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A novel method for the preparation of crystalline perindopril erbumine

机译:一种制备培哚普利晶状蛋白精的新方法

摘要

A process for preparation of crystalline perindopril erbumine of formula (II) which exhibits the X-ray (powder) diffraction pattern like that shown in FIG. 2 The process comprises reacting a solution of perindopril of formula (I), in a solvent selected from N,N-dimethylformamide, dimethyl acetals of lower aliphatic aldehydes, dimethyl ketals of lower aliphatic ketones and 1,2-dialkoxyethane with tertiary butylamine and crystallization of the erbumine salt thus obtained by heating the reaction mixture to reflux, filtering hot, cooling gradually to 20° C. to 30° C., and further cooling to 0° C. to 15° C. for 30 minutes to 1 hour and finally filtering off and drying the crystals.
机译:制备式(II)的培哚普利晶状精蛋白的方法,该方法表现出如图3所示的X射线(粉末)衍射图。 2该方法包括使式(I)的培哚普利的溶液在选自N,N-二甲基甲酰胺,低级脂族醛的二甲基缩醛,低级脂族酮的二甲基缩酮和1,2-二烷氧基乙烷的溶剂中与叔丁胺反应并结晶通过加热反应混合物至回流,热过滤,逐渐冷却至20℃至30℃,并进一步冷却至0℃至15℃持续30分钟至1小时,从而获得所得到的精胺盐。最后过滤并干燥晶体。

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