H,s), 2.60(3H,s), 2.30(3H,s)CDCl3164~166157.81(1H,d,J=8.6), 7.37(1H,d,J=8.6), 7.28(2H,d,J=9.0), 6.92(2H,d,J=9.0), 2.71(3H,s), 2.41(3H,s), 2.29(3H,s)CDCl3125~127167.87(1H,d,J=9.0), 7.26(1H,d,J=9.0), 7.25(2HJ=9.0), 2.71(3H,s), 2.59(3H,s), 2.44(3H,s), 2.23(3H,s)CDCl3185~187198.10(1H,d,J=9.3), 7.32(2H,d,J=9.0), 7.24(1H,d,J=9.3), 6.92(2H,d,J=9.0), 2.72(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl3122~123218.40(1H,s), 7.36(2H,d,J=8.8), 7.01(1H,s), 7.02(2H,d,J=8.8), 2.72(3H,s), 2.33(3H,s), 2.24(3H,s)CDCl3130~131228.15(1H,s), 7.33(2H,d,J=8.9),7.19(1H,s), 6.93(2H,d,J=8.9), 2.71(3H,s), 2.38(3H,s),2.23(3H,s)CDCl3160~162238.16(1H,s), 7.32(2H,d,J=8.8), 7.27(1H,s), 6.94(2H,d,J=8.8), 3.91(3H,s), 2.71(3H,s), 2.29(3H,s),CDCl3169~171248.12(1H,s), 7.37(2H,d,J=8.8), 7.04(2H,d,J=8.8), 6.88(1H,s), 2.69(3H,s), 2.18(3H,s), 1.29(9H,s)CDCl3164~165258.14(1H,s), 7.32(2H,d,J=8.8), 7.11(1H,s), 6.93(2H,d,J=8.8), 2.75(3H,s), 2.69(2H,q,J=7.2), 2.37(3H.s), 1.18(3H,t,J=7.2)CDCl3120~121268.14(1H,s), 7.32(2H,d,J=7.2), 7.11(1H,s), 6.94(2H,d,J=7.2), 2.74(3H,s), 2.64(2H,t,J=8.4), 2.37(3H,s), 1.60-1.37(4H.m), .0.96(3H,t,J=7.4)CDCl3114~115
    [0150] Table 16 278.18(1H,s), 7.39(1H,s), 7.33(2H,d,J=8.0), 7.20(1H,s), 6.93(2H,d,J=8.0), 2.73(3H,s), 2.36(3H,s)CDCl3-288.19(1H,s), 7.32(2H,d,J=8.8), 7.20(1H,s), 6.92(2H,d,J=8.8), 3.00(2H,q,J=7.2), 2.38(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.2)CDCl3143~144298.23(1H,s), 7.40(1H,s), 7.32(2H,d,J=9.0), 0.93(2H,d,J=9.0), 3.24(1H,m,J=6.5), 2.38(3H,s), 1.40(6H,d,J=6.5)CDCl3-308.18(1H,s), 7.32(2H,d,J=7.0), 7.19(1H,s), 6.93(2H,d,J=7.0), 2.97(2H,t,J=7.8), 2.38(3H,s), 2.25(3H,s), 1.76(2H,m), 1.50(2H,m), 0.99(3H,t,J=7.1)CDCl3123~125317.77(1H,d,J=11.4), 7.32(2H,d,J=8.8), 7.26(1H,d,J=8.1), 6.96(2H,d,J=8.8), 2.71(3H,s), 2.41(3H,s), 2.23(3H,s)CDCl3150~152327.89(1H,s), 7.30(2H,d,J=9.0), 7.05(1H,s), 6.90(2H,d,J=9.0), 2.70(3H,s), 2.39(3H,s), 2.37(3H,s), 2.22(3H,s)CDCl3148~150347.48'(1H,s), 7.28(2H,d,J=8.8), 7.15(1H,s), 6.91(2H,d,J=8.8), 3.93(3H,s), 2.69(3H,s), 2.38(3H,s), 2.21(3H,s)CDCI3128.5~129.5357.70(1H,s), 7.36(2H,d,J=8.8), 7.32(1H,s), 6.99(2H,d,J=8.8), 2.75(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl3149~151387.98(1H,d,J=9.3), 7.32(1H,d,J=9.3), 7.27(2H,d,9.0), 6.87(2H,d,J=9.0), 3.42(1H,m), 2.45(3H,s), 2.31(3H,s), 1.35(6H,d,J=6.1)CDCI3123~124.5407.96(1H,d,J=9.0), 7.36(1H,d,J=9.0), 7.28-6.80(4H,m), 2.72(3H,s), 2.46(3H,s), 2.28(3H,s)CDCI3107~108418.16(1H,s), 7.26(1H,s), 7.30-6.84(4H,m), 2.72(3H,s), 2.40(3H,s), 2.24(3H,s)CDCl3125~126427.92(1H,d,J=9.0), 7.49(1H,d,J=9.0), 7.26-6.82(4H,m), 2.71(3H,s), 2.47(3H,s), 2.27(3H,s)CDCI3100~102438.16(1H,s), 7.53-6.88(4H,m), 7.05(1H,s), 2.70(3H,s), 2.33(3H,s), 2.22(3H,s)CDCl3159~161448.01(1H,d,J=9.0), 7.62(2H,d,J=8.8), 7.40(1H,d,J=9.0), 6.96(2H,d,J=8.8), 2.74(3H,s), 2.45(3H,s), 2.28(3H,s)CDCl3194~195458.19(1H,s), 7.63(2H,d,J=8.8), 7.40(1H,s), 6.98(2H,d,J=8.8), 2.73(3H,s), 2.44(3H,s), 2.26(3H,s)CDCI3189~192467.91(1H,d,J=9.0), 7.50(1H,d,J=9.0), 7.04(2H,m), 6.93(2H,m), 2.71(3H,s), 2.47(3H,s) 2.27(3H,s)CDCl3128~132478.14(1H,s),7.26(1H.s), 7.11(4H,m), 2.70(3H,s), 2.34(3H,s), 2.22(3H,s)CDCl3130~134487.89(1H,d,J=9.3), 7.30(1H,d,J=9.3), 7.15(2H,d,J=8.2), 6.88(2H,d,J=8.2), 2.71(3H,s), 2.47(3H,s), 2.34(3H,s), 2.27(3H,s)CDCl3118~120498.13(1H,s), 7.17(2H,d,J=8.3), 7.10(1H,s), 6.92(2H,d,J=8.3), 2.69(3H,s), 2.35(3H,s), 2.32(3H,s), 2.21(3H,s)CDCl3138~140507.87(1H,d,J=9.0), 7.25(1H,d,J=9.0), 6.96(2H,d,J=9.2), 6.89(2H,d,J=9.2), 3.80(3H,s), 2.70(3H,s), 2.48(3H,s), 2.27(3H,s)CDCl3120~121518.12(1H,s), 7.01(2H,d,J=9.0), 6.97(1H,s), 6.93(2H,d,J=9.0), 3.83(3H,s), 2.69(3H,s), 2.30(3H,s), 2.21(3H,s)CDCl3150~152527.92(1H,d,J=9.5), 7.35(1H,d,J=9.5), 7.25-6.51(4H,m), 3.77(3H,s), 2.71(3H,s), 2.46(3H,s), 2.27(3H,s)CDCl375~78538.14(1H,s)., 7.20(1H,s), 7.28-6.55(4H,m), 3.79(3H,s), 2.71(3H,s), 2.36(3H,s), 2.23(3H,s)CDCl397~98
    [0151] Table 17 547.84(1H,d,J=9.0), 7.19(1H,d,J=9.0), 7.16-6.87(4H,m), 3.83(3H,s), 2.69(3H,s), 2.48(3H,s), 2.27(3H,s)CDCl354~55558.12(1H,s), 7.03(1H,s), 7.22-6.87(4H,m), 3.81(3H,s), 2.68(3H,s), 2.26(3H,s), 2.20(3H,s)CDCl3179~180567.99(1H,d,J=8.9), 7.58(2H,d,J=8.6), 7.39(1H,d,J=8.9), 8.99(2H,d,J=8.6), 2.73(3H,s), 2.45(3H,s), 2.28(3H,s)CDCl3167~168618.16(1H,d,J=9.2), 7.62(2H,d,J=8.7), 7.28(1H,d,J=9.2), 7.04(2H,d,J=8.7), 2.74(3H,s), 2.42(3H,s), 2.27(3H,s)CDCl3105~107648.18(1H,s), 7.60(2H,d,J=8.6), 7.33(1H,s), 7.01(2H,d,J=8.6), 2.73(3H,s), 2.41(3H,s), 2.25(3H,s)CDCl3172~172.5688.44(1H,s), 7.65(2H,d,J=8.6), 7.18(1H,s), 7.13(2H,d, J=8.6), 2.75(3H,s), 2.36(3H,s), 2.27(3H,s)CDCl3138~139.5768.14(1H,d,J=9.0), 7.50-7.26(4H,m), 7.12(1H,d,J=9.0), 2.73(3H,s), 2.42(3H,s), 2.27(3H,s)CDCl391~93808.43(1H,s), 7.56-7.25(4H,m), 7.10(1H,s), 2.73(3H,s), 2.32(3H,s), 2.26(3H,s)CDCl372~74837.95(1H,d,J=8.9), 7.35(1H,d,J=8.9), 7.19(2H,d,J=9.2), 6.95(2H,d,J=9.2), 2.72(3H,s), 2.46(3H,s), 2.28(3H,s)CDCl3145~146867.88(1H,d,J=9.1),7.28(1H,d,J=9.1), 7.15(2H,d,J=8.8), 6.86(2H,d,J=8.8), 2.71(3H,s), 2.60(3H,s), 2.45(3H,s), 2.24(3H,s)CDCl3160~162867.76(1H,d,J=9.3),7.36(3H,m),7.00(2H,d,J=9.3),2.35(3H,s),1.94(3H,s)DMSO-d6-877.91(1H,d,J=9.1), 7.28(1H,d,J=9.1), 7.15(2H,d,J=8.8), 6.87(2H,d,J=8.8), 3.97(3H,s), 3.02(2H,q,J=7.4), 2.59(3H,s), 2.33(3H,s), 1.38(3H,t,J=7.4)CDCl3106~107908.10(1H,d,J=8.9), 7.28-7.20(4H,m), 6.99(1H,d,J=8.9), 2.73(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl3100~101.5918.13(1H,br,d),7.27-7.21(3H,m),6.99(2H,d,J=9),2.76(2H,q,J=7.4), 2.73(3H,s),2.25(3H,s),1.30(3H,t,J=7.6)CDCl3-928.12(1H,br.d),7.30-7.21(3H,m),6.99(2H,d,J=9.0),2.73(5H,m), 2.25(3H,s),1.76(2H,m),1.47(2H,m),0.99(3H,t,J=7.3)CDCl3-938.14(1H,br.d),7.27-7.22(3H,m),6.92(2H,d,J=9.3),2.73-2.69(5H,m), 2.35(2H,m),2.25(3H,s),1.78(2H,m),1.63(2H,m), 1.43-1.29(6H,m) 0.81(3H,t,J=9,2)CDCl3-958.11(1H,br.d),7.26-7.22(3H,m),6.99(2H,d,J=9.3),2.73(3H,s), 2.55(2H,d,J=7.1),2.26(3H,s),1.07(6H,d,J=6.6),0.91(1H,m)CDCl3-968.10(1H,br,d),7.26-7,22(3H,m),6,99(2H,d,J=9.0),2.72(3H,s),2.26(3H,s), 2.05(1H,m),1.19(2H,m),1.11(2H,m)CDCl3-978.10(1H,br.d),7.26-7.20(3H,m),6.99(2H,d,J=9.0),3.57 (1H,m),2.75(3H,s),2.52-2.38 (4H,m),2.25(3H,s),2.12 (2H,m),CDCl3-988.14(1H,br.d),728-7.20(3H,m),6.99(2H,d,J=9.3).6.71(1H,dd,J1=17.3, J2=1.2),6.43(1H,dd,J1=17.3,J2=10.5),6.13(1H,dd,J1=10.2,J2=1.0), 2.74(3H,s),2.25(3H,s),CDCl3-998.13(1H,br.d),7.27-7.20(3H,m),7.00(2H,d,J=9.3),6.48(1H,s),5.87(1H,s) 2.72(3H,s),2.24(3H,s),2.11(3H,s)CDCl3-1018.16(1H,br.d),7.30-7.21(3H,m),7.00(2H,d,J=9.3),3.96(3H,s), 2.75(3H,s),2.34(3H,s),CDCl3-1028.15(1H,br.d),7.30-7.21(3H,m),7.00(2H,d,J=9.0),4.36(2H,q,J=7.0), 2.74(3H,s),2.34(3H,s),1.41(3H,t,J=7.2)CDCl3-
