WO2005042474A1 - ジアミン誘導体、その製造方法およびそれらを有効成分とする植物病害防除剤 - Google Patents
ジアミン誘導体、その製造方法およびそれらを有効成分とする植物病害防除剤 Download PDFInfo
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- WO2005042474A1 WO2005042474A1 PCT/JP2004/015471 JP2004015471W WO2005042474A1 WO 2005042474 A1 WO2005042474 A1 WO 2005042474A1 JP 2004015471 W JP2004015471 W JP 2004015471W WO 2005042474 A1 WO2005042474 A1 WO 2005042474A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/20—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
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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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
- C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/44—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/43—Y being a hetero atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D307/85—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
Definitions
- Diamine derivatives process for producing the same, and plant disease control agents containing them as active ingredients
- the present invention relates to a novel diamine derivative, a method for producing the same, and a plant disease controlling agent containing them as an active ingredient.
- Pest control plays an important role in rice cultivation, and rice blast is an important disease, and various plant disease control agents have been developed and used. However, there is no sufficient activity in controlling plant diseases or harm to useful crops. In recent years, due to the frequent use of plant disease control agents, drug-resistant bacteria have emerged, and existing drugs may not show sufficient activity. In view of the above, a new plant disease control agent capable of controlling harmful bacteria at a low concentration is required.
- JP-A-2003-096046 discloses a diamine derivative different from the compound of the present invention and a plant disease controlling agent containing the same as an active ingredient. However, the usefulness of a diamine derivative having an oxycarbol group having a halogen-substituted hydrocarbon is described here.
- Patent Document 1 JP 2003-096046 (WO2003008372)
- An object of the present invention is to provide a diamine derivative having an excellent control effect on rice blast.
- the present inventors have now found that among diamine derivatives, particularly a diamine derivative having an oxycarbol group having a halogen-substituted hydrocarbon, rice has high and controlling effects on rice blast. . This control effect was found to be significantly superior to the effect obtained by other diamine derivatives as disclosed in, for example, JP-A-2003-096046, and the present invention was completed. [0005] That is, the present invention is as follows.
- R 1 represents a halogen-substituted hydrocarbon having 16 carbon atoms
- R 2 and R 7 each independently represent a hydrogen atom, a hydrocarbon having 16 carbon atoms or an acyl group
- R3 and R4 each independently include a hydrogen atom, a substituted or unsubstituted hydrocarbon having 16 carbon atoms, or an optionally substituted heteroaryl group or a bonding carbon atom
- R5 and R6 each independently represent a hydrogen atom or a hydrocarbon having 16 carbon atoms
- R8 represents an optionally substituted arylalkyl group
- a plant disease control agent comprising the diamine derivative according to the above [1] as an active ingredient.
- a compound represented by the formula (2) is converted to a compound represented by the formula (4)
- the diamine derivative according to the present invention has an excellent control effect on rice blast by having an oxycarbol group having a halogen-substituted hydrocarbon.
- hydrocarbons having 16 carbon atoms substituted with halogen include chloromethyl, 2-chloroethyl, 2,2,2-trichloroethyl, 3-chloro-1-propyl, 4-chloro mouth- Chlorine-substituted alkyl group such as 1-butyl group, 2-fluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,1,3,3,3-hexafluoro mouth- 2-propyl group, 1,3-difluoro-2-propyl group, 5-fluoro-1-pentyl group, 6,6,6,5,5,4,4,3,3-nonafluoro-1-hexyl group , 1-ethoxy-2,2,2-trifluoroethyl group, etc., fluorine-substituted alkyl group, 2-bromo
- Alkyl groups containing two or more halogens such as iodine-substituted alkyl groups, 3-bromo-1,1,1,1-trifluoro-2-propyl groups, cyclopropyl cyclopropyl groups, 2-chlorocyclobutyl groups, and 2-chlorocyclyl groups
- Chlorine-substituted cycloalkyl groups such as pentyl, 2-chlorocyclohexyl, 3-chlorocyclohexyl and 4-chlorocyclohexyl, 2-fluorocyclohexyl, 2,2,3,3-tetrafluoro Fluoro-substituted cycloalkyl such as rocyclopropyl, bromine-substituted cycloalkyl such as 2-bromocyclohexyl, iodine-substituted cycloalkyl such as 2-cyclohexyl, 2-chloro-2-propyl
- hydrocarbon having a carbon number of 16 examples include methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, butyl, and propyl.
