Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
  • C07D213/72—Nitrogen atoms
  • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
• • 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
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • 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
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
  • A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
• • 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
  • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
  • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
  • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
  • C07D215/38—Nitrogen atoms
  • C07D215/42—Nitrogen atoms attached in position 4
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

• the present invention relates to novel pesticidal compounds of formula I
• R* t and R 2 are each independently of the other Cx- alkyl, halo-C r C 6 alkyl containing 1-5 halogen atoms, C 1 -C 2 alkoxy-C 1 -C 6 alkyl, nitro-C r C 6 alkyl, cyano-C j -Cgalkyl,
• Rj and R 2 taken together, form a saturated or unsaturated 5- to 7-membered unsubstituted or substituted carbocyclic or heterocyclic ring which may contain one or two hetero atoms selected from O and S;
• R 3 and R 4 are each independently of the other hydrogen, C r C 6 alkyl or halogen;
• R 5 is hydrogen, C r C 6 alkyl which is unsubstituted or substituted by cyano, nitro, halogen, carboxyl, C 1 -C 2 alkoxycarbonyl, C 1 -C 2 alkanesulfonyl or phenylsulfonyl,
• Y is an unsubstituted or substituted 5-8-membered carbocyclic or heterocyclic ring which can be saturated or unsaturated, aromatic or nonaromatic and which may contain 1 or 2 hetero atoms selected from O, S and/or N and to which a further aromatic group can be fused.
• n is 1,2,3 or 4; or tautomers thereof, in the free form or in the form of a salt.
• the invention further relates to the preparation of these compounds, to agrochemical compositions comprising at least one of said compounds as active ingredient, and to the use of said compounds or compositions for pest control, preferably as microbicides, insecticides and acaricides in agriculture, horticulture and in the hygiene sector.
• the compounds of formula I and their possible tautomers may be obtained in salt form.
• the compounds of formula I contain at least one basic centre, they may typically form acid addition salts.
• These salts may conveniently be formed with a mineral acid such as sulfuric acid, a phosphoric acid or a hydrohalic acid, with an organic carboxylic acid such as acetic acid, oxalic acid, malonic acid, maleic acid, fumaric acid or phthalic acid, with a hydroxycarboxylic acid such as ascorbic acid, lactic acid, malic acid, tartaric acid or citric acid, or with benzoic acid, or with an organic sulfonic acid such as methanesulfonic acid or p-toluenesulfonic acid.
• a mineral acid such as sulfuric acid, a phosphoric acid or a hydrohalic acid
• an organic carboxylic acid such as acetic acid, oxalic acid, malonic acid, maleic acid, fumaric acid or phthalic
• Suitable salts with bases are typically metal salts such as alkali metal salts or alkaline earth metal salts, e.g. sodium, potassium or magnesium salts, or salts with ammonia or an organic amine such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower alkylamine typically ethylamine, diethylamine, triethylamine or dimethylpropylamine, or a mono-, di- or trihydroxy-lower alkylamine, e.g. mono-, di- or triethanolamine.
• Corresponding inner salts may also be formed. Agrochemically acceptable salts are preferred within the scope of this invention.
• the compounds of formula I contain asymmetrical carbon atoms, then the compounds are obtained in optically active form. Owing to the presence of double bonds the compounds may be obtained in the [E] or [Z] form. Atropisomerism can also occur.
• the invention relates not only to the pure isomers, e.g. enantiomers and diastereoisomers, but also to all possible mixtures of isomers, e.g. mixtures of diastereoisomers, racemates or mixtures of racemates.
• Alkyl groups are, in accordance with the number of carbon atoms, straight-chain or branched and will typically be methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-amyl, tert-amyl, 1-hexyl or 3-hexyl.
• Alkenyl will be understood as meaning straight-chain or branched alkenyl such as allyl, ethallyl, 1-methylvinyl or but-2-en-l-yl.
• Preferred alkenyl radials contain 3 to 4 carbon atoms in the chain.
• Alkynyl can likewise, in accordance with the number of carbon atoms, be straight-chain or branched and is typically propargyl, but-1-yn-l-yl or but-l-yn-3-yl. The preferred meaning is propargyl.
