EP0719260A1 - Derives de butenol-triazolyle, leur preparation et leur utilisation comme microbicides - Google Patents

Derives de butenol-triazolyle, leur preparation et leur utilisation comme microbicides

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Publication number
EP0719260A1
EP0719260A1 EP94928316A EP94928316A EP0719260A1 EP 0719260 A1 EP0719260 A1 EP 0719260A1 EP 94928316 A EP94928316 A EP 94928316A EP 94928316 A EP94928316 A EP 94928316A EP 0719260 A1 EP0719260 A1 EP 0719260A1
Authority
EP
European Patent Office
Prior art keywords
carbon atoms
halogen
formula
alkyl
alkoxy
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.)
Ceased
Application number
EP94928316A
Other languages
German (de)
English (en)
Inventor
Michael Lindemann
Stefan Dutzmann
Heinz-Wilhelm Dehne
Gerd Hänssler
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 AG
Original Assignee
Bayer AG
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
Priority claimed from DE4419812A external-priority patent/DE4419812A1/de
Application filed by Bayer AG filed Critical Bayer AG
Publication of EP0719260A1 publication Critical patent/EP0719260A1/fr
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/40—Halogenated unsaturated alcohols
    • C07C33/50—Halogenated unsaturated alcohols containing six-membered aromatic rings and other rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/75—Reactions with formaldehyde
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/527—Unsaturated compounds containing keto groups bound to rings other than six-membered aromatic rings
    • C07C49/567—Unsaturated compounds containing keto groups bound to rings other than six-membered aromatic rings containing halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/08—Compounds containing oxirane rings with hydrocarbon radicals, substituted by halogen atoms, nitro radicals or nitroso radicals

