WO2017043386A1 - 有害生物防除組成物 - Google Patents

有害生物防除組成物 Download PDF

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WO2017043386A1
WO2017043386A1 PCT/JP2016/075448 JP2016075448W WO2017043386A1 WO 2017043386 A1 WO2017043386 A1 WO 2017043386A1 JP 2016075448 W JP2016075448 W JP 2016075448W WO 2017043386 A1 WO2017043386 A1 WO 2017043386A1
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group
compound
present
reaction
composition
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PCT/JP2016/075448
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French (fr)
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直延 西口
栄力 砂村
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住友化学株式会社
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Definitions

  • the present invention relates to a pest control composition and a control method.
  • Non-Patent Document 1 a pest control agent treated with an insecticidal active compound is known (for example, see Non-Patent Document 1).
  • Non-Patent Document 1 a pest control agent treated with an insecticidal active compound
  • An object of the present invention is to provide a pest control composition having excellent efficacy.
  • R 1 is a hydrogen atom, a C1-C3 alkyl group optionally having one or more halogen atoms, a halogen atom, a C1-C3 alkoxy group, a C2-C4 alkoxycarbonyl group, S (O) m R 2 , NR 3 R 4 represents a nitro group or a cyano group, R 2 represents a C1-C3 alkyl group, R 3 and R 4 are the same or different and each represents a hydrogen atom or a C1-C3 alkyl group, n represents 0, 1 or 2, m represents 0, 1 or 2.
  • a pest control composition comprising the condensed heterocyclic compound represented by the formula (1) and one solvent selected from the following group (A).
  • R 1 is a hydrogen atom, a chlorine atom, a bromine atom, a methyl group, a trifluoromethyl group, a methoxy group, a methylsulfanyl group, a methylsulfinyl group, or a methylsulfonyl group;
  • a method for controlling pests which comprises applying the pest control composition according to [1] or [2] to a pest or a habitat of the pest.
  • pests can be controlled.
  • composition of the present invention contains a condensed heterocyclic compound represented by the formula (1) (hereinafter referred to as the present compound).
  • R 1 is a hydrogen atom, a C1-C3 alkyl group optionally having one or more halogen atoms, a halogen atom, a C1-C3 alkoxy group, a C2-C4 alkoxycarbonyl group, S (O) m R 2 , NR 3 R 4 represents a nitro group or a cyano group, R 2 represents a C1-C3 alkyl group, R 3 and R 4 are the same or different and each represents a hydrogen atom or a C1-C3 alkyl group, n represents 0, 1 or 2, m represents 0, 1 or 2. ]
  • halogen atom means a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
  • examples of the “C1-C3 alkyl group” include a methyl group, an ethyl group, a propyl group, and an isopropyl group.
  • the “C1-C3 alkyl group optionally having one or more halogen atoms” means C1-C3 in which at least one hydrogen atom of the C1-C3 alkyl group may be substituted with a halogen atom.
  • Represents an alkyl group for example, fluoromethyl group, chloromethyl group, bromomethyl group, iodomethyl group, difluoromethyl group, trifluoromethyl group, trichloromethyl group, 2-fluoroethyl group, 2,2,2-trifluoroethyl group, Examples include a pentafluoroethyl group and a heptafluoroisopropyl group.
  • examples of the “C1-C3 alkoxy group” include a methoxy group, an ethoxy group, a propyloxy group, and an isopropyloxy group.
  • C2-C4 alkoxycarbonyl group represents a group in which a C1-C3 alkoxy group and a carbonyl group are bonded, and represents a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, or an isopropoxycarbonyl group.
  • S (O) m R 2 represents a C1-C3 alkylsulfanyl group in which m is 0, an alkylsulfinyl group in which m is 1 and an alkylsulfonyl group in which m is 2.
  • the C1-C3 alkylsulfanyl group represents a methylsulfanyl group, an ethylsulfanyl group, a propylsulfanyl group, and an isopropylsulfanyl group.
  • the C1-C3 alkylsulfinyl group represents a methylsulfinyl group, an ethylsulfinyl group, a propylsulfinyl group, and an isopropylsulfinyl group.
  • the C1-C3 alkylsulfonyl group represents a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, and an isopropylsulfonyl group.
  • R 1 is a hydrogen atom, a chlorine atom, a bromine atom, a trifluoromethyl group, a methoxy group, a methylsulfanyl group, a methylsulfinyl group, or a methylsulfonyl group, and n is 2.
  • a certain compound is preferable, and a compound in which R 1 is a hydrogen atom and n is 2 is more preferable.
  • the present compound and its production intermediate compound can be produced, for example, by the following method.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include aliphatic halogenated hydrocarbons such as dichloromethane and chloroform, nitriles such as acetonitrile, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used in the reaction include sodium periodate, m-chloroperbenzoic acid, and hydrogen peroxide. When hydrogen peroxide water is used as the oxidizing agent, it can be carried out in the presence of a base or a catalyst as necessary. Examples of the base used for the reaction include sodium carbonate.
  • Examples of the catalyst used for the reaction include tungstic acid and sodium tungstate.
  • an oxidizing agent is usually used in a proportion of 1 to 1.2 mol.
  • the hydrogen peroxide solution is usually used in a proportion of 1 to 1.2 mol and the base is usually used in an amount of 0.01 to 1 per 1 mol of the compound (1a). Used in molar proportions.
  • the hydrogen peroxide solution is usually 1 to 1.2 mol per 1 mol of the compound (1a), and the catalyst is usually 0.01 to 0. Used in a proportion of 5 moles.
  • the reaction temperature is usually in the range of ⁇ 20 to 80 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite and sodium thiosulfate) and an aqueous solution of a base (for example, sodium bicarbonate) as necessary.
  • a reducing agent for example, sodium sulfite and sodium thiosulfate
  • a base for example, sodium bicarbonate
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include aliphatic halogenated hydrocarbons such as dichloromethane and chloroform, nitriles such as acetonitrile, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used for the reaction include m-chloroperbenzoic acid and aqueous hydrogen peroxide.