- a heteroaryl group includes a pyridyl group, a pyrimidyl group, a cyenyl group, a furanyl group, a pyrazolyl group, an imidazolyl group, an isothiazolyl group, an isoxazolyl group, an indolyl group, Quinolyl group, benzofuranyl group, benzochenyl group, benzoxazolyl group, benzisoxazolyl group, benzimidazolyl group Benzothiazoly
- alkyl group such as propyl group or butyl group
- cycloalkyl group such as cyclopropyl group, cyclobutyl group, cyclopentyl group or cyclohexyl group
- trifluoromethyl group difluoromethyl group, bromodifluoromethyl group or trifluoromethyl group.
- Halogen-substituted alkyl groups such as chloroethyl group, alkoxy groups such as methoxy group, ethoxy group, propoxy group or butoxy group, and halogen-substituted alkoxy groups such as trifluoromethoxy group, difluoromethoxy group, or trifluoroethoxy group.
- Alkyloxycarbamino groups such as lumino group, methyloxycarbo-amino group, ethyloxycarbo-amino group, propyloxycarbo-amino group, butyloxycarbo-amino group, cyclopropylo group, etc. Kisika Cycloalkyloxycarbo-amino, such as boroamino, cyclobutyloxycarbo-amino, cyclopentyloxycarbo-amino, cyclohexylcarboxy-amino, methylthio, ethylthio, propylthio or butylthio. Alkylthio groups such as groups
- Halogen-substituted alkylthio groups such as trifluoromethylthio, difluoromethylthio, or trifluoroethylthio; alkylsulfurs such as methanesulfiel, ethanesulfiel, polyesterpansulfiel, or butanesulfiel; Halogen-substituted alkylsulfyl groups such as fiell group, trifluoromethanesulfiel group, difluoromethanesulfiel group or trifluoromethanesulfiel group, methanesulfol group, ethanesulfol group, propanesulfol group or butanesulfol group Halogen-substituted alkylsulfol groups such as alkylsulfonyl groups such as trifluoromethylsulfonyl group, trifluoromethanesulfuryl group, difluoromethanesulfuryl group or trifluor
- Examples of the leaving group include a halogen atom represented by a chlorine atom, and an alkoxy represented by a methoxy group and an ethoxy group.
- Examples thereof include arylcarbonyl group represented by -loxy group, alkylthio group represented by methylthio group, 2,5-dioxopyrrolidi-loxy group, benzotriazolyloxy group and imidazolyl group. it can.
- the compound of the present invention represented by the formula (1) is a novel compound, and the compound represented by the formula (1) can be produced by the method described in the following reaction formula (1). .
- R1, R2, R3, R4, R5, R6 and R7 have the same meaning as in formula (2), and R8 and X have the same meaning as in formula (3).
- a diamine derivative represented by the formula (2) or a salt thereof is combined with a known carbonitrile conjugate represented by the formula (3) in the absence of a solvent or a base in a solvent.
- a diamine derivative represented by the formula (1) can be produced.
- Examples of the base used in the reaction represented by the reaction formula (1) include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, magnesium hydroxide, calcium hydroxide and the like.
- DMAP dimethylamino
- the amount of these bases to be used is not particularly limited. In such a case, it can be used as a solvent.
- a halogen such as water, dichloromethane, and chloroform is used unless it reacts with the formulas (1), (2) and (3).
- Hydrocarbons aromatic hydrocarbons such as benzene, toluene and xylene, aliphatic hydrocarbons such as hexane and heptane, dimethylformamide (DMF), dimethylacetamide (DMA), dimethyl sulfoxide (DMSO)
- Aprotic polar solvents such as 1,3-dimethyl-2-imidazolidinone (DMI), 1-methyl-2-pyrrolidone (NMP), getyl ether, diisopropyl ether, 1,2-dimethoxyethane Ethers such as (DME), tetrahydrofuran (THF) and dioxane; and -tolyls such as acetonitrile and propio-tolyl.
- the equivalent of the carbonyl compound represented by the formula (3) is preferably 11 equivalents to the compound represented by the formula (2), more preferably 11 1.2 equivalents.
- the reaction temperature and reaction time of the above reaction can be varied over a wide range.
