EP0789691A1 - Derives heterocyclyl-amino et heterocyclyl-oxy-cycloalcenyle et leur utilisation comme pesticides et comme fongicides - Google Patents

Derives heterocyclyl-amino et heterocyclyl-oxy-cycloalcenyle et leur utilisation comme pesticides et comme fongicides

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Publication number
EP0789691A1
EP0789691A1 EP95935945A EP95935945A EP0789691A1 EP 0789691 A1 EP0789691 A1 EP 0789691A1 EP 95935945 A EP95935945 A EP 95935945A EP 95935945 A EP95935945 A EP 95935945A EP 0789691 A1 EP0789691 A1 EP 0789691A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
halogen
compounds
formula
radicals
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.)
Withdrawn
Application number
EP95935945A
Other languages
German (de)
English (en)
Inventor
Martin Märkl
Wolfgang Schaper
Werner Knauf
Ulrich Sanft
Manfred Kern
Dieter Bernd Reuschling
Adolf Heinz Linkies
Werner Bonin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Original Assignee
Hoechst Schering Agrevo GmbH
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hoechst Schering Agrevo GmbH filed Critical Hoechst Schering Agrevo GmbH
Publication of EP0789691A1 publication Critical patent/EP0789691A1/fr
Withdrawn legal-status Critical Current

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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
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88—Oxygen atoms
    • 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
    • C07D239/42—One nitrogen atom