    [0152] Table 18 1038.16(1H,br.d),7.30-7.21(3H,m),7.00(2H,d,J=9.3),4.30(2H,t,J=6.6), 2.75(3H,s),2.34(3H,s),1.76(2H,m),1.50(2H,m),0.98(3H,t,J=7.4)CDCl3-1048.16(1H,br.d),7.30-7.21(3H,m),7.00(2H,d,J=9.3),4.30(2H,t,J=6.7), 2.74(3H,s),2.34(3H,s),1.76(2H,m),1.50-1.0(10H,m),0.88(3H,t,J=7.1)CDCl3-1058.19(1H,br.d),7.43(2H,t,J=8.0),7.32-7.22(6H,m),7.00(2H,d,J=9.0), 2.77(3H,s),2.44(3H,s),CDCl3-1068.16(1H,br.d),7.30-7.21(3H,m),6.99(2H,d,J=8.8),4.07(2H,d,J=6.6), 2.75(3H,s),2.34(3H,s),2.08(1H,m),1.01(6H,d,J=6.6)CDCl3-1078.14(1H,bd.d),7.30-7.21(3H,m).6.99(2H,d,J=9.0),6.01(1H,m), 5.46(1H,dd,J1=17.3,J2=1.5),5.36(1H,dd,J1=10.5,J2=1.2), 4.78(2H,dt,J1=5.8,J2=1.2),2.74(3H,s),2.34(3H,s),CDCl3-1088.20(1H,br.d),7.32-7.22(3H,m),7.00(2H,d,J=9.0),4.91(2H,s), 2.76(3H,s),2.37(3H,s),CDCl3-1108.17(1H,br.d),7.30-7.21(3H,m),6.99(2H,d,J=9.3),2.75(3H,s), 2.47(3H,s),2.32(3H,s)CDCl3-1117.79(1H,d,J=9.3),7.38-7.35(3H,m),7.01(2H,d,J=8),2.67(2H,q,J=7.5), 1.97(3H,s),1.22(3H,t,J=7.5)DMSO-d6-1128.16(1H,d,J=9.1), 7.28(1H,d,J=9.1), 7.21(2H,d,J=9.0), 6.99(2H,d,J=9.0), 3.94(3H,s), 3.03(2H,q,J=7.2), 2.35(3H,s), 1.39(3H,t,J=7.2)CDCl3oil1148.16(1H,d,J=9.3), 7.30-6.97(5H,m), 3.23(2H,t,J=7.7), 2.97(2H,t,J=7.4), 2.39(3H,s), 2.30-2.20(2H,m)CDCl3108.5~1101158.11(1H,d,J=9.3), 7.28-6.96(5H,m), 3.12(2H,broad), 2.62(2H,broad), 2.41(3H,s), 2.00(2H,broad), 1.90(2H,broad)CDCl3105~1071168.16(1H,s), 7.23(2H,d,J=8.8), 7.14(1H,s), 7.01(2H,d,J=8.8), 2.71(3H,s), 2.35(3H,s), 2.23(3H,s)CDCl3145~1471187.90(1H,s), 7.21(2H,d,J=8.8), 7.01(1H,s), 6.98(2H,d,J=8.8), 2.70(3H,s), 2.40(3H,s), 2.34(3H,s), 2.22(3H,s)CDCl3141~1431207.94(1H,s), 7.20(2H,d,J=8.8), 7.14(1H,s), 6.97(2H,d,J=8.8), 3.88(3H,s), 3.01(2H,q,J=7.6), 2.41(3H,s), 2.31(3H,s), 1.38(3H,t,J=7.6)CDCl3118.5~1201217.94(1H,s), 7.20(2GH,d,J=8.8, 6.99(1H,s), 6.97(2H,d,J=8.8), 3.00(2H,q,J=7.5), 2.40(3H,s), 2.35(3H,s), 2.25(3H,s), 1.37(3H,t,J=7.5)CDCl3-1228.41(1H,s), 7.28(2H,d,J=8.9), 7.12(2H,d,J=8.9), 6.98(1H,s), 2.73(3H,s), 2.30(3H,s), 2.25(3H,s)CDCl3109~110.51238.45(1H,s), 7.26(2H,d,J=8.7), 7.13(1H,s), 7.11(2H,d,J=8.7), 3.86(3H,s), 3.02(2H,q,J=7.7), 2.33(3H,s), 1.40(3H,t,J=7.7)CDCl3117~118.51248.60(1H,s), 7.31(2H,d,J=8.9), 7.19(2H,d,J=8.9), 6.92(1H,s), 2.41(3H,s), 2.30(6H,s)CDCl3163~164.51258.42(1H,s), 7.28-7.09(5H,m), 3.22(2H,t,J=7.8), 2.95(2H,t,J=7.5), 2.30(3H,s), 2.26-2.19(2H,m)CDCl3135~1371268.40(1H,s), 7.27(2H,d,J=7.0), 7.12(2H,d,J=7.0), 6.99(1H,s), 3.14(2H,t,J=6.4), 2.74(2H,t,J=6.3), 2.29(3H,s), 2.05-1.83(4H,m)CDCl3155~1571278.15(1H,s), 7.15(2H,d,J=9.0), 6.83(2H,d,J=9.0), 2.74(3H,s), 2.43(3H,s), 2.26(3H,s)CDCl3160~1621327.79(1H,s), 7.11(2H,d,J=9.0), 6.74(2H,d,J=9.0), 2.70(3H,s), 2.51(3H,s), 2.41(3H,s), 2.26(3H,s), 2.22(3H,s)CDCl3159~1611337.79(1H,s), 7.11(2H,d,J=9.0), 6.74(2H,d,J=8.0), 3.94(3H,s), 2.71(3H,s), 2.50(3H,s), 2.28(3H,s), 2.26(3H,s)CDCl3146~148
    [0153] Table 19 1357.83(1H,s), 7.11(2H,d,J=8.8), 6.75(2H,d,J=8.8), 3.94(3H,s), 3.01(2H,q,J=7.6), 2.50(3H,s), 2.30(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.6)CDCl3140~1421368.35(1H,s),7.15(2H,d,J=8.7), 6.81(2H,d,J=8.7), 2.74(3H,s), 2.40(3H,s), 2.26(3H,s)CDCl3110~1131377.20(2H,d,J=9.0), 7.10(1H,s), 6.96(2H,d,J=9.0), 2.72(6H,s), 2.40(3H,s), 2.25(3H,s)CDCl3110~111.51388.40(1H,s), 7.14(2H,d,J=8.8), 6.80(2H,d,J=8.8), 2.76(3H,s), 2.42(3H,s), 2.30(3H,s)CDCl3135~1371417.89(1H,d,J=9.1), 7.31-6.74(5H,m), 2.70(3H,s), 2.59(3H,s), 2.44(3H,s), 2.24(3H,s)CDCI386~871438.14(1H,d,J=9.3), 7.36-6.86(5H,m), 2.73(3H,s), 2.42(3,s), 2.27(3H,s)CDCl364~661457.92(1H,s), 7.36-6.74(5H,m), 2.69(3H,s), 2.39(3H,s), 2.37(3H,s), 2.22(3H,s)CDCl3-1478.42(1H,s), 7.42-6.70(5H,m), 2.73(3H,s), 2.33(3H,s), 2.26(3H,s)CDCl389~911517.98(1H,d,J=9.1), 7.60(2H,d,J=8.7), 7.39(1H,d,J=9.1), 6.94(2H,d,J=8.7), 2.73(3H,s), 2.45(3H,s), 2.28(3H,s)CDCl3147~1511568.16(1H,d,J=9.2),7.64(2H,d,J=8.5), 7.30(1H,d,J=9.2), 6.99(2H,d,J=8.5), 2.74(3H,s), 2.42(3H,s), 2.27(3H,s)CDCl387~891598.17(1H,s). 7.64(2,d,J=8.6), 7.28(1H,s), 6.99(2H,d,J=8.6), 2.72(3H,s), 2.39(3H,s), 2.24(3H,s)CDCl3109~1101637.69(1H,s), 7.69(2H,d,J=8.7), 7.11(2H,dd,J=8.7,J=1.6), 2.74(3H,s), 2.33(3H.s), 2.26(3H,s)CDCl3115~1171657.84(1H,s), 7.55(2H,d,J=8.7), 6.79(2H,d,J=8.7), 3.94(3H,s), 3.01(2H,q,J=7.7), 2.50(3H,s), 2.31(3H,s), 2.25(3H,s), 1.38(3H,t,J=7.7)CDCl3137~1381678.24(1H,d,J=9.2), 8.02(2H,d,J=8.8), 7.33(1H,d,J=9.2), 7.15(2H,d,J=8.8), 2.76(3H,s), 2.42(3H,s), 2.28(3H,s)CDCl3131~1331688.49(1H,s), 8.02(2H,d,J=8.8), 7.36(1H,s), 7.20(2H,d,J=8.8), 2.77(3H,s), 2.42(3H,s), 2.30(3H,s)CDCl3193~1951827.88(1H,d,J=9.0), 7.28(1H,d,J=9.0), 7.14(2H,d,J=8.8), 6.86(2H,d,J=8.8), 5.99(1H,tt,J=53.1,J=2.8),2.71(3H,s), 2.61(3H,s), 2.45(3H,s), 2.24(3H,s)CDCl3146~1481837.91(1H,d,J=9.1), 7.29(1H,d,J=9.1), 7.14(2H,d,J=9.0), 6.86(2H,d,J=9.0), 5.90(1H,tt,J=52.9,J=2.3), 3.97(3H,s), 3.02(2H,q,J=7.2), 2.60(3H,s), 2.33(3H.s). 1.38(3H,t,J=7.2)CDCI3103~104.51858.12(1H,d,J=9.2), 7.27(1H,d,J=9.2), 7.21(2H,d,J=9.0), 6.99(2H,d,J=9.0), 5.92(1H,tt,J=53.1,J=2.7), 2.73(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl388~911868.16(1 H,s,J=9.4), 7.28(1 H,d,J=9.4), 7.20(2H,d,J=9.0), 6.98(2H,d,J=9.0), 5.91(1H,tt,J=53.1,J=2.8), 3.95(3H,s), 3.03(2H,q,J=7.7), 2.35(3H,s), 1.38(3H,t,J=7.7)CDCl3oil1897.89(1H,s), 7.20(2H,d,J=8.9), 7.01(1H,s), 6.98(2H,d,J=8.9), 5.92(1H,tt,J=53.4,J=2.8), 2.70(3H,s), 2.41(3H,s), 2.34(3H,s), 2.22(3H,s)CDCl3126~1281907.94(1H,s), 7.20-6.95(5H,m), 5.92(1H,tt,J=53.1,J=2.9), 3.88(3H,s), 3.00(2H,q,J=7.7), 2.42(3H,s), 2.31(3H,s), 1.37(3H,t,J=7.7)CDCl3106.5~108.51928.40(1H,s), 7.27(2H,d,J=9.1), 7.12(2H,d,J=9.1), 6.96(1H,s), 5.94(1H,tt,J=53.1,J=2.8), 2.72(3H,s), 2.29(3H,s), 2.25(3H,s)CDCl3122~1241938.45(1H,s), 7.26-7.08(5H,m), 5.93(1H,tt,J=53.0,J=2.8), 3.86(3H,s), 3.02(2H,q,J=7.4), 2.33(3H,s), 1.40(3H,t,J=7.4)CDCl3104~106
