EP1784383A1 - Procede pour produire des amines biphenyle - Google Patents

Procede pour produire des amines biphenyle

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Publication number
EP1784383A1
EP1784383A1 EP05790368A EP05790368A EP1784383A1 EP 1784383 A1 EP1784383 A1 EP 1784383A1 EP 05790368 A EP05790368 A EP 05790368A EP 05790368 A EP05790368 A EP 05790368A EP 1784383 A1 EP1784383 A1 EP 1784383A1
Authority
EP
European Patent Office
Prior art keywords
formula
meanings given
chlorine
fluorine
anilides
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Withdrawn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
EP05790368A
Other languages
German (de)
English (en)
Inventor
Wolfgang JÖRGES
Jens-Dietmar Heinrich
Reinhard Lantzsch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Original Assignee
Bayer CropScience 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
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP1784383A1 publication Critical patent/EP1784383A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
    • C07C233/15—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/62—Preparation of compounds containing amino groups bound to a carbon skeleton by cleaving carbon-to-nitrogen, sulfur-to-nitrogen, or phosphorus-to-nitrogen bonds, e.g. hydrolysis of amides, N-dealkylation of amines or quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C211/44—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
    • C07C211/52—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00—Preparation of carboxylic acid amides
    • C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/24—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • 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
    • C07D231/14—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 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

