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EP1613633A1 - 7-alkinylamino-triazolopyrimidines, leurs procedes de production et leur utilisation pour lutter contre les champignons nuisibles et les produits les contenant - Google Patents

7-alkinylamino-triazolopyrimidines, leurs procedes de production et leur utilisation pour lutter contre les champignons nuisibles et les produits les contenant

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Publication number
EP1613633A1
EP1613633A1 EP04724256A EP04724256A EP1613633A1 EP 1613633 A1 EP1613633 A1 EP 1613633A1 EP 04724256 A EP04724256 A EP 04724256A EP 04724256 A EP04724256 A EP 04724256A EP 1613633 A1 EP1613633 A1 EP 1613633A1
Authority
EP
European Patent Office
Prior art keywords
formula
compounds
methyl
alkyl
chlorine
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Withdrawn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
EP04724256A
Other languages
German (de)
English (en)
Inventor
Jordi Tormo I Blasco
Carsten Blettner
Bernd Müller
Markus Gewehr
Wassilios Grammenos
Thomas Grote
Andreas Gypser
Joachim Rheinheimer
Peter Schäfer
Frank Schieweck
Anja Schwögler
Maria Scherer
Siegfried Strathmann
Ulrich Schöfl
Reinhard Stierl
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.)
BASF SE
Original Assignee
BASF SE
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Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP1613633A1 publication Critical patent/EP1613633A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Definitions