    [0154] Table 20 1977.82(1H,s), 7.09(2H,d,J=9.0), 6.74(2H,d,J=9.0), 5.89(1H,tt,J=53.1,J=2.6), 3.94(3H,s), 3.01(2H,q,J=7.2), 2.51(3H,s), 2.30(3H,s), 2.26(3H.s). 1.38(3H,t,J=7.2)CDCl3155~1572087.83(1H,s), 7.27-6.63(4H,m), 5.85(1H,tt,J=53.1,J=2.9), 3.94(3H,s), 3.01(2H,q,J=7.8), 2.50(3H,s), 2.31(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.8)CDCl396~97.52098.06(1H,d,J=9.3), 7.22(1H,d,J=9.3), 6.97(4H,s,), 4.34(2H,q,J=8.4), 2.71(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl390.5~91.52128.38(1H,s), 7.11-6.99(4H,m), 6.93(1H,s), 4.38(2H,q,J=8.5), 2.71(3H,s), 2.29(3H,s, 2.24(3H,s)CDCl3149.5~1502138.03(1H,d,J=9,4), 7.25-6.87(5H,m), 4.49(1H,m,J=6.0), 2.71(3H,s), 2.42(3H,s), 2.25(3H,s), 1.34(6H,d,J=6.0)CDCl3115~1172148.36(1H,s), 7.06(2H,d,J=9.0), 6.94(2H,d,J=9.0), 6.89(1H,s), 4.54(1H,m,J=6.1) 2.70(3H,s), 2.27(3H,s), 2.23(3H,s), 1.36(6H,d,J=6.1)CDCl3113~1152158.10(1H,d,J=9.0), 7.50(1H,s), 7.23-7.12(2H,m), 6.81(1H,d,J=9.0), 2.72(3H,s), 2.43(3H,s), 2.26(3H,s)CDCl392~942168.42(1H,s), 7.55-7.00(3H,m), 6.86(1H,s), 2.72(3H,s), 2.33(3H,s), 2.24(3H,s)CDCl3145~146.52178.20(1H,d,J=9.0), 7.64(1H,s), 7.37(2H,s), 7.28(1H,d,J=9.0), 2.75(3H,s), 2.42(3H,s), 2.28(3H,s)CDCI3125~1272188.47(1H,s), 7.67(1H,s), 7.49(2H,s), 7.24(1H,s), 2.76(3H,s), 2.37(3H,s), 2.28(3H,s)CDCl3134~1362228.17(1H,d,J=9,2), 7.77(1H,s), 7.45(1H,d,J=8.6), 7.21(1H,d,J=9.2), 6.85(1H,d,J=8.6), 2.74(3H,s), 2.42(3H,s), 2.27(3H,s)CDCl3110~1122288.45(1H,s), 7.81(1H,s), 7.50(1H,d,J=8.6), 7.04(1H,s), 7.01(1H,d,J=8.6), 2.74(3H,s), 2.34(3H,s), 2.27(3H,s)CDCl3123~1252478.15(1H,d,J=9.1), 7.28-6.76(4H,m), 2.73(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl3100~101.52488.42(1H,s), 7.18-6.86(4H,m), 2.74(3H,s), 2.36(3H,s), 2.27(3H,s)CDCl3104~1052497.89(1H,d,J=9.0), 7.39-6.99(3H,m), 6.64(1H,d,J=9.0), 2.71(3H,s), 2.62(3H,s), 2.45(3H,s), 2.24(3H,s)CDCl3149~1512507.91(1H,d,J=9.2), 7.39-6.99(3H,m), 6.63(1H,d,J=9.0), 3.97(3H,s), 3.02(2H,q,J=7.1), 2.61(3H,s), 2.33(3H,s), 1.38(3H,t,J=7.1)CDCl3112~1142527.77-7.76(2H,m),7.36-7.33(2H,m),6.88(1H,d,J=9.2), 2.35(3H,s),1.95(3H,s)DMSO-d6-2538.12(1H,d,J=9.2), 7.41-7.10(4H,m), 6.88(1H,d,J=9.2), 2.73(3H,s), 2.43(3H,s), 2.27(3H,s)CDCl378~802548.17(1H,d,J=9.1), 7.41-7.09(3H,m), 6.87(1H,d,J=9.1), 3.96(3H,s), 3.03(2H,q,J=7.2), 2.36(3H,s), 1.39(3H,t,J=7.2)CDCl3oil2567.91(1H,s), 7.42-6.85(4H,m), 2.70(3H,s), 2.42(3H,s), 2.34(3H,s), 2.22(3H,s)CDCl3126~1282577.95(1H,s), 7.41-6.85(4H,m), 3.88(3H,s), 3.00(2H,q,J=7.7), 2.44(3H,s), 2.31(3H,s),1.37(3H,t,J-7.7)CDCl3117~118.52598.42(1H,s), 7.46-7.11(4H,m), 6.80(1H,s), 2.72(3H,s), 2.28(3H,s), 2.25(3,s)CDCl3110~1112608.46(1H,s), 7.44-7.09(3H,m), 6.93(1H,s), 3.86(3H,s), 3.02(2H,q,J=7.5), 2.33(3H,s), 1.39(3H,t,J=7.5)CDCl3119~121
    [0155] Table 21 2627.84(1H,s), 7.39(1H,d,J=1.7), 6.92(1H,dd,J=9.0,J=1.7), 6.32(1 H,d,J=9.0), 3.94(3H,s), 30.1(2H,q,J=7.5), 2.50(3H,s), 2.31(3H,s), 2.26(3H,s)1.38(3H,t,J=7.5)CDCl3116~1172698.16(1H,d,J=9.1), 7.32-6.85(4H,m), 2.74(3H,s), 2.42(3H,s), 2.27(3H,s)CDCl3115~1172758.43(1H,s), 7.35-6.96(4H,m), 2.74(3H,s), 2.37(3H,s), 2.27(3H,s)CDCl3116~1182777.84(1 H,s), 7.20(1H,d,J=8.9), 6.87(1 H.d,J=2.8). 6.65(1H,dd,J=8.9,J=2.8), 3.95(3H,s), 3.01(2H,q,J=7.3), 2.50(3H,s), 2.31(3H,s), 2.26(3H,s), 1.38(3H,t,J=7,3)CDCl3164~1652798.12(1H,d,J=9.1), 7.31-6.97(4H,m), 2.72(3H,s), 2.42(3H,s), 2.26(3H,s)CDCl371~72.52808.41(1H,s), 7.32-6.87(4H,m), 2.72(3H,s), 2.28(3H,s), 2.24(3H,s)CDCl3119.5~1212818.17(1H, d, J=9.1), 7.94(1H,s), 7.51(1H,d,J=8.3), 7.22(1H,d,J=9.1), 6.81(1H,d,J=8.3), 2.74(3H,s), 2.43(3H,s), 2.27(3H,s)CDCl3ooil2828.46(1H,s), 7.97(1H,s),7.55(1H,d,J=8.5), 7.06(1H,s),6.98(1H,d,J=8.5), 2.74(3H,s), 2.35(3H,s), 2.27(3H,s)CDCl3108~1093088.08(1H,d,J=9.1), 7.16-7.01(3H,m), 6.75(1H,d,J=9.1), 2.72(3H,s), 2.43(3H,s), 2.33(3H,s), 2.26(3H,s)CDCl385.5~86.53128.40(1H,s), 7.21-7.04(3H,m), 6.67(1H,s), 2.71(3H,s). 2.23(9H,s)CDCl3103~1043147.83(1H,s), 7.12(1H,s), 6.81(1H,d,J=8.8), 6.16(1H,d,J=8.8), 3.94(3H,s), 3.01(2H,q,J=7.5), 2.48(3H,s), 2.47(3H,s), 2.31(3H,s), 2.23(3H,s), 1.28(3H.t.J=7.5)CDCl3126~1273247.91(1H,d,J=9.2), 7.38(1H,d,J=2.4), 7.24(H1,d,J=9.2), 7.00(1H,tt,J=8.9,J=2.4), 6.64(1H,d,J=8.9), 5.90(1H,tt,J=53.1,J=2.8), 3.97(3H,s,), 3.02(2H,g,J=7.3), 2.62(3H.s). 2,33(3H,s), 1.38(3H,t,J=7.3)CDCl394~95.53288.15(1H,d,J=9.1), 7.40-6.97(3H,m), 6.86(1H,d,J=9.1), 5.92(1 H,tt,J=53.0,J=2.6), 3.03(2H,q,J=7.4), 2.43(3H,s), 2.29(3H,s), 1.38(3H,t,J=7.4)CDCl3oil3327.95(1 H,s), 7.40(1H,d,J=2.6), 7.08(1 H,dd,J=9.0,J=2.6), 7.01(1 H,s), 6.88(1H,d,J=9.0), 5.93(1H,tt,J=52.9,J=2.5), 3.88(3H,s), 3.00(2H,g,J=7,5), 2.45(3H,s), 2.31(3H,s), 1.37(3H,t,J=7.5)CDCl3116~1173377.84(1 H,s), 7.38(1 H,d,J=2.4), 6.90(1H,dd,J=9.0,J=2.4), 6.31(1H,d,J=9.0), 5.89(1 H,tt,J=53.0,J=2.7), 3.94(3H,s), 3.01(2H,g,J=7.6), 2.51(3H,s), 2.31(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.6)CDCl3157.5~1593518.05(1H,br,d),7.71(2H,s),6.82(1H,d),2.71(3H,s),2.45(3H,s),2.26(3H,s)CDCl3-3528.45(1H,br,d),7.76(2H,s),6.45(2H,s),2.71(3H,s),2.23(6H,s)CDCl3-3538.05(1H,d,J=9.3), 7.35(2H,s), 6.84(1H,d,J=9.3), 2.71(3H,s), 2.45(3H,s), 2.26(3H,s)CDCl3116~1183548.43(1H,s), 7.41(2H,s), 6.45(1H,s), 2.71(3H,s), 2.23(6H,s)CDCl3139~140.53638.11(1H,d,J=9.2), 7.60-7.00(9H,m), 2.72(3H,s), 2.43(3H,s), 2.26(3H,s)CDCl3129~1303648.41(1H,s), 7.60-7.04(9H,m), 2.73(3H,s), 2.34(3H,s), 2.26(3H,s)CDCl3120~1243658.13(1H,d,J=9.2), 7.68-7.07(8H,m), 2.73(3H,s), 2.43(3H,s), 2.27(3H,s)CDCl3132~1343668.43(1H,s), 7.70-7.16(8H,m), 2.74(3H,s), 2.32(3H,s), 2.26(3H,s)CDCl3180~181
    [0156] Table 22 3677.91(1H,d,J=9.0),7.44-7.35(5H,m), 5.21(2H,s), 2.68(3H,s), 2.47(3H,s), 2.25(3H,s)CDCl3132~1343688.07(1H,s), 7.44(2H,s,J=8.3), 7.39(2H,d,J=8.3), 6.97(2H,s), 5.49(2H,s), 2.67(3H,s), 2.46(3H,s), 2.22(3H,s)CDCl3195~1973698.06(1H,d,J=8.6), 7.76(2H,d,J=8.3), 7.51(1H,d,J=8.6), 7.44(2H,d,J=8.3), 2.76(3H,s), 2.41(3H,s), 2.28(3H,s)CDCl3179~1813708.12(1H,s), 7.76(2H,d,J=8.3), 7.75(1H,s), 7.46(2H,d,J=8.3), 2.76(3H,s), 2.44(3H,s), 2.27(3H,s)CDCl3186~1883717.75(1H,d,J=9.0), 7.45(2H,d,J=8.6), 7.40(2H,d,J=8.6), 7.08(1H,d,J=9.0), 2.68(3H,s), 2.48(3H,s), 2.25(3H,s)CDCl3143~1443728.05(1H,s), 7.43(4H,s), 7.02(1H,s),2.68(3H,s), 2.23(3H,s), 2.19(3H,s)CDCl3162~1633738.21(1H,d,J=8.7), 8.15(1H,d,J=8.7), 7.70(2H,d,J=8.7), 7.42(2H,d,J=8.7), 2.72(3H,s), 2.46(3H,s), 2.24(3H,s)CDCl3158~159.53748.56(1H,d,J=9.0), 8.13(1H,d,J=9.0), 7.87,2H,d,J=8.3), 7.48(2H,d,J=8.3), 2.74(3H,s), 2.40(3H,s), 2.23(3H,s)CDCl3234~2373758.60(1H,d,J=8.9), 8.21(1H,d,J=8.9), 7.87(2H,d,J=8.5), 7.49(2H,d,J=8.5), 5.39(2H,s), 2.42(3H,s), 2.26(3H,s), 2.20(3H,s)CDCl3163~1653768.78(1H,s), 8.06(1H,s), 7.89(2H,d,J=8.7), 7.49(2H,d,J=8.7), 2.75(3H,s), 2.59(3H,s), 2.29(3H,s)CDCl3161~1643777.88(1H,d,J=8.7), 7.41(1H,d,J=8.7), 7.25(2H,d,J=8.3), 7.11(2H,d,J=8.3), 4.24(2H,s), 2.70(3H,s), 2.46(3H,s), 2.25(3H,s)CDCl3173~1743788.06(1H,s), 7.30-7.11(5H,m), 4.20(2H,s), 2.70(3H,s), 2.38(3H,s), 2.23(3H,s)CDCl3178~1803977.71(1H,s), 7.57(2H,d,J=8.7), 7.01(2H,d,J=8.7), 4.32(2H,t,J=6.0), 3.98-3.94(5H,m), 2.97(2H,q,J=7.2), 2.59(3H,s), 2.39(3H,s), 2.34-2.31(2H,m), 2.27(3H,s), 1,34(3H,s)CDCl3101.5~102.54247.90(1H,br.s), 7.44(1H,d,J=8.3), 7.30(1H,d,J=9.0), 7.13(1H,d,J=2.9), 6.93(1H,dd,J=9.0,J=2.9), 3.95(3H,s), 2.76(3H,s), 2.31(3H,s)CDCl3-4257.81(1H,d,J=11.5), 7.35(1H,d,J=6.3), 7.29(1H,dq,J=9.0,J=1.2), 7.10(1H,d,J=2.9), 6.91(1H,dd,J=9.0,J=2.9), 2.73(3H,s). 