Practical Synthesis of N-anilinyl phenothiazines using a cyclic hypervalent iodine coupling reagent

Synthesis Pub Date : 2024-08-08 DOI:10.1055/a-2383-0958
Kana Yanase, K. Morimoto, T. Dohi, Y. Kita
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Abstract

An improved protocol for the synthesis of N-anilinylphenothiazines based on the coupling reaction of anilines with phenothiazines using cyclic iodine(III) reagents is presented in this study. In the improved method, the product can be isolated and purified without using column chromatography, and the cyclic hypervalent iodine reagent can be quantitatively recovered by aliquot manipulation. Our workup procedure is simpler compared to previously reported ones, facilitating large-scale synthesis. We also successfully performed the para-selective phenothiazination of nitrogen-containing heterocycles such as hydroquinoline, which is important in pharmacology.
使用环状高价碘偶联试剂合成 N-苯胺基吩噻嗪的实用方法
本研究提出了一种基于苯胺与吩噻嗪的偶联反应的 N-苯胺基吩噻嗪的改进合成方法,该方法使用环状碘(III)试剂。在改进的方法中,无需使用柱层析即可分离和纯化产物,并可通过等分操作定量回收环状高价碘试剂。与之前报道的方法相比,我们的操作步骤更简单,有利于大规模合成。我们还成功地进行了氢喹啉等含氮杂环的对位选择性吩噻嗪化反应,这在药理学中非常重要。
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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