- the reaction temperature is preferably -20 to 200 ° C, more preferably 0 to 100 ° C, and the reaction time is preferably 0.01 to 150 hours, more preferably 0.1 to 15 hours. It is.
- the amine derivative represented by the formula (2) in the reaction formula (1) and a salt thereof other than those commercially available include, for example, Gabriel method, Delpin method, cyano group, amide, imine, oxime and the like. It can be easily produced by a method described in a known method for synthesizing an amine, such as the reduction of tetrahedron asymmetry (Tetrahedron Asymmetry), Vol. 11, p. 1907 (2000).
- the compound represented by the formula (3) in the reaction formula (1) can be obtained by converting a known carboxylic acid derivative represented by the formula (4) to thionyl chloride, oxalyl chloride, phosgene, phosphorus oxychloride, It can be produced by a conventional method of reacting with phosphorus chloride, phosphorus pentachloride, thionyl bromide, phosphorus tribromide, getylaminosulfur trifluoride, 1,1, -carbonylbis-1H-imidazole and the like.
- the compound represented by the formula (3) in the reaction formula (1) can be obtained by converting a known carboxylic acid derivative represented by the formula (4) to alcohols such as methyl alcohol and ethyl alcohol, phenol, nitrophenol and the like. Can also be produced by a conventional method of reacting with phenols.
- the compound represented by the formula (3) in the reaction formula (1) can be obtained by converting a known carboxylic acid derivative represented by the formula (4) to a methyl formate such as methyl chloroformate or phenyl chloroformate. When reacted with esters It can also be manufactured by the conventional method.
- the compound represented by the formula (3) in the reaction formula (1) is obtained by reacting a known carboxylic acid derivative represented by the formula (4) with N-hydroxysuccinimide, 1-hydroxybenzotriazole and the like. Let's do it!
- It can also be manufactured by a conventional method.
- the compound of the present invention represented by the formula (1) can also be produced by the method described in the reaction formula (2).
- R1, R2, R3, R4, R5, R6 and R7 have the same meaning as in formula (2), and R8 is a formula
- the diamine derivative represented by the formula (2) or a salt thereof is condensed with a known carboxylic acid derivative represented by the formula (4) in a solvent or in a solvent to obtain a compound represented by the formula
- the diamine derivative represented by (1) can be produced.
- the condensing agent includes N, ⁇ '-dicyclohexylcarbodiimide, 1,1, -carbylbis-1H-imidazole, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide ' Hydrochloride, 2-chloro-1,3-dimethylimidazolidum chloride and the like can be used.
- the amount of the condensing agent to be used is 112 equivalents, preferably 1 1.2 equivalents, to the compound represented by the formula (4).
- the organic solvent in this case is the same as that used in the method represented by the reaction formula (1), unless it reacts with the formulas (1), (2) and (4). Can be used.
- the amount of the carboxylic acid derivative represented by the formula (4) to be used is 112 equivalents, preferably 11.1.2 equivalents to the diamine derivative represented by the formula (2).
- reaction temperature and reaction time of the above reaction can be varied over a wide range. Generally, the reaction temperature is between -20 and 200 ° C, preferably between 0 and 100 ° C. The reaction time is 0.01 to 50 hours, preferably 0.1 to 15 hours. [0039]
- the compound of the present invention represented by the formula (1) can also be produced by the method described in the reaction formula (3).
- R2, R3, R4, R5, R6, R7 and R8 have the same meaning as in formula (5), and R1 and X have the same meaning as in formula (6).
- the diamine derivative represented by the formula (5) or a salt thereof is mixed with a known compound represented by the formula (6) in the absence of a solvent or a solvent in the presence of a base or a base.
- a diamine derivative represented by the formula (1) can be produced.
- the compound represented by the formula (6) in the reaction formula (3) reacts the corresponding alcohol with phosgene such as phosgene and triphosgene, and chloroformate such as phenol chloroformate. It can be manufactured by the usual method of letting it go.
- phosgene such as phosgene and triphosgene
- chloroformate such as phenol chloroformate
- the use amount of these bases is not particularly limited, and when the above-mentioned organic bases are used, they can be used as a solvent.
- the organic solvent may be the same as that used in the method represented by the reaction formula (1) as long as it does not react with the formulas (1), (5) and (6). Can be used.
- the amount of the compound represented by the formula (6) to be used is 114 equivalents, preferably 112 equivalents, to the diamine derivative represented by the formula (5).