Definitions

  • Heterocyciyl-amino and heterocyclyl-oxy-cycloalkenyl derivatives their use as pesticides and fungicides
  • the invention relates to heterocycyl-amino and heterocyclyl-oxy-cycloalkenyl derivatives, processes for their preparation and their use as pesticides and fungicides.
  • R 1 is hydrogen, halogen, (C r C 4 ) alkyl, (C r C 4 ) haloalkyl, (C 3 -C 5 ) cycloalkyl or (C 3 -C 5 ) halocycloalkyl;
  • R 2 and R 3 are the same or different and are each independently hydrogen, halogen, (C r C 4 ) alkyl, (C r C 4 ) haloalkyl, (C 3 -C 8 ) cycloalkyl, (C 3 -C 8 ) -Halogenocycloalkyl, (C r C 4 ) -alkoxy, (C r C 4 ) - haloalkoxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkyl, (C r C 4 ) - Haloalkoxy (C r C 4 ) alkyl, (C r C 4 ) alkoxy- (C r C 4 ) haloalkyl, (C r C 4 ) - haloalkoxy- (CC 4 ) haloalkyl, (C r C 4 ) - Alkylamino, (C, -C 4 ) al
  • R 2 and R 3 together with the carbon atoms to which they are attached form a saturated 5-, 6- or 7-membered isocyclic ring which may contain oxygen and / or sulfur instead of one or two CH 2 groups and which is optionally substituted by 1, 2 or 3 (C, -C 4 ) alkyl groups;
  • A represents CH or N
  • E represents a direct bond or a straight-chain or branched (C 1 -C 4 ) alkanediyl group, preferably a direct bond;
  • a and b are the same or different and independently of one another represent the numbers 0, 1, 2 or 3, where a and b do not simultaneously mean 0;
  • R 4 halogen, (C r C 4 ) alkyl, (C 3 -C 7 ) cycloalkyl, (C r C 4 ) haloalkyl, (C r C 4 ) alkoxy, (CC 4 ) haloalkoxy or optionally substituted Phenyl; v represents 0, 1 or 2;
  • R 7 and R 8 are (C r C 4 ) alkyl and R 9 are alkyl, cycloalkyl, aryl and arylalkyl; and the alkyl, alkenyl, alkynyl or R 5 , R 7 , R 8 and R 9 mentioned
  • Alkyloximino radicals optionally at least one of the following
  • R 6 has the meanings given and where R 7 and R 8 have the meanings given above for R 7 and R 8 ; ii. 3 to 12 atoms of these residues form an up to 12-membered
  • radicals are optionally with one or more, preferably up to three, in the case of halogen up to the maximum number of identical or different radicals from the series halogen, alkyl,
  • R 4 is halogen, preferably fluorine, chlorine and bromine, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkoxy, (C 1 -C 4 ) haloalkoxy or (CC 4 ) - alkylthio; and
  • R 5 (C r C 20 ) alkyl, (C 2 -C 20 ) alkenyl, (C 2 -C 20 ) alkynyl, optionally substituted aryl, optionally substituted heterocyclyl, cyano, halogen, hydroxy, carboxy, nitro, ( C 1 -C 20 ) -Alkyloximino or a group SiR 7 R 8 R 9 can mean, where R 7 and R 8 (C r C 4 ) -alkyl and R 9 -C-C 0 ) alkyl or optionally substituted aryl ; and the alkyl, alkenyl, alkynyl or alkyloximino radicals mentioned for R 5 , R 7 , R 8 and R 9 , optionally have at least one of the following features: i. one or more, preferably up to three, not adjacent
  • the radicals are optionally with one or more, preferably up to three, in the case of halogen up to the maximum number of identical or different radicals from the series halogen, [C ' -C * i 2 ) - alkyl, ⁇ C 3 -C 8 ) -Cycloalkyl, aryl, aryloxy, arylthio, heterocyclyl, heterocyclyloxy, heterocyclylthio, (C, -C 12 -haloalkyl, aryl- (C 1 -C 4 ) -alkyl, (C 3 -C 8 -cycloalkyl- (C r C 4 ) alkyl, (C r C 12 ) alkoxy, (C r C 12 ) - Haloalkoxy, (C., - C 12 ) -Alky ⁇ th.o, (C 3 -C 8 ) -cycloalkoxy, (C ⁇ C ⁇ ) - alkanoyl
  • R 1 represents hydrogen or fluorine
  • R 2 (C 1 -C 4 ) alkyl, cyclopropyl, halocyclopropyl, halogen (C.
  • R 3 is hydrogen, halogen, methyl, ethyl, methoxy, ethoxy, cyano or
  • A represents CH or N;
  • X represents NH or oxygen;
  • E stands for a direct bond; a is 1 and b is 2;
  • R 4 represents hydrogen, (C 1 -C 4 ) alkyl / trifluoromethyl or (C r C 4 ) alkoxy; and the remaining residues and variables are as defined above; and their salts; in particular those compounds in which R 1 is hydrogen; R 2 represents methyl, ethyl, propyl, isopropyl, 1-fluoroethyl, trifluoromethyl, cyclopropyl or methoxymethyl; R 3 halogen, methyl, ethyl, methoxy, ethoxy, cyano or (C r C 4 ) -
  • U represents a direct bond or oxygen
  • V represents a direct bond
  • R 1 represents hydrogen
  • R 2 represents ethyl, propyl, isopropyl, 1-fluoroethyl, trifluoromethyl or methoxymethyl
  • R 3 represents fluorine, chlorine, bromine or methoxy
  • Form quinazoline system which may be substituted with a fluorine atom, or R 2 and R 3 together with the ring system to which they are attached, the
  • U represents a direct bond or oxygen
  • V represents a direct bond
  • R 1 is hydrogen
  • R 2 represents ethyl or methoxymethyl
  • R 5 is (C r C 20 ) alkyl, (C 2 -C 20 ) alkenyl or (C 2 -C 20 ) alkynyl, where 3 to 6 carbon atoms of these hydrocarbon radicals can form a cycle and / or this hydrocarbon Radicals may optionally be substituted with a phenyl radical which may be unsubstituted or may have up to three, in the case of fluorine, up to the maximum number of identical or different substituents;