  • the reaction can be carried out in the presence of a base or a catalyst as necessary. Examples of the base used for the reaction include sodium carbonate. Examples of the catalyst used in the reaction include sodium tungstate.
  • the oxidizing agent is usually used at a ratio of 1 to 4 mol.
  • the oxidizing agent is used in a proportion of 1 to 2 moles relative to 1 mole of the compound (1b).
  • the hydrogen peroxide solution is usually used in a proportion of 1 to 4 mol and the base is usually used in an amount of 0.01 to 1 mol with respect to 1 mol of the compound (1b). Used in proportions.
  • the hydrogen peroxide solution is usually 1 to 4 mol per 1 mol of the compound (1b), and the catalyst is usually 0.01 to 0.5 mol. Used in molar proportions.
  • the reaction temperature is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite and sodium thiosulfate) and an aqueous solution of a base (for example, sodium bicarbonate) as necessary.
  • a reducing agent for example, sodium sulfite and sodium thiosulfate
  • a base for example, sodium bicarbonate
  • Compound (1c) can be produced in a one-step reaction (one pot) by reacting compound (1a) with an oxidizing agent.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include aliphatic halogenated hydrocarbons such as dichloromethane and chloroform, nitriles such as acetonitrile, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used for the reaction include m-chloroperbenzoic acid and aqueous hydrogen peroxide. When hydrogen peroxide is used as the oxidizing agent for the reaction, it is carried out in the presence of a base or a catalyst as necessary.
  • Examples of the base used for the reaction include sodium carbonate.
  • Examples of the catalyst used for the reaction include tungstic acid and sodium tungstate.
  • an oxidizing agent is usually used at a ratio of 2 to 5 moles.
  • the hydrogen peroxide solution is usually in a proportion of 2 to 5 mol and the base is usually 0.01 to 1 mol with respect to 1 mol of the compound (1a). Used in proportions.
  • the hydrogen peroxide solution is usually 2 to 5 mol per 1 mol of the compound (1a), and the catalyst is usually 0.01 to 0.5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite and sodium thiosulfate) and an aqueous solution of a base (for example, sodium bicarbonate) as necessary.
  • a reducing agent for example, sodium sulfite and sodium thiosulfate
  • a base for example, sodium bicarbonate
  • Manufacturing method 2 This compound comprises reacting a compound represented by the formula (M1) (hereinafter referred to as the compound (M1)) with a compound represented by the formula (M2) (hereinafter referred to as the compound (M2)). Can be manufactured.
  • M1 a compound represented by the formula (M1)
  • M2 a compound represented by the formula (M2)
  • Compound (M2) is known or can be produced according to a known method.
  • Compound (1a) can be produced by reacting compound (M1a) in which n is 0 in compound (M1) with compound (M2).
  • Compound (1b) can be produced by reacting compound (M1b) wherein n is 1 in compound (M1) with compound (M2).
  • Compound (1c) can be produced by reacting compound (M1c) wherein n is 2 in compound (M1) with compound (M2). The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran and tert-butyl methyl ether, and halogenated carbonization such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane and chlorobenzene.
  • ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran and tert-butyl methyl ether
  • halogenated carbonization such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane and chlorobenzene.
  • Hydrogen aromatic hydrocarbons such as toluene, benzene and xylene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, N, N-dimethylformamide, N-methylpyrrolidone, 1,3-dimethyl- Examples include aprotic polar solvents such as 2-imidazolidinone and dimethyl sulfoxide, nitrogen-containing aromatic compounds such as pyridine and quinoline, and mixtures thereof.
  • aromatic hydrocarbons such as toluene, benzene and xylene
  • esters such as ethyl acetate and butyl acetate
  • nitriles such as acetonitrile
  • N, N-dimethylformamide N-methylpyrrolidone
  • 1,3-dimethyl- Examples include aprotic polar solvents such as 2-imidazolidinone and dimethyl sulfoxide, nitrogen-containing aromatic compounds such as
  • Examples of the base used in the reaction include alkali metal hydrides such as sodium hydride and potassium hydride, alkaline earth metal hydrides such as calcium hydride, and alkali metal carbonates such as sodium carbonate and potassium carbonate. Examples thereof include salts or organic bases such as triethylamine, diisopropylpyroethylamine, pyridine and 4-dimethylaminopyridine.
  • the compound (M2) is usually used in a proportion of 1 to 2 mol
  • the base is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the reaction mixture is poured into water and extracted with an organic solvent and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture.
  • the compound can be isolated by collecting the resulting solid by filtration.
  • the isolated compound can be further purified by recrystallization, chromatography or the like.
  • a compound represented by formula (M7) (hereinafter referred to as compound (M7)) is obtained by reacting a compound represented by formula (M6) (hereinafter referred to as compound (M6)) with a chlorinating agent.
  • a compound represented by formula (M6) (hereinafter referred to as compound (M6))
  • a chlorinating agent such as 3,6-difluoropyridine-2-carboxylic acid and 3,6-dichloropyridine-2-carboxylic acid, both of which are commercially available compounds.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include aromatic hydrocarbons such as toluene and xylene, aliphatic halogenated hydrocarbons such as dichloromethane and chloroform, and mixtures thereof.
  • Examples of the chlorinating agent used in the reaction include thionyl chloride, oxalyl dichloride, phosphorus oxychloride and the like.
  • a chlorinating agent is usually used at a ratio of 1 to 15 mol with respect to 1 mol of the compound (M6).
  • the reaction temperature is usually in the range of 0 to 150 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours. After completion of the reaction, the compound (M7) can be isolated by removing the solvent.
  • a compound represented by formula (M9) (hereinafter referred to as compound (M9)) is obtained by reacting compound (M7) with a compound represented by formula (M8) (hereinafter referred to as compound (M8)).
  • compound (M8) a compound represented by formula (M8)
  • N2-methyl-5- (trifluoromethyl) pyridine-2,3-diamine represented by compound (M8) can be produced by the method described in WO 2010/125985. The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as tetrahydrofuran, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as tetrahydrofuran, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Aprotic polarities such as aromatic hydrocarbons, halogenated hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, N, N-dimethylformamide, N-methylpyrrolidone and dimethyl sulfoxide Examples include solvents and mixtures thereof.