- the reaction temperature and reaction time of the above reaction can be varied over a wide range.
- the reaction temperature is between -20 and 200 ° C, preferably between 0 and 100 ° C.
- the reaction time is 0.01 to 50 hours, preferably 0.1 to 15 hours.
- the diamine derivative represented by the formula (1) has an asymmetric carbon depending on the type of the substituent, and may exist as an optical isomer, a diastereoisomer, a racemate, and a mixture at an arbitrary ratio.
- the And all isomers of this kind as well as mixtures thereof are also included in the present invention.
- the plant disease controlling agent containing the diamine derivative represented by the formula (1), which is the compound of the present invention, as an active ingredient shows an excellent controlling effect against rice blast (Pyricularia oryzae) and the like.
- the diamine derivative represented by the formula (1) which is the compound of the present invention, is used in combination with other plant disease control agents, pesticides, herbicides, plant growth regulators and other pesticides, soil conditioners or fertilizers. Not only can they be mixed and used, but also mixed preparations with these can be used.
- the compound of the present invention may be used as it is, but is preferably applied in the form of a composition mixed with a carrier containing a solid or liquid diluent.
- a carrier refers to a synthetic or natural inorganic or organic substance formulated to assist in reaching the active ingredient at the site to be treated or to facilitate storage, transport, and handling of the active ingredient compound. I do.
- Suitable solid carriers include clays such as montmorillonite, kaolinite and bentonite, diatomaceous earth, terra alba, talc, vermiyukirite, gypsum, calcium carbonate, white carbonate, ammonium sulfate and other inorganic substances, soy flour, flour and the like. And urea.
- Suitable liquid carriers include aromatic hydrocarbons such as toluene, xylene and cumene, paraffinic hydrocarbons such as kerosene and mineral oil, and halogenated hydrocarbons such as carbon tetrachloride, chloroform and dichloroethane. , Ketones such as acetone and methyl ethyl ketone, ethers such as dioxane, tetrahydrofuran, diethylene glycol dimethyl ether, alcohols such as methanol, ethanol, propanol and ethylene glycol, dimethylformamide, dimethyl sulfoxide, 1-methyl-2 Aprotic polar solvents such as -pyrrolidone and water;
- aromatic hydrocarbons such as toluene, xylene and cumene
- paraffinic hydrocarbons such as kerosene and mineral oil
- halogenated hydrocarbons such as carbon tetrachloride, chloroform and dichloroethane.
- the following adjuvants may be used alone or in combination according to the purpose, taking into account the dosage form of the preparation, the application scene, and the like. Monkey
- Auxiliaries include, for the purpose of emulsification, dispersion, spreading, wetting, binding and stabilization, ligninsulfonate, alkylbenzenesulfonate, alkylsulfate, polio, and the like.
- Aeon surfactants such as xylanolylene quinolequinole sulfate and polyxylene olenoquinolelate phosphate, polyoxyalkylene alkyl ether, polyoxyalkylene alkyl aryl ether, polyoxyalkylene Nonionics such as alkylamines, polyoxyalkylene alkylamides, polyoxyalkylene alkylthioethers, polyoxyalkylene fatty acid esters, glycerin fatty acid esters, sorbitan fatty acid esters, polyoxyalkylene sorbitan fatty acid esters, and polyoxypropylene polyoxyethylene block polymers
- Surfactants calcium stearate, lubricants such as waxes, stabilizers such as isopropyl hydrogen phosphate, other methylcellulose, carboxymethylcellulose Loin, casein, gum arabic, and the like.
- these ingredients are not limited to the above!
- the amount of the active ingredient of the compound of the present invention is usually 0.5 to 20% by weight for powders, 5 to 50% by weight for emulsions, 10 to 90% by weight for wettable powders, and 0.1 to 20% for granules. % And 10-90% by weight for flowable products.
- the amount of carrier in each dosage form is usually 60-99% by weight for powders, 40-95% by weight for emulsions, 10-90% by weight for wettable powders, 80-99% by weight for granules and flowable preparations. Then it is 10-90% by weight.
- the amount of adjuvants is usually 0.1-20% by weight for powders, 120% by weight for emulsions, 0.1-20% by weight for wettable powders, and 0.1-20% by weight for granules.