  • A represents CH or N;
  • X represents NH or oxygen; E stands for a direct bond;
  • R 2 is methoxymethyl and R 3 is methoxy, or R 2 is ethyl and R 3 is chlorine or bromine, X is NH;
  • R 5 is (C ⁇ C ⁇ .- alkyl or (C 2 -C 20 ) -alkenyl, where 3-6
  • Carbon atoms of this radical can form a cycle and / or this may optionally be substituted with a phenyl radical which may be unsubstituted or may have up to three, in the case of fluorine, up to the maximum number of identical or different substituents; and the remaining radicals and variants are as defined above; as well as their salts.
  • halogen means a fluorine, chlorine, bromine or iodine atom, preferably a fluorine, chlorine or bromine atom; under the expression “(C 1 -C 4 ) alkyl” an unbranched or branched
  • Hydrocarbon residue with 1 - 4 carbon atoms such as. B. the methyl
  • Butyl radical under the expression "(C 1 -C 20 ) alkyl" the aforementioned alkyl radicals, and z.
  • alkyl group in which one or more hydrogen atoms are replaced by the above-mentioned halogen atoms, preferably chlorine or fluorine, such as the trifluoromethyl group, the 1-fluoroethyl group, the 2,2,2-
  • Cyclobutyl or cyclopentyl group under the expression "(C 3 -C 8 ) cycloalkyl" preferably the cyclopropyl,
  • Hydrogen atoms are replaced by the above-mentioned halogen atoms, preferably chlorine or fluorine; under the expression "(C 1 -C 4 ) alkoxy" an alkoxy group whose
  • Halogen hydrocarbon radical has the meanings given under the expression "(C 1 -C 4 ) haloalkyl”; for example, under the expression “(C 1 -C 4 ) alkoxy- (C 1 -C 4 ) alkyl”
  • Decyloxycarbonyl or dodecyloxycarbonyl group under the expression "cyano- (C-
  • Hydrocarbon radical that specified under the expression "(C 1 -C 4 ) alkyl” Has meanings; under the expression “(C ⁇ C ⁇ alkylidene” for example the exo-methylene, ethylidene, propylidene, 1-methyl-propylidene, butylidene, octylidene or dodecylidene group; under the expression “(C ⁇ C ⁇ .- alkyloximino "an oximino group on the oxygen with one of the expression””is etherified mentioned alkyl groups, the term " (C j -C ⁇ .- alkyl aryl "an isocyclic aromatic radical having preferably 6 to 14, in particular 6 to 12 carbon atoms, such as, for example, phenyl, naphthyl or biphenylyl, preferably phenyl; under the expression “heterocyclyl” a heteroaromatic or heteroaliphatic ring system, under “heteroaro
  • Heterocyclyloxy can be provided; the term "substituted heterocyclyl” is to be understood as meaning a heteroaromatic or heteroaliphatic ring system which is linked to one or more, preferably up to three, in the case of fluorine also up to
  • substituted aryl may be provided by substituents; under optionally provided with substituents "cycloaliphatic, aromatic and heterocyclic radicals", radicals are to be understood, such as. B.
  • substituted aryl In the case of fluorine, the same or different substituents listed under “substituted aryl” can also be provided up to the maximum number; under the term “aryl- (C 1 -C 4 ) alkyl” one under the term “(C 1 -C 4 ) -
  • alkyl "called alkyl group which is substituted by an aryl radical; the term” aryloxy ", for example, the phenoxy or 1- or 2-naphthyloxy
  • heterocyclyloxy or “heterocyclylthio” one of the heterocyclic radicals mentioned above which are linked via an oxygen or sulfur atom.
  • the substituents with which the various aliphatic, aromatic and heterocyclic ring systems can be provided include, for. B. Halogen, (C 1 -C 4 ) alkyl, trimethylsilyl, ⁇ C r C 4 ) haloalkyl, (C r C 4 > alkoxy, (C r C 4 )) haloalkoxy, (C 1 -C 4 ) -Alkoxy- (C 1 -C 4 ) -alkyl, (C r C 4 ) -alkylthio, alkylsulfinyl, alkylsulfonyl, phenyl, phenoxy, halophenoxy, (C 1 -C 4 ) -alkylphenoxy, (C 1 -C 4 ) - Alkoxyphenoxy, (C., - C 4 ) -haloalkoxyphenoxy, (C., - C 4 ) - haloalkylphenoxy, phen
  • Residues are optionally with one or more, preferably up to three, in the case of halogen up to the maximum number of identical or different residues from the series halogen, alkyl, cycloalkyl, aryl, aryloxy, arylthio, heterocyclyl, heterocyclyloxy, heterocyclylthio, haloalkyl, arylalkyl, Cycloalkylalkyl, alkoxy, haloalkoxy, alkylthio, cycloalkoxy, alkanoyloxy, haloalkane oyloxy, cycloalkanoyloxy, cycloalkylalkanoyloxy, aroyloxy, arylalkanoyloxy, alkylsulfonyloxy, arylsulfonyloxy, heterocyclylcarbonyloxy, hydroxy, cyano or
  • alkyl-dialkylsilyl-alkyl radicals such as. B. the trimethylsilylmethyl or ethyldimethylsilylethyl Group; or alkyl-cycloalkyl radicals such as. B. the 4-methyl-cyclohexyl, 3-ethyl-cyclopentyl or the 4-tert-butyl-cyclohexyl group; or cycloalkyl-alkyl radicals such as. B.
  • cyclohexylmethyl, cyclohexylethyl, cyclohexylpropyl, cyclohexylbutyl or 1-cyclohexyl-1-methylethyl group or aryl-alkyl radicals such as. B. the benzyl, the 2-phenylethyl, the 1-phenylethyl, the 1-methyl-1 - phenylethyl group, the 3-phenylpropyl, the 4-phenylbutyl group, the 2-methyl-2-phenylethyl group or the 1-methyl or 2-methyl-naphthyl group; or heterocyclylalkyl radicals such as, for. B.
