EP0882025A1 - Derives de pyrimidine, procede et intermediaires servant a les preparer et compositions pesticides ou fongicides les contenant - Google Patents

Derives de pyrimidine, procede et intermediaires servant a les preparer et compositions pesticides ou fongicides les contenant

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Publication number
EP0882025A1
EP0882025A1 EP97901621A EP97901621A EP0882025A1 EP 0882025 A1 EP0882025 A1 EP 0882025A1 EP 97901621 A EP97901621 A EP 97901621A EP 97901621 A EP97901621 A EP 97901621A EP 0882025 A1 EP0882025 A1 EP 0882025A1
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European Patent Office
Prior art keywords
alkyl
formula
alkoxy
hydrogen
compounds
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP97901621A
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German (de)
English (en)
Inventor
Wassilios Grammenos
Herbert Bayer
Thomas Grote
Reinhard Kirstgen
Bernd Müller
Ruth Müller
Klaus Oberdorf
Arne Ptock
Hubert Sauter
Franz Röhl
Michael Rack
Gisela Lorenz
Eberhard Ammermann
Siegfried Strathmann
Volker Harries
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BASF SE
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BASF SE
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • 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
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/34—One oxygen atom

Definitions

  • the present invention relates to pyrimidine derivatives of the formula I.
  • R 1 and R 2 are independent of each other
  • R 3 is hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, phenoxy- C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, cyano, C 1 -C 4 -alkoxy, hydroxy, Halogen;
  • R 4 is hydrogen, C 1 -C 8 alkyl, C 1 -C 4 haloalkyl,
  • C 1 -C 6 cyanoalkyl C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 2 -C 4 alkenyloxy-C 1 -C 4 alkyl, C 1 -C 4 haloalkoxy-C 1 -C 4 alkyl,
  • R 1 and R 2 are independent of each other
  • R 3 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenoxyC 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, cyano, hydroxy, halogen;
  • R 4 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl,
  • C 2 -C 4 alkynyl C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 3 -C 6 cycloalkoxy, C 1 -C 4 alkylthio, C 3 -C 6 cycloalkyl, C 5 -C 8 cycloalkenyl, heterocyclyl, aryl, aryloxy, arylthio, aryl C 1 -C 4 alkyl, aryl C 2 -C 4 alkenyl, Aryloxy-C 1 -C 4 alkyl,
  • NR f -CO-DR 9 benzyl, benzyloxy, aryl, aryloxy, hetaryl or hetaryloxy, where the 6 latter substituents can be partially or completely halogenated and / or can carry one to three of the following groups: cyano, C 1 -C 6 -Alkyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 4 -alkoxy, nitro, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkyl, hydroxy, rhodano, formyl, aminocarbonyl ⁇ unino, methylsulfonylamino, aminocarbonyl, C 1 -C 6 alkylaminocarbonyl;
  • Z is oxygen, sulfur or nitrogen, the nitrogen carrying hydrogen or C 1 -C 6 alkyl
  • D is a direct bond, oxygen or NR h n 0 or 1;
  • R b and R c independently of one another are hydrogen, C 1 -C 6 -alkyl,
  • R f is hydrogen, hydroxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl,
  • R g , R h independently of one another are hydrogen, C 1 -C 6 alkyl,
  • R 9 is hydrogen or C 1 -C 6 alkyl.
  • the cyclic radicals can be partially or completely halogenated and / or can carry one to three of the following groups: cyano, nitro, hydroxy, mercapto, amino, carboxyl,
  • C 1 -C 6 alkylaminocarbonyl di-C 1 -C 6 alkylamino, C 1 -C 6 alkylaminocarbonyl, di-C 1 -C 6 alkylaminocarbonyl, C 1 -C 6 alkylaminothiocarbonyl, di-C 1 -C 6- alkylaminothiocarbonyl, C 2 -C 6 alkenyl, C 2 -C 6 alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, hetaryl, hetaryloxy,
  • Z is oxygen, sulfur or nitrogen, the nitrogen carrying hydrogen or C 1 -C 6 alkyl
  • D is a direct bond, oxygen or NR h n 0 or 1;
  • R b and R c are independently hydrogen or C 1 -C 6 alkyl;
  • R f is hydrogen, hydroxy, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, C 2 -C 6 -alkenyloxy,
  • R g , R h independently of one another are hydrogen, C 1 -C 6 alkyl,
  • the invention also relates to processes and intermediates for the preparation of these compounds and compositions containing them for controlling animal pests and harmful fungi.
  • Phenylacetic acid derivatives for pest control are known from the literature (EP-A 422 597; EP-A 463 488; EP-A 370 629;
  • the present invention was based on new compounds with improved activity as an object.
  • the compounds I can be obtained in various ways by processes known per se in the literature.
  • EP-A 534 216, EP-A 658 541, EP-A 658 542 and EP-A 658 543 are known.
  • Hal in the formulas IIc and IId is iodine, bromine, chlorine and fluorine, preferably iodine, bromine and chlorine, and Ph is phenyl.
  • Hal is bromine, chlorine or fluorine, preferably chlorine or fluorine, with nucleophiles of the formula YAH (IIIa), in which Y and A have the meaning given, if appropriate in the presence of a diluent and if appropriate in the presence of a reaction auxiliary.