• Halogen and halo substituents will be understood generally as meaning fluoro, chloro, bromo or iodo. Fluoro, chloro or bromo are preferred meanings.
• Haloalkyl can contain identical or different halogen atoms, typically fluoromethyl, difluoromethyl, difluorochloromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, 2,2,2-trichloroethyl, 3 ,3 ,3-trifluoropropyl.
• halogen atoms typically fluoromethyl, difluoromethyl, difluorochloromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, 2,2,2-trichloroethyl, 3 ,3 ,3-trifluoropropyl.
• Alkoxy is typically methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy. Methoxy and ethoxy are preferred.
• Haloalkoxy is typically difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy and 2,2-difluoroethoxy.
• Cycloalkyl depending on the size of the ring, is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl.
• alkanoyl is straight-chain or branched and is typically formyl, acetyl, propionyl, butyryl or pivaloyl.
• Carbocyclic and heterocyclic rings can be saturated or unsaturated, aromatic or nonaromatic.
• Cyclic unsaturated hydrocarbon radicals can be aromatic, e.g. phenyl or naphthyl, or nonaromatic, e.g. cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctadienyl, or partially aromatic, e.g. tetrahydronaphthyl and indanyl.
• heterocyclyl groups are pyridyl, pyrimidinyl, imidazolyl, thiazolyl, 1,3,4-thiadiazolyl, triazolyl, thienyl, furanyl, pyrrolyl, morpholinyl, oxazolyl and the corresponding partially or completely hydrogenated rings.
• preferred compounds are pyridyl, pyrimidinyl, imidazolyl, thiazolyl, 1,3,4-thiadiazolyl, triazolyl, thienyl, furanyl, pyrrolyl, morpholinyl, oxazolyl and the corresponding partially or completely hydrogenated rings.
• Ri and R 2 are each independently of the other containing 1-5 haloatoms, C 1 -C 2 alkoxy-C ⁇ -C 4 alkyl, nitro-C 1 -C alkyl, cyano-C r C 4 alkyl, C ⁇ -C 2 alkanoyl-
• Rj and R 2 taken together, form a saturated or unsaturated 5-7-membered, unsubstituted or substituted carbocyclic or heterocyclic ring which may contain one or two hetero atoms selected from O and/or S;
• R 3 and R 4 are each independently of the other hydrogen, C r C 6 alkyl or halogen;
• R 5 is hydrogen or C r C 4 alkyl
• X, Y and n have the given meanings; among these compounds in particular those, wherein
• R 5 is hydrogen, C r C 6 alkyl or benzyl
• R- is C r C 4 alkyl, halo-C r C 4 alkyl containing 1-5 haloatoms, C 1 -C 2 alkoxy-C 1 -C 4 alkyl or
• R 2 is halogen
• R 3 and R 4 are hydrogen
• R 5 is hydrogen or C r C 4 alkyl
• X, Y and n have the given meanings.
• Y is phenyl or pyridine, each of which is unsubstituted or substituted and to which a further aromatic group can be fused.
• Y is phenyl substitued by an unsubstituted or substituted aryloxy group.
• Y is naphthyl, tetrahydronaphthyl, indanyl, indenyl, quinolinyl, isoquinolinyl, quinoxalinyl, quinazolinyl, tetrahydroquinolinyl, indolyl, indolinyl, chromanyl, benzodioxyl, benzofuryl, benzodioxolyl, benzothienyl, benzodithianyl, benzothiophene, 2,3-dihydrobenzothiophenyl.
• R*( is C r C 4 alkyl, containing 1-5 haloatoms, C 1 -C 2 alkoxy-C 1 -C alkyl or
• R 2 is halogen
• Z is phenyl, naphthyl, pyridyl or quinolyl, which aromatic groups are unsubstituted or substituted by C j -C 4 alkyl, trifluoromethyl, halogen or cyano.
