阿哌沙班关键中间体的实用综述

Wenwen Dong, Tengfei Gong, Chaoyang Liu, Jia Lin, Qiang Jia, Changhu Chu
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摘要

阿哌沙班是一种高效、选择性和有效的凝血因子Xa抑制剂。开发了一种实用高效的阿哌沙班关键中间体的制备工艺。从廉价的4-氯硝基苯和哌啶开始,开发了一个八步的中间体工艺。在这种情况下,使用亚氯酸钠两次在CO2气氛下将哌啶循环氧化为相应的内酰胺,从而构建两个内酰胺。此外,这些反应大多是在温和的条件下进行的,效率高,实用性强。大部分中间体可通过简单的浆液或再结晶得到,不需要柱层析纯化。图形抽象
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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A practical synthesis for the key intermediate of apixaban

Apixaban is a highly potent, selective, and efficacious inhibitor of blood coagulation factor Xa. A practical and efficient process has been developed for the preparation of the key intermediate of apixaban. Starting from inexpensive 4-chloronitrobenzene and piperidine, an eight-step procedure for the intermediate has been developed. In this case, sodium chlorite is used twice to oxidize the piperidine cycle to the corresponding lactam under a CO2 atmosphere, resulting in the construction of two lactams. Furthermore, most of these reactions are highly efficient and practical as they occur under mild conditions. Most of the intermediates can be obtained through simple slurry or recrystallization, and column chromatography purification is not necessary.

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