摘要
本文以对硝基苯乙胺及取代苯甲醛为原料,经席夫氏碱还原,N取代反应、铁粉盐酸还原硝基、甲烷磺酰化五步反应,设计合成了12个甲烷磺酰胺苯乙胺类衍生物。初步药理研究结果表明,这些化合物显示不同程度的抗心律失常活性。
Started from pnitrophenylethylamine and varied substituted benzaldehydes, twelve Nsubstituted methylsulfonamido phenylethylamino derivatives were designed and synthesized through five step chemical reactions. Their chemical structures were determined by IR, 1HNMR and MS. The pharmacological study showed that the target compounds exhibit antiarrhythmic activity to varying degrees in arrhythmic rats induced by aconitine.
出处
《中国药科大学学报》
CAS
CSCD
北大核心
1998年第3期161-166,共6页
Journal of China Pharmaceutical University
基金
江苏省应用基础研究项目
关键词
甲烷磺酰胺苯乙胺
Ⅲ类抗心律失常药
合成
Methylsulfonamidophenylethylamino
Class Ⅲ antiarrhythmic agents
Synthesis