Definitions

  • the present invention relates to new hydroxyethyl azolyl derivatives, a process for their preparation and their use as microbicides in crop protection and in protecting material.
  • X represents hydrogen, halogen, alkyl having 1 to 4 carbon atoms or
  • Z represents halogen, alkyl having 1 to 4 carbon atoms, haloalkyl having 1 to
  • n 0, 1, 2 or 3
  • the substances according to the invention contain an asymmetrically substituted carbon atom. They can therefore occur in optical isomer forms.
  • the present invention relates both to the individual isomers and to their mixtures.
  • the fungicidal properties of the substances according to the invention exceed 2- (2-chlorophenyl) -3- (2,4-dichlorophenyl) -3-hydroxy-4- (l, 2,4-t-riazole-l) -yl) -but-l-ene and the 2- (2-fluorophenyl) -3- (4-chlorophenyl) -3-hydroxy-4- (l, 2,4-triazol-l-yl) -but-l -en.
  • Formula (I) provides a general definition of the hydroxyethyl azolyl derivatives according to the invention.
  • X preferably represents hydrogen, fluorine, chlorine, methyl, ethyl, n-propyl, isopropyl, methoxy and ethoxy.
  • Z preferably represents fluorine, chlorine, bromine, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, trichloromethyl, trifluoromethyl, difluoromethyl, methoxy, Ethoxy, trifluoromethoxy, difluoromethoxy, nitro or for phenyl which is optionally mono- or disubstituted, identical or different, by fluorine and / or chlorine.
  • n preferably represents the numbers 0, 1, 2 or 3. If m represents 2 or 3, Z can represent the same or different radicals.
  • Preferred substances according to the invention are also addition products of acids and those hydroxyethyl azolyl derivatives of the formula (I) in which X, Z and m have the meanings given as preferred.
  • the acids that can be added preferably include hydrohalic acids, e.g. hydrochloric acid and hydrobromic acid, especially hydrochloric acid, also phosphoric acid, nitric acid, sulfuric acid, mono- and bifunctional carboxylic acids and hydroxycarboxylic acids, e.g. Acetic acid, maleic acid, succinic acid, fumaric acid, tartaric acid, citric acid, salicylic acid, sorbic acid and lactic acid as well as sulfonic acids, e.g. p-toluenesulfonic acid, 1,5-naphthalenedisulfonic acid or camphorsulfonic acid,
  • hydrohalic acids e.g. hydrochloric acid and hydrobromic acid, especially hydrochloric acid, also phosphoric acid, nitric acid, sulfuric acid, mono- and bifunctional carboxylic acids and hydroxycarboxylic acids, e.g. Acetic acid, maleic acid, succinic acid, fumaric acid, tartaric
  • preferred compounds according to the invention are addition products from salts of metals of the II. To IV. Main and of the I. and II. And IV. To VIII. Subgroup of the Periodic Table of the Elements and those hydroxyethyl azolyl derivatives of the formula (I) in which X, Z and m have the meanings indicated as preferred.
  • Salts of copper, zinc, manganese, magnesium, tin, iron and nickel are particularly preferred.
  • Anions of these salts are those which are derived from acids which lead to physiologically tolerable addition products.
  • Particularly preferred acids in this context are the hydrohalic acids, such as, for example, hydrochloric acid and bromine, and also phosphoric acid, nitric acid and sulfuric acid.
  • Formula (II) provides a general definition of the butenol derivatives required as starting materials in variant (a) of the process according to the invention.
  • X, Z and m preferably have those meanings which have already been mentioned preferably in connection with the description of the substances of the formula (I) according to the invention for these radicals or this index.
  • Shark stands for chlorine or bromine.
  • butenol derivatives of the formula (II) have hitherto not been known. They can be prepared by using cyclopropyl ketones of the formula
  • organometallic compounds required in the above process for the preparation of butenol derivatives of the formula (II) as reaction components Formula (VI) are known or can be prepared by methods known in principle (cf. J. Org. Chem. 41 (1976), 3725). So you get these substances by using styrene derivatives of the formula
  • bromine in the presence of a diluent, such as carbon tetrachloride, chloroform or dichloromethane, at temperatures between 0 ° C. and 30 ° C., the resulting bromides of the formula
  • a diluent e.g. Toluene, tetrahydrofuran or
  • Dioxane and in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or potassium hydroxide in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or potassium hydroxide in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or potassium hydroxide in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or potassium hydroxide in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or potassium hydroxide in the presence of a base, e.g. Diazabicyclonones (DBN), Diazabicycloundecen (DBU) or
  • Phase transfer catalyst at temperatures between 0 ° C and 130 ° C and the resulting bromostyrene derivatives of the formula
  • magnesium shavings in the presence of a diluent such as diethyl ether or tetrahydrofuran, at temperatures between 0 ° C and 70 ° C.
