发明申请
US20080248952A1 Substituted 6-Phenyl-7-Aminotriazolopyrimidines, Method for the Production Thereof, Their Use for Controlling Pathogenic Fungi, and Agents Containing These Compounds
审中-公开
取代的6-苯基-7-氨基三唑并嘧啶,其制备方法,其用于控制致病真菌和含有这些化合物的试剂
- 专利标题: Substituted 6-Phenyl-7-Aminotriazolopyrimidines, Method for the Production Thereof, Their Use for Controlling Pathogenic Fungi, and Agents Containing These Compounds
- 专利标题(中): 取代的6-苯基-7-氨基三唑并嘧啶,其制备方法,其用于控制致病真菌和含有这些化合物的试剂
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申请号: US11631004申请日: 2005-07-06
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公开(公告)号: US20080248952A1公开(公告)日: 2008-10-09
- 发明人: Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
- 申请人: Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
- 申请人地址: DE Ludwigshafen
- 专利权人: BASF Aktiengesellschaft
- 当前专利权人: BASF Aktiengesellschaft
- 当前专利权人地址: DE Ludwigshafen
- 优先权: DE102004033239.8 20040708
- 国际申请: PCT/EP2005/007277 WO 20050706
- 主分类号: C07D487/04
- IPC分类号: C07D487/04 ; A01N43/90 ; A01N25/00
摘要:
Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, 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, R2 is hydrogen or a group R1, R1 and R2 together with the nitrogen atom, to which they are attached, may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and which may comprise one to three further heteroatoms from the groups consisting of O, N and S as ring member and/or may be substituted according to the description; L is fluorine, chlorine or methyl; X is cyano, C1-C4-alkyl, C1-C4-alkoxy or C1-C2-haloalkoxy, where X is not methyl if R1 and R2 together are n-pentylene or 3-methyl-n-pentylene and L is fluorine, or R1 and R2 together are 3-methyl-n-pentylene and L is chlorine; processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
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