  • the present invention relates to 7-alkynylamino-triazolopyrimidines of the formula I.
  • a 1 is hydrogen, hydroxy, d-Cs-alkyl, CC 8 -alkylamino or di- (C r C 8 -alkyl) amino
  • n 0, 1 or 2;
  • n 1, 2, 3, 4 or 5, at least one group L being ortho to the bond with the triazolopyrimidine skeleton;
  • R 1 is hydrogen or CC 4 alkyl
  • R 2 C 3 -C 10 alkynyl which may be unsubstituted or partially or completely halogenated or may carry one to three groups R a :
  • R a halogen, cyano, nitro, hydroxy, -CC 6 alkylcarbonyl, C 3 -C 6 cycloalkyl, d-Ce-alkoxy, Ci-Ce-haloalkoxy, -C-C 6 -alkoxycarbonyl, -C-C 6 -alkylthio , C ⁇ -C 6 -alkylamino, di-C ⁇ -C 6 -alkylamino, C 2 -C 6 alkenyl, C 2 -C 6 alkenyloxy,
  • R b halogen, cyano, nitro, hydroxy, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, alkyl, haloalkyl, alkenyl, alkenyloxy, alkynyloxy, alkoxy, haloalkoxy, alkylthio, alkylamino, dialkylamino, formyl, alkylcarbonyl, alkylsulfonyl, Alkylsulfoxyl, alkoxycarbonyl, alkylcarbonyloxy, alkylaminocarbonyl, dialkylaminocarbonyl, alkylamino thiocarbonyl, dialkylaminothiocarbonyl, the alkyl groups in these radicals containing 1 to 6 carbon atoms and the alkenyl or alkynyl groups mentioned in these radicals containing 2 to 8 carbon atoms.
  • the invention also relates to processes for the preparation of these compounds, compositions containing them and their use for controlling phytopathogenic harmful fungi.
  • the present invention is based on the object of providing compounds with improved activity and / or broadened spectrum of activity.
  • the compounds of the formula I differ from those from the abovementioned publications by the configuration of the substitution of the 6-phenyl group, which is necessarily substituted in the ortho position.
  • the compounds of the formula I have an increased activity against harmful fungi compared to the known compounds.
  • the compounds according to the invention can be obtained in various ways. They are advantageous by reacting the dihalotriazolopyrimidines Formula II, obtained in the shark for a halogen atom, such as bromine or, in particular chlorine, with amines of the formula III under conditions generally known from WO 98/46608.
  • a halogen atom such as bromine or, in particular chlorine
  • reaction of II with amines III is advantageously carried out at 0 ° C to 70 ° C, preferably 10 ° C to 35 ° C, preferably in the presence of an inert solvent such as ether, e.g. B. dioxane, diethyl ether or in particular tetrahydrofuran, halogenated hydrocarbons such as dichloromethane and aromatic hydrocarbons such as toluene.
  • ether e.g. B. dioxane, diethyl ether or in particular tetrahydrofuran
  • halogenated hydrocarbons such as dichloromethane
  • aromatic hydrocarbons such as toluene.
  • a base such as tertiary amines, for example triethylamine or inorganic bases, such as potassium carbonate, is preferred; Excess amine of formula III can also serve as a base.
  • Amines of the formula III are known in some cases or can be prepared by known methods, for example from the corresponding alcohols via the tosylates and phthalimides [cf. J. Am. Chem. Soc, Vol. 117, p. 7025 (1995); WO 93/20804], by reducing the corresponding nitriles [cf. Heterocycles, vol. 35, p. 2 (1993); Synthetic Commun. 25: 413 (1995); Tetrahedron Lett., P. 2933 (1995)], or reductive amination of ketones [cf. J. Am. Chem. Soc, Vol. 122, p. 9556 (2000); Org. Lett. P. 731 (2001); J. Med.
  • the reaction temperature is usually from 0 to 120 ° C., preferably from 10 to 40 ° C. [cf. J. Heterocycl. Chem., Vol. 12, pp. 861-863 (1975)].
  • Suitable solvents include ethers such as dioxane, diethyl ether and, preferably tetrahydrofuran, halogenated hydrocarbons such as dichloromethane and aromatic hydrocarbons such as toluene.
  • Compounds of the formula IC, in which X is "-C-alkyl, can be obtained by coupling 5-halotriazolopyrimidines of the formula IA with organometallic reagents of the formula V.
  • the reaction takes place with transition metal catalysis, such as Ni or Pd catalysis.
  • X stands for CC 4 -alkyl and M for a metal ion of valence Y, such as B, Zn or Sn.
  • This reaction can be carried out, for example, analogously to the following methods: J. Chem. Soc. Perkin Trans. 1, 1187 (1994), ibid. 1, 2345 (1996); WO 99/41255; Aust. J. Chem., Vol. 43, S.733 (1990); J. Org. Chem., Vol. 43, S.358 ( 1978); J. Chem. Soc. Chem. Commun. S.866 (1979); Tetrahedron Lett., Vol. 34, S.8267 (1993); ibid., Vol. 33, P.413 (1992).
  • 5-alkyl-7-hydroxy-6-phenyltriazolopyrimidines VIII are obtained.
  • R represents a CC alkyl group, in particular methyl or ethyl.
  • Chlorination or bromination agents such as phosphorus oxybromide, phosphorus oxychloride, thionyl chloride, thionyl bromide or sulfuryl chloride are preferably used.
  • the reaction can be carried out in bulk or in the presence of a solvent. Usual reaction temperatures are from 0 to 150 ° C or preferably from 80 to 125 ° C.
  • the reaction of IX with amines III is advantageously carried out at 0 ° C. to 70 ° C., preferably 10 ° C. to 35 ° C., preferably in the presence of an inert solvent, such as ether, e.g. B. dioxane, diethyl ether or in particular tetrahydrofuran, halogenated hydrocarbons such as dichloromethane and aromatic hydrocarbons such as toluene [cf. WO 98/46608].
  • ether e.g. B. dioxane, diethyl ether or in particular tetrahydrofuran
  • halogenated hydrocarbons such as dichloromethane
  • aromatic hydrocarbons such as toluene [cf. WO 98/46608].
  • a base such as tertiary amines, for example triethylamine or inorganic bases, such as potassium carbonate, is preferred; Excess amine of formula III can also serve as a base.
  • the malonates XI are known in the literature [J. At the. Chem. Soc, Vol. 64, 2714 (1942); J. Org. Chem., Vol. 39, 2172 (1974); Helv. Chim. Acta, Vol. 61, 1565 (1978)] or can be prepared according to the literature cited.
  • the subsequent saponification of the ester XII takes place under generally customary conditions, depending on the various structural elements, the alkaline or acidic saponification of the compounds XII can be advantageous. Under the conditions of ester hydrolysis, the decarboxylation to I.C can already take place in whole or in part.
  • the decarboxylation is usually carried out at temperatures from 20 ° C. to 180 ° C., preferably 50 ° C. to 120 ° C., in an inert solvent, optionally in the presence of an acid.
  • Suitable acids are hydrochloric acid, sulfuric acid, phosphoric acid, formic acid, acetic acid, p-toluenesulfonic acid.
  • Suitable solvents are water, 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.
  • the reaction mixtures are usually worked up, e.g. by mixing with water, separation of the phases and, if necessary, chromatographic purification of the crude products.
  • the intermediate and end products fall in part. in the form of colorless or slightly brownish, viscous oils, which are freed from volatile components or cleaned under reduced pressure and at a moderately elevated temperature. If the intermediate and end products are obtained as solids, they can also be purified by recrystallization or digesting.
  • isomer mixtures are obtained in the synthesis, however, a separation is generally not absolutely necessary, since the individual isomers are in some cases during preparation for use or during use (for example under light, acid). or base action) can convert into each other. Corresponding conversions can also take place after use, for example in the treatment of plants in the treated plant or in the harmful fungus to be controlled.
  • Halogen fluorine, chlorine, bromine and iodine
  • Alkyl saturated, straight-chain or branched hydrocarbon radicals with 1 to 4, 6 or 8 carbon atoms, for example dC 6 alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1- Dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 1-methylpentyl, 2- Methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1, 3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1- Ethyl butyl, 2-ethyl buty
  • Haloalkyl straight-chain or branched alkyl groups with 1 to 2 or 4 carbon atoms (as mentioned above), where the hydrogen atoms in these groups can be partially or completely replaced by halogen atoms as mentioned above: in particular d -haloalkyl such as chloromethyl, bromomethyl, dichloromethyl, Trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl or chlorodifluoromethyl;
  • Alkynyl straight-chain or branched hydrocarbon groups with 2 to 4, 6, 8 or 10 carbon atoms and one or two triple bonds in any position, e.g. C 2 -C 6 alkynyl such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2 -Butinyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl -3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl , 1-methyl-2-
  • R 2 has a chiral center
  • the (R) and (S) isomers and the racemates of the compounds of the formula I are included in the scope of the invention.
  • the particularly preferred embodiments of the intermediates in terms of the variables correspond to those of the radicals L m , R 1 , R 2 and X of the formula I.
  • R 21 is methyl or halomethyl
  • R 22 is hydrogen, methyl or halomethyl
  • R 23 is C 2 -C 8 -alkynyl, which may be unsubstituted or partially or completely halogenated and / or may carry one to three groups R a .
  • the remaining variables are defined as in Formula I.
