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公开(公告)号:CA2520579A1
公开(公告)日:2004-10-14
申请号:CA2520579
申请日:2004-03-24
Applicant: BASF AG
Inventor: GEWEHR MARKUS , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD , GYPSER ANDREAS , TORMO I BLASCO JORDI , GROTE THOMAS , BLETTNER CARSTEN , SCHAEFER PETER , RHEINHEIMER JOACHIM , MUELLER BERND , SCHERER MARIA , GRAMMENOS WASSILIOS , SCHWOEGLER ANJA , SCHIEWECK FRANK
IPC: A01N43/90 , C07D487/04
Abstract: The invention relates to 7-alkenylamino-triazolopyrimidines of formula (I) wherein the substituents have the following meaning: L represents halogen, alkyl, halogenalkyl, alkoxy, amino, NHR or NR2; R represents alkyl or alkyl- carbonyl; m represents 1, 2, 3, 4 or 5; X represents halogen, cyano, alkyl, halogenalkyl or alkoxy; R1 represents alkyl or halogenalkyl; R2 represents hydrogen, alkyl or halogenalkyl; R3 represents alkenyl which is unsubstitut ed or partially or totally halogenated or can be substituted according to the description; R4 represents hydrogen or alkyl, R3 and R4 can form, together with the nitrogen atom whereon they are bound, a five or six-membered unsaturated ring which can be interrupted by an atom from the groups O, N an d S and/or can include one or several substituents. The invention also relates to methods for producing said compounds, agents containing said compounds an d the use thereof in controlling plant pathogenic harmful fungi.
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公开(公告)号:HU0400439A2
公开(公告)日:2004-09-28
申请号:HU0400439
申请日:2002-05-17
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM DR , GYPSER ANDREAS , ROSE INGO , GROTE THOMAS , SCHAEFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , SPEAKMAN JOHN-BRYAN , STRATHMANN SIEGFRIED , LORENZ GISELA DR
IPC: A01N43/86 , A01N43/90 , C07D265/24 , C07D498/04 , C07D513/04
Abstract: Oxazin(ethi)one compounds of the formula I: in which the variables Z, R 1 , R 2 , R 3 and n are as defined in claim 1 and A is a 5- or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1, 2 or 3 heteroatoms selected from the group consisting of N, O and S, each of which cycles is attached via two carbon atoms to the oxazin(ethi)one ring, and the agriculturally useful salts of the oxazin(ethi)one compounds I are described. Moreover, the invention describes the use of compounds I and their salts for controlling phytopathogenic fungi, compositions which comprise the compounds I and/or their salts in a fungicidally effective amount and a method for controlling phytopathogenic fungi which comprises treating the fungi or the materials, plants, seeds or the soil threatened by fungal attack with a fungicidally effective amount of at least one compound of the formula I as claimed in claim 1 and/or a salt of I.
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公开(公告)号:AT274518T
公开(公告)日:2004-09-15
申请号:AT02727534
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 , C07D249/00 , C07D239/00
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:AT273981T
公开(公告)日:2004-09-15
申请号:AT00987356
申请日:2000-12-06
Applicant: BASF AG
Inventor: PEES KLAUS-JUERGEN , SCHIEWECK FRANK , TORMO I BLASCO JORDI , SAUTER HUBERT , CULLMANN OLIVER , MUELLER BERND , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL RHEINHARD DR
IPC: A01N43/90 , C07D487/04 , C07D239/00 , C07D249/00
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公开(公告)号:AU2003296662A1
公开(公告)日:2004-07-22
申请号:AU2003296662
申请日:2003-12-17
Applicant: BASF AG
Inventor: MULLER BERND , BLASCO JORDI TORMO I , GROTE THOMAS , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , SCHOFL ULRICH , STIERL REINHARD
IPC: A01N43/90 , C07D487/04
Abstract: Triazolopyrimidines of the formula I in which the index n and the substituents R 1 , R 2 and R 3 are as defined in the description, and processes for preparing these compounds, compositions comprising them and their use for controlling harmful fungi are described.
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公开(公告)号:SK14002003A3
公开(公告)日:2004-06-08
申请号:SK14002003
申请日:2002-05-17
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , GYPSER ANDREAS , ROSE INGO , GROTE THOMAS , SCHAFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , SPEAKMAN JOHN-BRYAN , STRATHMANN SIEGFRIED , LORENZ GISELA
IPC: A01N43/86 , A01N43/90 , C07D265/24 , C07D498/04 , C07D513/04
Abstract: Oxazin(ethi)one compounds of the formula I: in which the variables Z, R 1 , R 2 , R 3 and n are as defined in claim 1 and A is a 5- or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1, 2 or 3 heteroatoms selected from the group consisting of N, O and S, each of which cycles is attached via two carbon atoms to the oxazin(ethi)one ring, and the agriculturally useful salts of the oxazin(ethi)one compounds I are described. Moreover, the invention describes the use of compounds I and their salts for controlling phytopathogenic fungi, compositions which comprise the compounds I and/or their salts in a fungicidally effective amount and a method for controlling phytopathogenic fungi which comprises treating the fungi or the materials, plants, seeds or the soil threatened by fungal attack with a fungicidally effective amount of at least one compound of the formula I as claimed in claim 1 and/or a salt of I.
