Cocrystal of Codeine and Cyclopentobarbital

IF 0.6 Q4 CHEMISTRY, ORGANIC
Molbank Pub Date : 2023-09-11 DOI:10.3390/m1722
Thomas Gelbrich, Jascha Schinke, Ulrich J. Griesser
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引用次数: 0

Abstract

The two-component compound formed by codeine and cyclopentobarbital was produced using grinding techniques and through evaporation from alcoholic solutions. The cocrystal nature of this phase was established unequivocally through single crystal X-ray structure determination. The asymmetric unit contains one formula unit. In the cyclopentobarbital molecule, the cyclopentenyl ring is disordered over two positions related by a rotation of approximately 180° about its C—C bond to the pyrimidine ring. The two NH groups of the cyclopentobarbital molecule form N—H⋯N and N—H⋯O bonds to piperidine and hydroxyl groups, respectively, belonging to different codeine molecules. In addition, the hydroxyl and methoxy groups of neighboring codeine molecules are linked by O—H⋯O interactions, resulting in a H-bonded framework structure of codeine and cyclopentobarbital molecules. The cocrystal was also characterized using thermal analysis, X-ray powder diffraction and IR spectroscopy.
可待因与环戊巴比妥共晶
这种由可待因和环戊巴比妥组成的双组分化合物是通过研磨技术和从酒精溶液中蒸发得到的。通过单晶x射线结构测定,明确确定了该相的共晶性质。非对称单元包含一个公式单元。在环戊巴比妥分子中,环戊基环在两个位置上是无序的,这两个位置是围绕其C-C键与嘧啶环旋转约180°。环戊巴比妥分子的两个NH基团分别与属于不同可待因分子的哌啶和羟基形成N - h⋯N和N - h⋯O键。此外,邻近的可待因分子的羟基和甲氧基通过O - h⋯O相互作用连接,形成可待因和环戊巴比妥分子的h键框架结构。并用热分析、x射线粉末衍射和红外光谱对共晶进行了表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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