  • a particularly preferred subject matter is compounds I in which R 23 represents straight-chain or branched C 2 -C 8 -alkynyl which is unsubstituted or partially or completely halogenated.
  • L m is fluorine, chlorine, methyl, Ci-haloalkyl, methoxy, amino, NHR or NR 2 , in which R is methyl or acetyl.
  • # is the point of attachment to the triazolopyrimidine backbone
  • L 2 , L 4 independently of one another are hydrogen or fluorine
  • L 3 is hydrogen, fluorine, chlorine, CH 3 , OCH 3 , amino, NHR or NR 2 ;
  • L 5 is hydrogen, chlorine, fluorine or CH 3 .
  • Table 7 Compounds of the formula I in which X is chlorine, L m is pentafluoro and the combination of R 1 and R 2 for each compound corresponds to one row of Table A.
  • the compounds I are suitable as fungicides. They are characterized by excellent activity against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes, Deuteromycetes, Oomycetes and Basidiomycetes. Some of them are systemically effective and can be used in plant protection as leaf and soil fungicides.
  • Rhizoctonia species on cotton, rice and lawn are Rhizoctonia species on cotton, rice and lawn.
  • the compounds I are also suitable for combating harmful fungi such as Pacilomyces variotii in the protection of materials (e.g. wood, paper, dispersions for painting, fibers or fabrics) and in the protection of stored products.
  • harmful fungi such as Pacilomyces variotii in the protection of materials (e.g. wood, paper, dispersions for painting, fibers or fabrics) and in the protection of stored products.
  • the compounds I are used by treating the fungi or the plants, seeds, materials or the soil to be protected against fungal attack with a fungicidally active amount of the active compounds.
  • the application can take place both before and after the infection of the materials, plants or seeds by the fungi.
  • the fungicidal compositions generally contain between 0.1 and 95, preferably between 0.5 and 90% by weight of active ingredient.
  • the application rates in crop protection are between 0.01 and 2.0 kg of active ingredient per ha.
  • amounts of active compound of 0.001 to 0.1 g, preferably 0.01 to 0.05 g, are generally required per kilogram of seed.
  • the amount of active ingredient applied depends on the type of application and the desired effect. Usual application rates in material protection are, for example, 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active ingredient per cubic meter of treated material.
  • the compounds I can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the form of application depends on the respective purpose; in any case, it should ensure a fine and uniform distribution of the connection according to the invention.
  • the formulations are prepared in a known manner, e.g. by stretching the active ingredient with solvents and / or carriers, if desired using emulsifiers and dispersants, and in the case of water as diluent other organic solvents can also be used as auxiliary solvents.
  • auxiliaries 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.
  • Carriers such as natural powdered rock (e.g. kaolins, clays, talc, chalk) and synthetic powdered rock (e.g. highly disperse silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (e.g. polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste liquors and methyl cellulose.
  • Carriers such as natural powdered rock (e.g. kaolins, clays, talc, chalk) and synthetic powdered rock (e.g. highly disperse silica, silicates)
  • Emulsifiers such as nonionic and anionic emulsifiers (e.g. polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste
  • Suitable surfactants are alkali metal, alkaline earth metal salts, sulfonic acid ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates and fatty acids and their alkali and alkaline earth metal salts, salts of sulfated fatty alcohol glycol ethers, condensates of sulfonated naphthalene and naphthalene derivatives with Formaldehyde, condensation products of naphthalene or naphthalene sulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alky
  • Mineral oil fractions with a medium to high boiling point such as kerosene or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example benzene, toluene, are used to produce directly sprayable solutions, emulsions, pastes or oil dispersions.
  • 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 , into consideration.
  • Powders, materials for broadcasting and dusts can be prepared by mixing or grinding the active substances together with a solid carrier.
  • Granules e.g. Coating, impregnation and homogeneous granules can be produced by binding the active ingredients to solid carriers.
  • Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attack clay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers, e.g. 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 gels, silicates, talc, kaolin, attack clay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics,
  • 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).
  • V. 80 parts by weight of a compound according to the invention are combined with 3 parts by weight of the sodium salt of diisobutylnaphthalene sulfonic acid, 10 parts by weight of the sodium salt of lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of powdered silica gel mixed and ground in a hammer mill (active ingredient content 80% by weight).
  • the 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, old dispersions, pastes, dusts, sprinkling agents, granules by spraying, atomizing, dusting, scattering or pouring.
  • 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.
  • Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (wettable powders, old dispersions) by adding water.
  • 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. But it can concentrates consisting of an active substance, wetting agents, adhesives, dispersants or emulsifiers and possibly solvents or oil are also suitable and are suitable for dilution with water.
  • the active ingredient concentrations in the ready-to-use preparations can be varied over a wide range. In general, they 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.
  • UUV ultra-low-volume process
  • 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.
  • compositions according to the invention can also be present together with other active compounds which, e.g. with herbicides, insecticides, growth regulators, fungicides or also with fertilizers. Mixing the compounds I or the compositions containing them in the use form as fungicides with other fungicides results in an enlargement of the fungicidal spectrum of action in many cases.
  • Acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl, amine derivatives such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidine, guazatine, iminoctadine, spiroxamine, tridemorph,
  • Anilinopyrimidines such as pyrimethanil, mepanipyrim or cyrodinyl,
  • Antibiotics such as cycloheximide, griseofulvin, kasugamycin, natamycin, or streptomycin Penconazole, propiconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol, triflumizole, triticonazole,
  • Dicarboximides such as iprodione, myclozolin, procymidone, vinclozolin, Dithiocarbamates such as Ferbam, Nabam, Maneb, Mancozeb, Metam, Metiram, Propinerb, Polycarbamat, Thiram, Ziram, Zineb,
  • Heterocyclic compounds such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, famoxadone, fenamidon, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolan, mepronil, nuar
  • Copper fungicides such as Bordeaux broth, copper acetate, copper oxychloride, basic copper sulfate, nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthal-isopropyl,
  • Phenylpyrroles such as fenpiclonil or fludioxonil
  • fungicides such as acibenzolar-S-methyl, benthiavalicarb, carpropamide, chlorothalonil, cyflufenamid, cymoxanil, Dazomet, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamide, fentin acetate, fenoxanil,
  • Ferimzone fluazinam, fosetyl, fosetyl aluminum, iprovalicarb, hexachlorobenzene, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamide,
  • Strobilurins such as azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin or trifloxystrobin,
  • Sulfenoic acid derivatives such as captafol, captan, dichlofluanid, folpet, tolylfluanid,
  • Cinnamic acid amides and analogues such as dimethomorph, flumetover or flumorph.
  • the active ingredients were prepared separately as a stock solution with 0.25% by weight of active ingredient in acetone or DMSO. 1% by weight of the emulsifier Uniperol® EL (wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) was added to this solution and diluted with water to the desired concentration.
  • emulsifier Uniperol® EL wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
  • Leaves of potted plants of the "Large meat tomato St. Pierre" were sprayed with an aqueous suspension in the active ingredient concentration given below to the point of dripping wet. The following day, the leaves were infected with an aqueous spore suspension of Alternaria solani in 2% biomalt solution with a density of 0.17 x 10 6 spores / ml. The plants were then placed in a water vapor-saturated chamber at temperatures between 20 and 22 ° C. After 5 days the leaf infestation on the untreated but infected control plants had developed so strongly that the infestation could be determined visually in%.