  • a base may be added as necessary.
  • the base used in the reaction include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and N, N-diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M7) is usually used in a proportion of 1 to 3 mol
  • the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M9) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M9) can be further purified by chromatography, recrystallization and the like.
  • Compound (M9) can also be produced by reacting compound (M6) and compound (M8) in the presence of a condensing agent.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran, and tert-butyl methyl ether, and halogenations such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, and chlorobenzene.
  • Hydrocarbons aromatic hydrocarbons such as toluene, benzene, xylene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, N, N-dimethylformamide, N-methylpyrrolidone, 1,3-dimethyl
  • aprotic polar solvents such as -2-imidazolidinone and dimethyl sulfoxide
  • nitrogen-containing aromatic compounds such as pyridine and quinoline, and mixtures thereof.
  • Examples of the condensing agent used in the reaction include carbodiimides such as 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride and 1,3-dicyclohexylcarbodiimide.
  • a catalyst may be added as necessary.
  • Examples of the catalyst used in the reaction include 1-hydroxybenzotriazole.
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the reaction mixture is poured into water and extracted with an organic solvent and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture.
  • the collected solid can be collected by filtration to isolate compound (M9).
  • the isolated compound (M9) can be further purified by recrystallization, chromatography or the like.
  • the compound represented by the formula (M10) (hereinafter referred to as the compound (M10)) can be produced by intramolecular condensation of the compound (M9).
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran and tert-butyl methyl ether, and halogenated carbonization such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane and chlorobenzene.
  • Hydrogen aromatic hydrocarbons such as toluene, benzene and xylene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, N, N-dimethylformamide, N-methylpyrrolidone, 1,3-dimethyl- Examples include aprotic polar solvents such as 2-imidazolidinone and dimethyl sulfoxide, nitrogen-containing aromatic compounds such as pyridine and quinoline, and mixtures thereof.
  • a condensing agent, an acid, a base, or a chlorinating agent may be added as necessary.
  • Examples of the condensing agent used in the reaction include acetic anhydride, trifluoroacetic anhydride, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride, triphenylphosphine and base, and carbon tetrachloride or carbon tetrabromide. And mixtures of triphenylphosphine and azodiesters (eg diethyl azodicarboxylate).
  • Examples of the acid used for the reaction include sulfonic acids such as paratoluenesulfonic acid, carboxylic acids such as acetic acid, and polyphosphoric acid.
  • Examples of the base used in the reaction include pyridine, picoline, 2,6-lutidine, 1,8-diazabicyclo [5.4.0] -7-undecene (hereinafter referred to as DBU), 1,5-diazabicyclo [ 4.3.0] nitrogen-containing heterocyclic compounds such as 5-nonene, tertiary amines such as triethylamine and N, N-diisopropylethylamine, inorganic bases such as tripotassium phosphate, potassium carbonate and sodium hydride. Can be mentioned.
  • Examples of the chlorinating agent used in the reaction include phosphorus oxychloride.
  • the ratio of the condensing agent is usually 1 to 5 mol, and when an acid is used, the acid is usually 0.1 mol to 5 mol.
  • the base is usually used in a proportion of 1 to 5 mol
  • the chlorinating agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • reaction mixture After completion of the reaction, the reaction mixture is poured into water and extracted with an organic solvent and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture.
  • the collected solid can be collected by filtration to isolate compound (M10).
  • the isolated compound (M10) can be further purified by recrystallization, chromatography or the like.
  • the compound represented by the formula (M1a) (hereinafter referred to as the compound (M1a)) can be produced by reacting the compound (M10) with ethyl mercaptan in the presence of a base. The reaction is usually performed in the presence of a solvent.
  • Examples of the solvent used in the reaction include ethers such as tetrahydrofuran, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, N, Examples thereof include aprotic polar solvents such as N-dimethylformamide, N-methylpyrrolidone and dimethyl sulfoxide, water, and mixtures thereof.
  • Examples of the base used in the reaction include alkali metal carbonates such as sodium carbonate and potassium carbonate, and alkali metal hydrides such as sodium hydride.
  • ethyl mercaptan is usually used in a proportion of 1 to 10 mol
  • base is usually used in a proportion of 1 to 10 mol
  • ethyl mercaptan is used in a proportion of 1.0 to 1.1 mol
  • a base is used in a proportion of 1 to 2 mol with respect to 1 mol of compound (M10).
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 ° C. to 150 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (M1a) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M1a) can be further purified by chromatography, recrystallization and the like.
  • the composition of the present invention contains one type of solvent selected from the group (A) (hereinafter referred to as the present solvent).
  • Group (A) includes pentanol having a hydroxyl group, heptanol, octanol, cyclopentanol, butylene glycol, glycerin, tetrahydrofurfuryl alcohol, ethylene glycol monomethyl ether, tripropylene glycol monomethyl ether and propylene glycol phenyl ether, and an ester solvent.
  • ATBC tributyl acetyl citrate
  • dimethyl succinate and fatty acid linoleic acid any commercially available product or any one produced by a known method can be used.
  • composition of the present invention can be obtained by mixing the present compound and the present solvent.
  • the composition of the present invention includes both the state in which the present compound is completely dissolved in the present solvent and the state in which it is not dissolved but dispersed.
  • the content of the present compound in the composition of the present invention is 0.001 to 60% by weight, preferably 0.01 to 40% by weight.
  • the content of the present solvent in the composition of the present invention is 40 to 99.999% by weight, preferably 60 to 99.99% by weight.
  • pests for which the composition of the present invention is effective include harmful arthropods such as harmful insects and harmful mites. Specific examples of such pests include the following.
  • Hemiptera stink bugs such as Halyomorpha mista, bed bugs such as bed bugs (Cimex electrarius), and killer whales.
  • Lepidoptera Japanese medaka such as Plodia interpuntella, Hirosukoga such as iga (Tinea translucens), Koiga (Tineola bisselliella), etc.