Definitions

  • the present invention relates to a novel process for preparing substituted biphenylamines, novel intermediates and their preparation, and to a process for preparing fungicidally active carboxamides.
  • biphenyl derivatives can be prepared from phenylboronic acids and phenyl halides by Suzuki or Stille coupling (cf., for example, WO 01/42223, WO 02/064562, WO 03/070705, Robertson and Hansen (eds.) PCBs, The University Press of Kentucky 2001, 57-60).
  • a disadvantage of these methods are the high production costs.
  • the preparation of a boronic acid requires a Grignard reaction, and the transition metal catalyzed cross-coupling (eg, Suzuki) requires relatively high levels of palladium catalysts or (Bull. Korean Chem. Soc. 2000, 21, 165-166) the use of nearly equivalent amounts Zinc, which must be disposed of as waste and requires the carcinogenic dibromomethane to activate the zinc.
  • PCBs polychlorinated biphenyls
  • the second phenyl ring is specifically produced by a Diels
  • the object of the present invention was therefore to provide a new, economic lent method by which biphenylamines can be obtained with high overall yield and high purity.
  • the present invention thus relates to a process for the preparation of biphenylamines of the general formula (I) in which
  • R 1 represents hydrogen, fluorine, chlorine, C r C 4 alkyl, C r C 4 alkoxy, Ci-Q-alkylthio, or C 1 -C 4 -
  • Haloalkyl X 1 is fluorine, chlorine or bromine, X 2 is fluorine, chlorine or bromine,
  • Hal is chlorine, bromine or iodine
  • R 2 is hydrogen, C 1 -C 4 -AuCyI or Ci-C 4 -Akoxy
  • R 1 has the meanings given above, with 2-methylbut-3-yn-2-ol of the formula (HI)
  • the biphenylamines of the formula (I) can be prepared in good yields from inexpensive starting materials without a Grignard reaction by means of this reaction sequence.
  • the transition-metal-catalyzed coupling with butynol requires only very small amounts of catalyst, which are below the amounts necessary for Suzuki coupling.
  • process A according to the invention can be used all 4 levels are illustrated by the following formula scheme.
  • Hal is preferably chlorine.
  • HaI is also preferred for bromine.
  • HaI is also preferred for iodine.
  • Hal is particularly preferably bromine.
  • R 1 is preferably hydrogen.
  • R 1 furthermore preferably represents fluorine, where fluorine is particularly preferably in the 3-, 4- or 5- position, very particularly preferably in the 3- or 5-position, in particular in the 5-position of the respective compound [cf. eg formula (I)].
  • R 1 furthermore preferably represents chlorine, chlorine being particularly preferably in the 3- or 5-position of the respective compound.
  • R 1 also preferably represents methyl or iso-propyl, with methyl or iso-propyl particularly preferably being in the 6-position of the respective compound.
  • R 1 furthermore preferably represents trifluoromethyl, trifluoromethyl being particularly preferably in the 4- or 5-position of the respective compound.
  • R 1 furthermore preferably represents methoxy or methylthio, with methoxy or methylthio being particularly preferably in the 4-, 5- or 6-position of the respective compound.
  • R 2 is preferably hydrogen, methyl, ethyl, isopropyl, tert-butyl, methoxy, ethoxy, isopropoxy or tert-butoxy.
  • R 2 particularly preferably represents methyl, tert-butyl, methoxy or tert-butoxy.
  • R 2 is very particularly preferably methyl.
  • X 1 is preferably fluorine.
  • X 1 is also preferably chlorine.
  • X 1 is also preferably bromine.
  • X is preferably fluorine.
  • X 2 is also preferably chlorine.
  • X 2 is also preferably bromine.
  • the starting materials are anilides of the formula (II-a)
  • the anilides of the formula (II) to be used as starting materials in carrying out the process A according to the invention in the first stage are known in some cases or can be obtained by known processes [cf. e.g. Synlett, 2003, (14), 2231; Recl. Trav. Chim. Pay-Bas. 1964, 83, 1142 ;. J. Het. Chem. 1969, 6, 243].
  • the 2-methylbut-3-yn-2-ol of the formula (HI) to be used as starting material in carrying out the process A according to the invention in the first stage is known and commercially available.
  • the alkynyl anilides of the formula (TV) to be used as starting materials in carrying out the process A according to the invention in the second stage are novel and likewise the subject of this application.
  • Alkynyl anilides of the formula (IV) are obtained by the first step of the process A according to the invention.
  • ethinyl anilides of the formula (V) to be used as starting materials in carrying out the process A according to the invention in the third stage are partly novel (in the case where R 1 is fluorine) and are likewise the subject of this application.
  • Ethynyl anilides of the formula (V) are obtained by the second step of the process A according to the invention.
  • the thiophene dioxides of the formula (VI) to be used as starting materials in carrying out the process A according to the invention in the third stage are known (cf., for example, J. Org. Chem. 1961, 26, 346-351, J. Fluorine Chem , 88, 143-151; J. Amer. Chem. Soc. 2000, 122, 2440-2445).