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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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne les 7-alkinylamino-triazolopyrimidines de la formule (I) où les substituants ont la signification suivante: L représente un halogène, alkyle, halogène-alkyle, alcoxy, amino, NHR, NR2, cyano, S(O)nA1 ou C(O)A2 ; R représente alkyle ou alkylcarbonyle; A1 représente un hydrogène, hydroxy, alkyle, alkylamino ou dialkylamino ; n vaut 0, 1 ou 2; A2 représente alcényle, alcoxy, halogènealcoxy ou un groupe cité en A1; m vaut 1, 2, 3, 4 ou 5, au moins un groupe L étant en position « ortho » par rapport à la liaison avec le squelette triazolopyrimidine; X représente un halogène, cyano, alkyle, halogènealkyle ou alcoxy; R1 représente un hydrogène ou alkyle; R2 représente un alkinyle non substitué ou substitué conformément à la description. L'invention concerne également les procédés de production de ces composés, les produits les contenant et leur utilisation pour lutter contre les champignons nuisibles phytopathogènes.
EP04724256A 2003-04-02 2004-03-30 7-alkinylamino-triazolopyrimidines, leurs procedes de production et leur utilisation pour lutter contre les champignons nuisibles et les produits les contenant Withdrawn EP1613633A1 (fr)

