摘要
以氯乙酸乙酯为起始原料,经过格氏反应、还原、铵化、水解及拆分等五步反应,合成了左旋肉毒碱盐酸盐。优点是避开有毒的氰化物或氯化汞,且无需离子交换树脂.操作安全、简单。
l-Carnitine hydrochloride was synthesized primarily from chloroethyl acetate via the Grignard reaction,reducton,amination, hydrolysis and resolution. The dibenzoyl-d-tartaric acid was used as a resolutive agent. By this method,a poisonous cyanide or mercuric chloride could be avoided ,and basic ion-exchange resin could be avoided, too.
出处
《中国药物化学杂志》
CAS
CSCD
1995年第4期276-278,共3页
Chinese Journal of Medicinal Chemistry
基金
上海市科学技术发展基金
关键词
肉毒碱盐酸盐
合成
药物化学
Carnitine hydrochloride
Synthesis
Resolution