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抗骨质疏松药雷尼酸锶的合成
引用本文:丁翔宇,蒋晔,贾湘曼,刘丰华.抗骨质疏松药雷尼酸锶的合成[J].中国药学杂志,2008,43(11):874-876.
作者姓名:丁翔宇  蒋晔  贾湘曼  刘丰华
作者单位:河北医科大学药学院,石家庄,050017
摘    要: 目的研究雷尼酸锶的化学合成。方法以枸橼酸为起始原料,经过脱羧、酯化、环合、烷基化、水解成盐等多步反应生成终产物雷尼酸锶。结果雷尼酸锶的结构经IR,1H-NMR,13C-NMR得到证实,总产率约为42.6%。结论本合成路线操作简单、成本低,适合工业化生产。

关 键 词:雷尼酸锶  合成  骨质疏松
文章编号:1001-2494(2008)11-0874-03
收稿时间:2007-02-11;
修稿时间:2007年2月11日

Synthesis of Strontium Ranelate, an Antiosteoporosis Drug
DING Xiang-yu,JIANG Ye,JIA Xiang-man,LIU Feng-hua.Synthesis of Strontium Ranelate, an Antiosteoporosis Drug[J].Chinese Pharmaceutical Journal,2008,43(11):874-876.
Authors:DING Xiang-yu  JIANG Ye  JIA Xiang-man  LIU Feng-hua
Affiliation:Institute of Pharmacy,Hebei Medical University,Shijiazhuang 050017,China
Abstract:OBJECTIVE To study the synthesis route of strontium ranelate,an antiosteoporosis drug.METHODS Strontium ranelate was synthesized from citric acid via decarboxylation,esterification,cyclization,alkylation,hydrolysis and salification.RESULTS The structure of strontium ranelate was confirmed by IR,1H-NMR,13C-NMR,the total yield was 42.6% approximately.CONCLUSION The synthesis route was simple,low cost and could be used in industry.
Keywords:strontium ranelate  synthesis  osteoporosis
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