  • alkynyl anilides of the formula (IV) can dehydrate, according to which it is no longer possible to remove acetone to form ethynylanilides of the formula (V) (compare the following scheme).
  • the second side reaction is the formation of indoles according to the following scheme:
  • the first step of the process A according to the invention is carried out in the presence of a transition metal catalyst, preferably in the presence of dichlorobis (triphenylphosphine) palladium (.pi.).
  • a transition metal catalyst preferably in the presence of dichlorobis (triphenylphosphine) palladium (.pi.).
  • dichlorobis triphenylphosphine
  • other catalysts may also be used, e.g. Tetrakis (triphenylphosphine) palladium (O).
  • the first step of the process A according to the invention is preferably carried out in the presence of copper halides and triphenylphosphine as co-catalyst, particular preference is given to copper iodide.
  • the first stage of process A according to the invention can also be carried out without copper salts, which significantly increases the amount of Pd catalyst.
  • the reaction is carried out in the presence of a base, preferably in the presence of secondary or tertiary amines.
  • a base preferably in the presence of secondary or tertiary amines.
  • amines preferably diethylamine, dipropylamine, dibutylamine, piperidine, triethylamine, tripropylamine, tributylamine, more preferably triethylamine.
  • alkali metal carbonates may also be used as base in e.g. Nitriles are used as solvent.
  • the second stage of process A according to the invention is preferably carried out in a diluent which boils higher than acetone so that it can be removed from the reaction mixture continuously, if appropriate under reduced pressure.
  • Suitable solvents are all solvents inert to bases, such as hydrocarbons, chlorinated hydrocarbons, ethers or amides. Preference is given to using cyclohexane, toluene, xylene, chlorobenzene, 1,2-dimethoxyethane, dioxane, dimethylformamide, dimethylacetamide, N-methylpyrrolidinone, particularly preferably toluene and xylene.
  • the second stage of process A according to the invention is carried out in the presence of bases.
  • bases are alkali metal hydroxides, e.g. Sodium hydroxide, potassium hydroxide; Alcoholates, such as Sodium methylate, sodium ethylate, sodium butylate; Carbonates, such as sodium carbonate, potassium carbonate.
  • Indole ring closure can not be completely avoided as it also proceeds in a base-catalyzed manner (see, for example, Tetrahedron 2003, 59, 1571, J. Chem. Soc., Perkin Trans., 1, 2000, 1045-1075). By rapid cooling after completion of the reaction indole formation can still be largely suppressed suppression.
  • the third stage of process A according to the invention is preferably carried out in the presence of a solvent at elevated temperatures.
  • Suitable solvents for carrying out the third step of the process A according to the invention are: hydrocarbons, chlorinated hydrocarbons, nitriles, alcohols, ketones, ethers, amides or esters. Specifically, there may be mentioned: toluene, xylene, mesitylene, decalin, chlorobenzene, dichlorobenzene, butyronitrile, valeronitrile, propionitrile, cyclohexanone, ethylene glycol monoethyl ether, Anisole, dimethylformamide, butylacetate. Preferably used are xylene, butyronitrile or valeronitrile.
  • an ethinyl anilide of the formula (V) is preferably initially charged in a solvent and a thiophene dioxide of the formula (VI) is metered in at elevated temperature.
  • the thiophene dioxide of formula (VI) is used in excess. However, a deficit can also be used. Usually, 0.9 mol to 1.5 mol, preferably 1.05 mol to 1.25 mol, of thiophene dioxide of the formula (VI) are used per mole of ethynyl anilide of the formula (V). It is also possible to use per mole of ethynyl anilide of the formula (V) 0.5 mol to 1.5 mol, preferably 0.9 mol to 1, 25 mol, of thiophene dioxide of the formula (VI). The purification is carried out by crystallization.
  • the cleavage of the protecting group [-C (OO) R 2 ] on the nitrogen can be either basic or acidic according to known methods (cf., for example, TW Greene, PGM Wuts, Protective Groups in Organic Synthesis, Ed 3, New York, Wiley & Sons, 1999).
  • the biphenylamines of the formula (I) are valuable intermediates for the preparation of fungicidal active compounds.
  • R 1 represents hydrogen, fluorine, chlorine, C r C 4 alkyl, C r C 4 alkoxy, C, -C 4 alkylthio or C 1 -C 4 -HaIo- genalkyl
  • X 1 is fluorine, chlorine or bromine
  • X 2 is fluorine, chlorine or bromine
  • A is one of the following radicals A 1 to A 7: A ri3J
  • R 3 is C r C 3 -alkyl
  • R 4 is hydrogen, halogen, Ci-C 3 alkyl or C r C is 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms
  • R 5 is hydrogen, halogen or Q-Ca-alkyl
  • R 6 is hydrogen, halogen, Ci-C3 alkyl, amino, mono- or di (C r C 3 alkyl) amino,
  • R 7 is hydrogen, halogen, C r C 3 alkyl or C r C is 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms,
  • R 8 represents halogen, C r C 3 alkyl or C r C is 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms,