  • a diluent such as diethyl ether or tetrahydrofuran
  • Suitable diluents in the above process for the preparation of butenol derivatives of the formula (II) are all inert organic solvents which are customary for such reactions.
  • Ethers such as diethyl ether, tetrahydrofuran and dioxane can preferably be used.
  • reaction temperatures can be varied within a certain range. Generally one works at temperatures between -80 ° C and + 60 ° C.
  • the processing takes place according to usual methods. In general, the procedure is first to acidify and add water, then to separate the organic phase, to wash and to concentrate after drying.
  • Formula (III) provides a general definition of the oxiranes required as starting materials in variant (b) of the process according to the invention.
  • X, Z and m preferably have those meanings which are already in connection with the description of the substances of the formula according to the invention
  • the oxiranes of the formula (III) have hitherto not been known. They can be made by c) butenol derivatives of the formula
  • the bases used in the preparation of oxiranes of the formula (III) by process (c) above are all those which are customarily suitable for such reactions inorganic and organic bases.
  • Alkali metal carbonates such as sodium and potassium carbonate, furthermore alkali metal hydroxides, such as sodium and potassium hydroxide, furthermore alkali metal alcoholates, such as sodium and potassium methylate and ethylate, and potassium tert-butoxide, and furthermore lower tertiary alkyl amines, cycloalkyl amines and aralkyl amines, are preferably usable , such as triethylamine in particular.
  • Suitable diluents for the preparation of oxiranes of the formula (DI) according to process (c) above are all customary inert, organic solvents.
  • Nitriles such as acetonitrile, furthermore aromatic hydrocarbons such as benzene, toluene and dichlorobenzene, preferably also formamides such as dimethylformamide and strongly polar solvents such as dimethyl sulfoxide and hexamethylphosphoric acid triamide can be used.
  • reaction temperatures can be varied within a certain range in the preparation of oxiranes of the formula (III) according to process (c) above. In general, temperatures between 0 ° C and 100 ° C, preferably between 20 ° C and 60 ° C.
  • reaction When carrying out process (c) above for the preparation of oxiranes of the formula (III), the reaction is generally carried out under atmospheric pressure. However, it is also possible to work under increased or reduced pressure.
  • Formula (X) provides a general definition of the ketones required as starting materials in carrying out process (d) above for the preparation of oxiranes of the formula (III).
  • X, Z and m preferably have those
  • ketones of formula (X) are not yet known. They can be prepared by using benzyl ketones of the formula
  • Formula (XII) provides a general definition of the benzyl ketones required as starting materials in the preparation of the ketones of the formula (X) by the above process.
  • X, Z and m preferably have those meanings which have already been mentioned preferably in connection with the description of the substances of the formula (I) according to the invention for these radicals or for this index.
  • the benzyl ketones of the formula (XII) are known or can be prepared by methods known in principle (cf. EP-OS 0 461 483 and EP-OS 0 461 502).
  • the substances required as reaction components in carrying out the above process (d), namely bis (dimethylamino) methane of the formula (XIII) or paraformaldehyde or formalin (aqueous formaldehyde solution with a formaldehyde content of 37%) are known.
  • reaction temperatures can be varied within a substantial range. In general, temperatures between 20 ° C and 120 ° C, preferably between 30 ° C and 110 ° C.
  • the processing takes place according to usual methods.
  • Suitable catalysts for carrying out variant ( ⁇ ) of the above process for the preparation of ketones of the formula (X) are all reaction accelerators customary for such reactions.
  • Alkali metal hydroxides such as sodium hydroxide or potassium hydroxide, can preferably be used.
  • Suitable diluents for carrying out variant ( ⁇ ) of the above process for the preparation of ketones of the formula (X) are all inert organic solvents which are customary for such reactions.
  • Alcohols such as methanol or ethanol, can preferably be used.
  • the reaction temperatures can be varied within a certain range. In general, temperatures between 10 ° C and 40 ° C, preferably at room temperature.
  • variant ( ⁇ ) of the above process for the preparation of ketones of the formula (X) is carried out, 1.5 to 2.5 equivalents of paraformaldehyde or formalin and one equivalent are generally employed per mole of benzyl ketone of the formula (XII) Amount of catalyst. - The processing takes place according to usual methods.
