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公开(公告)号:DE50103550D1
公开(公告)日:2004-10-14
申请号:DE50103550
申请日:2001-06-13
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS , SAUTER HUBERT , CULLMANN OLIVER , GEWEHR MARKUS , MUELLER BERND , TORMO I BLASCO JORDI , GOETZ NORBERT , VOLK THORSTEN , LORENZ GISELA , AMMERMANN EBERHARD , STIERL REINHARD , STRATHMANN SIEGFRIED
IPC: A01N37/18 , A01N37/36 , A01N37/38 , C07C231/02 , C07C233/22 , C07C233/69
Abstract: Use of phenethylacrylamides of the formula I:in which the substituents have the following meanings:X is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy and -O-C(R ,R )-C=C-R ;R ,R and R have the meanings given in the description;m,n independently of one another are 1 to 4, it being possible for the radicals X or Y to be different if m or n is greater than 1;Y is halogen, nitro, cyano, alkyl, CF3, alkoxy and phenyl;R ,R independently of one another are hydrogen, halogen, alkyl, alkoxy, haloalkoxy and CF3;R ,R ,R ,R independently of one another are hydrogen, halogen, alkyl, alkoxy, orR and R together form a cyclopropyl ring, it being possible for the C-R - and C-R bonds can be in the E- or Z-position relative to each other;for controlling phytopathogenic fungal pests, novel phenethylacrylamides, their preparation, and compositions comprising them.
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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:DE60201089D1
公开(公告)日:2004-09-30
申请号:DE60201089
申请日:2002-04-06
Applicant: BASF AG
Inventor: TORMO I BLASCO JORDI , SAUTER HUBERT , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC: A01N25/02 , A01N25/08 , A01N43/90 , C07D487/04
Abstract: 6-(2-Chloro-6-fluoro-phenyl)-triazolopyrimidines of formula (I), in which R 1 and R 2 independently denote hydrogen or alkyl, alkenyl, alkynyl, alkadienyl, or haloalkyl, cycloalkyl, bicycloalkyl, 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 1 and R 2 radicals may be unsubstituted or partially or fully halogenated or may be substituted as defined in the description. R 1 and R 2 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; X is cyano, 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: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:AU2003298117A1
公开(公告)日:2004-06-15
申请号:AU2003298117
申请日:2003-11-14
Applicant: BASF AG
Inventor: SCHOFL ULRICH , STIERL REINHARD , BLASCO JORDI TORMO I , BLETTNER CARSTEN , MULLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED
IPC: A01N43/90 , C07D487/04 , C07D249/00
Abstract: 2-Substituted triazolopyrimidines of the formula I, in which the substituents are as defined below: L are halogen, cyano, nitro, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, -C(-O)-A or S(-O) p A'; A and A' are as defined in the description; p is 0, 1 or 2; m is 0, 1, 2, 3, 4 or 5; X is cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; R 1 ,R 2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl or cycloalkynyl, phenyl, naphthyl or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R 1 and R 2 together with the nitrogen atom to which they are attached may also form a five- or six-membered ring which may be interrupted by an atom from the group consisting of O, N and S, where R 1 and/or R 2 may be substituted as defined in the description; and R 3 is cyano, hydroxyl, alkoxy, alkenyloxy, haloalkoxy, haloalkenyloxy, NR 1 R 2 or S(O) n R 31 , where n and R 31 are as defined in the description; Processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi are described.