  • YAH bromine, chlorine or fluorine, preferably chlorine or fluorine
  • nucleophiles of the formula YAH (IIIa) in which Y and A have the meaning given, if appropriate in the presence of a diluent and if appropriate in the presence of a reaction auxiliary.
  • Y and A have the meaning given, if appropriate in the presence of a diluent and if appropriate in the presence of a reaction auxiliary.
  • R 3 and R 4 have the meaning given above, optionally in the presence of a diluent and optionally in the presence of a reaction auxiliary.
  • L 1 and L 2 are e.g. B. for halogen, for example chlorine, bromine or iodine, or alkyl or aryl sulfonate, for example methyl sulfonate, trifluoromethyl sulfonate, phenyl sulfonate or methylphenyl sulfonate.
  • the reduction of V to hydroxylamine X usually takes place at temperatures from -30 ° C.
  • the reaction of the hydroxylamine X with XIII usually takes place at temperatures from -20 ° C. to 60 ° C., preferably 0 ° C. to 30 ° C., in an inert organic solvent in the presence of a base [cf. WO-A 93/15046].
  • the reaction of the pyrimidine carbamate XIV with XV usually takes place at temperatures from -20 ° C. to 80 ° C., preferably 0 ° C. to 60 ° C., in an inert organic solvent in the presence of a base [cf. WO-A 93/15046].
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol and
  • Dimethyl sulfoxide and dimethylformamide particularly preferably cyclohexane, toluene, methylene chloride, tert-butyl methyl ether and water. Mixtures of the solvents mentioned can also be used
  • inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide are used as bases,
  • alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide
  • alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and
  • alkali metal amides such as lithium amide, sodium amide and potassium amide
  • alkali metal and alkaline earth metal carbonates such as
  • alkali metal alkyls such as methyl lithium, butyllithium and phenyllithium
  • alkyl magnesium halides such as methyl magnesium chloride and alkali metal and alkaline earth metal alcoholates such as sodium methoxide, sodium ethanolate, potassium ethanolate, potassium tert-butoxide and dimethoxymagnesium
  • the organic bases for example tertiary amines such as trimethylamine, triethylamine, tri-isopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines. Potassium carbonate, sodium hydroxide and triethylamine are particularly preferred.
  • the bases are generally used in catalytic amounts, but they can also be used in equimolar amounts, in excess or, if appropriate, as a solvent.
  • Alkyl is expediently C 1 -C 4 -alkyl, such as methyl, ethyl or n-propyl. These can then with nucleophiles of the formula YAH, in which Y has the meaning given above and A for oxygen f, or
  • Suitable diluents are e.g. aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and Tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and also dimethyl sulfoxide and dimethyl formamide, particularly preferably acetone, dimethyl formamide, tetrahydrofuran and dimethyl sulfoxide.
  • the process can also be carried out in a two-phase system such as water / toluene or water / dichloromethane, optionally in the presence of a phase transfer catalyst such as e.g. Tetrabutylammonium iodide, tetrabutylammonium bromide, tetrabutylammonium chloride, trimethylbenzylammonium chloride, 15-crown-5, 18-crown-6 or tris- [2- (2-methoxyethoxy) ethyl] amine.
  • a phase transfer catalyst such as e.g. Tetrabutylammonium iodide, tetrabutylammonium bromide, tetrabutylammonium chloride, trimethylbenzylammonium chloride, 15-crown-5, 18-crown-6 or tris- [2- (2-methoxyethoxy) ethyl] amine.
  • the process is preferably carried out in
  • inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide are used as bases,
  • alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide
  • alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and
  • alkali metal amides such as lithium amide, sodium amide and potassium amide
  • alkali metal and alkaline earth metal carbonates such as
  • alkali metal alkyls such as methyl lithium, butyllithium and phenyllithium
  • alkyl magnesium halides such as methyl magnesium chloride
  • alkali metal and alkaline earth metal alcoholates such as sodium methoxide, sodium ethanolate, potassium ethanolate, potassium tert-butanolate and dimethoxymagnesium
  • organic bases for example tertiary amines such as trimethylamine, triethylamine, tri-isopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines.
  • Potassium carbonate, sodium hydroxide, triethylamine and sodium methylate are particularly preferred.
  • the bases are generally used in catalytic amounts, but they can also be used in equimolar amounts, in excess or, if appropriate, as a solvent.
  • temperatures can be varied within a wide range when carrying out the method described above. In general, temperatures between 0 and 150 ° C, preferably between 20 and 130 ° C.
  • the process is usually carried out at normal pressure. However, it is also possible to work under increased or reduced pressure.
  • nucleophile Y-A-H 2.0 moles of nucleophile Y-A-H and optionally 1.0 to 3.0 moles, preferably 1.0 to 2.0 moles, of reaction auxiliary.
  • the acid chlorides VIIa are expediently obtained from the compounds VII in such a way that the carbalkoxy group of VII is first saponified in a manner known per se in a first place and the carboxylic acid obtained is expediently converted into the acid chloride VIIa in a manner known per se using thionyl chloride ( Houben-Weyl, Supplement 5, p. 225ff, p. 59ff and p. 604ff.)