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公开(公告)号:AT261433T
公开(公告)日:2004-03-15
申请号:AT99970386
申请日:1999-10-01
Applicant: BASF AG
Inventor: GEWEHR MARKUS , GRAMMENOS WASSILIOS , SAUTER HUBERT , BAYER HERBERT , GYPSER ANDREAS , MUELLER BERND , PTOCK ARNE , CULLMANN OLIVER , GROTE THOMAS , AMMERMANN EBERHARD , LORENZ GISELA , STRATHMANN SIEGFRIED , HARRIES VOLKER
IPC: A01N25/02 , A01N25/08 , A01N43/72 , A01N43/88 , A61K31/539 , A61P31/10 , C07D273/00 , C07D273/01
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公开(公告)号:AU2003232227A1
公开(公告)日:2003-11-17
申请号:AU2003232227
申请日:2003-04-30
Applicant: BASF AG
Inventor: GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD , BLASCO JORDI TORMO I , BLETTNER CARSTEN , MULLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS
IPC: A01N43/90 , C07C69/65 , C07D487/04 , C07C69/612 , C07C69/738
Abstract: Disclosed are a method for producing fungicidal triazolopyrimidine compounds, agents containing said compounds, and the use thereof for controlling harmful fungi. Also disclosed are triazolopyrimidines of formula (1), in which the substituents have the following meaning: L 1 represents alkyl; L 2 represents halogen; L 3 represents hydrogen or halogen; X represents halogen, cyano, alkyl, alkoxy, or haloalkoxy; R 1 , R 2 represent hydrogen, alkyl, haloalkyl, cycloalkyl, alkenyl, alkadienyl, alkinyl, or cycloalkinyl, phenyl, naphthyl, or a five-unit to ten-unit saturated, partially unsaturated, or aromatic heterocycle containing one to four heteroatoms from the group O, N, or S. R 1 and R 2 can also form a five-unit or six-unit ring along with the nitrogen atom to which they are linked. Said ring can be interrupted and/or substituted by an atom from the group O, N, and S while R 1 and/or R 2 can be substituted according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing said compounds, and the use thereof for controlling harmful fungi.
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公开(公告)号:CA2482809A1
公开(公告)日:2003-11-13
申请号:CA2482809
申请日:2003-04-30
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , TORMO I BLASCO JORDI , STRATHMANN SIEGFRIED , MUELLER BERND , GEWEHR MARKUS , BLETTNER CARSTEN , GRAMMENOS WASSILIOS , GYPSER ANDREAS , AMMERMANN EBERHARD , SCHWOEGLER ANJA , SCHIEWECK FRANK , GROTE THOMAS , LORENZ GISELA , SCHAEFER PETER , STIERL REINHARD
IPC: A01N43/90 , C07C69/65 , C07D487/04 , C07D239/00 , C07D249/00 , C07C69/612 , C07C69/738
Abstract: Disclosed are a method for producing fungicidal triazolopyrimidine compounds , agents containing said compounds, and the use thereof for controlling harmfu l fungi. Also disclosed are triazolopyrimidines of formula (I), in which the substituents have the following meaning: L1 represents alkyl; L2 represents halogen; L3 represents hydrogen or halogen; X represents halogen, cyano, alkyl, alkoxy, or haloalkoxy; R1, R2 represent hydrogen, alkyl, haloalkyl, cycloalkyl, alkenyl, alkadienyl, alkinyl, or cycloalkinyl, phenyl, naphthyl, or a five-unit to ten-unit saturated, partially unsaturated, or aromatic heterocycle containing one to four heteroatoms from the group O, N, or S. R1 and R2 can also form a five-unit or six-unit ring along with the nitrogen at om to which they are linked. Said ring can be interrupted and/or substituted by an atom from the group O, N, and S while R1 and/or R2 can be substituted according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing said compounds, and the use thereof for controlling harmful fungi.
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公开(公告)号:CA2467683A1
公开(公告)日:2003-05-30
申请号:CA2467683
申请日:2002-11-15
Applicant: BASF AG
Inventor: ROSE INGO , GEWEHR MARKUS , MUELLER BERND , GROTE THOMAS , STIERL REINHARD , SCHIEWECK FRANK , GYPSER ANDREAS , LORENZ GISELA , AMMERMANN EBERHARD , TORMO I BLASCO JORDI , SCHWOEGLER ANJA , GRAMMENOS WASSILIOS , STRATHMANN SIEGFRIED , SCHAEFER PETER , RHEINHEIMER JOACHIM
IPC: A01N43/54 , C07D239/42 , C07D239/46 , C07D239/47 , C07D239/48 , C07D239/52 , C07D401/06 , C07D401/14 , C07D403/12
Abstract: 5-Phenylpyrimidines of formula (I), where the substituents and the indices have the following meanings: R1, R2 = H, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkinyl or haloalkinyl, where R1 and R 2 together with the nitrogen atom to which they are bonded may form a saturate d or unsaturated ring, interrupted by an ether, thio, sulphoxy or sulphonyl group and which can be substituted by one to four groups Ra and/or Rb, R3 = H, halo, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy or alkenyloxy, R4 = H, hal o, cyano, hydroxy, mercapto, azido, alkyl, alkenyl, alkinyl, haloalkyl, alkoxy, alkenyloxy, alkinyloxy, haloalkoxy, alkylthio, alkenylthio, alkinylthio, haloalkylthio, -ON=CRaRb, -CRc=NORa, -NRcN=CRaRb, -NRaRb, -NRcNRaRb, -NORa, - NRcC (=NRc') NRaRb, -NRcC (=0) NRaRb, -NRaC (=0) Rc, -NRaC (=NORc)Rc', -OC (=0) Rc, -C (=NORc) NRaRb, -CRc (=NNRaRb), -C (=0) NRaRb or -C (=0) Rc, wher e Ra,Rb,Rc are as defined in the description, X = halo, alkyl, alkoxy or haloalkyl and m = a whole number from 1 to 5. The invention further relates to methods for production of the above compounds, agents containing the same an d use thereof for the treatment of noxious mycoses.
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