马来酰亚胺衍生物及苯并[1,4]氧烷衍生物的合成:含胺类药物的改性方法

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Lu Yin, , , Meitian Fu, , , Sihan Zhao, , , Qiong Wu, , , Ruize Jiang, , and , Chao Huang*, 
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引用次数: 0

摘要

马来酰亚胺修饰的药物分子可以提高药物的稳定性和选择性释放。本研究开发了一种易于操作、温和、安全的合成药物分子修饰策略。该策略利用了底物氨基酰亚胺和各种含胺分子在无催化剂条件下易于取代的特性。此法适用于各种类型的伯胺和仲胺。当与n -甲基苄胺反应时,通过温度调节可得到苯并[1,4]恶氮杂烷衍生物。同时,该方法对底物官能团具有良好的耐受性,获得了7个马来酰亚胺修饰的药物分子片段,产率较高(80-85%)。本文证实了用该方法修饰的药物分子仍然具有活性反应位点,可以进一步修饰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of Maleimide Derivatives and Benzo[1,4]oxetane Derivatives: a Modification Method of Amine-Containing Pharmaceuticals

Synthesis of Maleimide Derivatives and Benzo[1,4]oxetane Derivatives: a Modification Method of Amine-Containing Pharmaceuticals

Maleimide-modified drug molecules can improve the stability and selective release of drugs. This study developed an easy-to-operate, mild, and safe synthetic drug-molecule modification strategy. This strategy employs the easily substituted characteristics of the substrate aminomaleimide and various amine-containing molecules under catalyst-free conditions. This method is suitable for various types of primary amines and secondary amines. When reacting with N-methylbenzylamine, benzo[1,4]oxazepane derivatives can be obtained by temperature adjustment. At the same time, the method has good tolerance for substrate functional groups, and 7 maleimide-modified drug molecular fragments were obtained in high yield (80–85%). This article has confirmed that the drug molecules modified by this method still have active reaction sites and can be further modified.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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