  • the pyrimidinecarboxylic acid cyanides of the formula VIIb are obtained by reacting the acid chlorides of the formula VIIa with metal cyanides, for example with copper (I) or sodium cyanide, if appropriate in the presence of a diluent, such as e.g. Acetonitrile, appropriately at temperatures between 10 and 100 ° C in a conventional manner (EP-A-493 711).
  • metal cyanides for example with copper (I) or sodium cyanide, if appropriate in the presence of a diluent, such as e.g. Acetonitrile, appropriately at temperatures between 10 and 100 ° C in a conventional manner (EP-A-493 711).
  • a-oxo-pyrimidinyl-acetic acid derivatives of the formula IIa are advantageously obtained by hydrolyzing the pyrimidinecarboxylic acid cyanides of the formula VIIIb with aqueous acids, for example with hydrochloric acid at temperatures between 10 and 100 ° C., then by reaction with alcohols, for example methanol, if appropriate in the presence of a reaction auxiliary such as sulfuric acid and optionally in the presence of a diluent such as Toluene esterified at temperatures between 10 and 150 ° C, analogous to known processes (EP-A-493 711).
  • ⁇ -oxo-pyrimidinyl-acetic acid derivatives of the formula IIa are obtained by reacting the ⁇ -ketosulfoxides of the formula VIIc with a halogenating agent, for example N-bromosuccinimide, optionally in the presence of a diluent, such as e.g. Acetone, and then in a manner known per se with an alcohol, e.g. Methanol, treated at temperatures between 0 and 150 ° C (EP-A-493 711).
  • a halogenating agent for example N-bromosuccinimide
  • a diluent such as e.g. Acetone
  • dimethylamino-methylene derivatives of the formula VIIIb are known or can be prepared by processes known from the literature [J. Heterocyclic Chem. 21, 301 (1984)].
  • acetoacetic ester derivatives of the formula VIIIa are either either known or can be prepared by a process known per se
  • the further conversion of the pyrimidine carboxylic acid esters of the formula VII into the ⁇ -oxopyrimidinyl acetic acid derivatives of the formula IIa, in which Y, R 1 , R 2 have the meaning given above, and A for -O-CH 2 -, -C (R 3 ) STILL 2 - or is then done as described for Scheme 1.
  • Suitable diluents are, for example, aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, Dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, as well as dimethyl sulfoxide and dimethyl formamide, particularly preferably tetrahydrofuran, acetone, dimethyl formamide, acetonitrile and dimethyl
  • the process can also be carried out in a two-phase system such as water / toluene or water / dichloromethane, optionally in the presence of a phase transfer catalyst such as e.g. Tetrabutylammonium iodide, tetrabutylammonium bromide, tetrabutylammonium chloride, trimethylbenzylammonium chloride, 15-crown-5, 18-crown-6 or tris [2- (2-methoxyethoxy) ethyl] amine, can be implemented.
  • the process is preferably carried out in the presence of a suitable inorganic or organic base.
  • inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide are used as bases,
  • alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and
  • alkali metal amides such as lithium amide, sodium amide and potassium amide
  • alkali metal and alkaline earth metal carbonates such as
  • alkali metal alkyls such as methyl lithium, butyllithium and phenyllithium
  • alkyl magnesium halides such as methyl magnesium chloride and alkali metal and alkaline earth metal alcoholates such as sodium methoxide, sodium ethanolate, potassium ethanolate, potassium tert-butoxide and dimethoxymagnesium as well as organic bases, e.g. organic bases, Tertiary amines such as trimethylamine, triethylamine, tri-isopropylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines. Potassium carbonate, sodium hydroxide, triethylamine and sodium methylate are particularly preferred.
  • the bases are generally used in catalytic amounts, but they can also be used in equimolar amounts, in excess or, if appropriate, as a solvent.
  • the temperatures can vary within a wide range when carrying out the method described above. In general, temperatures between 0 and 150 ° C, preferably between 20 and 130 ° C.
  • the process is usually carried out at normal pressure. However, it is also possible to work under increased or reduced pressure.
  • 1.0 to 3.0 mol, preferably 1.0 to 2.0 mol, of nucleophile YAH and optionally 1.0 to 3.0 mol, preferably 1.0 to 2 are generally employed per mol of Xlc , 0 moles of reaction aids.
  • the products are carried out, worked up and isolated using methods known per se.
  • halopyrimidine derivatives of the formula Xlc in which R 1 and R 2 have the meaning given above, can be prepared in a known manner from the corresponding hydroxypyrimidine derivatives of the formula Xlb, for example by reaction with POCl 3 .
  • the dimethylamino-methylene derivatives of the formula XIIb can be prepared from the known halogen-nitroderivatives of the formula XII or Hal, which is expediently bromine or chlorine in the formula XII, by reaction with nucleophiles of the formula YAH, in which Y has the meaning given above and A for . or
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and also dimethyl sulfoxide and dimethyl formamide, particularly preferably tetrahydrofuran, acetone, dimethyl formamide, acetonitrile and dimethyl sulfoxide.
  • the process can also be carried out in a two-phase system such as water / toluene or water / dichloromethane, optionally in the presence of a phase transfer catalyst such as e.g. Tetrabutylammonium chloride, 15-crown-5, 18-crown-6 or tris- [2- (2-methoxyethoxy) ethyl] amine.
  • a phase transfer catalyst such as e.g. Tetrabutylammonium chloride, 15-crown-5, 18-crown-6 or tris- [2- (2-methoxyethoxy) ethyl] amine.