2.44(3H,s), 2.25(3H,s)CDCl3-4337.52(1H,s), 7.38(1H,d,J=1.7), 7.21(1H,s), 7.04(1H,d,J=9.0), 6.79(1H,d,J=9.0), 3.95(3H,s), 3.91(3H,s), 3.01(2H,q,7.4). 2.30(3H,s), 1.38(3H,t,J=7.4)CDCl3107~1084358.40(1H,s), 7.49(2H,d,J=8.4), 7.29(2H,d,J=8.4), 7.25(1H,s), 2.72(3H,s), 2.24(3H,s), 2.22(3H,s)CDCl3126.5~128.54368.46(1H,s), 7.58(1H,s), 7.42(2H,d,J=8.6), 7.28(2H,d,J=8.6), 2.78(3H,s), 2.47(3H.s). 2.30(3H.s)CDCl3183~1854378.90(1H,s), 8.51(1H,s), 7.89(2H,d,J=8.5), 7.32(2H,d,J=8.5),2.81(3H,s), 2.60(3H,s), 2.36(3H,s)CDCl3173~1754388.38(1H, s), 7.28(2H, d, J=9.2), 7.15(2H, d, J=9.2), 7.00(1H,s), 3.03(3H,s), 2.94(3H,s), 2.71(3H,s), 2.28(3H,s)CDCl388~89.54398.40(1H,s), 7.32-7.18(5H,m), 3.18(3H,s), 2.74(3H,s), 2.46(3H,s)CDCI3148~1494408.33(1H,s), 7.52(2H,d,J=8.6), 7.27(2H,d,J=8.6),5.25(2H,s), 2.71(3H,s), 2.48(3H,s), 2.26(3H,s)CDCI3183~1844418.39(1H,s), 7.42(1H,s), 7.25(2H,d,J=9.1), 7.11(2H,d,J=9.1), 3.80(3H,s), 2.69(3h,s), 2.38(3H,s)CDCI3106~108
    [0157] Table 23 4428.35(1H,s), 7.29-6.87(5H,m), 2.72(3H,s), 2.30(3H,s), 2.24(3H,s)CDCl395~964438.40(1H,s), 7.27-6.88(5H,m), 3.86(3H,s), 3.02(2H,q,J=7.5), 2.33(3H,s), 1.40(3H,t,J=7.5)CDCl3115~116.54448.64(1H,s), 7.26-7.16(3H,m), 6.99(2H,d,J=8.9), 3.84(3H,s), 2.73(3H,s), 2.26(3H,s), 2.26(3H,s)CDCl3165~1674477.76(1H,s), 7.29-7.26(1H,d), 7.23(2H,d,J=9.1), 7.03(2H,d,J=9.1), 2.73(3H,s), 2.39(3H,s), 2.24(3H,s)CDCl3-44811.60(1H,s), 7.67(1H,d,J=9.0), 7.42-7.38(3H,m), 7.14(2H,d,J=9.3), 2.36(3H,s), 1.93(3H,s)DMSO-d6-4497.81(1H,br.s), 7.34(1H,d,J=9.5), 7.22(2H,d,J=8.9), 7.04(2H,d,J=8.9), 3.92(3H,s), 2.73(3H,s), 2.36(3H,s)CDCl3-4507.67(1H,d,J=10.2), 7.17(2H,d,J=8.8), 6.97(2H,d,J=8.8), 3.94(3H,s), 2.73(3H,s), 2.34(3H,s)CDCl3-4517.65(1H,br.s), 7.17(2H,d,J=9.0), 6.95(2H,d,J=9.0), 2.73(3H,s), 2.41(3H,s), 2.28(3H,s)CDCl3 4527.26(2H,d,J=8.8), 7.04(2H,d,J=8.8), 7.01(1H,s), 2.79(3H,s), 2.31(3H,s), 2.26(3H,s)CDCl3123.5~125.54537.88(1H, d,J=9.0), 7.49(2H,d,J=8.7), 7.27-7.22(3H,m), 2.70(3H,s), 2.42(3H,s), 2.24(3H,s)CDCl3104.5~106.54548.16(1H,d,J=8.7), 7.52(1H,d,J=8.7), 7.43(2H,d,J=8.6), 7.29(2H,d,J=8.6), 2.76(3H,s), 2.43(3H,s), 2.28(3H,s)CDCl3128~1304558.45(1H,d,J=8.9), 8.31(1H,d,J=8.9), 8.01(2H,J=8.6), 7.37(2H,d,J=8.69, 2.77(3H,s), 2.41(3H,s), 2.26(3H,s)CDCl3131~1334568.11(1H,d,J=9.4), 7.26-6.96(5H,m), 3.24(3H,s), 3.04(3H,s), 2.71(3H,s), 2.29(3H,s)CDCl3110~1124578.08(1H,d,J=9.2), 7.32-7.02(5H,m), 3.28(3H,s), 2.73(3H,s), 2.54(3H,s)CDCl3123~1254588.07(1H,d,J=9.2), 7.24(1H,d,J=9.2), 7.21(2H,d,J=8.2), 7.00(2H,d,J=8.2), 3.73(3H,s9, 2.69(3H,s), 2.44(3H,s)CDCl393~854598.03(1H,d,J=9.0), 7.26-7.02(5H,m), 3.95(3H,s), 2.72(3H,s), 2.40(3H,s), 2.22(3H,s)CDCl3113~1144607.85(1H,d,J=8.8), 7.38(1H,t,J=8.8), 7.18(2H,d,J=9.1), 6.98(2H,d,J=9.1), 2.73(3H,s), 2.42(3H,s), 2.30(3H,s)CDCl3-4618.15(1H,d,J=9.3), 7.28(1H,d,J=9.3), 7.22(2H,d,J=8.8), 6.99(2H,d,J=8.8), 4.45(2H,s), 3.56(3H,s), 2.74(3H,s), 2.27(3H,s)CDCl3-4628.15(1H,d,J=8.9), 7.28(1H,d,J=8.9), 7.22(2H,d,J=9.2), 6.99(2H,d,J=9.2), 4.98(2H,s), 2.74(3H,s), 2.30(3H,s), 2.21(3H,s)CDCl3-4647.77(1H,s), 7.52(2H,d,J=8.6), 7.27(2H,d,J=8.6), 4.82(2H,s), 3.97(3H,s), 2.99(2H,q,J=7.3), 2.63(3H,s), 2.46(3H,s), 2.29(3H,s), 1.36(3H,t,J=7.3)CDCl3121~1224657.94(1H,s), 7.20(2H,d,J=8.6), 6.99(2H,d,J=8.6), 3.00(2H,q,J=7.2), 2.59(2H,t,J=7.6), 2.41(3H,s), 2.23(3H,s), 1.70(2H,m), 1.39-1.28(10H,m), 0.89(3H,t,J=7.2)CDCl3-4667.96(1H,s), 7.21(2H,d,J=8.8), 6.99(2H,d,J=8.8), 6.97(1H,s), 4.33(2H,s), 3.46(3H,s), 3.01(2H,q,J=7.5), 2.42(3H.s), 2.25(3H,s), 1.38(3H,t,J=7.5)CDCl3-4677.95(1H,s), 7.21(2H,d,J=8.8), 7.08(1H,s), 6.98(2H,d,J=8.8), 4.86(2H,s), 3.00(2H,q,J=7.6), 2.41(3H,s), 2.26(3H,s), 2.14(3H,s),1.37(3H,t,J=7.6)CDCl3-
    [0158] Table 24 4687.94(1H,s), 7.46(1H,s), 7.19(2H,d,J=8.9), 6.98(2H,d,J=8.9), 4.51(2H,s), 3.75(3H,s), 2.98(2H,q,J=7.5), 2.41(3H,s), 2.40(3H,s), 1.36(3H,t,J=7.5)CDCl3-4697.92(1 H,s), 7.22(2H,d,J=8.8), 7.02(2H,d,J=8.8), 6.98(1 H,s), 3.00(2H,q,J=7.6), 2.42(3H,s), 2.25(3H,s), 1.89(1H,m), 1.36(3H,t,J=7.6), 1.10(2H.m). 1,02(2H.m)CDCl3-4707.94(1H,s), 7.41(1H,s), 7.19(2H,d,J=8.8), 6.97(2H,d,J=8.8), 3.83(3H,s), 3.99(2H,q,J=7.6), 2.40(3H,s), 2.38(3H,s), 1.36(3H,t,J=7.6)CDCl3-4717.94(1H,s), 7.38(1H,s), 7.19(2H,d,J=8.8), 6.99(2H,d,J=8.8), 5.17(2H,s), 3.83(2H,t,J=4.6), 3.47(2H,t,J=4.6), 3.33(3H,s), 3.00(2H,q,J=7.6), 2.41(3H,s), 2.39(3H,s), 1.36(3H,t,J=7.6)CDCl3-4727.49(1H,s), 7.19(2H,s,J=8.7), 7.12(1H,s), 6.98(2H,d,J=8.7), 3.95(3H,s), 2.70(3H,s), 2.36(3H,s), 2.21(3H,s)CDCl3126~1284737.52(1H,s), 7.24(1H,s), 7.18(2H,d,J=8.8), 6.98(2H,d,J=8.8), 3.96(3H,s), 3.90(3H,s), 3.01(2H,q,J=7.3), 2.30(3H,s), 1.38(3H,t,J=7.3)CDCl3115~1164968.45(1H,s), 7.45-7.10(3H,m), 6.78(1H,s), 5.95(1H,tt,J=53.1,J=2.8), 3.01(2H,q,J=7.7), 2.28(3H,s), 2.27(3H,s), 1.39(3H,t,J=7.7)CDCl3126~1284977.62(1H,s), 7.22(1H,s), 7.17(2H,d,J=9.1), 6.99(2H,d,J=9.1), 5.91(1H,tt,J=52.9,J=2.3), 3.97(3H,s), 3.90(3H,s), 3.01(2H,q,J=7.3), 2.30(3H.s). 1.38(3H,s,J=7.3)CDCl3107.5~108.55397.90(1H,d,J=9.0),7.29(1H,d,J=9.0), 7.11(2H,d,J=9.0), 6.86(2H,d,J=9.0), 6.06(1H,dt,J=53.4,J=2.5), 3.97(3H,s), 3.02(2H,q,J=7.7), 2.60(3H,s), 2.32(3H.s). 1.38(3H.t.J=7.7)CDCl3oil5407.94(1H,s), 7.17(1H,s), 7.13(2H,d,J=7.2), 6.97(2H,d,J=7.2), 6.08(1H,dt,J=53.4,J=2.5), 3.87(3H,s), 3.00(2H,q,J=7.6),2.41(3H,s), 2.31(3H,s), 1.37(3H,t,J=7.6)CDCI384~865417.83(1H,s), 7.07(2H,d,J=8.9), 6.74(2H,d, J=8.9), 6.05(1H,dt,J=53.4,J=2.4), 3.94(3H,s), 3.01(2H,q,J=7.2), 2.50(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.2).CDCI386~885697.81(1H,J=11.2), 7.43(1H,d,J=8.3), 7.41(1H,d,J=8.9), 7.12(1H,d,J=2.9), 6.88(1H,dd,J=8.9,J=2.9), 3.96(3H,s), 2.74(3H,s), 2.30(3H,s)CDCI3-5728.04(2H,d,J=8.9), 7.83(1H,br,s), 7.40(1H,d,J=8.5), 7.01(2H,d,J=8.9), 4.73(2H,q,J=7.2), 2.73(3H,s), 2.43(3H,s), 2.25(3H,s), 1.39(3H,t,J=7.2)CDCI3-5738.01(2H,d,J=8.9), 7.87(1H,dd,J=9.0,J=1.5), 7.42(1H,t,J=9.0), 6.97(2H,d,J=8.9), 4.36(2H,q,J=7.1), 2.73(3H,s), 2.40(3H,s), 2.30(3H,s), 1.38(3H,t,J=7.1)CDCl3-5747.83(1H,d,J=9.0), 7.26(1H,d,J=9.0), 7.10(2H,d,J=8.5), 6.78(2H,d,J=8.5), 2.70(3H,s). 2.62(3H,s), 2.44(3H,s), 2.31(3H,s), 2.23(3H,s)CDCl3106~1075757.87(1H,s), 7.15(2H,d,J=8.6), 6.99(1H,s), 6.87(2H,d,J=8.6), 2.68(3H,s), 2.42(3H,s), 2.34(3H,s), 2.32(3H,s),2.21(3H,s)CDCl3143~1445767.76(1H,d,J=11.7), 7.29(1H,d,J=8.5), 7.10(1H,d,J=8.3), 6.8(1H,d,J=2.7), 6.77(1H,dd,J=8.3,J=2.7), 3.90(3H,s), 2.71(3H,s), 2.27(3H,s), 2.25(3H,s), 2.24(3H,s)CDCl3-5777.76(1H,d,J=11.2), 7.19(2H,d,J=8.6), 7.16(1H,d,J=8.5), 6.96(2H,d,J=8.6), 2.70(3H,s), 2.65(2H,q,J=7.7), 2.35(3H,s), 2.22(3H,s), 1.24(3H,t.J=7.7)CDCl3-5787.83(1H,br.s), 7.64(2H,d,J=8.9), 7.47(1H,d,J=8.3), 7.03(2H,d,J=8.9), 3.94(3H,s), 2.74(3H,s), 2.30(3H,s)CDCl3-5797.68(1H,d,J=11), 7.61(2H,d,J=8.8), 6.99(2H,d,J=8.8), 3.94(3H,s), 2.74(3H,s), 2.34(3H,s)CDCl3-5807.65(1H,d,J=11), 7.61(2H,d,J=8.8), 6.99(2H,d,J=8.8), 2.72(3H,s), 2.40(3H,s), 2.28(3H,s)CDCl3-5817.82(1H,d,J=11.0), 7.64(2H,d,J=8.5), 7.34(1H,d,J=8.3), 7.03(2H,d,J=8.5), 2.73(3H,s), 2.42(3H,s), 2.25(3H,s)CDCl3-5827.90(1H,br,s), 7.61(2H,d,J=8.8), 7.46(1H,t,J=6.8), 6.99(2H,d,J=8.8), 3.94(3H,s), 2.76(3H,s), 2.36(3H,s)CDCl3-