  • the dimethylsulfonium methylide of the formula (XI) required as reaction component when carrying out the above process (d) for the preparation of oxiranes of the formula (III) is known (cf. Heterocycles 8, 397 (1977)). It is used in the above implementation in a freshly prepared state, e.g. in situ. from trimethylsulfonium halide or trimethylsulfonium methylsulfate, in the presence of a strong base, e.g. Sodium hydride, sodium amide, sodium methylate, potassium tert-butoxide or potassium hydroxide, in the presence of a diluent, such as tert-butanol or dimethyl sulfoxide.
  • a strong base e.g. Sodium hydride, sodium amide, sodium methylate, potassium tert-butoxide or potassium hydroxide, in the presence of a diluent, such as tert-butanol or dimethyl sul
  • Alcohols such as tert-butanol, ethers, such as tetrahydrofuran or dioxane, and also aliphatic and aromatic hydrocarbons, such as benzene, toluene or xylene, and strongly polar solvents, such as dimethyl sulfoxide, can preferably be used.
  • reaction temperatures can be carried out when carrying out the above process
  • Alkali metal carbonates such as sodium and potassium carbonate
  • alkali metal hydroxides such as sodium and potassium hydroxide
  • alkali metal alcoholates such as sodium and potassium methylate and ethylate, and potassium tert-butoxide
  • alkali metal alcoholates such as sodium and potassium methylate and ethylate, and potassium tert-butoxide
  • furthermore lower tertiary alkylamines, cycloalkylamines and aralkylamines such as, in particular, triethylamine.
  • Nitriles such as acetonitrile, aromatic hydrocarbons such as benzene, toluene and dichlorobenzene, formamides such as dimethylformamide and strongly polar solvents such as dimethyl sulfoxide and hexamethylphosphoric triamide are preferably used.
  • reaction temperatures can be varied within a substantial range when carrying out the process according to the invention. In general, temperatures between 0 ° C and 130 ° C, preferably between 40 ° C and 120 ° C.
  • the process according to the invention is also generally carried out under normal pressure. However, it is also possible to work under increased or reduced pressure.
  • 1,2,4-triazole of the formula (IV) and 0 are generally employed per mol of butenol derivative of the formula (II) or of oxirane of the formula (III) , 3 to 3 moles of acid binder.
  • the processing takes place according to usual methods.
  • the procedure is such that the reaction mixture is concentrated, the remaining residue is taken up in an organic solvent which is not very miscible with water, washed with water and concentrated after drying.
  • the remaining product can optionally be subjected to further cleaning processes.
  • hydroxyethyl azolyl derivatives of the formula (I) according to the invention can be converted into acid addition salts or metal salt complexes.
  • the acid addition salts of the compounds of formula (I) can be easily prepared by conventional salt formation methods, e.g. by dissolving a compound of formula (I) in a suitable inert solvent and adding the
  • Acid e.g. Hydrochloric acid can be obtained and in a known manner, e.g. by filtration, isolated and, if necessary, cleaned by washing with an inert organic solvent.
  • metal salt complexes according to the invention were mentioned as preferred metal salts.
  • the metal salt complexes of the compounds of formula (I) can be obtained in a simple manner by conventional methods, e.g. by dissolving the metal salt in alcohol, e.g. Ethanol and adding to compounds of
  • Metal salt complexes can be prepared in a known manner, e.g. by filtering, isolating and, if necessary, cleaning by recrystallization.
  • the active compounds according to the invention have a strong microbicidal action and can be used to protect against undesirable microorganisms, such as fungi and bacteria, in crop protection and in the material.
  • Fungicides are used in crop protection to combat Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Deuteromycetes.
  • Xanthomonas species such as Xanthomonas oryzae
  • Pseudomonas species such as Pseudomonas lachrymans
  • Erwinia species such as Erwinia amylovora
  • Pythium species such as Pythium ultimum
  • Phytophthora species such as Phytophthora infestans
  • Pseudoperonospora species such as Pseudoperonospora humuli or Pseudoperonospora cubensis;
  • P 1 asm opara species such as Plasmopara viticola
  • Peronospora species such as Peronospora pisi or P. brassicae;
  • Erysiphe species such as Erysiphe graminis
  • Sphaerotheca species such as Sphaerotheca fuliginea
  • Podosphaera species such as Podosphaera leucotricha
  • Venturia species such as Venturia inaequalis
  • Pyrenophora species such as Pyrenophora teres or P. graminea;
  • Drechslera (Conidial form: Drechslera, Syn: Helminthosporium);
  • Cochliobolus species such as Cochliobplus sativus; (Conidial form: Drechslera, Syn: Helminthosporium);
  • Uromyces species such as Uromyces appendiculatus
  • Puccinia species such as Puccinia recondita
  • Tilletia species such as Tilletia caries
  • Ustilago species such as Ustilago nuda or Ustilago avenae
  • Pellicularia species such as Pellicularia sasakii
  • Pyricularia species such as Pyricularia oryzae
  • Fusarium species such as Fusarium culmorum
  • Botrytis species such as Botrytis cinerea