  • the process is preferably carried out in the presence of a suitable inorganic or organic base.
  • inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide are used as bases,
  • alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide
  • alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and
  • alkali metal amides such as lithium amide, sodium amide and potassium amide
  • alkali metal and alkaline earth metal carbonates such as
  • alkali metal alkyls such as methyllithium, butyllithium and phenyllithium
  • alkylmagnesium halides such as methyl magnesium chloride and alkali metal and alkaline earth metal alkoxides such as sodium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide and dimethoxymagnesium
  • organic bases for example tertiary amines such as trimethylamine, triethylamine, tri-isopropylamine and N-methylpiperidine, pyridine, sub substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines.
  • Potassium carbonate, sodium hydroxide, triethylamine and sodium methylate are particularly preferred.
  • the bases are generally used in catalytic amounts, but they can also be used in equimolar amounts, in excess or, if appropriate, as a solvent.
  • the temperatures can be varied within a wide range when carrying out the method described above. In general, temperatures between 0 and 150 ° C, preferably between 20 and 130 ° C. The process is usually carried out at normal pressure. However, it is also possible to work under increased or reduced pressure.
  • 1.0 to 3.0 mol, preferably 1.0 to 2.0 mol, of nucleophile YAH and optionally 1.0 to 3.0 mol, preferably 1.0 to 3.0 mol, are generally employed per mol of XIIa 2.0 moles of reaction aid.
  • the compounds of the formula XIIa can then be converted into the dimethylamino-methylene derivatives of the formula XIIb by a process known per se (1. Chem. Ber. 1081 (65), 2. Chem. Ber. 3407 (64), 3. Synth. Communications 939 (82)).
  • the compounds I can be obtained as E / Z isomer mixtures which, for example, can be separated into the individual compounds by crystallization or chromatography in the usual way.
  • halogen fluorine, chlorine, bromine and iodine
  • Alkyl straight-chain or branched alkyl groups with 1 to 4, 6 or 10 carbon atoms, for example C 1 -C 6 -alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methyl-propyl, 2-methylpropyl, 1,1 -Dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl,
  • Alkylamino an amino group which carries a straight-chain or branched alkyl group having 1 to 6 carbon atoms as mentioned above;
  • Dialkylamino an amino group which carries two independent, straight-chain or branched alkyl groups each having 1 to 6 carbon atoms as mentioned above;
  • Alkylcarbonyl straight-chain or branched alkyl groups with 1 to 10 carbon atoms, which have a carbonyl group
  • Alkylsulfonyl straight-chain or branched alkyl groups with 1 to 6 or 10 carbon atoms, which are bonded to the skeleton via a sulfonyl group (-SO 2 -);
  • Alkylsulfoxyl straight-chain or branched alkyl groups with 1 to 6 carbon atoms, which have a sulfoxyl group
  • Alkylaminocarbonyl alkylamino groups with 1 to 6 carbon atoms as mentioned above, which are bonded to the skeleton via a carbonyl group (-CO-);
  • Dialkylaminocarbonyl dialkylamino groups each having 1 to 6 carbon atoms per alkyl radical as mentioned above, which are bonded to the skeleton via a carbonyl group (-CO-);
  • Alkylaminothiocarbonyl alkylamino groups with 1 to 6 carbon atoms as mentioned above, which are bonded to the skeleton via a thiocarbonyl group (-CS-);
  • Dialkylaminothiocarbonyl dialkylamino groups each having 1 to 6 carbon atoms per alkyl radical as mentioned above, which are bonded to the skeleton via a thiocarbonyl group (-CS-);
  • Haloalkyl straight-chain or branched alkyl groups with 1 to 6 carbon atoms, in which case the hydrogen atoms in these groups can be partially or completely replaced by halogen atoms as mentioned above, for example C 1 -C 2 -haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl , Chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2.2 -Dichlor-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl;
  • Alkoxy straight-chain or branched alkyl groups with 1 to 4 or 6 carbon atoms as mentioned above, which are bonded to the skeleton via an oxygen atom (-O-), e.g.
  • C 1 -C 6 alkoxy such as methyloxy, ethyloxy, propyloxy, 1-methylethyloxy, butyloxy, 1-methylpropyloxy, 2-methylpropyloxy, 1,1-dimethylethyloxy, pentyloxy, 1-methylbutyloxy, 2-methylbutyloxy,
  • Halogenalkoxy straight-chain or branched alkyl groups with 1 to 6 carbon atoms, in which groups the hydrogen atoms can be partially or completely replaced by halogen atoms as mentioned above, and where these groups are bonded to the skeleton via an oxygen atom;
  • Alkylthio straight-chain or branched alkyl groups with 1 to 4 or 6 carbon atoms as mentioned above, which are bonded to the structure via a sulfur atom (-S-), e.g.
  • C 1 -C 6 alkylthio such as methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio, 1,1-dimethylethylthio, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2 2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio,
  • Cycloalkyl monocyclic alkyl groups with 3 to 6 carbon ring members, e.g. Cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl;
  • Alkenyl straight-chain or branched alkenyl groups with 2 to 6 or 10 carbon atoms and a double bond in any position, for example C 2 -C 6 alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2- Butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl,
  • Alkenyloxy straight-chain or branched alkenyl groups with 2 to 6 carbon atoms and a double bond in any position, which are bonded to the structure via an oxygen atom (-O-);
  • Alkenylthio or alkenylamino straight-chain or branched alkenyl groups with 2 to 6 carbon atoms and a double bond in any position which (alkenylthio) are bonded to the skeleton via a sulfur atom or (alkenylamino) a nitrogen atom.
