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4-(6-脱氧-β-D-吡喃葡萄糖基)-1-甲氧基-2-【(反式-4-正丙基环己基)甲基】苯的合成及其晶型研究.
引用本文:汪文锦,谢亚非,刘钰强,魏鹏,高志刚,汤立达,徐为人,赵桂龙.4-(6-脱氧-β-D-吡喃葡萄糖基)-1-甲氧基-2-【(反式-4-正丙基环己基)甲基】苯的合成及其晶型研究.[J].国外医药(植物药分册),2014(1):1-5.
作者姓名:汪文锦  谢亚非  刘钰强  魏鹏  高志刚  汤立达  徐为人  赵桂龙
作者单位:天津医科大学药学院;天津药物研究院天津市药物设计与发现重点实验室;齐鲁工业大学化学与制药工程学院;
基金项目:国家自然科学基金资助项目(21302141);天津市科技计划项目(10ZCKFSH01300)
摘    要:目的寻找一条合成目标化合物4-(6-脱氧-β-D-吡喃葡萄糖基)-1-甲氧基-2-【(反式-4-正丙基环己基)甲基】苯的简易路线,并研究其晶型。方法利用苯基溴化物片段和6-脱氧葡萄糖酸内酯片段作为起始原料合成目标化合物;采用有机混合溶剂和含水混合溶剂结晶的方式制备目标化合物的晶型,采用粉末X射线衍射分析和热重-差热分析技术对其进行表征,并对其进行了初步稳定性研究。结果目标化合物的总收率为74%,通过上述制备方法获得了同一种晶型,该晶型对光、热和湿均是稳定的。结论设计了一条合成目标化合物的简易路线,该路线操作简便、路线短、收率高,并制备了一种具有良好稳定性的目标化合物的晶型。

关 键 词:4-(6-脱氧-β-D-吡喃葡萄糖基)-1-甲氧基-2-【(反式-4-正丙基环己基)甲基】苯  苯基溴化物  6-脱氧葡萄糖酸内酯  晶型

Synthesis of 4-(6-deoxy-β-D-glucopyranosyl)-l-methosyl-2-[(trans-4-n- propylcyclohexyl) methyl] benzene and its polymorphic characteristics
Authors:WANG Wen-jin  XIE Ya-fei  LIU Yu-qiang  WEI Peng  GAO Zhi-gang  TANG Li-da  XU Wei-ren  ZHAO Gui-long
Institution:1. School of Pharmacy, Tianjin Medical University, Tianjin 300070, China 2. Tianjin Key Laboratory of Molecular Design and Drug Discovery, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, China 3. School of Chemical and Pharmaceutical Engineering, Qilu University of Technology, Jinan 250353, China)
Abstract:Abstract: Objective To search for a facile synthetic route for synthesis of target compound 4-(6-deoxy-β-D-glucopyranosyl)-l- methosyl-2-(trans-4-n-propylcyclohexyl)methyl] benzene and to study its polymorphic characteristics. Methods A phenyl bromide fragment and 6-deoxygluconolactone fragment were used as starting materials to synthesize the target compound. Polymorph of target compound was prepared from organic mixed solvents and aqueous mixed solvents, and was characterized by powder X ray diffraction (PXRD), and thermogravimetric analysis coupled with differential thermal analysis (TG-DTA), and the preliminary stability properties of the polymorph was also studied. Results The total yield of target compound was 74%. The same polymorph of the target compound was obtained by the above methods, and was stable to light, heat, and moisture. Conclusion A facile synthetic route for synthesis of target compound is developed, which has the advantages of simple operating procedure, easy post-processing and high yield, and a stable polymorph of target compound is obtained.
Keywords:4-(6-deoxy-β-D-glucopyranosyl)-l-methosyl-2-[(trans-4-n-propylcyclohexyl) methyl] benzene  phenyl bromide  6-deoxygluconolactone  polymorph
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