  • aryloxyalkyl radicals such as. B. the phenoxymethyl or naphthoxymethyl group; or cycloalkyl radicals which are monocyclic as listed above under the expression “(C 3 -C 8 ) cycloalkyl”, bicyclic such as, for. B.
  • haloalkyl derivatives of the corresponding groups such as haloalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, haloalkylcycloalkyl or halocycloalkyl radicals.
  • the present invention relates to the compounds of formula I in the form of the free base or an acid addition salt.
  • Acids that can be used for salt formation are inorganic acids such as hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid or organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, fumaric acid, adipic acid, stearic acid, oleic acid, methanesulfonic acid, benzenesulfonic acid or toluenesulfonic acid.
  • Some of the compounds of the formula I have one or more chirality elements. Racemates or diastereomers can therefore occur.
  • the invention encompasses both the pure isomers and their mixtures.
  • the mixtures of diasteromers can by conventional methods, for. B. by selective crystallization from suitable solvents or by chromatography in the components. Racemates can be separated into the enantiomers by customary methods, for. B. by salt formation with an optically active acid, separation of the diastereomeric salts and release of the pure enantiomers by means of a base.
  • the invention further relates to a process for the preparation of compounds of the formula I, which is characterized in that a compound of the formula II
  • A, R 1 , R 2 and R 3 have the meanings given under formula I and L is a leaving group, such as halogen, alkylthio, alkanesulfonyloxy or arylsulfonyloxy, alkylsulfonyl or arylsulfonyl, with a nucleophile of the formula III
  • X, E, a, b, v, U, V, R 4 and R 5 have the meanings given under formula I, and the compounds of the formula I obtained in this way or otherwise, if R 3 is hydrogen, are optionally in halogenated at position 5 of the heterocycle, preferably chlorinated or brominated, or further derivatized in the side chain R 5 .
  • the substitution reaction described above is known in principle.
  • the leaving group L can be varied within wide limits and can mean, for example, a halogen atom such as fluorine, chlorine, bromine or iodine or alkylthio such as methyl or ethylthio; or alkanesulfonyloxy, such as methane, trifluoromethane or ethanesulfonyloxy, or arylsulfonyloxy, such as benzenesulfonyloxy or toluenesulfonyloxy or alkylsulfonyl, such as methyl- or ethylsulfonyl or arylsulfonyl, such as phenyl- or toluenesulfonyl.
  • a halogen atom such as fluorine, chlorine, bromine or iodine or alkylthio such as methyl or ethylthio
  • the aforementioned reaction is carried out in a temperature range of 20-150 ° C., advantageously in the presence of a base and optionally in an inert organic solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, N-methylpyrrolidin-2-one, Dioxane, tetrahydrofuran, 4-methyl-2-pentanone, methanol, ethanol, butanol, ethylene glycol,
  • an inert organic solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, N-methylpyrrolidin-2-one, Dioxane, tetrahydrofuran, 4-methyl-2-pentanone, methanol, ethanol, butanol, ethylene glycol,
  • Suitable bases are, for example, alkali metal or alkaline earth metal carbonates, hydrogen carbonates, amides or hydrides such as sodium carbonate, sodium hydrogen carbonate, potassium carbonate, sodium amide or sodium hydride, organolithium compounds, such as n-butyllithium.
  • Suitable bases for the case where X is oxygen are, for example, alkali or alkaline earth metal carbonates, bicarbonates, amides or hydrides such as sodium carbonate, sodium bicarbonate, potassium carbonate, sodium amide or sodium hydride; if X is NH, these are, for example, alkali - Or alkaline earth metal carbonates, bicarbonates, hydroxides, amides or hydrides such as sodium carbonate, sodium bicarbonate, potassium carbonate, sodium hydroxide, sodium amide or sodium hydride or organic bases such as triethylamine or pyridine.
  • a second equivalent of an amine of formula III can also be used as an auxiliary base.
  • the starting compounds of the formula II are either known or they can be prepared analogously to known processes; see e.g. B.:
  • acetoacetic ester derivatives serve as starting products and are converted into the halopyrimidines via the corresponding hydroxypyrimidines:
  • the starting compounds of the formula II can also be obtained from malonic ester derivatives in analogy to known processes:
  • the compounds of the formula II in which R 3 is halogen can be obtained by known processes by halogenation. If X is oxygen, the nucleophiles of the formula III required as starting products can be prepared by known processes, for example by reducing a carbonyl group with a suitable reducing agent, for example a complex metal hydride or, in the case of an aldehyde or ketone, also with hydrogen and a Hydrogenation catalyst.