  • Diptera Culex pipiens palens, Culex quaters, and other squids such as Culex quinquefasciaus, etc .; Houseflies such as Anopheles, Chironomidae, Musca domestica, Muscina stabulans, etc. Steal acids, Nomibae such as Oki Mont Nomibae (Megaselia spiracularis), flies such as giant flies (Clogmia albipunctata), sciaridae acids, blackfly acids, Abu such as gadfly (Tabanus trigonus), keds acids and stable flies such.
  • Nomibae such as Oki Mont Nomibae (Megaselia spiracularis)
  • flies such as giant flies (Clogmia albipunctata), sciaridae acids, blackfly acids
  • Abu such as gadfly (Tabanus trigonus), ked
  • Coleoptera adzuki bean weevil (Callosobruchuys Kunststoffensis) weevils such as, Tenebrionidae such as red flour beetle (Tribolium castaneum), varied carpet beetle (Anthrenus verbasci), Hara Giro carpet beetle (Dermestes maculates) beetle such as, cigarette beetle (Lasioderma serricorne) Bark beetles such as, and bark beetles such as Lyctus bruneus.
  • Tenebrionidae such as red flour beetle (Tribolium castaneum), varied carpet beetle (Anthrenus verbasci), Hara Giro carpet beetle (Dermestes maculates) beetle such as, cigarette beetle (Lasioderma serricorne) Bark beetles such as, and bark beetles such as Lyctus bruneus.
  • Coleoptera Cat fleas (Ctenocephalides felis), Dog fleas (Ctenocephalides canis), Human fleas (Pulex irritans), Keops mud mines (Xenopsylla cheopeis), etc. *
  • Anoplura body louse (Pediculus humanus corporis), head lice (Pediculus humanus humanus), crab louse (Phthirus pubis), Ushijirami (Haematopinus eurysternus), Hitsujijirami (Dalmalinia ovis), Butajirami (Haematopinus suis), Inujirami (Linognathus setosus) and the like. *
  • Hymenoptera Monomorium phalaosis, Formica fusca japonica, Ruriari (Ochtellus pungens), Prisomylme puns. Ants such as Argentine ants (Linepithema humile) and wasps.
  • Cockroaches German cockroaches (Blatella germanica), Black cockroaches (Periplaneta fulignosa), Cockroach cockroach (Periplaneta americana), Japanese cockroach (Peripraneta brunet)
  • Isoptera Yamato termite (Reticulitermes speratus), Formosan subterranean termite (Coptotermes formosanus), the United States drywood termites (Incisitermes minor), Daikoku termites (Cryptotermes domesticus), Taiwan termites (Odontotermes formosanus), Kou Shun termite (Neotermes koshunensis), Satsuma termites (Glyptotermes satsumensis), white-tailed termites (Glyptotermes nakajimai), caterpillars (Glyptotermes fuscus), white-tailed termites (Glyptotermes kodamai), comb Toshiroari (Glyptotermes kushimensis), giant termite (Hodotermopsis japonica), Xiangzhou Ye termite (Coptotermes guangzhoensis), Amami termites (Reticulitermes amamianus), Miyatake, termites (Re
  • the pest control method of the present invention can be controlled by applying the composition of the present invention directly to pests by spraying, spraying, dipping, application, or by applying it to the habitat of pests.
  • This is a method for controlling a target pest (hereinafter referred to as the present invention control method).
  • the composition of the present invention is diluted, or the composition of the present invention is mixed with an inert carrier such as a solid carrier, a liquid carrier, or a gaseous carrier, and a surfactant or other adjuvant for formulation is added as necessary. Then, it may be applied to a pest or a pest habitat.
  • the habitat of a pest means the entire living sphere in which the pest is active, for example, a place including a pest nest, a feeding area, a path, and the like.
  • Examples of the preparation containing the composition of the present invention include solutions, oils, emulsions, wettable powders, flowables (suspensions in water, suspensions in oil, microcapsules, etc.), aerosols, carbon dioxide preparations, piezos.
  • a liquid agent an oil agent, a flowable agent, an aerosol agent, a resin kneading agent, a cellulose kneading agent, a paper impregnation agent, a nonwoven fabric impregnation agent, a knitted fabric impregnation agent, a resin impregnation agent, and a cellulose impregnation agent are exemplified.
  • solid carrier used in the preparation containing the composition of the present invention examples include clays (kaolin clay, diatomaceous earth, bentonite, fubasami clay, acidic clay), synthetic hydrous silicon oxide, talc, ceramic, and other inorganic minerals (sericite).
  • Resin kneading agent, cellulose kneading agent, paper impregnating agent, nonwoven fabric impregnating agent, knitted fabric impregnating agent, resin impregnating agent, cellulose impregnating agent, etc., as a substrate natural resin, polyethylene, polypropylene, polyacrylonitrile, (Polymethyl methacrylate, polyester resin such as polyethylene terephthalate, nylon resin such as nylon-6, nylon-11, nylon-66, polyamide resin, polyvinyl chloride, polyvinylidene chloride, vinyl chloride-propylene copolymer, polyurethane, etc.) Cellulose, paper, cloth (cotton, hemp, silk, etc.), non-woven fabric and the like are preferable.
  • liquid carrier examples include water, ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.), nitriles (acetonitrile, isobutyronitrile, etc.), acid amides (N, N-dimethylformamide, N, N-dimethylacetamide, etc.) Halogenated hydrocarbons (dichloromethane, trichloroethane, carbon tetrachloride, etc.), sulfoxides (dimethyl sulfoxide, etc.), propylene carbonate, vegetable oil, and the like.
  • ketones acetone, methyl ethyl ketone, cyclohexanone, etc.
  • nitriles acetonitrile, isobutyronitrile, etc.
  • acid amides N, N-dimethylformamide, N, N-dimethylacetamide, etc.
  • Halogenated hydrocarbons diichloromethane, trichloro
  • gaseous carrier examples include fluorocarbon, butane gas, LPG (liquefied petroleum gas), dimethyl ether, and carbon dioxide gas.
