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赛红霉素的合成工艺

Synthesis process of Cethromycin
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摘要 目的改进赛红霉素的合成工艺。方法以红霉素A为原料,经肟化、酯化、烃基化、脱保护、脱肟、环氨甲酸酯化、酸水解、氧化和去保护等10步反应合成目标化合物。结果和结论改进后的方法操作简便,成本降低。 OBJECTIVE To improve the synthetic process of Cethromycin(ABT-773).METHODS The target compound was synthesized through oximation,esterification,alkylation,deprotection,deoximation,cyclocarbamation,acid hydrolysis,oxidation and deprotection from erythromycin A.RESULTS and CONCLUSION Cethromycin was synthesized successfully.Modified method has the advantages of simple manipulation,lower cost.
出处 《华西药学杂志》 CAS CSCD 北大核心 2011年第1期20-23,共4页 West China Journal of Pharmaceutical Sciences
关键词 大环内酯类抗生素 酮内酯 赛红霉素 合成 Macrolide antibiotics Ketolide Cethromycin Synthesis
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参考文献9

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