  • Septoria species such as Septoria nodorum
  • Leptosphaeria species such as Leptosphaeria nodorum
  • Cercospora species such as Cercospora canescens
  • Alternaria species such as Alternaria brassicae
  • Pseudocercosporella species such as Pseudocercosporella he otrichoides.
  • the active compounds according to the invention are particularly suitable for combating Pyricularia oryzae and Pellicularia sasakii on rice and for combating Cereal diseases such as Leptosphaeria nodorum, Cochliobolus sativus, Pyrenophora teres, Pseudocercosporella herpotrichoides, Erysiphe and Fusarium species.
  • Cereal diseases such as Leptosphaeria nodorum, Cochliobolus sativus, Pyrenophora teres, Pseudocercosporella herpotrichoides, Erysiphe and Fusarium species.
  • the substances according to the invention have a very good and broad in vitro effect.
  • the substances according to the invention can be used to protect technical materials against attack and destruction by undesired microorganisms.
  • technical materials are to be understood as non-living materials that have been prepared for use in technology.
  • technical materials which are to be protected against microbial change or destruction by active substances according to the invention can be adhesives, glues, paper and cardboard, textiles, leather, wood, paints and plastic articles, cooling lubricants and other materials which are attacked by microorganisms or can be decomposed.
  • parts of production systems for example cooling water circuits, which may be impaired by the multiplication of microorganisms, may also be mentioned.
  • technical materials are preferably adhesives, glues, papers and cartons, leather, wood, paints, cooling lubricants and heat transfer fluids, particularly preferably wood.
  • Bacteria, fungi, yeasts, algae and mucilaginous organisms may be mentioned as microorganisms which can cause degradation or a change in the technical materials.
  • the active compounds according to the invention preferably act against fungi, in particular mold, wood-discoloring and wood-destroying fungi (Basidiomycetes) and against slime organisms and algae.
  • microorganisms of the following genera may be mentioned:
  • Alternaria such as Alternaria tenuis, Aspergillus, such as Aspergillus niger, Chaetomium, such as Chaetomium globosum, Coni ⁇ phora, such as Coniophora puetana, Lentinus, such as Lentinus tigrinus, Penicillium, such as Penicillium glaucum, Polyporus, such as Polyporus versicolor, Aureobasidium, such as Aureobasidium pullulans, Sclerophoma, such as Sclerophoma pityophila,
  • Trichoderma such as Trichoderma viride, Escherichia, such as Escherichia coli, Pseudomonas, such as Pseudomonas aeruginosa, Staphylococcus, such as Staphylococcus aureus.
  • the substances according to the invention can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in coating compositions for seeds, and ULV formulations.
  • customary formulations such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in coating compositions for seeds, and ULV formulations.
  • formulations are made in a known manner, e.g. by mixing the active ingredients with extenders, i.e. liquid solvents, under
  • liquefied gases and / or solid carriers optionally using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
  • water e.g. organic solvents can also be used as auxiliary solvents.
  • aromatics such as xylene, toluene, or alkylnaphthalenes
  • chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride
  • aliphatic hydrocarbons such as cyclohexane or paraffins, e.g. Petroleum fractions, alcohols, such as butanol or glycol, and their ethers and esters, ketones, such as acetone,
  • liquefied gaseous extenders or carriers mean liquids which are gaseous at normal temperature and under normal pressure, e.g. Aerosol propellants such as butane, propane, nitrogen and carbon dioxide; as fixed
  • Carrier materials are possible: for example natural rock powder, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock meals, such as highly disperse silica, aluminum oxide and silicates;
  • Possible solid carriers for granules are: for example broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules from inorganic and organic flours and granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stalks ;
  • suitable emulsifiers and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and
  • Adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-shaped polymers can be used in the formulations, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids.
  • Other additives can be mineral and vegetable oils.
  • Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc are used.
  • inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc are used.
  • the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
  • the active compounds according to the invention can also be used in a mixture with known fungicides, bactericides, acaricides, nematicides or insecticides, for example to to broaden the spectrum of activity or to prevent the development of resistance.
  • synergistic effects also occur, which means that the mixture has a higher effect than the sum of the effects of the individual components.
