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维库溴铵的合成工艺改进 被引量:3

Improved synthesis of vecuronium bromide
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摘要 以表雄酮为原料经磺酸酯化、消去、酯化、氧化、开环、还原、乙酰化,最后和溴甲烷成盐等8步反应合成维库溴铵,操作简捷、条件温和、成本低,适合工业化生产,产品结构经红外光谱、核磁共振谱、质谱确证,总收率19.6%。 Vecuronium bromide was synthesized from epiandrosterone through esterification, elimination, oxidation, ring opening, reduction, and acetylation, followed by reaction with bromomethane. This cost-saving and simplified method can be used in the commercial scale manufacture. The structure of this product was elucidated by IR, ^1HNMR, ^13CNMR, DEPT and MS, with an overall product yield reaching 19.6%.
出处 《化学试剂》 CAS CSCD 北大核心 2009年第7期568-570,共3页 Chemical Reagents
基金 徐州市科技局自然科学基金资助项目(XJ07066) 江苏省大型科学仪器设备共享服务平台理事会资助项目 徐州师范大学自然科学研究基金资助项目(07XLB20)
关键词 维库溴铵 肌松药 非去极化 合成 vecuronium bromide muscle relaxants non depolarizing synthesis
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参考文献6

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