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公开(公告)号:ES2196054T3
公开(公告)日:2003-12-16
申请号:ES95905614
申请日:1995-01-03
Applicant: BASF AG
Inventor: BAYER HERBERT , SAUTER HUBERT , MUELLER RUTH , GRAMMENOS WASSILIOS , HARREUS ALBRECHT , KIRSTGEN REINHARD
IPC: A01N37/50 , A01N37/52 , A01N43/06 , A01N43/36 , A01N43/40 , A01N43/54 , A01N43/80 , A01N43/82 , A01N43/824 , A01P3/00 , A01P7/04 , C07D249/08 , C07C251/38 , C07C251/40 , C07C251/44 , C07C251/48 , C07C251/52 , C07C251/54 , C07C251/56 , C07C251/58 , C07C255/11 , C07C327/44 , C07C327/48 , C07C327/58 , C07D207/32 , C07D207/333 , C07D207/36 , C07D213/30 , C07D213/53 , C07D213/62 , C07D213/64 , C07D213/79 , C07D233/64 , C07D237/14 , C07D239/34 , C07D239/46 , C07D241/18 , C07D261/08 , C07D261/10 , C07D261/12 , C07D263/32 , C07D263/34 , C07D271/06 , C07D271/10 , C07D277/24 , C07D307/42 , C07D333/32 , C07D521/00
Abstract: Phenylacetic acid derivatives of the formula I
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公开(公告)号:AU2003210217A1
公开(公告)日:2003-09-09
申请号:AU2003210217
申请日:2003-02-06
Applicant: BASF AG
Inventor: SCHIEWECK FRANK , BLASCO JORDI TORMO I , GROTE THOMAS , GYPSER ANDREAS , MULLER BERND , RHEINHEIMER JOACHIM , ROSE INGO , SCHAFER PETER , GRAMMENOS WASSILIOS , GEWEHR MARKUS , SCHWOGLER ANJA , BLETTNER CARSTEN , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC: A01N43/54 , C07D401/04
Abstract: The invention relates to 2-(2-pyridyl)-5-phenyl-6-amninopyrimidines of formula I, wherein the substitutes and the index have the following meaning: R 1 represents halogen, hydroxy, hyano, hxo, nitro, amino, mercapto, alkyl, halogenalkyl, alkenyl, alkinyl, cycloalkyl, alkoxy, halogenalkoxy, carboxyl, alkoxycarbonyl, carbamoyl, alkylaminocarbonyl, dialkylamincarbonyl, morpholinocarbonyl, pyrrolidinocarbonyl, alkylcarbonylamino, alkylamino. dialkylamino, alkylthio, alkylsulfinyl, alkylsulfonyl, hydroxysulfonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl; m=0 or 1-4; R 2 represents hydrogen, halogen, cyano, alkyl, halogenalkyl or alkoxy; R 3 , R 4 represents hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl, R 3 and R 4 together with the nitrogen atom to which they are connected, form a five or six-membered ring which is interrupted by an atom from the group O, N or S and/or can be substituted according to the description; R 5 represents halogen, alkyl or halogenalkyl; R 6 represents hydrogen or one of the known groups in R 5 ; R 7 , R 8 represent hydrogen, halogen, alkyl or halogenalkyl; R 9 represents hydrogen, halogen, hydroxy, cyano, alkyl, alkoxy, cycloalkoxy, halogenalkoxy, alkoxycarbonyl or alkylaminocarbonyl. The invention also relates to a method and intermediate product for the production of said compound in addition to the use thereof for combating undesirable plants.
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270.
公开(公告)号:HU0300650A2
公开(公告)日:2003-07-28
申请号:HU0300650
申请日:2001-06-13
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD , CULLMANN OLIVER , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GOETZ NORBERT , LORENZ GISELA , MUELLER BERND , SAUTER HUBERT , STIERL REINHARD , STRATHMANN SIEGFRIED , TORMO I BLASCO JORDI , VOLK THORSTEN
IPC: A01N37/18 , A01N37/36 , A01N37/38 , C07C231/02 , C07C233/22 , C07C233/69
Abstract: Use of phenethylacrylamides of the formula I:in which the substituents have the following meanings:X is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy and -O-C(R ,R )-C=C-R ;R ,R and R have the meanings given in the description;m,n independently of one another are 1 to 4, it being possible for the radicals X or Y to be different if m or n is greater than 1;Y is halogen, nitro, cyano, alkyl, CF3, alkoxy and phenyl;R ,R independently of one another are hydrogen, halogen, alkyl, alkoxy, haloalkoxy and CF3;R ,R ,R ,R independently of one another are hydrogen, halogen, alkyl, alkoxy, orR and R together form a cyclopropyl ring, it being possible for the C-R - and C-R bonds can be in the E- or Z-position relative to each other;for controlling phytopathogenic fungal pests, novel phenethylacrylamides, their preparation, and compositions comprising them.
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