    [0159] Table 25 6177.81(1H,d,J=11.2),7.43(1H.d,J=8.5), 7.36(1H,t,J=8.5), 7.00(1H,m), 6.93(2H,m), 3.93(3H,s), 2.73(3H,s), 2.29(3H,s)CDCl3-6187.87(1H,d,J=9.0), 7.42(1H,t,J=8.7), 7.33(1H,t,J=8.4), 6.96(1H,m), 6.89(3H,m), 3.95(3H,s), 2.74(3H,s), 2.36(3H,s)CDCl3-6347.81(1H,d,J=10.2), 7.43(1H,d,J=2.0), 7.42(1H,m), 7.41(1H,m), 7.34(1H,br.s), 7.14(1H,m), 3.92(3H,s), 2.73(3H,s), 2.29(3H,s)CDCl3-6357.81(1H,d,J=10.5), 7.44-7.41(2H,m), 7.34(1H,s), 7.29(1H,d,J=8.3), 7.14(1H,m), 2.72(3H,s), 2.39(3H,s), 2.24(3H,s)CDCl3-6367.88(1H,s), 7.39-7.36(3H,m), 7.28(1H,br.s), 7.10(1H,m), 3.95(3H,s), 2.75(3H,s), 2.36(3H,s)CDCl3-6447.89(1H,d,J=9.2), 7.31-6.74(5H,m), 2.72(3H,s), 2.59(3H,s), 2.45(3H,s), 2.24(3H,s)CDCl384~856457.91(1H,s), 7.36-7.74(5H,m), 2.70(3H,s), 2.38(3H,s), 2.37(3H,s), 2.22(3H,s)CDCl3-6468.10(1H,d,J=9.2), 7.40-7.14(4H,m), 6.89(1H,d,J=7.5), 2.72(3H,s), 2.43(3H,s), 2.26(3H,s)CDCl3-6478.41(1H,s), 7.44-7.11(4H,m), 2.72(3H,s), 2.28(3H,s), 2.24(3H,s)CDCl3118~1196487.95(1H,s), 7.19(1H,s), 7.10(1H,d,J=8.8), 6.79-6.74(2H,m), 3.90(3H,s), 3.01(2H,q,J=7.7), 2.39(3H,s), 2.31(3H,s), 1.38(3H,t,J=7.7)CDCl3132~133.56497.92(1H,d,J=9.2), 7.28(1H,d,J=9.2), 7.06(1H,d,J=8.9), 6.71-6.64), 3.97(3H,s), 3.02(2H,q,J=7.6), 2.58(3H,s), 2.33(3H,s9, 1.38(3H,t,J=7.6)CDCl3129~130.56507.80(1H,d,J=11.2), 7.41(1H,d,J=8.3), 7.13(1H,d,J=8.1), 6.83(1H,m), 6.81(1H,s), 2.73(3H,s), 2.30(3H,s),CDCl3-6517.80(1H,d,J=11), 7.33(1H,d,J=8.6), 7.12(1H,d,J=9.0), 6.81(1H,m), 6.79(1H,s), 2.72(3H,s), 2.43(3H,s), 2.25(3H,s)CDCl3-6527.87(1H,d,J=9.1), 7.40(1H,dd,J=9.1,J=8.3), 7.10(1H,d,J=8.8), 6.80(1H,dd,J=8.8,J=2.8), 6.77(1H,d,J=2.8), 3.95(3H,s), 2.74(3H,s), 2.36(3H,s)CDCl3-6537.83(1H,s), 7.03(1H,d,J=8.9), 6.59-6.53(2H,m), 3.95(3H,s), 3.01(2H,q,J=7.7), 2.49(3H,s), 2.30(3H,s), 2.26(3H,s), 1.38(3H,t,J=7.7)CDCl3127.5~128.56798.05-7.98(2H,m), 7.69(1H,d,J=8.8), 7.47(1H,d,J=9.4, 7.00(1H,d,J=8.8), 2.72(3H,s), 2.43(3H,s), 2.26(3H,s)CDCl3239~2406808.15(1H,s), 8.05(1H,s), 7.69(1H,d,J=8.7), 7.51(1H,s), 6.99(1H,d,J=8.7),2.72(3H,s), 2.46(3H,s), 2.25(3H,s)CDCl3170~171.56837.85(1 H,s), 7.74(1 H,s), 7.49(1H,dd,J=9.6,J=2.2), 6.66(1 H,d,J=9.6), 4.30(1H,t,J=7.3), 3.98(3H,s), 3.84(1H,t,J=5.7), 2.98(2H,q,J=7.2), 2.61(3H,s), 2.43(3H.s). 2.32(2H,tt,J=7.3,J=5.7), 2.28(3H,s),CDCl3140~1416858.19(1H,s), 8.02(1H,s), 7.84(1H,s), 3.94(3H,s), 3.01(2H,q,J=7.6), 2.48(3H,s), 2.30(3H,s), 2.24(3H,s), 1.36(3H,t,J=7.6)CDCl3185~186.56878.41(1H,s), 7.96(1H,s), 7.93(1H,dd,J=8.8,J=2.7), 7.52(1H,s), 7.05(1 H,d,J=8.8), 3.94(3H,s),2.73(3H,s), 2.32(3H,s),2.30(3H,s)CDCl3-6948.50(1H,d,J=2.7),8.00(1H,s),7.62(1H,d,J=8.7),7.31(1H,s),7.24(1H,dd,J= 8.7,J=2.7),3.92(3H,s),3.02(2H,q,J=7.5),2.38(3H,s),2.33(3H,s),1.39(3H,t, J=7.5)CDCl3-7008.23(1H,q,J=1.1), 8.02(1H,br.s), 7.80(1H,d,J=10.1), 7.70(1H,d), 3.98(3H,s), 2.74(3H,s), 2.31(3H,s)CDCl3- Reference Example 1 Synthesis of 4-nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene (compound represented by formula (7)
    [0160] A mixed solution composed of 44.3 g of 1-chloro-4-nitro-2-trifluoromethylbenzene, 98 mL of N,N-dimethylacetamide, 35 g of 4-trifluoromethoxyphenol, and 20.4 g of potassium carbonate was stirred with heating at 90 to 100°C for 3 hr. This reaction solution was concentrated under the reduced pressure. Ethyl acetate was then added to and dissolved in the residue, and the solution was washed with brine. The solution was then concentrated under the reduced pressure. n-Hexane was added to the residue, and the precipitated crystals were collected by filtration to give 66.9 g of 4-nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene (yield 92.7%). Reference Example 2 Synthesis of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethylaniline (compound represented by formula (5))
    [0161] Iron powder (72.7 g), 251 mL of ethanol, 103 mL of distilled water, and 0.55 mL of 35% hydrochloric acid were mixed together, and the mixture was heated to reflux. Subsequently, a solution of 66.9 g of 4-nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene dissolved in 77 mL of ethanol was added dropwise to the mixed solution, and the mixture was heated under reflux for 2.5 hr. The reaction solution was cooled to room temperature, sodium bicarbonate water was added thereto, and the mixture was filtered. The filtrate was concentrated under the reduced pressure, and ethyl acetate and brine were added to the residue, followed by separation. The ethyl acetate layer was washed with brine and was then concentrated under the reduced pressure to give 61.0 g of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethylaniline (yield 99%). Reference Example 3 Synthesis of 2-chloro-1-(4-chlorophenylthio)-4-nitrobenzene (compound represented by formula (7b))
    [0162] Potassium carbonate (10.4 g) was added to a mixture composed of 50 mL of N,N-dimethylacetamide, 19.2 g of 1,2-dichloro-4-nitrobenzene, and 14.5 g of 4-chlorobenzenethiol. This mixed solution was stirred at 35 to 40°C for 2.5 hr. This reaction solution was poured into 500 mL of iced water, and the precipitated crystals were collected by filtration to give 27.8 g of 2-chloro-1-(4-chlorophenylthio)-4-nitrobenzene (yield 92.5%). Reference Example 4 Synthesis of 1-(4-chlorobenzenesulfonyl)-4-nitrobenzene (compound represented by formula (7d))
    [0163] A 35% aqueous hydrogen peroxide solution (13.6 g) was added dropwise to a mixture composed of 14.0 g of 1-(4-chlorophenylthio)-4-nitrobenzene and 47 mL of acetic acid. The mixed solution was stirred with heating at 70 to 80°C for 1.5 hr. Thereafter, this reaction solution was cooled and was poured into water, and the precipitated crystals were collected by filtration to give 22.0 g of 1-(4-chlorobenzene sulfonyl)-4-nitrobenzene. Reference Example 5 Synthesis of 2-chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene (compound represented by formula (7e))