  • surfactant examples include nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, and polyethylene glycol fatty acid ester, and anions such as alkyl sulfonate, alkyl benzene sulfonate, and alkyl sulfate. Surfactant is mentioned.
  • formulation adjuvants include stickers, dispersants, colorants, antifreezes and stabilizers, such as casein, gelatin, sugars (starch, gum arabic, cellulose derivatives, alginic acid, etc.), cereals Powder, lignin derivative, bentonite, synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acids, etc.), glycerin, PAP (isopropyl acid phosphate), nordihydroguaiaretic acid, BHT (2,6-di-) by children and pets such as tert-butyl-4-methylphenol), BHA (mixture of 2-tert-butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol), dehydroacetic acid, pepper powder, etc.
  • Pest-attracting incense such as anti-fouling agent, cheese flavor, onion flavor peanut oil Etc. The.
  • the composition of the present invention or the preparation containing the composition of the present invention is pretreated on the path of pests.
  • Pests suitable for this embodiment include dwarf arthropods such as cockroaches, ants and spiders.
  • Formulations suitable for this embodiment include solutions, oils, emulsions, wettable powders, flowables (suspensions in water, suspensions in oil, microcapsules, etc.), aerosols and the like.
  • the composition of the present invention is mixed with dimethyl sulfoxide and the emulsion is mixed with the composition of the present invention and a surfactant such as polyoxyethylene styryl phenyl ether and calcium dodecylbenzenesulfonate.
  • a surfactant such as polyoxyethylene styryl phenyl ether and calcium dodecylbenzenesulfonate.
  • the wettable powder is prepared by mixing the composition of the present invention with a solid simple substance such as a synthetic hydrous silicon oxide fine powder or diatomaceous earth, and a surfactant such as sodium lauryl sulfate or calcium lignin sulfonate. be able to.
  • the flowable agent can be prepared by dispersing the composition of the present invention in an aqueous solution containing a surfactant such as polyoxyethylene alkyl ether sulfate ammonium salt using an emulsifier or a wet pulverizer.
  • a surfactant such as polyoxyethylene alkyl ether sulfate ammonium salt
  • the aerosol agent the composition of the present invention is used as it is, or a mixture of the composition of the present invention and an auxiliary solvent is put into an aerosol can, an aerosol valve is mounted, a gaseous carrier is filled, and an actuator is mounted. Can be prepared.
  • preparations such as a resin kneading agent, a cellulose kneading agent, a paper impregnating agent, a nonwoven fabric impregnating agent, a knitted fabric impregnating agent, a resin impregnating agent, and a cellulose impregnating agent are used as they are.
  • a station where pests can enter hereinafter referred to as the present extermination tool.
  • a pest habitat for example, near a pest nest or in a path.
  • this extermination tool are structures having a structure resembling pest nests, feeding grounds, etc.
  • Pests suitable for this embodiment include dwarf arthropods such as cockroaches, ants and spiders.
  • the resin kneading agent and the cellulose kneading agent go through a step of kneading the composition of the present invention or a preparation (solution, oil, etc.) containing the composition of the present invention on a substrate such as resin or cellulose using a normal kneading apparatus. It can be produced by molding by injection molding, extrusion molding, press molding or the like.
  • Paper impregnating agent, non-woven fabric impregnating agent, knitted fabric impregnating agent, resin impregnating agent, cellulose impregnating agent is a composition of the present invention or a preparation containing the composition of the present invention (liquid agent, oil agent, flowable agent, etc.), paper, non-woven fabric, resin, Manufactured by processing into a plate shape, film shape, tape shape, sheet shape, net shape, string shape, etc., through a process of supporting (impregnating, applying) on a substrate such as cellulose, a step of molding or cutting, etc. be able to.
  • these preparations may contain a target pest-inducing component.
  • a specific embodiment of the present extermination tool that can be used in the control method of the present invention is a structure having a doorway through which a pest can pass with a size that can be arranged in the vicinity of a pest nest or in a path
  • An extermination tool in which the composition of the present invention is treated on the inner surface of the structure may be mentioned.
  • the outer shape of the removal tool includes a rectangular parallelepiped, a hemisphere, a triangular pyramid, a quadrangular pyramid, a triangular prism, etc.
  • the size of the removal tool is 1 to 20 cm in length and 1 to 30 cm in width if it is a rectangular parallelepiped.
  • the size and number of doorways vary depending on the target pest, but if the target pest is a cockroach and the external shape of the extermination tool is a rectangular parallelepiped, the two places and one side in the longitudinal direction of the extermination tool are completely Or it is more preferable to set it as the shape opened partially.
  • the material of this extermination tool is not specifically limited, Paper and resin are preferable from a viewpoint of economical efficiency or workability.
  • composition of the present invention has excellent efficacy, one or more parts of the pest body (eg, antennae, feet, mouth, etc.) are brought into contact with the composition of the present invention for a short time to control the pest. be able to.
  • the composition of the present invention can be used on surfaces where pests frequently appear inside and outside buildings.
  • the control method of the present invention is suitable for controlling pests, particularly dwarf arthropods, inside, around and outdoors in buildings.
  • the present invention can be applied to a place where a pest is hidden (for example, the inside of a drawer, a pipe, a crack, or the like) and a place where a path for the pest is formed (for example, one corner, an edge, a cover plate, or the like).
  • the composition of the present invention is applied preferably in a linear or spot form.
  • the composition of the present invention is preferably applied only to places where children and pets do not touch.
  • the treatment amount of the composition of the present invention and the preparation containing the composition of the present invention may vary depending on the target pest, but is usually 1 to 5000 mg / m 2 , preferably 10 to 5000 mg / m 2 in terms of the present compound. More preferably, it is 20 to 1000 mg / m 2 .
  • the present composition can be used in combination with or in combination with known insecticides and synergists. Examples of active ingredients of such insecticides and synergists are shown below.
