摘要
通过氯化、酯化反应合成了β内酰胺类抗生素———头孢泊肟酯4位侧链1氯乙基异丙基碳酸酯,产品纯度达90%,收率为50%,接近文献值,工艺简单,适于工业化生产.
As an intermediate at the 4th position of the side chain of Cefpodoxime Proxetil,1chloroethyl isopropyl carbonate was synthesized by two steps: chlorination and esterification.The yield was 50%,and the purity was up to 90%which has never been reported.The process may be easily used in industry.
出处
《沈阳药科大学学报》
CAS
CSCD
1998年第3期206-207,共2页
Journal of Shenyang Pharmaceutical University
关键词
头孢泊肟酯
氯乙基
异丙基碳酸酯
侧链
cefpodoxime proxetil
1chloroethyl chloroformate
1chloroethyl isopropyl carbonate