    [0164] N,N-Dimethylacetamide (42 mL), 16.2 g of 1,2-dichloro-4-nitrobenzene, 12 g of 4-chlorobenzyl alcohol, and 8.7 g of potassium carbonate were mixed together, and the mixture was stirred with heating at 100 to 140°C for 30 hr. This reaction solution was concentrated under the reduced pressure. The residue was dissolved in 100 mL of ethyl acetate and 100 mL of toluene, and the solution was washed with water and brine. The organic layer was concentrated under the reduced pressure, and the residue was recrystallized from ethanol to give 11.77 g of 2-chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene (yield 46.9%). Reference Example 6 Synthesis of (2-chloro-4-nitrophenyl)-(4'-chlorophenyl)methanone (compound represented by formula (7f))
    [0165] 2-Chloro-4-nitrobenzoyl chloride (23.1 g) was added dropwise to a mixture composed of 11.8 g of monochlorobenzene and 13.3 g of aluminum chloride. The mixed solution was stirred with heating at 40°C for 6 hr and was then added dropwise to 45 mL of warm water. Further, toluene and ethyl acetate were added to the mixed solution followed by separation and washing with sodium bicarbonate water and brine. The organic layer was concentrated under the reduced pressure. n-Hexane was added to the residue, and the precipitated crystals were collected by filtration to give 24.0 g of (2-chloro-4-nitrophenyl)-(4'-chlorophenyl)methanone (yield 81%). Reference Example 7 Synthesis of (4-amino-2-chlorophenyl)-(4'-chlorophenyl)methanone (compound represented by formula (5f))
    [0166] Iron powder (12 g), 42 mL of ethanol, 17 mL of distilled water, and 0.09 mL of 35% hydrochloric acid were mixed together, and the mixture was heated to reflux. Subsequently, (2-chloro-4-nitrophenyl)-(4'-chlorophenyl)methanone (8.9 g) dissolved in 12.8 mL of ethanol was added dropwise to the mixed solution, and the mixture was heated under reflux for one hr. This mixed solution was then cooled to room temperature, sodium bicarbonate water was then added thereto, and the mixture was filtered. The filtrate was concentrated under the reduced pressure, and ethyl acetate and brine were added to the residue, followed by separation. The ethyl acetate layer was washed with brine and was then concentrated under the reduced pressure to give 7.56 g of (4-amino-2-chlorophenyl)-(4'-chlorophenyl)methanone (yield 95%). Reference Example 8 Synthesis of 3-chloro-4-(4-chlorobenzyl)aniline (compound represented by formula (5 g))
    [0167] Iodine (1 g) and 50 mL of acetic acid were mixed together, 2.53 g of 50% phosphoric acid was added thereto, and the mixture was heated with stirring to reflux. Subsequently, a mixture composed of 3.2 g of (4-amino-2-chlorophenyl)-(4'-chlorophenyl)methanone and 15 mL of acetic acid were added dropwise to the mixed solution. This solution was heated under reflux for 134 hr, was then cooled and was poured into water. Ethyl acetate was added to the mixed solution followed by separation and washing with brine. The ethyl acetate layer was concentrated to give 3.0 g of 3-chloro-4-(4-chlorobenzyl)aniline (yield 100%). Reference Example 9 Synthesis of 4-nitro-4'-trifluoromethoxy-2-trifluoromethylbiphenyl (compound represented by formula (7h))
    [0168] 1-Bromo-4-nitro-3-trifluorobenzene (2.5 g), 2.1 g of 4-trifluoromethoxyphenylboric acid, 9.3 mL of ethanol, and 18.3 g of toluene were mixed together to prepare a solution. An aqueous solution of 0.93 g of sodium carbonate dissolved in 9 g of water was added to the solution. Tetrakis(triphenylphosphine)palladium(0) (0.067 g) was added thereto, and the mixture was heated under reflux for 4 hr. The reaction mixture was cooled, ethyl acetate and distilled water were then added thereto, followed by separation and washing with brine. The ethyl acetate layer was concentrated to give 3.54 g of 4-nitro-4'-trifluoromethoxy-2-trifluoromethylbiphenyl (yield 100%). Reference Example 10 Synthesis of 3-chloro-2-(2,6-dimethyl-4-nitrophenoxy)-5-trifluoromethylpyridine (compound represented by formula (7a))
    [0169] 2,3-Dichloro-5-trifluoromethylpyridine (1.04 g), 0.8 g of 2,6-dimethyl-4-nitrophenol, and 0.5 g of potassium carbonate were added to 3 mL of dimethylacetamide, and the mixture was allowed to react at 155 to 165°C for one hr. The reaction mixture was cooled, ethyl acetate and distilled water were then added thereto, followed by separation and washing with brine. The ethyl acetate layer was concentrated to give 2.01 g of 3-chloro-2-(2,6-dimethyl-4-nitrophenoxy)-5-trifluoromethylpyridine (yield 100%). Reference Example 11 Synthesis of 5-chloro-2-(2-chloro-4-nitrophenoxy)pyridine (compound represented by formula (7a))
    [0170] 1,2-Dichloro-4-nitrobenzene (19.2 g), 12.9 g of 5-chloropyridine-2-ol, and 10.4 g of potassium carbonate were added to 50 mL of dimethylacetamide, and the mixture was allowed to react at 90 to 110°C for 15 hr. The reaction mixture was cooled, ethyl acetate and brine were then added thereto, followed by separation and washing with brine. The ethyl acetate layer was concentrated, and the precipitated crystals were collected by filtration. The filtrate was concentrated, and the crude product thus obtained was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 15.75 g of 5-chloro-2-(2-chloro-4-nitrophenoxy)pyridine (yield 55.2%). Reference Example 12 Synthesis of 1,3-Dimethyl-5-nitro-2-(3-(4-trifluoromethylphenoxy)-propoxy)benzene (compound represented by formula (7i))
    [0171] 2,6-Dimethyl-4-nitrophenol (5.2 g) and 12.6 g of 1,3-dibromopropane were added to 19 mL of distilled water, the mixture was stirred, and 7.51 g of a 16.6% aqueous sodium hydroxide solution was then added thereto. Further, the mixture was heated under reflux while adding 2.46 g of a 30% aqueous sodium hydroxide solution for 5 hr. The reaction mixture was cooled, and ethyl acetate and brine were added thereto, followed by separation and washing with brine. The ethyl acetate layer was concentrated under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 4.97 g of 2-(3-bromopropoxy)-1,3-dimethyl-5-nitrobenzene. Next, 1.0 g of the product, 0.57 g of 4-trifluoromethylphenol, 2 mL of dimethylacetamide, and 0.36 g of potassium carbonate were mixed together, and the mixture was heated at 90 to 100°C for one hr. The reaction solution was cooled and was then poured into water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with a 2% aqueous sodium hydroxide solution and brine and was then concentrated under the reduced pressure to give 1.28 g of 1,3-dimethyl-5-nitro-2-(3-(4-trifluoromethylphenoxy)propoxy)benzene.
