Sotorasib原料药的轴向手性,第一部分:制备Atropisomerically Pure Sotorasib中间体的经典决议的发展

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Andrew T. Parsons*, Seb Caille, Marc A. Caporini, Daniel J. Griffin, Michael A. Lovette, William Powazinik IV and Gabrielle St-Pierre, 
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引用次数: 9

摘要

本文描述的是在KRAS G12C抑制剂sotorasib的合成中制备atrosom异构中间体的发现和开发。通过高通量实验,(+)-2,3-二苯甲酰-d-酒石酸[(+)-DBTA]被确定为一种廉价且容易获得的溶解剂,可以通过经典的分离方法分离和分离所需的阿托品。随后的优化和表征研究导致了一个高度选择性的过程,提供了所需的阿托普二聚体作为一种独特的三组分共晶溶剂化物,选择性为>2000:1。这种经典的分辨率已经在500公斤的规模上成功地进行了,对sotorasib制造工艺的商业化至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Axial Chirality in the Sotorasib Drug Substance, Part 1: Development of a Classical Resolution to Prepare an Atropisomerically Pure Sotorasib Intermediate

Axial Chirality in the Sotorasib Drug Substance, Part 1: Development of a Classical Resolution to Prepare an Atropisomerically Pure Sotorasib Intermediate

Described herein is the discovery and development of a process to prepare an atropisomeric intermediate in the synthesis of the KRAS G12C inhibitor sotorasib. Using high-throughput experimentation, (+)-2,3-dibenzoyl-d-tartaric acid [(+)-DBTA] was identified as an inexpensive and readily available resolving agent that enables separation and isolation of the desired atropisomer through a classical resolution. Subsequent optimization and characterization studies led to a highly selective process, providing the desired atropisomer as a unique three-component cocrystal solvate with a selectivity of >2000:1. This classical resolution has been performed successfully on >500 kg scale and was critical to the commercialization of the sotorasib manufacturing process.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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