  • Alkenylcarbonyl straight-chain or branched alkenyl groups with 2 to 10 carbon atoms and a double bond in any position, which are bonded to the skeleton via a carbonyl group (-CO-);
  • Alkynyl straight-chain or branched alkynyl groups with 2 to 10 carbon atoms and a triple bond in any position, for example C 2 -C 6 -alkynyl such as ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentinyl,
  • Alkynyloxy or alkynylthio and alkynylamino straight-chain or branched alkynyl groups having 2 to 6 carbon atoms and a triple bond in any position which (alkynyloxy) via an oxygen atom or (alkynylthio) via a sulfur atom or (alkynylamino) via a nitrogen atom bonded to the skeleton are.
  • Alkynylcarbonyl straight-chain or branched alkynyl groups with 3 to 10 carbon atoms and a triple bond in any position, which are bonded to the skeleton via a carbonyl group (-CO-);
  • Cycloalkenyl or cycloalkenyloxy, cycloalkenylthio and cycloalkenylamino monocyclic alkenyl groups with 3 to 6 carbon ring members which are bonded to the structure directly or (cycloalkenyloxy) via an oxygen atom or (cycloalkenylthio) via a nitrogen atom, e.g. cycloalkenylamino) Cyclopropenyl, cyclobutenyl, cyclopentenyl or cyclohexenyl.
  • Cycloalkoxy or cycloalkylthio and cycloalkylamino monocyclic alkenyl groups with 3 to 6 carbon ring members which (cycloalkyloxy) are bonded to the skeleton via an oxygen atom or (cycloalkylthio) a sulfur atom or (cycloalkylamino) via a nitrogen atom, e.g. Cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;
  • Heterocyclyl or heterocyclyloxy, heterocyclylthio and heterocyclylamino three- to six-membered, saturated or partially unsaturated mono- or polycyclic heterocycles which contain one to three herero atoms selected from a group consisting of oxygen, nitrogen and sulfur, and which directly or (heterocyclyloxy) are bound to the structure via an oxygen atom or (heterocyclylthio) via a sulfur atom or (heterocyclylamino) via a nitrogen atom, for example 2-tetrahydrofuranyl, oxiranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazoldinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 3 -pyrazo
  • aromatic mono- or polycyclic hydrocarbon radicals which directly or (aryloxy) via an oxygen atom (-O-) or (arylthio) a sulfur atom (-S-), (arylcarbonyl) via a carbonyl group (-CO-) or (arylsulfonyl) via a Sulfonyl group (-SO 2 -) are bound to the skeleton, for example phenyl, naphthyl and phenanthrenyl or phenyloxy, naphthyloxy and phenanthrenyloxy and the corresponding carbonyl and sulfonyl radicals;
  • Arylamino aromatic mono- or polycyclic hydrocarbon residues, which are attached to the structure via a nitrogen atom.
  • Hetarylsulfonyl aromatic mono- or polycyclic radicals which, in addition to carbon ring members, also contain one to four nitrogen atoms or one to three nitrogen atoms and one oxygen or one sulfur atom or one oxygen or one
  • 1,3,4-triazol-2-yl - Benzo-condensed 5-membered heteroaryl, containing one to three nitrogen atoms or one nitrogen atom and / or one oxygen or sulfur atom: 5-ring heteroaryl groups which, in addition to carbon atoms, contain one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or
  • 5-membered heteroaryl which is bonded via nitrogen and contains one to three nitrogen atoms: 5-ring heteroaryl groups which, in addition to carbon atoms, contain one to four nitrogen atoms or one to three nitrogen atoms as ring members and in which two adjacent carbon ring members or a nitrogen and an adjacent carbon ring member can be bridged by a buta-1,3-diene-1,4-diyl group, these rings being bonded to the framework via one of the nitrogen ring members; 6-membered heteroaryl containing one to three or one to four nitrogen atoms: 6-ring heteroaryl groups which, in addition to carbon atoms, can contain one to three or one to four nitrogen atoms as ring members, for example 2-pyridinyl, 3-pyridinyl, 4- Pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl, 1,3,5-triazin-2
  • 6-ring heteroaryl groups in which two adjacent carbon ring members can be bridged by a buta-1,3-diene-1,4-diyl group, e.g.
  • Quinoline isoquinoline, quinazoline and quinoxaline, - pyrido [3,2-d] thiazol-2-yl or the corresponding oxy, thio, carbonyl or sulfonyl groups.
  • Hetarylamino aromatic mono- or polycyclic radicals which, in addition to carbon ring members, can additionally contain one to four nitrogen atoms or one to three nitrogen atoms and one oxygen or one sulfur atom and which are bonded to the structure via a nitrogen atom.
  • R 1 is hydrogen and R 2 is trifluoromethyl.
  • R 1 and R 2 are hydrogen.
  • compounds I are furthermore preferred in which X represents N (CO 2 CH 3 ) -OCH 3 .
  • R 3 is C 1 -C 4 alkyl, in particular methyl.