  • pyrethroid compounds acrinathrin, allethrin, benfluthrin, beta-cyfluthrin, bifenthrin, cycloprotorin, fluprothrin (cycloprothrin) , Cypermethrin, deltamethrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucitrate f lucytrinate, flufenprox, flumethrin, fluvalinate, halfenprox, imiprothrin, permethrin, praretrin, praretrin resmethrin, sigma-cypermethrin, silafluofen, tefluthrin, tralomethrin, transfluthrin, tetramethrin thrin), phenothrin, cyphenothrin, alpha-cypermethrin, zeta-
  • Neonicotinoid compounds imidacloprid (imidac1oprid), nitenpyram (nitenpyram), acetamiprid (acetamipride), thiamethoxam, thiacloprid (thiacloprid), dinoteurin (dinothurine) (6) Benzoylurea compound Chlorfluazuron, bistrifluron, diafenthiuron, diflubenzuron, fluazuron, flucycloxuron, flucyclolone (Flufenoxuron), hexaflumuron, lufenuron, novaluron, novifluuron, teflubenzuron, triflumuron, and triflumuron.
  • Phenylpyrazole compounds Acetoprole, ethiprole, vaniliprole, pyriprole, and pyrafluprole.
  • Bt toxin Live spores and produced crystal toxins derived from Bacillus thuringiensis, and mixtures thereof Other insecticide active ingredients chlorfenapyr, cyantraniliprole, cyromazine, Hydroprene, methoprene, indoxacarb, methoxadiazone, pyriproxyfen, spinosad, chlorantraniprolol ).
  • the organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate.
  • the obtained organic layer was dried under reduced pressure.
  • the obtained residue was subjected to silica gel chromatography to obtain 326 mg of the present compound 4 described below.
  • Table 1 shows the physical property values of the present compounds described in the above production examples.
  • Formulation Example 1 44 mg of the present compound 1 and 10 mL of n-pentanol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain Composition A of the present invention.
  • Formulation Example 2 44 mg of the present compound 1 and 10 mL of n-heptanol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain Composition B of the present invention.
  • Formulation Example 3 44 mg of the present compound 1 and 10 mL of n-octanol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain Composition C of the present invention.
  • Formulation Example 4 44 mg of the present compound 1 and 10 mL of cyclopentanol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition D of the present invention.
  • Formulation Example 5 44 mg of this compound 1 and 10 mL of butylene glycol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition E of the present invention.
  • Formulation Example 6 44 mg of the present compound 1 and 10 mL of glycerin [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition F of the present invention.
  • Formulation Example 7 44 mg of the present compound 1 and 10 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain a composition G of the present invention.
  • Formulation Example 8 44 mg of the present compound 1 and 10 mL of ethylene glycol monomethyl ether [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition H of the present invention.
  • Formulation Example 10 44 mg of the present compound 1 and 10 mL of propylene glycol phenyl ether [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition J of the present invention.
  • Formulation Example 13 Comparative composition C was obtained by mixing 44 mg of indoxacarb and 10 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.].
  • Formulation Example 10 44 mg of the present compound 2 and 10 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] are mixed to obtain the composition K of the present invention.
  • Formulation Example 11 44 mg of the present compound 3 and 10 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] are mixed to obtain the present composition L.
  • Formulation Example 12 44 mg of the present compound 4 and 10 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] are mixed to obtain the composition M of the present invention.
  • Formulation Example 13 5 g of any of the present compounds 1 to 4 is mixed with 40 g of tetrahydrofurfuryl alcohol and 55 g of N, N-dimethylformamide to obtain a solution.
  • Formulation Example 14 27 mg of the present compound 1 and 7 mL of tetrahydrofurfuryl alcohol are mixed, and 0.7 mL of the mixture is dropped onto a 6 ⁇ 9 cm cardboard.
  • the cardboard is folded in three and formed into a cylindrical shape having a triangular cross section (2 cm on a side, 9 cm in length), and the outside is covered with vinyl tape to obtain a paper impregnating agent.
  • Formulation Example 15 44 mg of the present compound 1 and 10 mL of isopropyl acetate [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain Composition N of the present invention.
  • Formulation Example 16 44 mg of the present compound 1 and 10 mL of octyl acetate [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition O of the present invention.
  • Formulation Example 17 44 mg of the present compound 1 and 10 mL of methyl laurate [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain the present composition P.
  • Formulation Example 18 44 mg of the present compound 1 and 10 mL of methyl myristate [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition Q of the present invention.
  • Formulation Example 19 44 mg of the present compound 1 and 10 mL of ATBC [manufactured by Taoka Chemical Co., Ltd.] were mixed to obtain the present composition R.
  • Formulation Example 20 44 mg of the present compound 1 and 10 mL of dimethyl succinate [manufactured by Tokyo Chemical Industry] were mixed to obtain the present composition S.
  • Formulation Example 21 44 mg of the present compound 1 and 10 mL of linoleic acid [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed to obtain composition T of the present invention.
  • Formulation Example 22 27 mg of the present compound 1 and 7 mL of linoleic acid [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (2 cm on a side of a triangle, 9 cm in length), and the outside was covered with vinyl tape to obtain a paper impregnating agent 1.
  • Formulation Example 23 27 mg of this compound 1 and 7 mL of ATBC [manufactured by Taoka Chemical Co., Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (2 cm on a side, 9 cm in length), and the outside was covered with vinyl tape to obtain a paper impregnating agent 2.
  • Formulation Example 24 27 mg of this compound 1 and 7 mL of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and molded into a cylindrical shape with a triangular cross section (2 cm on a side, 9 cm in length), and the outside was covered with vinyl tape to obtain a paper impregnating agent 3.
  • Formulation Example 25 27 mg of this compound 1 and 7 mL of propylene glycol phenyl ether [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (2 cm on a triangle, 9 cm in length), and the outside was covered with vinyl tape to obtain a paper impregnating agent 4.
  • Formulation Example 26 27 mg of this compound 1 and 7 mL of ethylene glycol monomethyl ether [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (triangle side 2 cm, length 9 cm), and the outside was covered with vinyl tape to obtain a paper impregnating agent 5.
