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公开(公告)号:DE59910677D1
公开(公告)日:2004-11-04
申请号:DE59910677
申请日:1999-11-12
Applicant: BASF AG
Inventor: VON DEYN WOLFGANG , GEBHARDT JOACHIM , RACK MICHAEL , LOCHTMAN RENE , GOETZ NORBERT , KEIL MICHAEL , WITSCHEL MATTHIAS , HAGEN HELMUT , MISSLITZ ULF , BAUMANN ERNST
IPC: C07C251/40 , C07C251/48 , C07C319/14 , C07C323/09 , C07D261/04 , C07D261/08 , C07D413/10
Abstract: The present invention describes a process for preparing isoxazoles of the formula Iwhere:R is hydrogen, C1-C6-alkyl,R is hydrogen, C1-C6-alkyl,R , R , R are each hydrogen, C1-C6-alkyl or R and R together form a bond,R is a heterocyclic ring,n is 0, 1 or 2;which comprises preparing an intermediate of the formula VIwhere R , R , R and R are each as defined above, followed by halogenation, thiomethylation, oxidation and acylation to give compounds of the formula I.Furthermore, the invention describes novel intermediates for preparing the compounds of the formula I and novel processes for preparing the intermediates.
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公开(公告)号:CA2519990A1
公开(公告)日:2004-10-07
申请号:CA2519990
申请日:2004-03-20
Applicant: BASF AG
Inventor: GROTE THOMAS , MUELLER BERND , GEWEHR MARKUS , SCHIEWECK FRANK , RETHER JAN , GYPSER ANDREAS , GRAMMENOS WASSILIOS , TORMO I BLASCO JORDI , STIERL REINHARD , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , RACK MICHAEL , SCHWOEGLER ANJA , BLETTNER CARSTEN , RHEINHEIMER JOACHIM
IPC: C07D333/38 , C07D333/12
Abstract: The invention relates to trifluoromethyl-thiophene carboxylic acid anilides of general formulas I, II, and III, wherein the substituents have the following meaning: R1, R4 independently represent C1-C4alkyl, C3-C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, C1-C4 alkoxy, said groups being optionally substitut ed by halogen, H, halogen, nitro, CN; R2 represents H, OH, C1-C4 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, said groups being optionally substituted by haloge n; R3 represents C1-C12 alkyl, C3-C12 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C2-C12 alkinyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups bei ng optionally substituted by R7; phenyl, phenyl-C1-C6 alkyl, phenyl-C2-C6 alkenyl, phenyl-C2-C6 alkinyl, phenyloxy-C1-C6 alkyl, phenyloxy-C2-C6 alkeny l, phenyloxy-C2-C6 alkinyl, the alkyl portion, alkenyl portion, and alkinyl portion being optionally substituted by R7 and the phenyl ring being optionally substituted by R5; -C(R8)=NOR6; X represents O, S, or a direct bond; R5 represents H, C1-C4alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, halogen, nitro, CN, phenyl which can be substituted by R1, phenoxy that can be substituted by R1, C1-C6 alkyl-phenyl, the alkyl portion being optionally substituted by halogen andthe phenyl ring being optionally substituted by R1 ; R6 represents C1-C4 alkyl, C3-C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, phenyl which can be substituted by R1; R7 represents C1-C4 alkyl, C1-C8 alkoxy, C2-C8 alkenyloxy , C2-C8 alkinyloxy, C1-C4 alkoxy-C1-C8 alkoxy, said groups being optionally substituted by halogen, halogen; R8 represents H, R7, or C1-C12 alkyl, C3-C1 2 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups being optionally substituted by halogen; phenyl which can be substituted by R5; n represents 0 to 4; and m represents 0, 1. Also disclosed is the use of the inventive trifluoromethyl-thiophene carboxylic acid anilides as fungicides and agents containing said trifluoromethyl- thiophene carboxylic acid anilides.
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公开(公告)号:AU2004224205A1
公开(公告)日:2004-10-07
申请号:AU2004224205
申请日:2004-03-20
Applicant: BASF AG
Inventor: GROTE THOMAS , MULLER BERND , RETHER JAN , SCHWOGLER ANJA , SCHOFL ULRICH , SCHIEWECK FRANK , STRATHMANN SIEGFRIED , BLASCO JORDI TORMO I , GYPSER ANDREAS , BLETTNER CARSTEN , STIERL REINHARD , RHEINHEIMER JOACHIM , GRAMMENOS WASSILIOS , GEWEHR MARKUS , RACK MICHAEL
IPC: C07D333/38 , C07D333/12
Abstract: The invention relates to novel biphenyl carboxamides of formula (I), wherein A, R, Z, X, Y, m and n have the meanings given in the description, to multiple methods for producing these substances, to their use for combating unwanted micro-organisms and to novel intermediate products and the production thereof.