  • R 3 is C 1 -C 4 alkoxy, in particular methoxy.
  • compounds I are also preferred in which Y is aryl, in particular, if appropriate, subst. Phenyl.
  • compounds I are particularly preferred in which Y represents cycloalkyl, in particular cyclohexyl.
  • compounds I are particularly preferred in which Y is hetaryl, in particular optionally subst.
  • R 4 is C 1 -C 4 alkyl, in particular methyl and ethyl, are also particularly preferred.
  • R 4 is C 3 -C 4 alkenyl, in particular allyl.
  • R 4 is C 3 -C 4 -alkynyl, in particular propargyl.
  • R 4 represents haloalkenyl, in particular trans-chloroallyl.
  • the compounds I are suitable as fungicides.
  • the compounds I are notable for excellent activity against a broad spectrum of phytopathogenic fungi, in particular from the classes of the Ascomycetes and Basidiomycetes. Some of them are systemically effective and can be used as leaf and soil fungicides. They are particularly important for combating a large number of fungi on various crops such as wheat, rye, barley, oats, rice, corn, grass, cotton, soybeans, coffee, sugar cane, wine, fruit and ornamental plants and vegetable plants such as cucumbers, beans and pumpkin family, as well as on the seeds of these plants.
  • Erysiphe graminis in cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea on pumpkin plants, Podosphaera leucotricha on apples, Uncinula necator on vines, Puccinia species on cereals, Rhizoctonia species and Rhizoctonia Ustilago species on cereals and sugar cane, Venturia inaequalis (scab) on apples, Helminthosporium species
  • Cereals Septoria nodorum on wheat, Botrytis cinerea (gray mold) on strawberries, vines, Cercospora arachidicola on peanuts, Pseudocercosporella herpotrichoides on wheat, barley, Pyricularia oryzae on rice, Phytophthora infestans on potatoes and tomatoes, Fusarium and various plants , Plasmopara viticola on vines, Alternaria species
  • the compounds I are applied by making the mushrooms
  • Materials or the soil are treated with a fungicidally effective amount of the active ingredients. It is used before or after the infection of the materials, plants or seeds by the fungi.
  • auxiliary agents come there The following are essentially considered: solvents such as aromatics (e.g. xylene), chlorinated aromatics (e.g.
  • chlorobenzenes paraffins (e.g. petroleum fractions), alcohols (e.g. methanol, butanol), ketones (e.g. cyclohexanone), amines (e.g. ethanolamine, dimethylformamide) and water ;
  • Carriers such as natural stone powder (eg kaolins, clays, talc, chalk) and synthetic stone powder (eg highly disperse silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste liquors and methyl cellulose.
  • nonionic and anionic emulsifiers eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates
  • dispersants such as lignin sulfite waste
  • the fungicidal compositions generally contain between 0.1 and 95, preferably between 0.5 and 90% by weight of active ingredient. Depending on the type of effect desired, the application rates are between 0.01 and 2.0 kg of active ingredient per ha.
  • active ingredient 0.001 to 0.1 g, preferably 0.01 to 0.05 g, per kg of seed are generally required.
  • agents according to the invention can also be present in the use form as fungicides together with other active ingredients, which e.g. with herbicides, insecticides, growth regulators,
  • Fungicides or with fertilizers are Fungicides or with fertilizers.
  • Sulfur, dithiocarbamates and their derivatives such as iron, zinc dimethyldithiocarbamate, zinc ethylenebisdithiocarbamate, manganese ethylenebisdithiocarbamate, manganese zinc ethylenediamine bisdithiocarbamate, Tetramethylthiuramdisulfide, ammonia complex of zinc (N, N-ethylene-bis-dithiocarbamate), ammonia complex of zinc (N , N'-propylene-bis-dithiocarbamate), zinc (N, N'-propylene-bis-dithiocarbamate), N, N'-polypropylene-bis- (thiocarbamoyl disulfide;
  • Nitroderivatives such as dinitro- (1-methylheptyl) phenylcrotonate
  • the compounds of the formula I are also suitable for effectively controlling pests from the class of the insects, arachnids and nematodes. You can in crop protection as well as on the
  • Hygiene storage protection and veterinary sector are used as pesticides.
  • the harmful insects from the order of the butterflies include, for example, Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobisturaumumone, Cheimatobisturaumumone Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus,
  • Eupoecilia ambiguella Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cuninellellia, hyponomeutella malaria, Hyponomeutella, Hyponomeutella
  • brasiliensis Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus,
  • Leptinotarsa decemlineata Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae,
  • Diptera From the order of the two-winged species (Diptera), for example, Aedes aegypti, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Contarinia sorghicola, Cordylobia anthropucitae, Cordylobia anthropucaga, brassylaciaacropucita, brassylaciaacropucita, brassylaciaacropucita, brassylaciaacropacea, brassylaciaacropaceacita, brassylaciaacropia , Fannia canicularis, Gasterophilus intestinalis,
  • Hoplocampa minuta Hoplocampa testudinea, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta.