  • a suitable reducing agent for example a complex metal hydride or, in the case of an aldehyde or ketone, also with hydrogen and a Hydrogenation catalyst.
  • the starting materials for the particularly preferred cis-cyclohexyloxy derivatives the catalytic hydrogenation of appropriately substituted phenols or the reduction of appropriately substituted cyclohexanone derivatives with complex hydrides which carry substituents with a large amount of space, such as e.g. B. L-Selectride ® .
  • the nucleophiles of the formula III required as starting products can, if NH is NH, be prepared by known processes, for example by reducing an oxime or a nitrile with a suitable reducing agent, for example a complex metal hydride or hydrogen in the presence of a hydrogenation catalyst, reductive amination or Leuckart-Wallach reaction of an aldehyde or ketone or Gabriel reaction of an alkyl halide or tosylate.
  • a suitable reducing agent for example a complex metal hydride or hydrogen in the presence of a hydrogenation catalyst, reductive amination or Leuckart-Wallach reaction of an aldehyde or ketone or Gabriel reaction of an alkyl halide or tosylate.
  • the reductive amination of appropriately substituted cyclohexanones with ammonium salts and sodium cyanoborohydride or with ammonia and hydrogen in the presence of metal catalysts such as nickel, ruthenium, rhodium or palladium is particularly suitable for the preparation of the cyclohexylamines, the starting materials for the particularly preferred cyclohexylamino derivatives
  • metal catalysts such as nickel, ruthenium, rhodium or palladium
  • the proportion of desired cis amine is particularly high.
  • Another method is the hydrogenation of amines in the presence of hydrogenation catalysts.
  • the active ingredients are suitable for good plant tolerance and cheaper
  • Hygiene sector occur. They are effective against normally sensitive and resistant species as well as all or individual stages of development.
  • Pests include:
  • Rhipicephalus spp. Amblyomma spp., Hyalomma spp., Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Br ⁇ obia praetiosa,
  • Pediculus humanus corporis Haematopinus spp., Linognathus spp .. From the order of the Mallophaga z.
  • B. Trichodectes pp., Damalinea spp .. From the order of the Thysanoptera z.
  • B. Hercinothrips femoralis, Thrips tabaci. From the order of Heteroptera z.
  • B. Eurygaster spp. Dysdercus intermedius, Piesma quadrata, Cimex lectularius, Rhodnius prolixus, Triatoma spp .. From the order of Homoptera z. B.
  • the plant-parasitic nematodes that can be controlled according to the invention include, for example, the root-parasitic soil nematodes, such as, for. B. those of the genera Meioidogyne (root gall nematodes, such as Meioidogyne incognita, Meioidogyne hapla and Meioidogyne javanica), heterodera and globodera (cytogenetic nematodes, such as Globodera rostochiensis, Globodera pallida, Heterodera trattoliophenolathenolatheus, and Radiolusidolatheolatheus, as well as Radiatusus radifolate osteolate and Radiolusus yolica) and Simplastus trattoliophenolatheolatyolatheidus Pratylenchus penetrans and Pratylenchus curvitatus; Tylenchulus such as Tylenchulus semipenetrans
  • the compounds of the invention can also be used to combat the nematode genera Ditylenchus (stem parasites such as Ditylenchus dipsaci and Ditylenchus destructor), Aphelenchoides (leaf nematodes such as Aphelenchoides ritzemabosi) and Anguina (flower nematodes such as Anguina tritici).
  • Ditylenchus stem parasites such as Ditylenchus dipsaci and Ditylenchus destructor
  • Aphelenchoides leaf nematodes such as Aphelenchoides ritzemabosi
  • Anguina flower nematodes such as Anguina tritici
  • the invention also relates to compositions, in particular insecticidal and acaricidal compositions, which contain the compounds of the formula I in addition to suitable formulation auxiliaries.
  • the agents according to the invention generally contain the active ingredients of the formula I in an amount of 1 to 95% by weight.
  • WP wettable powder
  • EC emulsifiable concentrates
  • SL aqueous solutions
  • emulsions emulsions
  • sprayable solutions dispersions based on oil or water
  • SO suspoemulsions
  • SE suspoemulsions
  • DP dusts
  • mordants Granules in the form of micro, spray, elevator and adsorption granules
  • water-dispersible granules WG
  • ULV formulations microcapsules, waxes or baits.
  • combinations with other pesticidally active substances, fertilizers and / or growth regulators can also be prepared, e.g. B. in the form of a finished formulation or as a tank mix.
  • Spray powders are preparations which are uniformly dispersible in water and which, in addition to the active substance, are also a wetting agent, in addition to a diluent or inert substance.