- N- (4-Methylbenzoyl) -3-methyl-1,2-butanediamine hydrochloride 0.59 g of triethylamine was added to 6 ml of a solution of dichloromethane in 6 ml of dichloromethane under ice-cooling. A 25 g dichloromethane solution (2 ml) was stirred at room temperature for 4 hours under ice cooling. The reaction solution was purified by silica gel column chromatography (ethyl acetate Z hexane) to obtain 0.43 g of the title compound as white crystals.
- reaction solution was allowed to stand at room temperature for 1 hour, concentrated under reduced pressure, and 50 ml of ethyl acetate was added to the obtained residue, followed by washing with water.
- the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain a solid.
- the obtained solid was washed with diisopropyl ether, and then purified by silica gel column chromatography (ethyl acetate Z hexane) to obtain 0.34 g of the title compound as white crystals.
- N- (4-Methylbenzoyl) -3-methyl-1,2-butanediamine hydrochloride 0.45 g of triethylamine was added to 5 ml of a solution of 0.550 g of dichloromethane in ice-cooled water, and chloroformate 2,2 0.41 g of 2-trichloromethyl ether was stirred at room temperature for 4 hours under ice cooling.
- the reaction solution was purified by silica gel column chromatography (ethyl acetate Z hexane) to obtain 0.52 g of the title compound as white crystals.
- a mixture of 0.65 g of 1,1,1,3,3,3-hexafluoro-2-propanol and 0.43 g of triethylamine was added to 6 ml of a dichloromethane solution of 0.78 g of chloroformic acid 4-nitrophenyl in 0.4 ml of triethylamine. Added under cooling. After the reaction solution was stirred for 1 hour under ice cooling, 0.50 g of N- (4-methylbenzoyl) -3-methyl-1,2-butanediamine hydrochloride was added under ice cooling. After the reaction solution was stirred under ice cooling for 15 minutes, 0.21 g of triethylamine was added under ice cooling.
- the reaction solution was stirred for 1 hour under ice cooling and for 1 hour at room temperature, and then left for 1 hour.
- the reaction solution was washed with 50 ml of dichloromethane with water and water. .
- the organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure.
- the obtained solid was purified by silica gel column chromatography (ethyl acetate Z hexane) to obtain 0.38 g of the title compound as white crystals. .
- Table 1 The compounds represented by the formula (1) which can be produced in the same manner as in Examples 11 to 15 are shown in Table 1 (Tables 11 to 13). Some physical properties are shown in Table 2 (Table 2-1 Table 1-2 Table 9).
- Me represents a methyl group
- Et represents an ethyl group
- n-Pr represents a normal propyl group
- i-Pr represents an isopropyl group
- cyclohexyl represents a cyclohexyl group.
- Example 8 [0079] wettable powder
- Compound of the present invention (4) 30 parts, kaolinite 63 parts, solpol 5039 (mixture of aionic surfactant and white carbon: trade name of Toho Chemical Co., Ltd.) 5 parts and white carbon 2 parts are uniformly mixed and pulverized. To obtain a wettable powder.
- Emulsion was prepared by uniformly mixing 20 parts of compound (5) of the present invention, 55 parts of xylene, 20 parts of ⁇ , ⁇ -dimethylformamide, and 5 parts of Solpol 2680 (surfactant).
- Compound of the present invention (6) 40 parts, Solpol 3353 (Nonionic surfactant: trade name of Toho Chemical Co., Ltd.) 5 parts, 1 part aqueous solution of xanthan gum 5 parts, water 40 parts, ethylene glycol 10 parts effective The components other than the components were uniformly dissolved, then the compound of the present invention was added, and the mixture was thoroughly stirred and wet-ground with a sand minole to obtain a flowable agent.
- Solpol 3353 Nonionic surfactant: trade name of Toho Chemical Co., Ltd.
- a rice pot (variety: Koshihikari; 2 leaf stage) was sprayed with a diluent of a wettable powder prepared to 200 ppm according to Example 9 and air-dried. Plants were placed in a climate chamber (setting conditions: 22 ° C, 12 hours dark cycle) and sprayed with a blast spore suspension. Keep the weather chamber humid, 7 days Later, a survey was conducted. The control value was calculated according to the following formula, and indicated based on the criteria shown in Table 3 below. The results are shown in Tables 41 and 42.
- Control value (%) (1—number of cases in treated plot Z number of cases in non-treated plot) X I 0 0
- control drugs used were those of the following formulas (7) and (8) contained in WO2003008372.