  • Heteroptera for example Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps,
  • suckers for example Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis pomi, Aphis sambuci, Brachycaudus cardui, Brevicoryne brassicae, Cerosipha gossypyusiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaiaia, Dreyfusiaiaiaiaia , Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Metopolophium dirhodum, Myzodes persicae, Myzus cerasi, Nilaparvata lugens, Pemphigus bursarius
  • Arachnoid for example, arachnids
  • Acarina such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Brevipalpus phoenicis, Bryobia praetiosa, Dermacentor silvarum, Eotetranychus carpini, Eriophyes sheldoni, Hyinommobusuncus, Iinoblus, I megnini, Paratetranychus pilosus, Dermanyssus gallinae, Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, Tetranychus cinnabarinus, Tetranychuschusus, Tetranychuschuschusch.
  • Carina such as Amblyomma americanum, Am
  • root gall nematodes e.g. Meloidogyne hapla, Meloidogyne incognita
  • active ingredients as such, in the form of their formulations or the use forms prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or
  • Dispersions emulsions, oil dispersions, pastes, dusts, scattering agents, granules by spraying, atomizing, dusting, scattering or pouring can be used.
  • the application forms depend entirely on the purposes; in any case, they should ensure the finest possible distribution of the active compounds according to the invention.
  • Preparations can be varied in larger areas.
  • active ingredients are between 0.0001 and 10%, preferably between 0.01 and 1%.
  • the active ingredients can also be used with great success in the ultra-low-volume process (ULV), it being possible to apply formulations with more than 95% by weight of active ingredient or even the active ingredient without additives.
  • the amount of active ingredient used to control pests is 0.1 to 2.0, preferably under outdoor conditions
  • Mineral oil fractions come from to produce directly sprayable solutions, emulsions, pastes or oil dispersions
  • medium to high boiling point such as kerosene or diesel oil, also coal tar oils as well as oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, strongly polar
  • Solvents for example dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, into consideration.
  • Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (wettable powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances as such or dissolved in an oil or solvent can be homogenized in water by means of wetting agents, adhesives, dispersants or emulsifiers.
  • wetting, adhesive wetting, adhesive,
  • Dispersants or emulsifiers and possibly solvents or oil existing concentrates are prepared which are suitable for dilution with water.
  • Formaldehyde polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octy
  • Powders, materials for broadcasting and dusts can be prepared by mixing or grinding the active substances together with a solid carrier.
  • the formulations generally contain between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight, of the active ingredient.
  • the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR spectrum).
  • formulations are: I. 5 parts by weight of a compound according to the invention are intimately mixed with 95 parts by weight of finely divided kaolin. In this way, a dust is obtained which contains 5% by weight of the active ingredient. II. 30 parts by weight of a compound according to the invention are mixed with a mixture of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil based on the top surface of this silica gel was sprayed, intimately mixed. In this way, a preparation of the active ingredient with good adhesiveness (active ingredient content 23% by weight) is obtained.
  • Castor oil consists (active ingredient content 9% by weight).
  • V. 80 parts by weight of a compound according to the invention are mixed well with 3 parts by weight of the sodium salt of diisobutylnaphthalenalphasulfonic acid, 10 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of powdered silica gel and in milled in a hammer mill (active ingredient content 80% by weight).
  • VIII.20 parts by weight of a compound according to the invention are mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene- ⁇ -sulfonic acid, 17 parts by weight of the sodium salt of a lignin sulfonic acid from a sulfite waste liquor and 60 parts by weight of powdered silica gel well mixed and in one Grind the hammer mill.
  • a spray liquor is obtained which contains 0.1% by weight of the active ingredient.
  • Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers.
  • Solid carriers are, for example, mineral earths, such as silica gel, silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers, such as For example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder and other solid carriers.
  • mineral earths such as silica gel, silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers, such as For example, ammonium sulfate, ammonium
  • Oils of various types, herbicides, fungicides, other pesticides, bactericides can be added to the active compounds, if appropriate also only immediately before use (tank mix). These agents can be added to the agents according to the invention in a weight ratio of 1:10 to 10: 1.
  • the mixture is then neutralized with solid sodium bicarbonate, extracted with ether, dried and concentrated again.
  • the residue is taken up in 80 ml of dimethylformamide (DMF) without further purification, and 0.55 g (4 mmol) of K 2 CO 3 and 0.5 g (4 mmol) of dimethyl sulfate are added with cooling.
  • the mixture is then stirred at room temperature for 3 h, extracted with MtBE, the org. Phases dried over sodium sulfate and concentrated.
  • the residue is chromatographed on silica gel with n-heptane / ethyl acetate (1: 1) as the eluent. 0.7 g of the title compound 2 remain as a resin.
  • Leaves of potted vines of the "Müller-Thurgau" variety were sprayed to runoff point with aqueous active compound preparation which was prepared with a stock solution of 10% active compound, 63% cyclohexanone and 27% emulsifier.
  • the plants were drying the spray coating for 7 days in a greenhouse. Only then were the leaves inoculated with an aqueous suspension of zoospores from Plasmopara viticola.
  • the vines were then placed for 48 hours in a steam-saturated chamber at 24 ° C and then for 5 days in a greenhouse at temperatures between 20 and 30 ° C. After this time, the plants were again placed in a moist chamber for 16 hours in order to accelerate the sporangium carrier outbreak. The extent of the development of the infestation on the undersides of the leaves was then determined visually.
