醋酸巴多昔芬的合成工艺改进 |
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作者姓名: | 张春来 姜琦 宣景安 李国贤 |
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作者单位: | 扬子江药业集团有限公司,扬子江药业集团有限公司,扬子江药业集团有限公司,扬子江药业集团有限公司 |
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摘 要: | 目的:改进醋酸巴多昔芬的合成工艺。方法:以对羟基苄醇和环己亚胺基乙基氯盐酸盐为起始原料,经过亲核取代、氯代得到侧链,4-苄氧基苯丙酮和4-苄氧基苯肼盐酸盐经缩合得母核,侧链和母核缩合后,经成盐,氢解、中和,与乙酸成盐总计6步得目标化合物。结果:目标化合物经质谱、核磁共振确证其结构。总收率可达53%,产品HPLC纯度99.5%以上。结论:改进后的工艺步骤大大缩短,且操作简单,收率和纯度较高,适合工业化生产。
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关 键 词: | 醋酸巴多昔芬 选择性雌激素受体调节剂 骨质疏松症 合成工艺 |
收稿时间: | 2014/8/4 0:00:00 |
修稿时间: | 2014/10/20 0:00:00 |
An improved process for synthesis of bazedoxifene acetate |
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Institution: | Yangtze River Pharmaceutical Group Co.,Ltd.,Yangtze River Pharmaceutical Group Co.,Ltd.,Yangtze River Pharmaceutical Group Co.,Ltd. |
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Abstract: | Objective: To improve the synthetic process of bazedoxifene acetate. Methods: The side chain was synthesized from 4-hydroxybenzyl alcohol and 2-(hexamethyleneimino) ethyl chloride hydrochloride as starting materials through nucleophilic substituent and chlorination. The stemnucleus was obtained by condensation taking 4-Benzyloxypropiophenone and 4-Methoxyphenylhydrazine hydrochloride as raw materials; The side chain and the stemnucleus were condensed and process by acidification, hydrogenolysis, neutralization and acidification with acetic acid to get the target compound via total six steps. Result: The structure of the target compound was confirmed by MS and 1H-NMR. The total yield was 53%, and the HPLC purity was more than 99.5%. Conclusion: The improved process with short steps, simple operation, good yield and purity is feasible for industralization. |
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Keywords: | bazedoxifene acetate selective estrogen receptor momulator synthetic process |
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