  • Emulsifiable concentrates are obtained by dissolving the active ingredient in an organic solvent, e.g. B. butanol, cyclohexanone, dimethylformamide, xylene or higher-boiling aromatics or hydrocarbons with the addition of one or more emulsifiers.
  • organic solvent e.g. B. butanol, cyclohexanone, dimethylformamide, xylene or higher-boiling aromatics or hydrocarbons
  • emulsifiers that can be used are: alkylarylsulfonic acid calcium salts such as cadodecylbenzene sulfonate or nonionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide-ethylene oxide condensation products.
  • Dusts are obtained by grinding the active ingredient with finely divided solid substances, e.g. B. talc, natural clays such as kaolin, bentonite, pyrophillite or diatomaceous earth.
  • Granules can either be produced by spraying the active ingredient onto adsorbable, granulated inert material or by applying active ingredient concentrates by means of adhesives, e.g. As polyvinyl alcohol, sodium polyacrylic acid or mineral oils, on the surface of carriers such as sand, kaolinite or granulated inert material.
  • Suitable active ingredients can also be granulated in the manner customary for the production of fertilizer granules, if desired in a mixture with fertilizers.
  • the active ingredient concentration is e.g. B. about 10 to 90 wt .-% the rest of 100 wt .-% consists of conventional formulation ingredients.
  • the active substance concentration can be approximately 5 to 80% by weight.
  • Dust-like formulations usually contain 5 to 20 wt .-% of active ingredient, sprayable solutions about 2 to 20 wt .-%.
  • the active ingredient content depends in part on whether the active compound is in liquid or solid form and which granulation aids, fillers, etc. are used.
  • the active ingredient formulations mentioned may contain the customary adhesives, wetting agents, dispersants, emulsifiers, penetrants, solvents, fillers or carriers.
  • the concentrates present in the commercial form are optionally diluted in the customary manner, for. B. with wettable powders, emulsifiable concentrates, dispersions and sometimes also with microgranules using water. Dust-like and granulated preparations as well as sprayable solutions are usually no longer diluted with other inert substances before use.
  • the application rate required varies with the external conditions such as temperature, humidity and others. It can fluctuate within wide limits, e.g. B. between 0.0005 and 10.0 kg / ha or more of active substance, but it is preferably between 0.001 and 5 kg / ha.
  • the active compounds according to the invention can be present in their commercially available formulations and in the use forms prepared from these formulations in mixtures with other active compounds, such as insecticides, attractants, sterilants, acaricides, nematicides, fungicides, growth-regulating substances or herbicides.
  • the pesticides include, for example, phosphoric acid esters, carbamates, carboxylic acid esters, formamidines, tin compounds, substances produced by microorganisms and the like. a .. Preferred mixing partners are
  • the active substance content of the use forms prepared from the commercially available formulations can be from 0.00000001 to 95% by weight of active substance, preferably between 0.00001 and 1% by weight.
  • the application takes place in a customary manner adapted to the application forms.
  • the active compounds according to the invention are also suitable for controlling endo- and ectoparasites in the veterinary field or in the field of animal husbandry.
  • the active compounds according to the invention are used here in a known manner, such as by oral use in the form of, for example, tablets, capsules, drinkers, granules, by dermal use in the form of, for example, dipping (dipping), spraying (spraying), pouring on (pour-on and spot) -on) and powdering and by parenteral use in the form of, for example, injection.
  • the novel compounds of the formula I according to the invention can accordingly also be used particularly advantageously in animal husbandry (for example cattle, sheep, pigs and poultry such as chickens, geese, etc.).
  • the animals are given the new compounds, if appropriate in suitable formulations (cf. above) and if appropriate with the drinking water or feed orally.
  • the compounds of the formula I according to the invention are also notable for an excellent fungicidal action.
  • Fungal pathogens that have already penetrated into the plant tissue can be successfully combated curatively. This is particularly important and advantageous in the case of those fungal diseases which can no longer be effectively combated with the usual fungicides after infection has occurred.
  • the spectrum of activity of the claimed compounds covers various economically important phytopathogenic fungi, such as. B. Plasmopara viticola, Erysiphe graminis, Phytophthora infestaus, Pyricularia oryzae, Pyrenophora teres, Leptosphaera notorum, Pelliskularia sasatrii and Puccinia recondita.
