...
首页> 外文期刊>International Research Journal of Pure and Applied Chemistry >Synthesis and Characterization of Impurities of aCommon and Advanced Intermediate ofCandesartan and Azilsartan Antihypertensive Drugs
【24h】

Synthesis and Characterization of Impurities of aCommon and Advanced Intermediate ofCandesartan and Azilsartan Antihypertensive Drugs

机译:坎地沙坦和奥美沙坦降压药的普通和高级中间体的杂质的合成与表征

获取原文
           

摘要

Six impurities were identified in the lab development batches during the course of benzimidazole intermediate (1) synthesis by reverse phase HPLC method. Intermediate 1 is used as a common and advanced intermediate in the synthesis of candesartan and azilsartan. All the impurities were characterized by IR, NMR, LC/MS and CHN analyses, which included an isomer of intermediate 11 (impurity 19), desethyl analogue of 1 (impurity 20), desethoxy analogue of 1 (impurity 21), methyl analogue of 1 (impurity 22), cyanobiphenyl benzimidazole (impurity 25) and cyanobiphenyl derivative of 1 (impurity 26). The synthesis and characterization of these impurities are presented.
机译:在苯并咪唑中间体(1)合成过程中,通过反相HPLC方法在实验室开发批次中鉴定出六种杂质。中间体1在坎地沙坦和阿齐沙坦的合成中用作常见的高级中间体。所有杂质均通过IR,NMR,LC / MS和CHN分析进行表征,包括中间体11(杂质19)的异构体,1(杂质20)的去乙基类似物,1(杂质21)的去乙氧基类似物,1(甲基)21的甲基类似物。 1(杂质22),氰基联苯苯并咪唑(杂质25)和氰基联苯衍生物1(杂质26)。介绍了这些杂质的合成和表征。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号