• R- is C,-C 4 alkyl, halo-C r C 4 alkyl containing 1-5 haloatoms, or C 3 -C 7 cycloalkyl;
• R 2 is halogen
• Y is naphthyl, tetrahydronaphthyl, indanyl, indenyl, quinolinyl, isoquinolinyl, quinoxalinyl, quinazolinyl, tetrahydroquinolinyl, indolyl, indolinyl, chromanyl, benzodioxyl, benzofuryl, benzodioxolyl, benzothienyl, benzodithianyl, benzothiophene,
• R 10 and R ⁇ are each independently of the other hydrogen or halogen
• Z is phenyl which is unsubstituted or substituted by C r C 4 alkyl, trifluoromethyl, halogen or cyano.
• R 10 and R n are each independently of the other hydrogen or halogen
• Y is naphthyl, tetrahydronaphthyl, indanyl, indenyl, quinoliyl, isoquinolinyl, quinoxalinyl, quinazolinyl, tetrahydroquinolinyl, indolyl, indolynyl, chromanyl, benzodioxyl, benzofuryl, benzodioxolyl, benzothienyl, benzodithianyl, benzothiophene,
• Rj is methyl or ethyl
• R 2 is chloro
• Z is phenyl which is unsubstituted or substituted by one or two halogen atoms
• R j to R 5 have the meanings given for formula I, in the absence or in the presence of a suitable condensing agent and/or a base, to give a compound of formula I.
• Suitable condensing agents are N,N-dicyclohexylcarbodiimide, phosphorus pentachloride, phosgene, oxalyl chloride and thionyl chloride.
• Rj to R 5 , X and Y have the meanings given for formula I, is reacted with a thionating agent, typically with phosphorus pentasulfide or 4-methoxyphenylthio- phosphoric acid cyclodithioanhydride ("Lawesson reagent").
• Rj to R 5 have the meanings given for formula I, and Y is an aromatic group, can be prepared by reacting a compound of formula V
• the above described reactions are carried out in per se known manner, conveniently in the absence or in the presence of a suitable solvent or diluent or of a mixture thereof, and, as required, with cooling, at room temperature or with heating, suitably in the temperature range from c. -20°C to the boiling temperature of the reaction medium, preferably from c. -20°C to c. +150°C, and, if necessary, in a closed reactor under pressure, in an inert gas atmosphere and/or under anhydrous conditions.
• solvents or diluents are: aromatic, aliphatic and alicyclic hydrocarbons and halogenated hydrocarbons such as benzene, toluene, xylene, chlorobenzene, bromobenzene, petroleum ether, hexane, cyclohexane, dichloromethane, trichloromethane, dichloroethane or trichloroethane; ethers such as diethyl ether, tert-butylmethyl ether, tetrahydrofuran or dioxane; ketones such as acetone or methyl ethyl ketone; alcohols such as methanol, ethanol, propanol, butanol, ethylene glycol or glycerol; esters such as ethyl acetate or butyl acetate; amides such as N,N-dimethylformamide, N,N-dimethylacetamide, N
• Bases used in excess may also be used as solvents or diluents.
• suitable bases are hydroxides, hydrides, amides, alkanolates, carbonates, dialkylamides or alkylsilylamides of alkali metals or alkaline earth metals, alkylamines, alkylenediamines, cycloalkylamines or N-alkylated and unsaturated or saturated cycloalkylamines, basic heterocycles, ammonium hydroxides and carbocyclic amines.
• Typical examples of such bases are sodium hydroxide, sodium hydride, sodium amide, sodium methanolate, sodium carbonate, potassium tert-butanolate and potassium carbonate, lithium diisopropylamide, potassium bis(trimethylsilyl)amide, calcium hydride, triethylamine, triethylenediamine, cyclohexylamine, N-cyclohexyl-N,N-dimethylamine, N,N-diethylaniline, pyridine, 4-(N,N-dimethylamino)pyridine, N-methylmorpholine, benzyl trimethylammonium hydroxide as well as l,8-diazabicyclo[5.4.0]undec-5-ene (DBU).
• DBU l,8-diazabicyclo[5.4.0]undec-5-ene
• reaction can be carried out under phase transfer catalysis in an organic solvent, e.g. methylene chloride or toluene, in the presence of an aqueous basic solution, e.g. sodium hydroxide solution, and of a phase transfer catalyst, e.g. tetrabutylammonium hydrogen sulfate.
