A Highly Atroposelective Negishi Coupling Enables the Commercial Manufacturing Process of Divarasib.

IF 1.4 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Chimia Pub Date : 2026-08-19 DOI:10.2533/chimia.2026.450
Stephan Bachmann, Raphael Bigler, Danis Kaldre, