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公开(公告)号:PE20051164A1
公开(公告)日:2006-02-14
申请号:PE2005000271
申请日:2005-03-09
Applicant: BASF AG
Inventor: MULLER BERND , TORMO I BLASCO JORDI , GROTE THOMAS , SCHERER MARIA , STIERL REINHARD , SCHOFL ULRICH , SCHIEWECK FRANK , BLETTNER CARSTEN , NIEDENBRUCK MATTHIAS , GEWEHR MARKUS , GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , SCHAFER PETER , WAGNER OLIVER , STRATHMANN SIEGFRIED , SCHWOGLER ANJA
IPC: A01N43/90 , C07D487/04
Abstract: SE REFIERE A UN COMPUESTO DE FORMULA I DONDE R1 ES ALQUILO C1-C5, ALCOXI C1-C10-ALQUILO C1-C10; R2 ES ALQUILO C5-C12, ALCOXI C1-C10-ALQUILO C1-C10 PUDIENDO R1 Y/O R2 ESTAR SUSTITUIDOS POR 1-3 GRUPOS DE CN, NITRO, HIDROXI, CICLOALQUILO C3-C6, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 6-METIL-5-PENTIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA; 5-HEXIL-6-METIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA; 6-ETIL-5-n-OCTIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA, ENTRE OTROS. REFERIDA TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON EFECTIVOS CONTRA UN AMPLIO ESPECTRO DE HONGOS FITOPATOGENOS EN DIFERENTES PLANTAS DE CULTIVO TALES COMO TRIGO, CEBADA, AVENA, PASTO, SOYA, ENTRE OTROS
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公开(公告)号:PE11642005A1
公开(公告)日:2006-02-14
申请号:PE0002712005
申请日:2005-03-09
Applicant: BASF AG
Inventor: MULLER BERND , TORMO I BLASCO JORDI , GROTE THOMAS , SCHERER MARIA , STIERL REINHARD , SCHOFL ULRICH , SCHIEWECK FRANK , BLETTNER CARSTEN , NIEDENBRUCK MATTHIAS , GEWEHR MARKUS , GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , SCHAFER PETER , WAGNER OLIVER , STRATHMANN SIEGFRIED , SCHWOGLER ANJA
IPC: A01N43/90 , C07D487/04
CPC classification number: C07D487/04
Abstract: SE REFIERE A UN COMPUESTO DE FORMULA I DONDE R1 ES ALQUILO C1-C5, ALCOXI C1-C10-ALQUILO C1-C10; R2 ES ALQUILO C5-C12, ALCOXI C1-C10-ALQUILO C1-C10 PUDIENDO R1 Y/O R2 ESTAR SUSTITUIDOS POR 1-3 GRUPOS DE CN, NITRO, HIDROXI, CICLOALQUILO C3-C6, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 6-METIL-5-PENTIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA; 5-HEXIL-6-METIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA; 6-ETIL-5-n-OCTIL-[1,2,4]TRIAZOLO[1,5-a]PIRIMIDIN-7-ILAMINA, ENTRE OTROS. REFERIDA TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON EFECTIVOS CONTRA UN AMPLIO ESPECTRO DE HONGOS FITOPATOGENOS EN DIFERENTES PLANTAS DE CULTIVO TALES COMO TRIGO, CEBADA, AVENA, PASTO, SOYA, ENTRE OTROS
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公开(公告)号:AU2005254665A1
公开(公告)日:2005-12-29
申请号:AU2005254665
申请日:2005-06-14
Applicant: BASF AG
Inventor: WAGNER OLIVER , GROTE THOMAS , SCHERER MARIA , SCHAFER PETER , STRATHMANN SIEGFRIED , NIEDENBRUCK MATTHIAS , SCHWOGLER ANJA , STIERL REINHARD , MULLER BERND , GRAMMENOS WASSILIOS , SCHIEWECK FRANK , RHEINHEIMER JOACHIM , HUNGER UDO , SCHOFL ULRICH , BLETTNER CARSTEN , NAVE BARBARA , GEWEHR MARKUS
IPC: A01N43/653 , A01N43/90 , C07D487/04
Abstract: The use of substituted triazolopyrimidines of the formula I in which R 1 is alkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R 2 is hydrogen or a group R 1 , where R 1 and/or R 2 may be substituted according to the description, and X is halogen; as fungicides, novel 6-(2-tolyl)triazolopyrimidines, processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
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公开(公告)号:AU2005237235A1
公开(公告)日:2005-11-10
申请号:AU2005237235
申请日:2005-04-23
Applicant: BASF AG
Inventor: GEWEHR MARKUS , STIERL REINHARD , MULLER BERND , NIEDENBRUCK MATTHIAS , SCHERER MARIA , GROTE THOMAS , SCHOFL ULRICH , BLASCO JORDI TORMO I , SUAREZ-CERVIERI MIGUEL OCTAVIO , STRATHMANN SIEGFRIED