  • the compounds according to the invention are also suitable for use in technical fields, for example as wood preservatives, as preservatives in paints, in cooling lubricants for metalworking or as preservatives in drilling and cutting oils.
  • the active compounds according to the invention can be used either alone or in combination with other Fungicides known from the literature are used.
  • Drug concentration of use forms can range from 0.0001 to
  • active ingredient 95% by weight of active ingredient, preferably between 0.0001 and 1% by weight.
  • the application takes place in a customary manner adapted to the application forms
  • a dusting agent is obtained by mixing 10 parts by weight of active ingredient and 90 parts by weight of talc as an inert substance and comminuting them in a hammer mill.
  • a wettable powder which is readily dispersible in water is obtained by adding 25 parts by weight of active compound, 65 parts by weight of kaolin-containing quartz as the inert substance, 10 parts by weight of lignosulfonic acid potassium and 1 part by weight of oleoylmethyl tauric acid sodium as the wetting agent. and dispersant mixes and grinds in a pin mill.
  • a dispersion concentrate which is easily dispersible in water is prepared by mixing 40 parts by weight of active compound with 7 parts by weight of a sulfosuccinic acid half-ester, 2 parts by weight of a lignosulfonic acid sodium salt and 51 parts by weight of water and in a attritor ground to a fineness of less than 5 microns.
  • An emulsifiable concentrate can be prepared from 15 parts by weight Active ingredient, 75 parts by weight of cyclohexane as a solvent and 10 parts by weight of oxyethylated nonylphenol (10 AEO) as an emulsifier.
  • Granules can be produced from 2 to 15 parts by weight of active ingredient and an inert granule carrier material such as attapulgite, pumice granules and / or quartz sand.
  • a suspension of the wettable powder from example b) having a solids content of 30% is expediently used and sprayed onto the surface of an attapulgite granulate, dried and mixed intimately.
  • the proportion by weight of the wettable powder is approximately 5% and that of the inert carrier material approximately 95% of the finished granulate.
  • Spray powder concentrate with a concentration of 250 ppm (based on
  • the compounds according to Examples B and C produced 100% mortality in the test animals.
  • Larvae (L3) of the Southern Corn Rootworm (Diabrotica undecimpunctata) were placed on filter paper discs, which were impregnated with 1 ml of an acetone dilution of a wettable powder in a concentration of 250 ppm based on the active ingredient. After the acetone had been evaporated off, the dishes were closed, stored for 3 days at 28 ° C. and then the mortality of the larvae was determined. The compounds according to Examples B and C showed 100% mortality.
  • Filter paper discs with laying eggs (egg age: 2 days) of the American cotton bug (Oncopeltus fasciatus) were each treated with 1 ml of an aqueous preparation which contained 250 ppm of the respective active ingredient. After the covering had dried on, the filter paper disks were stored in petri dishes at room temperature and maximum atmospheric humidity. The ovicidal activity was determined after 7 days. 100% ovicidal activity (mortality of the eggs) was found in Examples B and C.
  • Apple plants heavily infested with fruit tree spider mites Panonychus ulmi, full population (Malus domestica) were sprayed with an aqueous preparation which contained 250 ppm of the respective active ingredient until they began to drip. After cultivating the plants in the greenhouse for 9 days, the mortality of the fruit tree spider mites (full population) was checked. 100% mortality was found in Examples A, B, C and D.
  • Petri dishes were covered with Jaan filter paper on the inside of the bottom and 20 pieces of 1 day old Manduca sexta eggs were placed on the paper. Then about 1 ml of an artificial insect feed diet was added to the middle of the Petri dish and the inside of the base was sprayed with eggs and feed diet with an aqueous spray powder suspension of the test products corresponding to 600 l / ha. After closing the petri dish and storing for 5 days at room temperature, the mortality of the eggs was determined. Compound B was 100% effective.
  • the active compounds were dissolved in 10% (w / v) in a mixture consisting of dimethylformamide (85 g), nonylphenol polyglycol ether (3 g) and oxyethylated castor oil (7 g), and the emulsion concentrates thus obtained were dissolved in water diluted a test concentration of 500 ppm.
  • the compounds according to Example C each have a 100% inhibition of oviposition in an active ingredient concentration of 500 ppm.
  • a Grignard solution was prepared from 100 g (0.49 mol) of 4-bromo-2-fluoroanisole and 13 g (0.53 mol) of magnesium shavings in 350 ml of tetrahydrofuran.