  • the action of the compounds of the general formula I against animal pests could be shown by the following experiments:
  • the active compounds were a) as a 0.1% solution in acetone or b) as a 10% emulsion in one Mixture of 70% by weight cyclohexanone, 20% by weight Nekanil® LN (Lutensol® AP6, wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) and 10% by weight Emulphor® EL (Emulan® EL, emulsifier on based on ethoxylated fatty alcohols) and diluted to the desired concentration with acetone in the case of a) or with water in the case of b).
  • the lowest concentration was determined at which the compounds still caused an 80-100% inhibition or mortality compared to untreated control tests (threshold of action or minimum concentration).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Dérivés de pyrimidine représentés par la formule (I), dans laquelle les substituants possèdent la signification suivante: X représente C(CO2CH3)=NOCH3, C(CONHCH3)=NOCH3, C(CO2CH3)=CHOCH3, C(CO2CH3)=CHCH3, N(CO2CH3)-OCH3; R<1> et R<2> indépendamment l'un de l'autre représentent hydrogène, alkyle C1-C4, halogenalkyle C1-C4 ou alcoxy C1-C4; A est (i) permettant d'effectuer la liaison désignée par * avec Y; R<3> représente hydrogène, alkyle C1-C4, halogenalkyle C1-C4, phenoxyalkyle C1-C4, cycloalkyle C3-C6, cyano, alcoxy C1-C4, hydroxy, halogène; R<4> représente hydrogène, alkyle C1-C8, halogenalkyle C1-C4, cyanoalkyle C1-C6, alcoxy-C1-C4-alkyle-C1-C4, alcényloxy-C1-C4-alkyle-C1-C4, haloalcoxy-C1-C4-alkyle-C1-C4, oxoalkyle C1-C4, alcényle C2-C4, alcinyle C2-C4, halogenalcényle C2-C4, halogenalcinyle C2-C4, cycloalkyle C3-C6, cycloalkyle-C3-C6-alkyle-C1-C4, alcoxy C1-C4; Y représente hydrogène, hydroxy, halogène, et éventuellement substitué, aryle, hétaryle, cycloalkyle, cycloalcényle, hétérocyclyle, alkyle, alcényle, alcinyle, halogenalkyle, alcoxy, aryloxy, arylthio, hétaryloxy, hétarylthio, alkylthio ou cycloalkyloxy. Dans le cas ou X représente C(CO2CH3)=CHOCH3, A ne signifie pas -O-. L'invention concerne également leurs sels, procédés et intermédiaires servant à les préparer et compositions pesticides et fongicides les contenant.
EP97901621A 1996-02-05 1997-01-31 Derives de pyrimidine, procede et intermediaires servant a les preparer et compositions pesticides ou fongicides les contenant Withdrawn EP0882025A1 (fr)

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DE19603990 1996-02-05
DE19603990 1996-02-05
PCT/EP1997/000423 WO1997029093A1 (fr) 1996-02-05 1997-01-31 Derives de pyrimidine, procede et intermediaires servant a les preparer et compositions pesticides ou fongicides les contenant

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DE19804486A1 (de) * 1998-02-05 1999-08-12 Basf Ag 2-(Pyrazolyloxy)-pyridin-3-ylessigsäure- Derivate, sie enthaltende Mittel und ihr
EP1987011A1 (fr) * 2006-02-15 2008-11-05 Basf Se Pyrimidines substituées en position 2 et leur utilisation comme pesticides
US10743535B2 (en) 2017-08-18 2020-08-18 H&K Solutions Llc Insecticide for flight-capable pests

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NZ213630A (en) 1984-10-19 1990-02-26 Ici Plc Acrylic acid derivatives and fungicidal compositions
ES2067570T3 (es) 1988-12-29 1995-04-01 Ciba Geigy Ag Esteres metilicos de acidos aldimino- o cetimino-oxi-ortotolilacrilicos, obtencion de los mismos y fungicidas que los contienen.
DE3917352A1 (de) 1989-05-27 1990-11-29 Basf Ag Neue oximether und diese enthaltende fungizide
US5286750A (en) 1989-10-11 1994-02-15 Basf Aktiengesellschaft Phenylacetic acid derivatives and fungicides containing them
PH11991042549B1 (fr) 1990-06-05 2000-12-04
ATE161007T1 (de) 1990-06-27 1997-12-15 Basf Ag O-benzyl-oximether und diese verbindungen enthaltende pflanzenschutzmittel
NZ242290A (en) 1991-04-15 1994-12-22 Zeneca Ltd Pyridyl and pyrimidinyl substituted oxime-o-benzyl ether derivatives; preparatory processes, fungicidal compositions and an intermediate
DE4116090A1 (de) 1991-05-17 1992-11-19 Basf Ag (alpha)-phenylacrylsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen und schadpilzen
DE4131311A1 (de) 1991-09-20 1993-04-01 Basf Ag Dihydropyranderivate und diese enthaltende pflanzenschutzmittel
RU94026277A (ru) * 1993-07-12 1996-05-27 Сандоз АГ (CH) Пиримидиниловые производные акриловой кислоты, способ их получения, способ подавления фитопатогенных грибов, фунгицидное средство
GB9400889D0 (en) 1994-01-18 1994-03-16 Sandoz Ltd Novel compounds
GB9519787D0 (en) * 1995-09-28 1995-11-29 Sandoz Ltd Organic compounds

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AU1546197A (en) 1997-08-28

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