  • copper preparations such as: copper hydroxide, copper naphthenate,
  • Mancopper Mancozeb, Maneb, Mepanipyrim, Mepronil, Metalaxyl, Metconazol, Methasulfocarb, Methfuroxam, Metiram, Metsulfovax, Myclobutanil,
  • Probenazole prochloraz, procymidone, propamocarb, propiconazole, propineb, pyrazophos, pyrifenox, pyrimethanil, pyroquilone, Quintozen (PCNB), sulfur and sulfur preparations,
  • Tebuconazole Tecloftalam, Tecnazen, Tetraconazole, Thiabendazole, Thicyofen, Thiophanat-methyl, Thiram, Tolclophos-methyl, Tolylfluanid, Triadimefon, Triadimenol, Triazoxid, Trichlamid, Tricyclazol, Tridemorph, Trifluminol, Trifluminol
  • Imidacloprid Iprobefos, Isazophos, Isofenphos, Isoprocarb, Isoxathion, Ivemectin, Lamda-cyHalothrin, Lufenuron,
  • Parathion A Parathion M, Permethrin, Phenthoat, Phorat, Phosalon, Phosmet, Phosphamdon, Phoxim, Pirimicarb, Pirimiphos M, Pirimiphos A, Profenofos, Promecarb, Propaphos, Propoxur, Prothiofos, Prothoat, Pymetrozin, Pyrachlophhion, Pyrachlophhion, Pyrachlophhion, Pyrachlophion, Pyrachlophion, Pyrachlophin, Pyrachlophion, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Pyrachlophin, Py
  • Tebufenozid Tebufenpyrad, Tebupirimphos, Tefiubenzuron, Tefluthrin, Temephos, Terbam, Terbufos, Tetrachlorvinphos, Thiafenox, Thiodicarb, Thiofanox, Thio-methon, Thionazin, Thuringiensin, Tralomenhria, triomononium, triomonethonium, triomonhronium, triomoshronium, triomoshronium, tri XMC, xylylcarb, zetamethrin.
  • the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, suspensions, wettable powders, pastes, soluble powders, dusts and granules. They are used in the customary manner, for example by watering, spraying, atomizing, scattering, dusting, foaming, brushing, etc. It is also possible to apply the active ingredients using the ultra-low-volume process or to prepare the active ingredient or the active ingredient itself in the Inject soil. The seeds of the plants can also be treated. - 23
  • the active compound concentrations in the use forms can be varied within a substantial range: they are generally between 1 and 0.0001% by weight, preferably between 0.5 and 0.001% by weight.
  • amounts of active ingredient are generally from 0.001 to
  • active ingredient concentrations of 0.00001 to 0.1% by weight, preferably 0.0001 to 0.02% by weight, are required at the site of action.
  • the means used to protect technical materials contain the
  • Active ingredients in general in an amount of 1 to 95%, preferably from 10 to 75%.
  • the application concentrations of the active compounds according to the invention depend on the type and the occurrence of the microorganisms to be controlled and on the composition of the material to be protected.
  • the amount used can be determined by test series.
  • the application concentrations are in the range from 0.001 to 5% by weight, preferably from 0.05 to 1.0% by weight, based on the material to be protected.
  • Concentrates or very general formulations can be increased if additional antimicrobial compounds, fungicides, bactericides, herbicides, insecticides or other active substances are used to increase the spectrum of activity or to achieve special effects such as e.g. added protection against insects.
  • additional antimicrobial compounds, fungicides, bactericides, herbicides, insecticides or other active substances are used to increase the spectrum of activity or to achieve special effects such as e.g. added protection against insects.
  • These blends can be a broader
  • Sulfenamides such as dichlorfluanid (Euparen), tolyfluanid (Methyleuparen), Folpet, Fluorfolpet;
  • Benzimidazoles such as Carbendazim (MBC), Benomyl, Fuberidazole, Thiabendazole or their salts;
  • Thiocyanates such as thiocyanatomethylthiobenzothiazole (TCMTB), methylene bisthiocyanate (MBT);
  • quaternary ammonium compounds such as benzyldimethyltetradecylammonium chloride, benzyldimethyldodecylammonium chloride, dodecyldimethylammonium chloride;
  • Morpholine derivatives such as C n -C 14 -4-alkyl-2,6-dimethyl-morpholine homologs (tridemorph), (+) - cis-4- [tert-butylphenyl) -2-methylpropyl] -2,6-dimethylmorpholine (Fen ⁇ propimorph), Falimorph;
  • Phenols such as o-phenylphenol, tribromophenol, tetrachlorophenol, pentachlorophenol, 3-methyl-4-chlorophenol, dichlorophen, chlorophen or their salts;
  • A-zoles such as triadimefon, triadimenol, bitertanol, tebuconazole, propiconazole, azaconazole, hexaconazole, prochloraz, cyproconazole, l- (2-chlorophenyl) -2- (l-chlorocyclopropyl) -3- (l, 2,4-triazol-l -yl) -propan-2-ol or l- (2-chlorophenyl) -2- (l, 2,4-triazol-l-yl-methyl) -3,3-dimethyl-butan-2-ol.
  • Iodopropargyl derivatives such as iodopropargyl butyl carbamate (? BC), chlorophenyl formal, phenyl carbamate, hexyl carbamate, cyclohexyl carbamate, iodopropargyloxyethylphenyl carbamate;
  • Iodine derivatives such as diiodomethyl-p-arylsulfones e.g. Diiodomethyl p-tolyl sulfone;
  • Bromine derivatives such as bromopol
  • Isothiazolines such as N-methylisothiazolin-3-one, 5-chloro-N-methylisothiazolin-3-one, 4,5-dichloro-N-octylisothiazolin-3-one, N-octylisothiazolin-3-one (octilinone); Benzisothiazolinones, cyclopentene isothazolines;