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公开(公告)号:NZ524049A
公开(公告)日:2004-09-24
申请号:NZ52404901
申请日:2001-07-17
Applicant: BASF AG
Inventor: LOCHTMAN RENE , KEIL MCIHAEL , GEBHARDT JOACHIM , RACK MICHAEL , VON DEYN WOLFGANG
IPC: C07B61/00 , C07C319/14 , C07C323/62 , C07D261/04 , C07D413/04 , C07C251/40 , C07D413/10
Abstract: A process for preparing 4-thioalkylbromobenzene derivatives such as 4-methylthio-3-(4,5-dihydroisoxazol-3-yl)-2-methylbromobenzene of the formula (I) is disclosed, wherein: R1 is C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C3-C8-cycloalkyl or a halogen; R2 is C1-C6-alkyl, C1-C6-alkoxy, C3-C8-cycloalkyl, C2-C6-alkenyl, cyano or a heterocyclic radical; R3 is C1-C6-alkyl; which comprises reacting a compound of the formula (II), in which R1 and R2 are as defined above, with a dialkyl disulfide of the formula (III) in the presence of a nitrite such as sodium nitrite and a catalyst such as copper powder in a suitable solvent. The reaction may be carried out at temperatures between 30-100 degree C
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公开(公告)号:BR0211180A
公开(公告)日:2004-08-10
申请号:BR0211180
申请日:2002-07-08
Applicant: BASF AG
Inventor: BLASCO JORDI TORMO I , SAUTER HUBERT , LLER BERND M , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHOFER PETER , SCHIEWECK FRANK , RACK MICHAEL , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC: A01N43/90 , C07D487/04
Abstract: Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R and R independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R and R radicals may be unsubstituted or substituted as defined in the description, or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
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公开(公告)号:BR0210858A
公开(公告)日:2004-06-29
申请号:BR0210858
申请日:2002-07-03
Applicant: BASF AG
Inventor: MUELLER BERND , SAUTER HUBERT , GEWEHR MARKUS , GRAMMENOS WASSILIOS , BLASCO JORDI TORMO I , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHOFER PETER , SCHIEWECK FRANK , RACK MICHAEL , LORENZ GISELA , STRATHMANN SIEGFRIED , AMMERMANN EBERHARD , STIERL REINHARD
IPC: A01N43/90 , C07D487/04 , A01N43/653
Abstract: 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines (I) are new. 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines of formula (I) are new. [Image] n : 0-5; R : halo, CN, OH or OCN, or alkyl, alkenyl, alkynyl, T', haloalkenyl, OT, alkenyloxy, alkynyloxy, OT', cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, CONH 2, mono- or dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkynyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, cycloalkylcarbonyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); T : 1-6C alkyl; T' : 1-6C haloalkyl; Het : 5-10 membered, saturated, partially unsaturated or aromatic heterocycle containing 1-4 of O, N and/or S heteroatoms; R 11-10C alkyl, alkenyl, alkynyl, 3-12C cycloalkyl, 3-10C cycloalkenyl, phenyl, naphthyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); R ahalo, CN, NO 2, OH, T, T', COT, cycloalkyl, OT, OT', COOT, NHT, NT 2, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C alkynyloxy, alkoximino, alkenyloximino, alkynyloximino, aralkoximino, alkynyl, alkynyloxycarbonyl, phenyl, naphthyl or Het (where all aliphatic, alicyclic or aromatic groups are optionally partially or completely halogenated and optionally substituted by 1-3 R aand/or 1-3 R c); R bhalo, CN, NO 2, OH, SH, NH 2, COOH, CONH 2, CSNH 2, T, T', 2-8C alkenyl, 2-8C alkenyloxy, 2-8C alkynyloxy, OT, OT', ST, NHT, NT 2, CHO, COT, SO 2T, SOT, COOT, OCOT, CONHT, CONT 2, CSNHT or CSNT 2; R