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头孢西丁钠的合成 被引量:4

Synthesis of Cefoxitin Sodium
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摘要 头孢西丁是一种具有长效、广谱抗菌特点的第二代头孢类抗生素。本文以头孢噻吩酸为原料,甲氧基化产物不需结晶提纯而直接用于去乙酰化,缩短了生产周期和节省了原料。本方法制备简便,适于工业化生产。 Cefoxitin, the second -generation cephalosporins, is permanence and has a broad spectrum of antibacterial activity . In this paper, starting from cephalotin, the cefoxitin was obtained via 3 steps including methoxylation, deacetylation and carbamoylation. The poduct of methoxylation could be used for deacetylation without crystallition and purification, and the materials were redused and production cycle was shorten. The method is simple and convenient and can be scaled up to indusrtrial production.
出处 《山东化工》 CAS 2008年第12期18-19,共2页 Shandong Chemical Industry
关键词 头孢噻吩 头孢西丁钠 合成 次氯酸叔丁酯 异辛酸钠 cephalotin cefoxitin sodium synthesis tert - butyl hypochlorite sodium 2 - ethylhexanoate
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  • 1卢红代,王超,魏曾光,等.头孢西丁钠的制备方法:中国,101235045A[P].2008-08-06.
  • 2Deshpande P B, Khadangale B P. Process for the preparation of cefoxitin: US, 2006252928 [ P ]. 2006 - 11 -09.
  • 3Manca A (IT) ,Monguzzi R (IT), Zenoni M (IT), et al. Process for preparing cefoxitin : EP, 1748049 A2 [ P]. 2007 -01 -31.
  • 4谭端明,张黎辉,叶澄海.抗菌药物头孢西丁的合成:中国,101007812A[P].2007-08-01.
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