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New crystalline forms of Racemic and Homochiral Atenolol with Cinnamic Acid

机译:新的结晶形式的外消旋和冠单编纂含有肉桂酸

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R- and S-Atenolol crystallize as a solid solution from which it is difficult to separate the enantiomers. Both RS- and R-Atenolol form a new crystalline phase in the presence of sufficient amounts of cinnamic acid in ethanol. The XRPD patterns of RS-Atenolol/Cinnamic acid and R-Atenolol/Cinnamic acid acid show distinct features indicating that these new crystalline phases have distinct crystalline structures. The solvent mediated transformation indicates considerable morphological differences between the two new crystalline phases. It is possible that the Atenolol solid solution is transformed into a racemic/homochiral crystal system via adduction with cinnamic acid. Other co-builders might change it to a conglomerate system.
机译:R-和S- ateoolol作为固溶体结晶,从中难以分离对映体。 RS-和R- ateNolol两者都在乙醇中存在足够量的肉桂酸存在的新结晶相。 RS-Atenolol /肉桂酸和R-·阿托啉/肉桂酸酸的XRPD模式显示出明显的特征,表明这些新的结晶相具有不同的晶体结构。溶剂介导的转化表明两种新的结晶相之间具有相当大的形态学差异。通过用肉桂酸的内加,可以将阿扎洛尔固体溶液转化为外消旋/冠细胞晶体系统。其他共建者可能会将其改变为集团系统。

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