ccycloalkyl, -O-cycloalkyl, heterocyclyl, -O-heterocyclyl, aryl, -O-aryl, -S-aryl, -O-T-aryl, -T-aryl, heteroaryl, -O-heteroaryl or -S-heteroaryl (where cycloalkyl or heterocyclyl rings are 3-10 membered, aryl rings are preferably 6-10 membered and heteroaryl rings are preferably 5-6 membered; and all rings are optionally partially or completely halogenated and optionally substituted by alkyl or haloalkyl); and R 21-4C alkyl, 2-4C alkynyl or 2-4C alkynyl (all optionally substituted by halo, CN, NO 2, OMe, OEt or 1-4C alkoxycarbonyl; Unless specified otherwise alkyl moieties have 1-8C, alkenyl or alkynyl moieties 2-10C and cycloalkyl or cycloalkenyl moieties 3-6C. Independent claims are also included for: (1) preparation of (I); and (2) dicarbonyl compound intermediates of formula (III), provided that n is not 0 and R 1and R 2are not both Me. [Image] ACTIVITY : Fungicide. 7-Cyclohexyl-5-methyl-6-(2-chloro-6-fluorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine (Ia) at a concentration of 63 ppm gave at least 90 % protection of tomato plants against Alternaria solani. MECHANISM OF ACTION : None given.
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公开(公告)号:ZA200300816B
公开(公告)日:2004-03-10
申请号:ZA200300816
申请日:2003-01-29
Applicant: BASF AG
Inventor: GERHARDT JOACHIM , KEIL MICHAEL , LOCHTMAN RENE , RACK MICHAEL , DEYN WOLFGANG VON
IPC: C07C209/74 , C07C211/52 , C07D261/04 , C07D , C07C
Abstract: The invention relates to a method for producing 4-bromine-aniline derivatives of formula (I), wherein the substituents have the following meanings: R : C1-C6-alkyl, C1-C6-halogenalkyl, C1-C6-alkoxy, C1-C6-halogen-alkoxy, C3-C8-cycloalkyl, halogen; R : C1-C6-alkyl, C1-C6-alkoxy, C3-C8-cycloalkyl, C2-C6-alkenyl, cyano or a heterocyclic radical.
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公开(公告)号:DE59906901D1
公开(公告)日:2003-10-09
申请号:DE59906901
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
IPC: C07B61/00 , C07D231/20
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公开(公告)号:SK462003A3
公开(公告)日:2003-07-01
申请号:SK462003
申请日:2001-07-17
Applicant: BASF AG
Inventor: LOCHTMAN RENE , KEIL MICHAEL , GEBHARDT JOACHIM , RACK MICHAEL , VON DEYN WOLFGANG
IPC: C07B61/00 , C07C319/14 , C07C323/62 , C07D261/04 , C07D413/04 , C07C251/40 , C07D413/10
Abstract: A process for preparing 4-thioalkylbromobenzene derivatives of the formula I where: R 1 is C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 3 -C 8 -cycloalkyl, halogen, R 2 is C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 3 -C 8 -cycloalkyl, C 2 -C 6 -alkenyl, cyano or a heterocyclic radical, R 3 is C 1 -C 6 -alkyl, which comprises reacting a compound of the formula II, in which R 1 and R 2 are as defined above, with a dialkyl disulfide of the formula III R 3 -S-S-R 3 III in the presence of a nitrite and a catalyst in a suitable solvent is described.
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公开(公告)号:DE59808163D1
公开(公告)日:2003-06-05
申请号:DE59808163
申请日:1998-01-08
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , DEYN WOLFGANG VON , GEBHARDT JOACHIM , HILL LUISE , RACK MICHAEL , KOENIG HARTMANN , GOETZ NORBERT , MAYWALD VOLKER , KARDORFF UWE
IPC: C07D231/20 , C07D261/04 , C07D261/20 , C07D413/10 , C07D417/10
Abstract: PCT No. PCT/EP98/00066 Sec. 371 Date Jul. 13, 1999 Sec. 102(e) Date Jul. 13, 1999 PCT Filed Jan. 8, 1998 PCT Pub. No. WO98/31676 PCT Pub. Date Jul. 23, 1998Sulfur-containing 2-chloro-3-(4,5-dihydro-3-isoxazolyl)-benzoic acids of the formula I in which the substituents have the meanings given in the description are prepared as described.
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