  • R 9 is halogen, Ci-C3 alkyl or Ci-C3 haloalkyl having 1 to 7 fluorine, chlorine and / or
  • R 10 is hydrogen, halogen, QQ-alkyl or C r C 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms,
  • Hal, R 2 and R 1 have the meanings given above, with 2-methylbut-3-yn-2-ol of the formula (IE) y CH 3
  • A has the abovementioned meanings and Y is halogen or hydroxyl, if appropriate in the presence of a catalyst, if appropriate in the presence of a condensing agent, if appropriate in the presence of an acid binder and, if appropriate, in
  • R 1 , R 2 , X 1 and X 2 have the preferred, particularly preferred and very particularly preferred meanings given above
  • A is preferably Al, A2, A3, A4 or A5.
  • A is particularly preferably Al or A2.
  • R 3 is preferably methyl.
  • R 4 is preferably iodine, methyl, difluoromethyl or trifluoromethyl.
  • R 4 particularly preferably represents methyl, difluoromethyl or trifluoromethyl.
  • R 5 is preferably hydrogen, fluorine, chlorine or methyl.
  • R 5 particularly preferably represents hydrogen or fluorine.
  • R 6 is preferably hydrogen, chlorine, methyl, amino or dimethylamino.
  • R 6 particularly preferably represents methyl.
  • R 7 is preferably methyl, difluoromethyl or trifluoromethyl.
  • R 8 is preferably chlorine, bromine, iodine, methyl, difluoromethyl or trifluoromethyl.
  • R 8 particularly preferably represents iodine, difluoromethyl or trifluoromethyl.
  • R 9 is preferably bromine or methyl.
  • R 9 particularly preferably represents methyl
  • R 10 is preferably methyl or trifluoromethyl.
  • R 10 particularly preferably represents methyl or trifluoromethyl.
  • Y is preferably chlorine or hydroxy.
  • the first to fourth stages of method B correspond to the first to fourth stages of the inventive method A and are carried out according to the above description.
  • the carboxylic acid derivatives of the formula (DC) to be used as starting materials in the fifth step of carrying out the process B according to the invention are known and / or can be prepared by known processes (cf., WO 03/066609, WO 03/066610, cf. EP-A 0 545 099, EP-A 0 589 301, EP-A 0 589 313 and US 3,547,917).
  • Suitable diluents for carrying out the fifth step of the process B according to the invention are all inert organic solvents. These include, preferably, aliphatic, alicyclic or aromatic hydrocarbons, such as, for example, petroleum ether, hexane, heptane, cyclohexane, methylcyclohexane, benzene, toluene, xylene or decalin; halogenated hydrocarbons, such as, for example, chlorobenzene, dichlorobenzene, dichloromethane, chloroform, tetrachloromethane, dichloroethane or trichloroethane; Ethers, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole
  • the fifth step of process B according to the invention is optionally carried out in the presence of a suitable acid acceptor.
  • a suitable acid acceptor all customary inorganic or organic bases are suitable. These preferably include alkaline earth metal or alkali metal hydrides, hydroxides, amides, alkoxides, acetates, carbonates or bicarbonates, such as, for example, sodium hydride, sodium amide, lithium diisopropylamide, sodium methoxide, sodium ethoxide, potassium tert-butoxide , Sodium hydroxide, potassium hydroxide, sodium acetate, sodium carbonate, potassium carbonate, potassium hydrogencarbonate, sodium bicarbonate or ammonium carbonate, and also tertiary amines, such as trimethylamine, triethylamine, tributylamine, N, N-dimethylaniline, N, N-dimethylbenzylamine, pyridine, N-methylpiperidine, N-methylmorpholine, N, N-di
  • the fifth stage of process B according to the invention is carried out in the presence of a suitable condensation agent.
  • a suitable condensation agent all condensing agents conventionally used for such amidation reactions are suitable.
  • acid halide generators such as phosgene, phosphorus tribromide, phosphorus trichloride, phosphorus pentachloride, phosphorus oxychloride or thionyl chloride;
  • Anhydride formers such as ethyl chloroformate, methyl chloroformate, isopropyl chloroformate, isobutyl chloroformate or methanesulfonyl chloride;
  • Carbodiimides such as N j N'-dicyclohexylcarbodiimide (DCC) or other customary Kondensa ⁇ tion agent such as phosphorus pentoxide, polyphosphoric acid, N, N'-carbonyldiimidazole, 2-ethoxy-N- ethoxycarbonyl-l,
  • the fifth step of process B according to the invention is carried out in the presence of a catalyst.
  • a catalyst examples which may be mentioned are 4-dimethylaminopyridine, 1-hydroxybenzotriazole or dimethylformamide.
  • reaction temperatures can be varied in carrying out the fifth step of the process B according to the invention in a wider range.
  • the reaction is carried out at temperatures from 0 ° C. to 150 ° C., preferably at temperatures from 0 ° C. to 80 ° C.
  • Step 1 N- [4-Fluoro-2-f3-hydroxy-3-methylbut-1-yn-1-phenyl] acetamide
  • Step 2 N- ( ⁇ 2-Ethynyl-4-fluorophenone acetamide
  • Triethylamine in vacuo the residue is dissolved in about 70 ml of toluene, washed 3 times with 30 ml x water, dried and the solvent is distilled off in vacuo. The residue is in
  • Step 3 N- (3 ', 4'-dichloro-5-fluorobiphenyl-2-ylV2.2-dimethylpropanamide

