Synthetic process of telavancin
Xiong Lun2; Guan Dongliang1; Li Jian2; Huang Wei1
刊名Journal of China Pharmaceutical University
2017
卷号48期号:2页码:172-177
关键词vancomycin telavancin synthetic process
ISSN号1000-5048
其他题名特拉万星合成工艺研究
文献子类Article
英文摘要New process reported the synthesis of telavancin using decyl alcohol as the starting material.After methanesulfonylation,nucleophilic substitution with ethanolamine,Fmoc protection,and Parikh-Doering oxidation,the intermdiate N-(9-fluorenyl-9-methoxycarbonyl) decylaminoethyl acetaldehyde (5) was obtained.Vancomycin hydrochloride and intermediate 5 were then subject to reductive amination reaction,Fmoc deprotection,and Mannich reaction to give the telavancin product.The process have been deeply studied on the two key reactions of reductive amination and Mannich reaction,and the reaction conditions have been optimized.The overall yield is 46% based on starting material vancomycin.
资助项目国家自然科学基金资助项目[00000000]
WOS研究方向Pharmacology & Pharmacy (provided by Clarivate Analytics)
语种中文
CSCD记录号CSCD:5964872
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/269208]  
专题药物安全性评价中心
作者单位1.Shanghai Institute of Materia Media,Chinese Academy of Sciences, Shanghai 201203, China.
2.College of Pharmacy,East China University of Science and Technology, Shanghai 200237, China.;
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GB/T 7714
Xiong Lun,Guan Dongliang,Li Jian,et al. Synthetic process of telavancin[J]. Journal of China Pharmaceutical University,2017,48(2):172-177.
APA Xiong Lun,Guan Dongliang,Li Jian,&Huang Wei.(2017).Synthetic process of telavancin.Journal of China Pharmaceutical University,48(2),172-177.
MLA Xiong Lun,et al."Synthetic process of telavancin".Journal of China Pharmaceutical University 48.2(2017):172-177.
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