• organic solvent e.g. methylene chloride or toluene
• a phase transfer catalyst e.g. tetrabutylammonium hydrogen sulfate.
• N-(4- ⁇ yridyl)carboxamides as pesticides, inter alia from patent application WO 93/04580.
• the compounds of formula I of this invention differ structurally from these compounds in characteristic manner.
• the compounds of formula I can be used in agriculture and related fields as pest control agents for controlling plant pests. They are distinguished by their excellent activity at low concentrations, they are well tolerated by plants and are environmentally safe. They have very useful curative, preventive and, in particular, systemic properties, and can be used for protecting numerous cultivated plants.
• the compounds of formula I can be used to inhibit or destroy the pests which occur on plants or parts of plants (fruit, blossoms, leaves, stems, tubers, roots) in different crops of useful plants, while at the same time the parts of plants which also grow later are protected from infestation, for example by phytopathogenic microorganisms.
• the compounds of formula I can also be used as seed dressing agents for protecting seeds (fruit, tubers, grains) and plant cuttings against fungal infections as well as against phytopathogenic fungi which occur in the soil.
• the compounds of formula I are effective against the phytopathogenic fungi belonging to the following classes: Fungi imperfecti (e.g. Botrytis, Pyricularia, Helminthosporium, Fusarium, Septoria, Cercospora, and Alternaria); and Basidiomycetes (e.g. Rhizocotonia, Hemileia, Puccinia). They are also effective against the class of the Ascomycetes (e.g. Venturia and Erysiphe, Podosphaera, Monilinia and Uncinula), and especially against that of the Oomycetes (e.g. Phytophthora, Pythium and Plasmopara).
• Fungi imperfecti e.g. Botrytis, Pyricularia, Helminthosporium, Fusarium, Septoria, Cercospora, and Alternaria
• Basidiomycetes e.g. Rhizocotonia, Hemileia, Puccinia
• They are also effective against
• the compounds of formula I are also useful pest control agents for controlling insects and/or acarina in crop plants and ornamentals in agriculture, especially in cotton, vegetable and fruit crops, in forestry and in the storage and material protection sectors as well as in the hygiene sector, and for controlling pests of animals, especially on domestic animals and productive livestock.
• the compounds of formula I are effective against various stages of development and their activity may be observed in an immediate kill of the pests or sometime later, for example in moulting or in diminished oviposition and/or hatching rate.
• the animal pests typically include those of the order Lepidoptera, Coleoptera, Orthoptera, Isoptera, Acarina (e.g. Boophilus spp.).
• Target crops suitable for the plant protective utility disclosed herein typically comprise within the scope of the present invention the following species of plants: cereals (wheat, barley, rye, oats, rice, maize, sorghum and related species), beet (sugar beet and fodder beet), pomes, drupes and soft fruit (apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries and blackberries), leguminous plants (beans, lentils, peas, soybeans), oil plants (rape, mustard, poppy, olives, sunflowers, coconut, castor oil plants, cocoa beans, groundnuts), cucurbits (cucumbers, marrows, melons), fibre plants (cotton, flax, hemp, jute), citrus fruit (oranges, lemons, grapefruit, mandarins), vegetables (spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, sweet peppers), lauraceae (avocados, cinnamon, camphor),
• the compounds of formula I are usually applied in the form of compositions and can be applied to the crop area or plant to be treated, simultaneously or in succession, with further compounds.
• These further compounds can be fertilisers or micronutrient donors as well as other preparations that influence plant growth. It is also possible in this connection to use selective herbicides, insecticides, fungicides, bactericides, nematicides, molluscicides or mixtures of several of these preparations, together with optional carriers, surfactants or application-promoting adjuvants commonly employed in the art of formulation.
• Suitable carriers and adjuvants may be solid or liquid and correspond to the appropriate substances ordinarily employed in formulation technology, including natural or regenerated mineral substances, solvents, dispersants, wetting agents, tackifiers, thickeners, binders or fertilisers.
• a preferred method of applying a compound of formula I, or an agrochemical composition which contains at least one of said compounds, is foliar application.
• the frequency of application and the rate of application will depend on the risk of infestation by the corresponding pathogen.