IPC: A01N43/653
Abstract: A fungicidal composition (A) comprising synergistic amounts of a 3-indolylsulfonyl-1-aminosulfonyl-triazole derivative (I) and a second active agent (2), is new. Fungicidal composition (A) comprising synergistic amounts of a 3-indolylsulfonyl-1-aminosulfonyl-triazole derivative of formula (I) and a second active agent (2), where (2) is any of: azoles (e.g. cyproconazole, difenoconazole, enilconazole, epoxiconazole, fluquiconazole, flusilazol, hexaconazole, imazalil, metconazole, mycolbutanil, penconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol or triflumizole); strobilurines (e.g. azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, cresoxime-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin or trifloxystrobin); acylalanines (e.g. benalaxyl, metalaxyl, mefenoxam, ofurace and oxadixyl); amine derivatives, e.g. spiroxamine; aniliniopyrimidines (e.g. pyrimethanil, mepanipyrim or cyprodinil); dicarboximides (e.g. iprodione, procymidone or vinclozolin); cinnamic acid amide and analogs (e.g. dimethomorph, flumetover or flumorph); dithiocarbamates (e.g. ferbam, nabam, maneb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb); heterocyclic compounds (e.g. benomyl, boscalide, carbendazim, dithianon, famoxadon, fenamidon, pentiopyrad, quinoxyfen, thiophanate-methyl, triforine); 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine (II); sulfur or copper fungicides (e.g. Bordeaux mixture, copper acetate, copper oxychloride or basic copper sulfate); nitrophenyl derivatives (e.g. dinocap); phenylpyrroles (e.g. fenpiclonil or fludioxonil); sulfenic acid derivatives (e.g. captafol, dichlorofluanide or tolylfluanide); other fungicides (e.g. benthiavalicarb, chlorothalonil, cyflufenamide, diclofluanide, ethaboxam, fenhexamide, fluazinam, iprovalicarb, namdipropamide, metrafenon, zoxamide); oxime-ether derivatives of formula (III) or heterocyclic compounds of formula (IV). R 1>= hydrogen, halo, cyano, 1-4C alkyl, alkoxy, alkylthio or alkoxycarbonyl, 1-2C haloalkyl, phenyl, benzyl, formyl or CH=NOA; A in (I)= hydrogen, 1-4C alkyl or alkylcarbonyl; R 2>= hydrogen, halo, cyano, 1-4C alkyl, 1-2C haloalkyl or 1-6C alkoxycarbonyl; R 3>= halo, cyano, nitro, 1-4C alkyl, alkoxy, alkylthio or alkoxycarbonyl, 1-2C haloalkyl, formyl or CH=NOA; n in (I)= 0-4; R 4>= hydrogen, halo, cyano, 1-4C alkyl or 1-2C haloalkyl; X= 1-4C haloalkoxy; n in (III)= 0-3; R= halo, 1-4C (halo) alkyl or (halo)alkoxy; A in (IV)= O or N; B= N or direct bond; G= C or N; R 41>= 1-4C alkyl; R 42>= 1-4C alkoxy; and R 43>= halo. An independent claim is also included for seeds treated with 1-1000 g (A) per 100 kg. [Image] [Image] [Image] ACTIVITY : Plant Antifungal. MECHANISM OF ACTION : None given.
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公开(公告)号:AU2005221805A1
公开(公告)日:2005-09-22
申请号:AU2005221805
申请日:2005-03-08
Applicant: BASF AG
Inventor: BLASCO JORDI TORMO I , GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , HUNGER UDO , SCHWOGLER ANJA , SCHAFER PETER , GEWEHR MARKUS , WAGNER OLIVER , NIEDENBRUCK MATTHIAS , BLETTNER CARSTEN , MULLER BERND , STIERL REINHARD , SCHIEWECK FRANK , GROTE THOMAS , SCHOFL ULRICH , SCHERER MARIA , STRATHMANN SIEGFRIED
IPC: C07D487/04
Abstract: The invention relates to 5,6 -dialkyl- 7 -amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R 1 represents alkyl, alkoxyalkyl, alkenyl or alkynyl; R 2 represents alkyl, alkoxyalkyl, alkenyl or alkynyl, R 1 and/or R 2 being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
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