- Control value (%) (1 number of cases in one treatment area / number of cases in non-treatment area) XI 0 0
- the diamine derivative according to the present invention exhibits an excellent control effect on rice blast, and is therefore useful as a plant disease control agent.
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- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
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- Engineering & Computer Science (AREA)
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Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04792637A EP1681285A4 (en) | 2003-10-31 | 2004-10-20 | DIAMINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF, AND PLANT DISEASE AGENT CONTAINING SAID DERIVATIVES AS AN ACTIVE INGREDIENT |
BRPI0415972-1A BRPI0415972A (pt) | 2003-10-31 | 2004-10-20 | derivados de diamina, processo para produção desses derivados, e agentes para controle de doenças de plantas os quais contêm esses derivados como ingredientes ativos |
US10/577,653 US20070049635A1 (en) | 2003-10-31 | 2004-10-20 | Diamine derivatives, process for producing the same, and plant disease control agents containing the same as active ingredients |
JP2005515112A JP4627496B2 (ja) | 2003-10-31 | 2004-10-20 | ジアミン誘導体、その製造方法およびそれらを有効成分とする植物病害防除剤 |
AU2004284997A AU2004284997B2 (en) | 2003-10-31 | 2004-10-20 | Diamine derivative, process for producing the same, and plant disease control agent containing the same as active ingredient |
IL174919A IL174919A0 (en) | 2003-10-31 | 2006-04-10 | Diamine derivatives, process for the production thereof and plant disease control compositions containing the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003-372467 | 2003-10-31 | ||
JP2003372467 | 2003-10-31 |
Publications (1)
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WO2005042474A1 true WO2005042474A1 (ja) | 2005-05-12 |
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PCT/JP2004/015471 WO2005042474A1 (ja) | 2003-10-31 | 2004-10-20 | ジアミン誘導体、その製造方法およびそれらを有効成分とする植物病害防除剤 |
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US (1) | US20070049635A1 (ja) |
EP (1) | EP1681285A4 (ja) |
JP (1) | JP4627496B2 (ja) |
KR (1) | KR100863849B1 (ja) |
CN (1) | CN100450997C (ja) |
AU (1) | AU2004284997B2 (ja) |
BR (1) | BRPI0415972A (ja) |
IL (1) | IL174919A0 (ja) |
TW (1) | TWI343786B (ja) |
WO (1) | WO2005042474A1 (ja) |
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WO2018159609A1 (ja) | 2017-02-28 | 2018-09-07 | 三井化学アグロ株式会社 | 植物病害防除組成物およびそれを施用する植物病害の防除方法 |
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- 2004-10-20 KR KR1020067009117A patent/KR100863849B1/ko active IP Right Grant
- 2004-10-20 WO PCT/JP2004/015471 patent/WO2005042474A1/ja active Application Filing
- 2004-10-20 JP JP2005515112A patent/JP4627496B2/ja active Active
- 2004-10-20 CN CNB2004800292555A patent/CN100450997C/zh active Active
- 2004-10-20 BR BRPI0415972-1A patent/BRPI0415972A/pt not_active IP Right Cessation
- 2004-10-20 EP EP04792637A patent/EP1681285A4/en not_active Withdrawn
- 2004-10-20 AU AU2004284997A patent/AU2004284997B2/en not_active Ceased
- 2004-10-27 TW TW093132510A patent/TWI343786B/zh active
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Also Published As
Publication number | Publication date |
---|---|
CN100450997C (zh) | 2009-01-14 |
US20070049635A1 (en) | 2007-03-01 |
TWI343786B (en) | 2011-06-21 |
AU2004284997B2 (en) | 2008-10-16 |
EP1681285A1 (en) | 2006-07-19 |
CN1863766A (zh) | 2006-11-15 |
JP4627496B2 (ja) | 2011-02-09 |
IL174919A0 (en) | 2006-08-20 |
BRPI0415972A (pt) | 2007-01-23 |
JPWO2005042474A1 (ja) | 2007-11-29 |
EP1681285A4 (en) | 2006-11-22 |
KR100863849B1 (ko) | 2008-10-15 |
TW200526116A (en) | 2005-08-16 |
KR20060088127A (ko) | 2006-08-03 |
AU2004284997A1 (en) | 2005-05-12 |
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