  • Formulation Example 27 27 mg of the present compound 1 and 7 mL of octyl acetate [manufactured by Wako Pure Chemical Industries, Ltd.] were mixed, and 0.7 mL of the mixture was dropped onto 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (2 cm on a triangle, 9 cm in length), and the outside was covered with vinyl tape to obtain a paper impregnating agent 6.
  • Formulation Example 28 27 mg of this compound 1 and 7 mL of acetone [manufactured by Nacalai Tesque] were mixed, and 0.7 mL of the mixture was dropped onto a 6 ⁇ 9 cm cardboard.
  • the cardboard was folded in three and formed into a cylindrical shape with a triangular cross section (2 cm on a side, 9 cm in length), and the outside was covered with vinyl tape to obtain a comparative paper impregnating agent 1.
  • Formulation Example 29 A mixture of 1 g of the present compound 1 and 39 g of linoleic acid [manufactured by Wako Pure Chemical Industries, Ltd.] is added to 60 g of 3.3 wt% aqueous solution of Gohsenol GH-17 [manufactured by Nippon Synthetic Chemical Industry, polyvinyl alcohol]. K.
  • the composition U of the present invention was obtained by emulsifying with a Robomix [manufactured by PRIMIX, an emulsification mixer] so that the volume median diameter of the droplets was about 30 ⁇ m.
  • Formulation Example 30 A mixture of 1 g of the present compound 1 and 39 g of ATBC [manufactured by Taoka Chemical] was added to 60 g of 3.3 wt% aqueous solution of Gohsenol GH-17 [manufactured by Nippon Synthetic Chemical Industry, polyvinyl alcohol]. K.
  • the composition V of the present invention was obtained by emulsifying using a Robomix [manufactured by PRIMIX, an emulsification mixer] so that the volume median diameter of the droplets was about 30 ⁇ m.
  • Formulation Example 31 A mixed solution of 1 g of the present compound 1 and 39 g of isopropyl myristate [Wako Pure Chemical Industries, Ltd.] was added to 60 g of a 3.3 wt% aqueous solution of GOHSENOL GH-17 [manufactured by Nippon Synthetic Chemical Industry, polyvinyl alcohol].
  • a comparative composition D was obtained by emulsifying using a Robomix [manufactured by Primex, an emulsifying mixer] so that the volume median diameter of the droplets was about 30 ⁇ m.
  • Formulation Example 32 0.02 part of the present compound 1, 60 parts of tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemical Industries, Ltd.] and 30 parts of 0.2% aqueous sodium benzoate solution are placed in an aerosol can (AE290WO, manufactured by Toyo Seikan Co., Ltd.).
  • An aerosol formulation A was obtained by attaching a valve part (push-down type valve with a stem having a hole diameter of 0.33 mm, manufactured by Nippon Precision Valve) and filling 10 parts of propellant (dimethyl ether) through the valve part. .
  • Formulation Example 33 0.02 part of the present compound 1, 60 parts of acetone [manufactured by Nacalai Tesque] and 30 parts of 0.2% aqueous sodium benzoate solution are placed in an aerosol can (AE290WO, manufactured by Toyo Seikan Co., Ltd.), and the valve part (pore size is reduced). A push-down valve equipped with a 0.33 mm stem (manufactured by Nippon Precision Valve) was attached, and 10 parts of propellant (dimethyl ether) was filled through the valve part to obtain a comparative aerosol preparation 1.
  • AE290WO manufactured by Toyo Seikan Co., Ltd.
  • Formulation Example 34 0.02 part of the present compound 1, 60 parts of ethanol [manufactured by Nacalai Tesque] and 30 parts of 0.2% sodium benzoate aqueous solution are placed in an aerosol can (AE290WO, manufactured by Toyo Seikan), and the valve part (pore size is A push-down valve equipped with a 0.33 mm stem (manufactured by Nippon Precision Valve) was attached, and 10 parts of propellant (dimethyl ether) was filled through the valve part to obtain a comparative aerosol preparation 2.
  • AE290WO manufactured by Toyo Seikan
  • Formulation Example 35 0.02 part of the present compound 1, 60 parts of propylene glycol monomethyl ether [manufactured by Wako Pure Chemical Industries, Ltd.] and 30 parts of 0.2% aqueous sodium benzoate solution are placed in an aerosol can (AE290WO, manufactured by Toyo Seikan Co., Ltd.). Attach a valve part (push-down valve with a stem with a hole diameter of 0.33 mm, manufactured by Nippon Precision Valve), and fill 10 parts of propellant (dimethyl ether) through the valve part to obtain comparative aerosol formulation 2 It was.
  • AE290WO manufactured by Toyo Seikan Co., Ltd.
  • Test Example 1 Contact test on German cockroach (Blattella germanica).
  • the composition of the present invention comparative composition, tetrahydrofurfuryl alcohol [manufactured by Wako Pure Chemicals], ATBC [manufactured by Taoka Chemical], or dimethyl succinate [manufactured by Wako Pure Chemicals]
  • the filter paper was uniformly dropped. After being placed in a room (about 25 ° C., relative humidity about 60%) for about 1 hour, the filter paper was laid on the bottom of a plastic cup having a bottom diameter of about 10 cm and a height of about 7 cm.
  • Control rate (%) (Number of dead and moribund insects on day 7 / number of samples) x 100
  • Test Example 2 Spray treatment test.
  • the solution described in Preparation Example 13 is diluted with water to a predetermined concentration.
  • the water dilution is sprayed with a sprayer from a distance of 10 to 100 cm onto a treated surface (15 ⁇ 15 cm) such as a decorative board or a plywood board, and the amount of the diluted liquid adhering to the treated board is 10 to 500 mg / m 2.
  • a ring made of a plastic plate (diameter: about 14 cm, height: about 5 cm) is placed on a processing plate stored for 24 hours under indoor conditions, and 10 cockroaches in a group (5 males, 5 females). Release.
  • Margarine is applied on the inner surface of the ring to prevent scooping up, and the cockroach is forcibly brought into contact with the processing plate. After 1 hour of contact, German cockroaches are collected in a clean cup and fed with food and water for storage. Seven days later, the state of German cockroaches is observed, and the control rate is calculated from the proportion of dead individuals using the following formula. As a result, it can be confirmed that the liquid preparation described in Preparation Example 13 exhibits an excellent effect.
