卡罗合成亚甲基蓝的机理研究

F. Sánchez-Viesca, Reina Gómez
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引用次数: 6

摘要

最近对亚甲基蓝作为一种有前途的药物治疗几种重要疾病的新应用的兴趣促使我们填补了与该化合物相关的未知方面。由于目前还没有卡罗合成亚甲基蓝的机理,我们提供了从N,N-二甲基苯基二胺到二苯并噻嗪衍生物的电子流,一步一步的。由于氯化铁的氧化性,它是一个自由基生成系统。我们指出了与硫化氢发生的替代反应,硫化氢是形成噻嗪环的还原剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On the Mechanism of the Caro Synthesis of Methylene Blue
The recent interest for new applications of methylene blue as a promising drug for several important ailments prompted us to fill unknown aspects related to this compound. Since there is no mechanism on the Caro synthesis of methylene blue, we provide the electron flow, step by step, from the starting N,N-dimethylphenylenediamine to the dibenzothiazine derivative. It is a free radical generation system due to the oxidizing properties of ferric chloride. We pointed out the alternative reactions that take place with hydrogen sulphide, the reducer from which the thiazine ring is formed.
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