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威伦贝酰胺法在瑞德西韦关键中间体的实用合成中的应用。

Weinreb Amide Approach to the Practical Synthesis of a Key Remdesivir Intermediate.

机构信息

Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, P. R. China.

Key Laboratory of Plant Resources and Chemistry in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, South Beijing Road 40-1, Urumqi, Xinjiang 830011, P. R. China.

出版信息

J Org Chem. 2021 Apr 2;86(7):5065-5072. doi: 10.1021/acs.joc.0c02986. Epub 2021 Mar 18.

Abstract

Currently, remdesivir is the first and only FDA-approved antiviral drug for COVID-19 treatment. Adequate supplies of remdesivir are highly warranted to cope with this global public health crisis. Herein, we report a Weinreb amide approach for preparing the key intermediate of remdesivir in the glycosylation step where overaddition side reactions are eliminated. Starting from 2,3,5-tri--benzyl-d-ribonolactone, the preferred route consisting of three sequential steps (Weinreb amidation, -TMS protection, and Grignard addition) enables a high-yield (65%) synthesis of this intermediate at a kilogram scale. In particular, the undesirable PhMgCl used in previous methods was successfully replaced by MeMgBr. This approach proved to be suitable for the scalable production of the key remdesivir intermediate.

摘要

目前,瑞德西韦是唯一经美国食品药品监督管理局批准用于治疗 COVID-19 的抗病毒药物。为应对这一全球公共卫生危机,瑞德西韦的充足供应是非常必要的。在此,我们报告了一种 Weinreb 酰胺方法,用于在糖基化步骤中制备瑞德西韦的关键中间体,该步骤消除了过度加成的副反应。从 2,3,5-三-O-苄基-D-核糖内酯开始,优选的路线包括三个连续步骤(Weinreb 酰胺化、-TMS 保护和格氏加成),能够以公斤级规模实现该中间体的高产率(65%)合成。特别是,成功用 MeMgBr 替代了先前方法中使用的不理想的 PhMgCl。该方法被证明适用于关键瑞德西韦中间体的规模化生产。

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