  • Pyridines such as l-hydroxy-2-pyridinthione (and their Na, Fe, Mn, Zn salts), tetrachloro-4-methylsulfonylpyridine;
  • Metal soaps such as tin, copper, zinc naphthenate, octoate, 2-ethylhexanoate, oleate, phosphate, benzoate, oxides such as TBTO, Cu 2 O, CuO, ZnO;
  • Organic tin compounds such as tributyltin naphtenate and tributyltin oxide;
  • Dialkyldithiocarbamates such as Na and Zn salts of dialkyldithiocarbamates, tetram ethyltiuramidisulfid (TMTD);
  • Nitriles such as 2,4,5,6-tetrachloroisophthalonitrile (chlorothalonil) etc.
  • Halogenated microbicides such as Cl-Ac, MCA, tectamer, bromopol, bromidox;
  • Benzothiazoles such as 2-mercaptobenzothiazoles; so. Dazomet;
  • Formaldehyde-releasing compounds such as benzyl alcohol mono (poly) hemiformal, oxazolidines, hexahydro-s-triazines, N-methylolchloroacetamide;
  • Tributyltin or K salts bis (N-cyclohexyl) diazinium - (dioxy copper or aluminum).
  • Phosphoric acid esters such as azinphos-ethyl, azinphos-m ethyl, l- (4-chlorophenyl) -4- (O-ethyl, S-propyl) phosphoryloxypyrazole (TIA-230), chlorpyrifos, Coumaphos, Demetomon, Demeton-S-methyl , Diazinon, Dichlorfos, Dimethoate, Ethoprophos, Etrim- fos, Fenitrothion, Fention, Heptenophos, Parathion, Parathion-methyl, Phosalone, Phoxim, Pirimiphos-ethyl, Pirimiphos-methyl, Profenofos, Prothiofos, Sulprofos, Triazophos and Trichlor. - 28 -
  • Carbamates such as aldicarb, bendiocarb, BPMC (2- (l-methylpropyl) phenylmethyl carbamate), butocarboxime, butoxycarboxim, carbaryl, carbofuran, carbosulfan, cloethocarb, isoprocarb, methomyl, oxamyl, pirimicarb, promecarb, propoxur and thiodine.
  • Pyrethroids such as allethrin, alphamethrin, bioresmethrin, byfenthrin (FMC 54800),
  • Organosilicon compounds preferably dimethyl (phenyl) silylmethyl-3-phenoxybenzyl ether such as e.g. Dimethyl (4-ethoxyphenyl) silylmethyl-3-phenoxybenzyl ether or dimethyl (phenyl) silylmethyl-2-phenoxy-6-pyridylmethyl ether such as e.g. Dimethyl (9-ethoxyphenyl) silylmethyl-2-phenoxy-6-pyridylmethyl ether or (phenyl) [3- (3-phenoxyphenyl) propyl] (dimethyl) silanes such as e.g. (4-ethoxyphenyl) - [3 (4-fluoro-3-phenoxyphenyl) propyl] dimethylsilane.
  • dimethyl (phenyl) silylmethyl-3-phenoxybenzyl ether such as e.g. Dimethyl (4-ethoxyphenyl) silylmethyl-3-phenoxybenzyl ether or dimethyl (phenyl) si
  • Algicides Algicides, molluscicides, active substances against "sea animals", which relate to e.g. Place ship floor paints.
  • a solution of 66 g (0.33 mol) of trimethylsulfonium iodide in 400 ml of dimethylsulfoxide is added dropwise to 400 ml of tetrahydrofuran at 0 ° C. while stirring.
  • the mixture is left to stir at 0 ° C. for 5 minutes and then 70 g (0.25 mol) of 2- (2-fluorophenyl) -3- (l-chloro-cycloprop-l-yl) -prop-l-en are added
  • Add -3-one in 100 ml of dimethyl sulfoxide is first stirred at 0 ° C. for 15 minutes and then at room temperature for a further 6 hours.
  • Solvent 10 parts by weight of N-methyl-pyrrolidone emulsifier: 0.6 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted with water to the desired concentration.
  • the plants remain in an incubation cabin at 20 ° C. and 100% relative atmospheric humidity for 48 hours.
  • the plants are placed in a greenhouse at a temperature of approx. 15 ° C and a relative humidity of approx. 80%.
  • Evaluation is carried out 10 days after the inoculation.
  • Solvent 10 parts by weight of N-methyl-pyrrolidone emulsifier: 0.6 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted with water to the desired concentration.
  • the plants are placed in a greenhouse under translucent incubation hoods at a temperature of about 20 ° C. and a relative humidity of about 100%.
  • Evaluation is carried out 4 days after the inoculation.
  • Emulsifier 0.3 part by weight alkyl aryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted with water to the desired concentration.
  • the plants are then placed in a greenhouse at 23 ° C. and a relative atmospheric humidity of approx. 70%.
  • Evaluation is carried out 10 days after the inoculation.
  • Emulsifier 0.3 part by weight of alkyl aryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted with water to the desired concentration.
  • the disease infestation is evaluated 4 days after the inoculation.
  • Solvent 12.5 parts by weight of acetone emulsifier: 0.3 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and the concentrate is diluted to the desired concentration with water and the stated amount of emulsifier.
  • the disease infestation is evaluated 5 to 8 days after the inoculation.
  • X represents hydrogen, halogen, alkyl having 1 to 4 carbon atoms or
  • Z for halogen, alkyl with 1 to 4 carbon atoms, haloalkyl with 1 to 4 carbon atoms and 1 to 5 halogen atoms, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms and 1 to 5 halogen atoms, nitro or optionally single to triple , is identical or different phenyl substituted by halogen and
  • n 0, 1, 2 or 3
  • X represents hydrogen, fluorine, chlorine, methyl, ethyl, n-propyl, isopropyl, methoxy or ethoxy,

