发明名称 |
Process for preparing tetrazole-substituted anthranilamide derivatives and novel crystal polymorphs of these derivatives |
摘要 |
The present invention relates to a process for preparing tetrazole-substituted anthranilamide derivatives of the formula (I);
in which R1, R2, R3, R4, R5 and Z are each as defined in the description, and to a novel crystal polymorph of these derivatives and to the use thereof in agrochemical formulations. |
申请公布号 |
US8969572(B2) |
申请公布日期 |
2015.03.03 |
申请号 |
US201113159961 |
申请日期 |
2011.06.14 |
申请人 |
Bayer Cropscience AG |
发明人 |
Pazenok Sergii;Lui Norbert;Volz Frank;Olenik Britta;Funke Christian;Fischer Rüdiger;Gaertzen Oliver;Hinz Martin-Holger;Neeff Arnd |
分类号 |
C07D401/14 |
主分类号 |
C07D401/14 |
代理机构 |
Miles & Stockbridge PC. |
代理人 |
Miles & Stockbridge PC. |
主权项 |
1. A process for preparing a compound of formula (I), or a N-oxide or a salt thereofin which
R1, R3 are each independently C1-C5-alkyl, R2 is halogen R4 is hydrogen, chlorine, or cyano, R5 is (C1-C3)perfluoroalkyl, Z is N, said process comprising reacting an N-aryl- and N-hetaryl-substituted pyrazole of formula (II) in which R is C1-C6-alkyl, aryl(C1-C6)alkyl or aryl and X is fluorine, chlorine, bromine, iodine, CH3SO2O, CF3SO3, or p-CH3—C6H4SO3, with a tetrazole of formula (III) to give a pyrazolecarboxylic ester of formula (IV) in which the latter are optionally hydrolysed under acidic or basic conditions without preceding isolation to a pyrazolecarboxylic acid of formula (V) and the latter are reacted with a compound of the formula (VI) to give an anthranilamide of the formula (I) |
地址 |
Monheim DE |