药学研究
藥學研究
약학연구
JOURNAL OF PHARMACEUTICAL RESEARCH
2014年
8期
492-493
,共2页
亚胺培南%合成%缩合%催化氢化
亞胺培南%閤成%縮閤%催化氫化
아알배남%합성%축합%최화경화
ImiPenem%Synthesis%Condensation%Catalytic hydrogenation
目的:合成亚胺培南。方法以碳青霉烯双环母核为起始原料,磷酰化后直接与巯基乙胺盐酸盐反应,所得产物经偶联,氢化得亚胺培南。结果亚胺培南工艺总收率62%,纯度98.6%。结论本工艺操作简单,收率高,纯度好,适合工业化生产。
目的:閤成亞胺培南。方法以碳青黴烯雙環母覈為起始原料,燐酰化後直接與巰基乙胺鹽痠鹽反應,所得產物經偶聯,氫化得亞胺培南。結果亞胺培南工藝總收率62%,純度98.6%。結論本工藝操作簡單,收率高,純度好,適閤工業化生產。
목적:합성아알배남。방법이탄청매희쌍배모핵위기시원료,린선화후직접여구기을알염산염반응,소득산물경우련,경화득아알배남。결과아알배남공예총수솔62%,순도98.6%。결론본공예조작간단,수솔고,순도호,괄합공업화생산。
Objective To synthesize imiPenem. Methods ImiPenem was PrePared from bicyclic keto ester,reacting with cysteamine hydrochloride after PhosPhrylation,then through the reaction of condensation,and catalytic hydrogenation. Results The Process had been successfully imPlemented to PrePare the target comPound in 62% overall yield and 98. 6% area Purity. Conclusion This Process was more suitable for industrial Production with simPle oPeration,high Purity and high yield.