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

L'invention concerne un nouveau procédé pour produire des amines biphényle substituées, de nouveaux produits intermédiaires et leur réalisation, ainsi qu'un procédé pour produire des carboxamides à effet fongicide.
EP05790368A 2004-08-27 2005-08-13 Procede pour produire des amines biphenyle Withdrawn EP1784383A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004041531A DE102004041531A1 (de) 2004-08-27 2004-08-27 Verfahren zum Herstellen von Biphenylaminen
PCT/EP2005/008838 WO2006024388A1 (fr) 2004-08-27 2005-08-13 Procede pour produire des amines biphenyle

Publications (1)

Publication Number Publication Date
EP1784383A1 true EP1784383A1 (fr) 2007-05-16

Family

ID=35615542

Family Applications (1)

Application Number Title Priority Date Filing Date
EP05790368A Withdrawn EP1784383A1 (fr) 2004-08-27 2005-08-13 Procede pour produire des amines biphenyle

Country Status (6)

Country Link
US (1) US7750186B2 (fr)
EP (1) EP1784383A1 (fr)
JP (1) JP2008510745A (fr)
DE (1) DE102004041531A1 (fr)
TW (1) TW200621684A (fr)
WO (1) WO2006024388A1 (fr)

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Publication number Priority date Publication date Assignee Title
DE102006014722A1 (de) * 2006-03-30 2007-10-04 Bayer Cropscience Ag Verfahren zum Herstellen von 2-Ethinylphenylacetamiden
DE102006016462A1 (de) * 2006-04-07 2007-10-11 Bayer Cropscience Ag Verfahren zum Herstellen von Biphenylaminen über Vinylaniline
DE102006036222A1 (de) * 2006-08-03 2008-02-07 Bayer Cropscience Ag 3-Difluormethyl-pyrazolylcarboxanilide
DE102007016971A1 (de) 2007-04-10 2008-10-16 Saltigo Gmbh 2-Nitro-5-fluor-3',4'-dichlorbiphenyl sowie ein Verfahren zu dessen Herstellung
EP2008991A1 (fr) * 2007-06-29 2008-12-31 Bayer CropScience AG Procédé destiné à la fabrication de bi-aryles
EP2119697A1 (fr) * 2008-05-09 2009-11-18 Bayer CropScience AG Procédé pour la synthèse de diphénylanilines substituées
WO2011023324A1 (fr) * 2009-08-31 2011-03-03 Bayer Cropscience Ag Procédé à base de tétraarylborates pour produire des biphényles substitués
WO2012065947A1 (fr) 2010-11-15 2012-05-24 Bayer Cropscience Ag 5-halogénopyrazolecarboxamides
EP2546229A1 (fr) 2011-07-15 2013-01-16 Friedrich-Alexander-Universität Erlangen-Nürnberg Procédé de synthèse d'aminobiphényles
EP2683682A1 (fr) 2011-03-07 2014-01-15 Basf Se Procédé de synthèse d'aminobiphényles
EP2723720A1 (fr) 2011-06-21 2014-04-30 Bayer Intellectual Property GmbH Procédé de préparation de pyrazolyl-carboxanilides
CN104220417B (zh) 2012-03-07 2017-10-13 巴斯夫欧洲公司 使用芳基肼合成氨基联苯类的方法
WO2015162144A1 (fr) * 2014-04-25 2015-10-29 Bayer Cropscience Ag Procédé de production de biphénylamides à partir d'anilides par catalyse au ruthénium
WO2019044266A1 (fr) 2017-08-28 2019-03-07 株式会社日本ファインケム Procédé de production d'un dérivé de pyrazole-4-carboxamide

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CA2081935C (fr) 1991-11-22 2004-05-25 Karl Eicken Derives d'anilide et leur emploi contre botrytis
DE4231517A1 (de) 1992-09-21 1994-03-24 Basf Ag Carbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen
DE4231519A1 (de) 1992-09-21 1994-03-24 Basf Ag Cyclohex(en)ylcarbonsäureamide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen
PL354102A1 (en) 1999-12-09 2003-12-29 Syngenta Participations Agsyngenta Participations Ag Pyrazolecarboxamide and pyrazolethioamide as fungicide
GB0103258D0 (en) 2001-02-09 2001-03-28 Syngenta Participations Ag Organic compounds
DE10204391A1 (de) 2002-02-04 2003-08-14 Bayer Cropscience Ag Difluormethylthiazolylcarboxanilide
DE10204390A1 (de) 2002-02-04 2003-08-14 Bayer Cropscience Ag Disubstituierte Thiazolylcarboxanilide
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Also Published As

Publication number Publication date
US7750186B2 (en) 2010-07-06
JP2008510745A (ja) 2008-04-10
TW200621684A (en) 2006-07-01
DE102004041531A1 (de) 2006-03-02
WO2006024388A1 (fr) 2006-03-09
US20080194835A1 (en) 2008-08-14

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