• the compound of formula I can also penetrate the plant through the roots via the soil (systemic action) by drenching the locus of the plant with a liquid formulation, or by applying the compounds in solid form to the soil, e.g. in granular form (soil application). In crops of water rice such granular formulations can be applied to the flooded rice field.
• the compounds of formula I may also be applied to seeds (coating) by impregnating the seeds either with a liquid formulation of the fungicide or coating them with a solid formulation.
• the compounds of formula I are used in unmodified form or, preferably, together with the adjuvants conventionally employed in the art of formulation. To this end they are conveniently formulated in known manner to emulsifiable concentrates, coatable pastes, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granulates, and also encapsulations in polymeric substances.
• the methods of application such as spraying, atomising, dusting, scattering, coating or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
• Advantageous rates of application are normally from 5 g to 2 kg of active ingredient (a.i.) per hectare, preferably from 10 g to 1 kg a.i ha, most preferably from 20 g to 600 g a.iJha.
• advantageous rates of application are from 10 mg to 1 g of active ingredient per kg of seeds.
• compositions, preparations or mixtures containing the compound of formula I and, where appropriate, a solid or liquid adjuvant are prepared in known manner, conveniently by homogeneously mixing and/or grinding the active ingredient with extenders, as with a solvent (mixture), a solid carrier and, in some cases, surface-active compounds (surfactants).
• Suitable solvents are: aromatic hydrocarbons, the fractions containing 8 to 12 carbon atoms, typically xylene mixtures or substituted naphthalenes, phthalates such as dibutyl or dioctyl phthalate, aliphatic hydrocarbons such as cyclohexane or paraffins; also alcohols and glycols and their ethers and esters, such as ethanol, diethylene glycol, 2-methoxyethanol or 2-ethoxyethanol, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, dimethyl sulfoxide or dimethyl formamide, as well as vegetable oils or epoxidised vegetable oils such as epoxidised coconut oil or soybean oil; or water.
• aromatic hydrocarbons the fractions containing 8 to 12 carbon atoms, typically xylene mixtures or substituted naphthalenes, phthalates such as dibutyl or dioctyl phthalate, aliphatic
• the solid carriers typically used for dusts and dispersible powders are usually natural mineral fillers such as calcite, talcum, kaolin, montmorillonite or attapulgite.
• natural mineral fillers such as calcite, talcum, kaolin, montmorillonite or attapulgite.
• highly dispersed silica or highly dispersed absorbent polymers such as calcite, talcum, kaolin, montmorillonite or attapulgite.
• Suitable granulated adsorptive carriers are porous types such as pumice, broken brick, sepiolite or bentonite; and suitable nonsorbent carriers are materials such as calcite or sand.
• pregranulated materials of inorganic or organic nature can be used, e.g. especially dolomite or pulverised plant residues.
• suitable surface-active compounds are nonionic, cationic and/or anionic surfactants having good emulsifying, dispersing and wetting properties.
• surfactants will also be understood as comprising mixtures of surfactants.
• Suitable anionic surfactants can be water-soluble soaps as well as water-soluble synthetic surface-active compounds.
• nonionic surfactants are nonylphenolpolyethoxyethanols, poly- ethoxylated castor oil, polyadducts of polypropylene and polyethylene oxide, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxy- ethanol.
• Fatty acid esters of polyoxyethylenesorbitane, e.g. polyoxyethylenesorbitane trioleate, are also suitable.
• Cationic surfactants are preferably quaternary ammonium salts carrying, as N-substituents, at least one C 8 -C 22 alkyl radical and, as further substituents, optionally halogenated lower alkyl, benzyl or hydroxy-lower alkyl radicals.
• the agrochemical compositions usually contain 0.1 to 99 % by weight, preferably 0.1 to 95 % by weight, of a compound of formula I, 99.9 % to 1 % by weight, preferably 99.8 to 5 % by weight, of a solid or liquid adjuvant, and 0 to 25 % by weight, preferably 0.1 to 25 % by weight, of a surfactant
• compositions may also contain further ingredients such as stabilisers, antifoams, viscosity regulators, binders, tackifiers as well as fertilisers or other chemical agents to obtain special effects.
• Emulsions of any desired concentration can be prepared by diluting such concentrates with water.
