手性(物理)
阿托品
共晶
酒石酸
化学
立体化学
选择性
分辨率(逻辑)
组合化学
纳米技术
材料科学
物理
有机化学
分子
计算机科学
催化作用
夸克
氢键
人工智能
量子力学
手征对称破缺
柠檬酸
Nambu–Jona Lasinio模型
作者
Andrew T. Parsons,Seb Caille,Marc A. Caporini,Daniel J. Griffin,Michael A. Lovette,William Powazinik,Gabrielle St‐Pierre
标识
DOI:10.1021/acs.oprd.2c00176
摘要
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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