    [0172] Preparation Example 1 [Wettable powder] Compound 90 30 wt% Clay 30 wt% Diatomaceous earth 35 wt% Calcium lignin sulfonate 4 wt% Sodium laurylsulfate 1 wt% The above ingredients were intimately mixed together, and the mixture was ground to prepare wettable powder.
    [0173] Preparation Example 2 [Dust] Compound 90 2 wt% Clay 60 wt% Talc 37 wt% Calcium stearate 1 wt% The above ingredients were intimately mixed together to prepare dust.
    [0174] Preparation Example 3 [Emulsifiable concentrate] Compound 90 20 wt% N,N-Dimethylformamide 20 wt% Solvesso 150 (Exxon Mobil Corporation) 50 wt% Polyoxyethylene alkylaryl ether 10 wt% The above ingredients were homogeneously mixed and dissolved to prepare emulsifiable concentrate.
    [0175] Preparation Example 4 [Granules] Compound 2 5 wt% Bentonite 40 wt% Talc 10 wt% Clay 43 wt% Calcium lignin sulfonate 2 wt% The above ingredients were homogeneously ground and intimately mixed together. Water was added to the mixture, followed by thorough kneading. Thereafter, the kneaded product was granulated and dried to prepare granules.
    [0176] Preparation Example 5 [Floables] Compound 2 25 wt% POE polystyrylphenyl ether sulfate 5 wt% Propylene glycol 6 wt% Bentonite 1 wt% 1% aqueous xanthan gum solution 3 wt% PRONAL EX-300 (Toho Chemical Industry Co., Ltd.) 0.05 wt% ADDAC 827 (K.I. Chemical Industry Co., Ltd.) 0.02 wt% Water 59.93 wt% All the above ingredients except for the 1% aqueous xanthan gum solution and a suitable amount of water were premixed together, and the mixture was then ground by a wet grinding mill. Thereafter, the 1% aqueous xanthan gum solution and the remaining water were added to the ground product to prepare 100 wt% floables. Test Example 1: Pesticidal effect against Plutella xylostella
    [0177] A cabbage leaf disk having a diameter of 5 cm was placed in a plastic cup. Test compounds, which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%), were spread over the cabbage leaf disk by means of a spray gun, and the cabbage leaf disk was then air dried. Five larvae at the second instar of Plutella xylostella were released in the cup. The cup was then lidded, and the larvae were reared in a chamber at a constant temperature (25°C). Three days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 200 ppm. Test Example 2: Pesticidal effect against Spodoptera litura
    [0178] A cabbage leaf disk having a diameter of 5 cm was placed in a plastic cup. Test compounds, which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%), were spread over the cabbage leaf disk by means of a spray gun, and the cabbage leaf disk was then air dried. Five larvae at the third instar of Spodoptera litura were released in the cup. The cup was then lidded, and the larvae were reared in a chamber at a constant temperature (25°C). Three days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 200 ppm. Test Example 3: Pesticidal effect against Myzus persicae
    [0179] A cabbage leaf disk having a diameter of 2.8 cm was placed in a plastic schale. Test compounds, which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%), were spread over the cabbage leaf disk by means of a spray gun, and the cabbage leaf disk was then air dried. Thereafter, ten larvae at the first instar of Myzus persicae were released in the schale. The schale was then lidded, and the larvae were reared in a chamber at a constant temperature (25°C). Two days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Test Example 4: Miticidal effect against Tetranychus cinnabarinus
    [0180] A kidney leaf disk having a diameter of 2 cm was placed on agar. Seven female adult mites of Tetranychus cinnabarinus were released on the kidney leaf disk. The female adult mites were allowed to oviposit in a chamber kept at a constant temperature (25°C) for 24 hr. The female adult mites were then removed from the kidney leaf disk. Test compounds, which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%), were spread over the leaf disk by means of a spray gun, and the leaf disk was then air dried. Thereafter, the leaf disk was stored in a constant-temperature chamber of 25°C. Seven days after the treatment, the test system was observed for hatching of eggs and survival or death of larva ticks and nymphs, and the unhatching rate of eggs and the death rate of larva ticks/nymphs were calculated based on the observation results. The sum of the unhatching rate of eggs and the death rate of larva ticks/nymphs was determined as the total death rate. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Test Example 5: Control effect against Laodel phax striatellus
    [0181] Test compounds, which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%), were spread over four rice seedlings (7 days after sowing) sowed in a plastic pot by means of a spray gun, followed by air drying. Thereafter, this pot was covered by a plastic cylinder, and ten larvae at the second instar of Laodel phax striatellus were released in the pot. The pot was then lidded, and the larvae were reared in a chamber at a constant temperature (25°C). Three days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Test Example 6: Control effect against Trigonotylus caelestialium
    [0182] One wheat seedling was immersed in test compounds which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%) for 30 sec. This wheat seedling was air dried and was then placed in a glass cylinder. Two larvae at the second instar of Trigonotylus caelestialium were released in the glass cylinder. Thereafter, the cylinder was lidded, and the larvae were reared in a chamber at a constant temperature (25°C). During the test, the wheat was allowed to suck water through the bottom of the glass cylinder for feeding water to the wheat. Three days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Test Example 7: Pesticidal effect against Bemisia tabaci Genn.