Applications Claiming Priority (2)

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DE10314930 2003-04-02
PCT/EP2004/003346 WO2004087706A1 (fr) 2003-04-02 2004-03-30 7-alkinylamino-triazolopyrimidines, leurs procedes de production et leur utilisation pour lutter contre les champignons nuisibles et les produits les contenant

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EP1613633A1 true EP1613633A1 (fr) 2006-01-11

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US (1) US20060211711A1 (fr)
EP (1) EP1613633A1 (fr)
JP (1) JP2006522046A (fr)
KR (1) KR20050111627A (fr)
CN (1) CN100355754C (fr)
AR (1) AR043975A1 (fr)
AU (1) AU2004226253A1 (fr)
BR (1) BRPI0408864A (fr)
CA (1) CA2520718A1 (fr)
CL (1) CL2004000713A1 (fr)
CO (1) CO5631446A2 (fr)
CR (1) CR7989A (fr)
EA (1) EA008920B1 (fr)
MX (1) MXPA05009820A (fr)
TW (1) TW200503623A (fr)
WO (1) WO2004087706A1 (fr)

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WO2005058900A1 (fr) * 2003-11-25 2005-06-30 Basf Aktiengesellschaft 6-(2,4,6-trifluorophenyl)-triazolopyrimidines, leur procede de production et leur utilisation pour lutter contre les champignons nuisibles, et agents contenant lesdits composes
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BRPI0408864A (pt) 2006-04-11
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JP2006522046A (ja) 2006-09-28
EA008920B1 (ru) 2007-08-31
WO2004087706A1 (fr) 2004-10-14
CA2520718A1 (fr) 2004-10-14
TW200503623A (en) 2005-02-01
EA200501533A1 (ru) 2006-04-28
CL2004000713A1 (es) 2005-05-06
CO5631446A2 (es) 2006-04-28
AU2004226253A1 (en) 2004-10-14
US20060211711A1 (en) 2006-09-21
CR7989A (es) 2006-05-30
CN1768062A (zh) 2006-05-03
CN100355754C (zh) 2007-12-19

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