• Example F-2 Emulsifiable concentrate
• Emulsions of any desired concentration can be prepared by diluting such a concentrate with water.
• N-methylpyrrolid-2-one epoxidised coconut oil white spirit (boiling ranges: 160-190°)
• Ready-for-use dusts are obtained by intimately the carriers with the compound.
• Wheat plants are sprayed to drip point 6 days after sowing with an aqueous spray mixture (0.02 % a.i.) prepared from a wettable powder formulation of the test compound and infected 24 hours later with a uredospore suspension of the fungus. After an incubation time of 48 hours (conditions: 95-100 % relative humidity at 20°C), the plants are stood at 22°C in a greenhouse. Evaluation of fungal infestation is made 12 days after infection.
• Wheat plants are drenched 5 days after sowing with an aqueous spray mixture (0.006 % a.i., based on the volume of the soil) prepared from a wettable powder formulation of the test compound. Care is taken that the spray mixture does not come in contact with the growing parts of plants. After 48 hours, the plants are infected with a uredospore suspension of the fungus. After an incubation period of 48 hours (conditions: 95-100 % relative humidity at 20°C), the plants are stood at 22°C in a greenhouse. Evaluation of fungal infestation is made 12 days after infection
• Example B-2 Action against Phytophthora infestans on tomatoes a) Residual-protective action
• tomato plants are sprayed to drip point with a spray mixture (0.02 % a.i.) prepared from a wettable powder formulation of the test compound.
• the tomato plants are treated 24 hours later with a conidia suspension of the fungus. Evaluation of fungal infestation is made after the plants have been incubated for 5 days at 20°C and 90-100°C relative humidity.
• Example B-3 Residual-protective action against Cercospora arachidicola on groundnut plants
• Groundnut plants 10-15 cm in height are sprayed to drip point with an aqueous spray mixture (0.02 ppm a.i.) prepared from a wettable powder formulation of the test compound and infected 48 hours later with a conidia suspension of the fungus.
• the infected plants are incubated for 72 hours at c. 21°C and high humidity and then stood in a greenhouse until the typical leaf specks occur. Evaluation of the fungicidal action is made 12 days after infection and is based on the number and size of the specks. Compounds of the Tables show good activity.
• Example B-4 Action against Plasmopara viticola on vines
• Vine seedlings in the 4- to 5-leaf stage are sprayed to drip point with an aqueous spray mixture (0.02 ppm a.i.) prepared from a wettable powder formulation of the test compound and infected 24 hours later with a sporangia suspension of the fungus.
• aqueous spray mixture (0.02 ppm a.i.) prepared from a wettable powder formulation of the test compound and infected 24 hours later with a sporangia suspension of the fungus.
• Example B-5 Action against Colletotrichum lagenarium on cucumbers
• Cucumber plants are sprayed with an aqueous spray mixture (0.002 ppm a.i.) prepared from a wettable powder formulation of the test compound and infected 2 days later with a spore suspension (l.SxlO 5 spores/ml) of the fiingus and incubated for 36 hours at 23 °C and high humidity Incubation is then continued at normal humidity and c. 22°C. Evaluation of fungal infestation is made 8 days after infection.
• an aqueous spray mixture 0.002 ppm a.i.
• a spore suspension l.SxlO 5 spores/ml
• Example B-6 Residual protective action against Venturia inaequalis on apple shoots Apple cuttings with 10-20 cm long fresh shoots are sprayed to drip point with a spray mixture (0.02 % a.i.) prepared from a wettable powder formulation of the test compound. The plants are infected 24 hours later with a conidia suspension of the fungus. The plants are then incubated for 5 days at 90-100 % relative humidity and stood in a greenhouse for a further 10 days at 20-24°C. Scab infestation is evaluated 12 days after infection. Compounds of the Tables show good activity.
• Example B7 Action against Erysiphe graminis on barley a) Residual protective action
• Barley plants about 8 cm in height are sprayed to drip point with a spray mixture (0.02 % a.i.) prepared from a wettable powder formulation of the test compound and the treated plants are dusted with conidia of the fungus 3 to 4 hours later.