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

Abstract

L'invention concerne des dérivés hétérocyclyl-amino et hétérocyclyl-oxy-cyloalcényle de formule (a) dans laquelle Ar désigne une 4-pyridyle ou une 4-pyrimidyle éventuellement substituée; X désigne NH, O, S, SO ou SO2; E désigne une liaison ou un alkane-diyle; a et b sont compris respectivement entre 0 et 3, sans être toutefois égaux à 0 en même temps; R4 désigne un halogène ou un alkyle, cycloalkyle, halogénoalkyle, alcoxy, halogénoalcoxy ou un phényle éventuellement substitué; v = 0 - 2; U désigne une liaison ou un O, S, SO, SO¿2? ou un imino éventuellement substitué; V désigne une liaison ou CO, -CQ-T- ou -C(T')=N-, avec Q, T et T' tels que définis dans la description; et R?5¿ désigne un alkyle, alcényle, alcinyle, un aryle ou un hétéroaryle éventuellement substitué, un cyano, NO¿2?, alkyloximino ou un groupe silyle. L'invention concerne en outre la fabrication de ces composés ainsi que leur utilisation comme pesticides et comme fongicides.
EP95935945A 1994-10-31 1995-10-18 Derives heterocyclyl-amino et heterocyclyl-oxy-cycloalcenyle et leur utilisation comme pesticides et comme fongicides Withdrawn EP0789691A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4438807 1994-10-31
DE4438807A DE4438807A1 (de) 1994-10-31 1994-10-31 Heterocyclyl-amino- und Heterocyclyl-oxy-cycloalkenyl-Derivate, ihre Verwendung als Schädlingsbekämpfungsmittel und Fungizide
PCT/EP1995/004088 WO1996013487A1 (fr) 1994-10-31 1995-10-18 Derives heterocyclyl-amino et heterocyclyl-oxy-cycloalcenyle et leur utilisation comme pesticides et comme fongicides

Publications (1)

Publication Number Publication Date
EP0789691A1 true EP0789691A1 (fr) 1997-08-20

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EP95935945A Withdrawn EP0789691A1 (fr) 1994-10-31 1995-10-18 Derives heterocyclyl-amino et heterocyclyl-oxy-cycloalcenyle et leur utilisation comme pesticides et comme fongicides

Country Status (14)

Country Link
EP (1) EP0789691A1 (fr)
JP (1) JP2002515007A (fr)
KR (1) KR970707104A (fr)
AU (1) AU3805895A (fr)
BR (1) BR9509499A (fr)
CA (1) CA2203998A1 (fr)
DE (1) DE4438807A1 (fr)
HU (1) HUT78087A (fr)
IL (1) IL115816A0 (fr)
MX (1) MX9703150A (fr)
PL (1) PL320007A1 (fr)
TR (1) TR199501334A2 (fr)
WO (1) WO1996013487A1 (fr)
ZA (1) ZA959154B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6326133B1 (en) 1997-11-19 2001-12-04 Fuji Photo Film Co., Ltd. Silver halide photographic material

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9810862D0 (en) * 1998-05-20 1998-07-22 Hoechst Schering Agrevo Gmbh Substitutedn pyridine and pyrimidines, processes for their preparation and their use as pesticides
GB9810860D0 (en) * 1998-05-20 1998-07-22 Hoechst Schering Agrevo Gmbh Substituted pyridine and pyrimidines, processes for their preparation and their use as pesticides
CN100592871C (zh) * 2008-03-14 2010-03-03 浙江林学院 一种杀虫剂组合物及其加工方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GT198900008A (es) * 1988-01-29 1990-07-17 Derivados de quinolina, quinazolina y cinolina.
IL89029A (en) * 1988-01-29 1993-01-31 Lilly Co Eli Fungicidal quinoline and cinnoline derivatives, compositions containing them, and fungicidal methods of using them
IL89027A (en) * 1988-01-29 1993-01-31 Lilly Co Eli Quinazoline derivatives, process for their preparation and fungicidal, insecticidal and miticidal compositions containing them
DE4208254A1 (de) * 1992-03-14 1993-09-16 Hoechst Ag Substituierte pyrimidine, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel und fungizid

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9613487A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6326133B1 (en) 1997-11-19 2001-12-04 Fuji Photo Film Co., Ltd. Silver halide photographic material

Also Published As

Publication number Publication date
MX9703150A (es) 1997-06-28
AU3805895A (en) 1996-05-23
CA2203998A1 (fr) 1996-05-09
KR970707104A (ko) 1997-12-01
JP2002515007A (ja) 2002-05-21
ZA959154B (en) 1996-05-27
HUT78087A (hu) 1999-08-30
DE4438807A1 (de) 1996-05-02
TR199501334A2 (tr) 1996-06-21
WO1996013487A1 (fr) 1996-05-09
BR9509499A (pt) 1997-10-14
IL115816A0 (en) 1996-01-19
PL320007A1 (en) 1997-09-01

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