    [0183] A cucumber leaf was cut into a size of 6.0 cm in diameter and was placed on a water-wetted absorbent cotton. Test compounds which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%) were sprayed in an amount of 2 mL over the cucumber leaf from a spraying tower. After air drying, this cucumber leaf was placed in a plastic cup, and 20 female adults of Bemisia tabaci Genn. were released in the cup. The cup was turned upside down and was allowed to stand in a chamber kept at a constant temperature (25°C). Five days after the treatment, the pests were observed for survival or death, and the death rate of the pests was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Test Example 8: Pestcidal effect against Thrips palmi KARNY
    [0184] A cucumber leaf was cut into a size of 2.5 cm square and was placed on a water-wetted absorbent cotton. Test compounds which had been diluted to designated concentrations by the addition of a 50% aqueous acetone solution (Tween 20, 0.05%) were sprayed in an amount of 2 mL over the cucumber leaf from an spraying tower. After air drying, this cucumber leaf was placed in a plastic cup, and ten larvae at the first instar of Thrips palmi KARNYU were released in the cup. The cup was allowed to stand in a chamber kept at a constant temperature (25°C). Two days after the treatment, the larvae were observed for survival or death, and the death rate of larvae was calculated based on the observation results. As a result, for the compounds according to the present invention shown in Tables 15 to 25 exhibited a death rate of not less than 80% at a concentration of not more than 500 ppm. Comparative Example
    [0185] Compound No. 136 described in WO 98/055460 and compound No. 46 described in Japanese Patent No. 2633377 were tested for insecticidal activity according to the methods described in Test Examples 1 to 5. The results were as shown in Table 26.
    [0186] Table 26 Death rate, %Plutella xylostellaSpodoptera lituraMyzus persicaeLaodelphax striatellusTetranychus cinnabarinusConcentration, ppm200200500500500 WO 98055460 Compund No. 136
    00000 JP 2633377 Compund No. 46
    010000
    权利要求:
    Claims (16)
    [0001] A compound represented by formula (I) or an agriculturally and horticulturally acceptable acid addition salt thereof:
    [0002] The compound according to claim 1, whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,optionally substituted C1-18 alkyl,COR4 wherein R4 represents optionally substituted C1-18 alkyl; optionally substituted C2-18 alkenyl; optionally substituted C3-10 cycloalkyl; optionally substituted C1-4 alkylthio; OR5 wherein R5 represents optionally substituted C1-18 alkyl, optionally substituted C2-18 alkenyl, or optionally substituted phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or optionally substituted C1-18 alkyl, orSO2R8 wherein R8 represents optionally substituted C1-18 alkyl,R2 represents a hydrogen atom or optionally substituted C1-4 alkyl,R3 represents optionally substituted C1-18 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy optionally substituted by halogen atom, C1-4 alkyloxycarbonyl optionally substituted by halogen atom, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0003] The compound according to claim 1, whereinR1 representsa hydrogen atom,an alkali metal,an alkaline earth metal,C1-18 alkyl optionally substituted by C1-4 alkyloxycarbonyl or C1-4 alkyloxy-C1-4 alkyloxy,COR4 wherein R4 represents C1-18 alkyl optionally substituted by C1-4 alkyloxy or acetyloxy; C2-18 alkenyl; C3-10 cycloalkyl; C1-4 alkylthio; OR5 wherein R5 represents C1-18 alkyl optionally substituted by halogen atom or C1-4 alkyloxy, C2-18 alkenyl, or phenyl; or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl, orSO2R8 wherein R8 represents C1-18 alkyl,R2 represents a hydrogen atom or C1-4 alkyl,R3 represents C1-18 alkyl optionally substituted by halogen atom or acetyloxy,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1, X2, and X3 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, C1-4 alkyloxycarbonyl, nitro, or cyano,provided that X1, X2, and X3 do not simultaneously represent a hydrogen atom, andZ represents a bond, an oxygen atom, a sulfur atom, SO, SO2, CH2, OCH2, O(CH2)3O, or CO.
    [0004] The compound according to claim 1, whereinW1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom, A', or B',provided that, when Z represents a bond, methylene optionally substituted by one or two methyl, or an oxygen atom, at least one of Y1, Y2, Y3, Y4, and Y5 represents A',wherein A' represents a group selected from the group consisting of:
    C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different;
    C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different;
    C1-8 alkyloxycarbonyl;
    C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different;
    C1-8 alkylsulfonyl which is subsituted by one or more halogen atoms which may be the same or different;phenyl which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different; andphenoxy which is substituted by one or more halogen atoms which may be the same or different, or C1-4 alkyl substituted by one or more halogen atoms which may be the same or different,B' represents a group selected from the group consisting of a halogen atom, C1-4 alkyl, C1-4 alkyloxy, and cyano,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0005] The compound according to claim 1, whereinany one of W1, W2, and W3 represents a nitrogen atom, and the other two groups represent the corresponding C-Y1, C-Y2, or C-Y3, andY1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl substituted by one or more halogen atoms which may be the same or different; or a halogen atom.
    [0006] The compound according to claim 1, whereinR1 represents a hydrogen atom; or COR4 wherein R4 represents C1-4 alkyl, OR5 wherein R5 represents C1-4 alkyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1 and X2 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, or C1-4 alkyloxycarbonyl,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom, andZ represents an oxygen atom, OCH2, or O(CH2)3O.
    [0007] The compound according to claim 1, whereinW1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, andY1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2.
    [0008] The compound according to claim 1, whereinR1 represents a hydrogen atom; or COR4 wherein R4 represents C1-4 alkyl, OR5 wherein R5 represents C1-4 alkyl, or NR6R7 wherein R6 and R7 each independently represent a hydrogen atom or C1-18 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,alternatively R2 and R3 together represent -(CH2)m- wherein m is 3 or 4,X1 and X2 each independently represent a hydrogen atom, a halogen atom, C1-4 alkyl optionally substituted by halogen atom, C1-4 alkyloxy, or C1-4 alkyloxycarbonyl,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom,W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively, andY1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyl which is substituted by one or more halogen atoms which may be the same or different; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or C1-8 alkylthio which is substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2, andZ represents an oxygen atom, OCH2, or O(CH2)3O.
    [0009] The compound according to claim 1, whereinR1 represents COR4' or COOR5 wherein R4' and R5 represent C1-4 alkyl,R2 represents C1-4 alkyl,R3 represents C1-4 alkyl,X1 and X2 each independently represent a hydrogen atom, or C1-4 alkyl optionally substituted by halogen atom,provided that X1 and X2 do not simultaneously represent a hydrogen atom,X3 represents a hydrogen atom,W1, W2, and W3 represent C-Y1, C-Y2, and C-Y3, respectively,Y1, Y2, Y3, Y4, and Y5 each independently represent a hydrogen atom; C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different; or a halogen atom,provided that at least one of Y1, Y2, Y3, Y4, and Y5 represents C1-8 alkyloxy which is substituted by one or more halogen atoms which may be the same or different, and/or C1-4 alkyloxy substituted by one or more halogen atoms which may be the same or different,alternatively adjacent two of Y1, Y2, Y3, Y4, and Y5 may together represent -O-(CH2)n-O- substituted by one or more halogen atoms, wherein n is 1 or 2, andZ represents an oxygen atom.
    [0010] An agricultural or horticultural insecticide comprising as an active ingredient a compound according to any one of claims 1 to 9 or an agriculturally and horticulturally acceptable acid addition salt thereof.
    [0011] An agricultural or horticultural insecticide comprising as an active ingredient a compound represented by formula (Ia) or an agriculturally and horticulturally acceptable acid addition salt thereof:
    [0012] A method for controlling an agricultural and horticultural insect pest, comprising the step of applying an effective amount of a compound according to any one of claims 1 to 9 or an agriculturally and horticulturally acceptable acid addition salt thereof to a plant or soil.
    [0013] A method for controlling an agricultural and horticultural insect pest, comprising the step of applying an effective amount of a compound represented by formula (Ia) as defined in claim 11 or an agriculturally and horticulturally acceptable acid addition salt thereof to a plant or soil.
    [0014] The method according to claim 12 or 13, wherein said insect pest is selected from the group consisting of Lepidoptera, Hemiptera, Coleoptera, Acari, Hymenoptera, Orthoptera, Diptera, Thysanoptera, and plant parasitic nematoda.
    [0015] Use of a compound according to any one of claims 1 to 9 or an agriculturally and horticulturally acceptable acid addition salt thereof, as an agricultural and horticultural insecticide.
    [0016] Use of a compound represented by formula (Ia) as defined in claim 11 or an agriculturally and horticulturally acceptable acid addition salt thereof, as an agricultural and horticultural insecticide.
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