• the infected plants are stood in a greenhouse at c. 22°C and fungus infestation is evaluated 10 days after infection.
• Compounds of the Tables show good activity.
• Barley plants about 8 cm in height are drenched with an aqueous spray mixture (0.002 % a.i., based on the volume of the soil) prepared from a wettable powder formulation of the test compound. Care is taken that the spray mixture does not come in contact with the growing parts of the plants.
• the treated plants are dusted 48 hours later with conidia of the fungus.
• the infected plants are then stood in a greenhouse at c. 22°C and evaluation of infestation is made 12 days after infection. Compounds of the Tables show good activity.
• Example B8 Action against Podosphaera leucotricha on apple shoots
• Apple cuttings with c. 15 cm fresh shoots are sprayed with a spray mixture (0.06 % a.i.) of the test compound.
• the plants are infected 24 hours later with a conidia suspension of the fungus and then stood in a humidity chamber at 70 % relative humidity at 20°C. Fungus infestation is evaluated 12 days after infection.
• Example B-9 Action against Nilaparvata lugens
• Rice plants are treated with an aqueous emulsion spray formulation containing the test compound in a concentration of 400 ppm. When the spray coating has dried, the rice plants are populated with cicada larvae in the 2nd and 3rd stage. Evaluation is made 21 days later. The percentage reduction in the population (percentage kill) is determined by comparing the number of surviving cicadas on the treated plants with those on the untreated plants.
• Example B-10 Action against Plutella xylostella caterpillars
• Young cabbage plants are sprayed with an aqueous emulsion spray formulation containing the test compound in a concentration of 400 ppm.
• the cabbage plants are populated with 10 caterpillars of Plutella xylostella in the 3rd stage and placed in a plastic container. Evaluation is made 3 days later. The percentage reduction of the population and of feeding damage (percentage kill) is determined by comparing the number of dead caterpillars and the feeding damage on the treated plants with those on the untreated plants.
• Example B-l 1 Action against Musca domestica
• a sugar lump is moistened with a solution of the test compound such that, after drying overnight, the concentration of test compound in the sugar is 250 ppm.
• the treated sugar lump is placed in an aluminium dish together with a most cotton wool swab and 10 adult
• Musca domestica of an OP-resistent strain The dish is then covered with a glass beaker and incubated at 25°C. The mortality rate is determined 24 hours later.
• Example B-l 2 Action against Tetranvchus urticae
• Young bean plants are populated with a mixed population of Tetranychus urticae and sprayed 1 day later with an aqueous emulsion spray formulation containing 400 ppm of test compound. The plants are then incubated for 6 days at 25 °C and afterwards evaluated.
• the percentage reduction in the population is determined by comparing the number of dead eggs, larvae and adults on the treated plants with those on the untreated plants.
• Example B-13 Action against a mixed population of Tetranychus cinnabarinus Dilution series
• Dwarf beans in the 2-leaf stage are populated with a mixed population (eggs, larvae/nymphs, adults) of an OP-tolerant strain of Tetranvchus cinnabarinus.
• the test compounds are sprayed on to the plants 24 hours after infection at rates of 200, 100, 50 mg a.i/litre in an automatic spray cabinet.
• the test compounds are formulated and diluted with water to the appropriate concentrations. The test is evaluated for the percentage kill 0f - eggs
• Replete adult female ticks are fixed with adhesive tape to a PVC sheet and covered with a cotton wool swab.
• the test organisms are then treated by impregnating the cotton wool swab with 10 ml of an aqueous solution containing the test compound in a concentration of 125 ppm.
• the cotton wool swab is then removed and the ticks are incubated for

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• 1995
  • 1995-10-09 TW TW084110636A patent/TW334337B/zh active
  • 1995-10-25 JP JP8515001A patent/JPH10508590A/ja active Pending
  • 1995-10-25 WO PCT/EP1995/004176 patent/WO1996014301A1/en not_active Application Discontinuation
  • 1995-10-25 AU AU38691/95A patent/AU3869195A/en not_active Abandoned
  • 1995-10-25 EP EP95937839A patent/EP0790983A1/en not_active Withdrawn
  • 1995-11-06 ZA ZA959366A patent/ZA959366B/xx unknown
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