  • Control rate (%) (number of dead individuals + number of moribund individuals) / number of test individuals x 100
  • Test Example 3 Insecticidal test by accidental contact with paper impregnating agent A large metal container (bottom about 180 x 120 cm, height about 15 cm), mouse solid feed, water, and 18 cm x 32 cm balls as nesting place A corrugated sheet prepared by folding a 32 cm side of the paper every 2 cm is installed as shown in FIG. After that, only one of the cockroaches, black-eyed cockroaches, and American cockroaches is released. The number of cockroaches released was 50 (25 males, 25 females) for German cockroaches, 20 (10 males, 10 females) for black cockroaches, and 20 (10 males, 10 females) for American cockroaches. Head).
  • one paper impregnating agent obtained in Formulation Example 14 is placed in the container as shown in FIG. Under these conditions, the test insects can obtain everything necessary for survival near the corrugated plate, so that most of the test period is active near the corrugated plate. Seven days after the paper impregnating agent is installed, the state of cockroaches is observed, and the control rate is calculated by the following formula. As a result, it can be confirmed that the paper impregnating agent obtained in Formulation Example 14 exhibits an excellent control effect.
  • Control rate (%) (number of dead individuals + number of moribund individuals) / number of test individuals x 100
  • Test Example 4 Contact Test to German Cockroaches (Blatella germanica)
  • the composition T1 mL of the present invention described in Formulation Example 21 was uniformly dropped onto a circular filter paper having a diameter of about 10 cm. After being placed in a room (about 25 ° C., relative humidity about 60%) for about 1 hour, the filter paper was laid on the bottom of a plastic cup having a bottom diameter of about 10 cm and a height of about 7 cm. 10 adult German cockroaches (Blatella germanica) (5 males, 5 females) were released into the cup and contacted with the filter paper for 1 minute. The German cockroaches were collected in a new cup and fed with food and water. 25 ° C. and relative humidity of about 60%). Seven days after the test, the state of German cockroaches was observed, and the control rate calculated using the following formula is shown in Table 3.
  • Control rate (%) (Number of dead and moribund insects on day 7 / number of samples) x 100
  • Test Example 5 Insecticidal test by accidental contact with paper impregnant 18 cm as solid feed for mice, water, and nesting place in resin container (bottom is about 25.5 ⁇ 37.5 cm, height is about 6.5 cm) A corrugated sheet prepared by folding a 32 cm side of a ⁇ 32 cm cardboard every 2 cm was installed as shown in FIG. Then, 50 adult German cockroaches (Blatella germanica) (25 males and 25 females) were released. After leaving the test insect to acclimatize to the test environment for one day or more, install one paper impregnating agent 1, paper impregnating agent 5 or comparative paper impregnating agent 1 in the container as shown in FIG. did.
  • test insects settled under the corrugated sheet, and the paper impregnating agent contained no attractant, so that most of the test period lived under or near the corrugated sheet.
  • the state of cockroaches was observed, and the control rate was calculated by the following formula.
  • Control rate (%) (number of dead individuals + number of moribund individuals) / number of test individuals x 100
  • Test Example 6 Contact test for Monomori phalaonis.
  • a diluted solution obtained by diluting the composition of the present invention described in the formulation example or the comparative composition with pure water so as to achieve the dilution ratio shown in Table 5 was obtained from a decorative board of about 15 cm square (Sunprint Normandy Pine No. 119 obtained from Tarutani Packaging Co., Ltd. ) Was uniformly sprayed so that the compound concentration was 50 mg / m 2, and dried at room temperature for 2 weeks.
  • Control rate (%) (Number of dead and moribund insects on day 7 / number of samples) x 100
  • Test Example 7 Aerosol spray test on Monomaria phalaonis. On the bottom of a plastic cup having a diameter of about 4.5 cm and a height of about 3.5 cm having a runaway prevention surface made of polytetrafluoroethylene on the inner wall, 10 tiger moths (Monomomori pharaonis) were placed. The plastic cup was placed on the bottom of a cylinder made of glass and plastic having an inner diameter of 16 cm and a height of 95 cm. Aerosol preparation A or comparative aerosol preparations 1 to 3 were sprayed from the upper part of the cylinder to the inside of the cylinder using an aerosol micro-spraying device so that the spray amount shown in Table 6 was obtained.
  • Aerosol preparation A or comparative aerosol preparations 1 to 3 were sprayed from the upper part of the cylinder to the inside of the cylinder using an aerosol micro-spraying device so that the spray amount shown in Table 6 was obtained.
  • the plastic cup was removed from the bottom of the cylinder, the house peas were transferred to a new cup, fed with food and water, and stored indoors (about 25 ° C., about 60% relative humidity). After 7 days, the state of the house moth was observed, and the control rate calculated using the following formula is shown in Table 6.
  • Control rate (%) (Number of dead and moribund insects on day 7 / number of samples) x 100
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WO2019013273A1 (ja) * 2017-07-13 2019-01-17 住友化学株式会社 複素環化合物及びそれを含有する有害節足動物防除剤
CN110914264A (zh) * 2017-07-13 2020-03-24 住友化学株式会社 杂环化合物及含有其的有害节肢动物防治剂
JPWO2019013273A1 (ja) * 2017-07-13 2020-05-07 住友化学株式会社 複素環化合物及びそれを含有する有害節足動物防除剤
US11203590B2 (en) 2017-07-13 2021-12-21 Sumitomo Chemical Company, Limited Heterocyclic compound and harmful-arthropod control agent containing same
CN110914264B (zh) * 2017-07-13 2022-02-11 住友化学株式会社 杂环化合物及含有其的有害节肢动物防治剂
JP7082978B2 (ja) 2017-07-13 2022-06-09 住友化学株式会社 複素環化合物及びそれを含有する有害節足動物防除剤
EP3453706A1 (en) 2017-09-08 2019-03-13 Basf Se Pesticidal imidazole compounds

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