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

Abstract

L'invention concerne de nouveaux dérivés de buténol-trizolyle de la formule (I), dans laquelle X désigne hydrogène, halogène, alkyle ayant entre 1 et 4 atomes de carbones, ou alcoxy entre 1 et 4 atomes de carbone, Z désigne halogène, alkyle ayant entre 1 et 4 atomes de carbone, halogénure d'alcoyle ayant entre 1 et 4 atomes de carbone et entre 1 et 5 atomes d'halogène, alcoxy ayant entre 1 et 4 atomes de carbone, halogénure d'alcoxy ayant entre 1 et 4 atomes de carbone et entre 1 et 5 atomes d'halogène, nitro ou phényle éventuellement substitué entre une et trois fois par halogène, de manière identique ou différente et m vaut 0, 1, 2 ou 3. L'invention concerne également leurs sels d'addition d'acide et leurs complexes de sels métalliques, un procédé permettant de préparer les nouvelles substances et leur utilisation comme microbicides dans la protection des végétaux et des matériaux. L'invention concerne par ailleurs de nouveaux dérivés de buténol de la formule (II), de nouveaux oxirannes de la formule (III), de nouvelles cétones de la formule (X), des procédés de préparation de ces substances et leur utilisation comme produits intermédiaires pour réaliser la synthèse des composés de la formule (I).
EP94928316A 1993-09-16 1994-09-06 Derives de butenol-triazolyle, leur preparation et leur utilisation comme microbicides Ceased EP0719260A1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE4331476 1993-09-16
DE4331476 1993-09-16
DE4419812 1994-06-07
DE4419812A DE4419812A1 (de) 1993-09-16 1994-06-07 Hydroxyethyl-azolyl-Derivate
PCT/EP1994/002964 WO1995007896A1 (fr) 1993-09-16 1994-09-06 Derives de butenol-triazolyle, leur preparation et leur utilisation comme microbicides

Publications (1)

Publication Number Publication Date
EP0719260A1 true EP0719260A1 (fr) 1996-07-03

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EP94928316A Ceased EP0719260A1 (fr) 1993-09-16 1994-09-06 Derives de butenol-triazolyle, leur preparation et leur utilisation comme microbicides

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US (1) US5786375A (fr)
EP (1) EP0719260A1 (fr)
JP (1) JPH09502710A (fr)
CN (1) CN1133590A (fr)
AU (1) AU7780194A (fr)
BR (1) BR9407482A (fr)
CA (1) CA2171754A1 (fr)
CZ (1) CZ70096A3 (fr)
HU (1) HU9600660D0 (fr)
PL (1) PL313448A1 (fr)
SK (1) SK36096A3 (fr)
TR (1) TR27956A (fr)
WO (1) WO1995007896A1 (fr)

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Publication number Priority date Publication date Assignee Title
BR9811018A (pt) * 1997-07-23 2000-09-26 Basf Ag Grânulos para a proteção de colheita, processos para sua preparação, para controle de nematódeos, insetos de infestação do solo, plantas germinativas, bactérias do solo e fungos de solo, e, uso de grânulos para a proteção do solo.
EP2509959A1 (fr) * 2009-12-08 2012-10-17 Kureha Corporation Dérivés azole et leurs procédés de production, composés intermédiaires pour synthétiser les dérivés et leurs procédés de production, et agents agro-horticoles et agents de protection de produits industriels contenant les dérivés

Family Cites Families (10)

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Publication number Priority date Publication date Assignee Title
US4927839A (en) * 1979-03-07 1990-05-22 Imperial Chemical Industries Plc Method of preventing fungal attack on wood, hides, leather or paint films using a triazole
AU542623B2 (en) * 1980-05-16 1985-02-28 Bayer Aktiengesellschaft 1-hydroxyethyl-azole derivatives
EP0117578A3 (fr) * 1983-02-23 1985-01-30 Shionogi & Co., Ltd. Dérivés d'alcool substitués par azole
US4952232A (en) * 1987-04-29 1990-08-28 E. I. Du Pont De Nemours And Company Antifungal carbinols
DE3784787T2 (de) * 1986-06-23 1994-01-20 Du Pont Merck Pharma Fungizide Karbinole.
US4980367A (en) * 1987-12-17 1990-12-25 E. I. Du Pont De Nemours And Company Antifungal carbinols
DE3812967A1 (de) * 1987-06-24 1989-01-05 Bayer Ag Azolylmethyl-cyclopropyl-derivate
DE3813874A1 (de) * 1987-07-10 1989-01-19 Bayer Ag Hydroxyalkyl-azolyl-derivate
DE3921481A1 (de) * 1989-06-30 1991-01-03 Bayer Ag Hydroxyethyl-cyclopropyl-azolyl-derivate
AU7184891A (en) * 1990-02-13 1991-09-03 E.I. Du Pont De Nemours And Company Aniline derivatives of alpha-styryl carbinols as antifungal agents

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9507896A1 *

Also Published As

Publication number Publication date
TR27956A (tr) 1995-11-06
BR9407482A (pt) 1996-11-12
HU9600660D0 (en) 1996-05-28
CA2171754A1 (fr) 1995-03-23
JPH09502710A (ja) 1997-03-18
PL313448A1 (en) 1996-07-08
CN1133590A (zh) 1996-10-16
SK36096A3 (en) 1996-09-04
AU7780194A (en) 1995-04-03
WO1995007896A1 (fr) 1995-03-23
CZ70096A3 (en) 1996-06-12
US5786375A (en) 1998-07-28

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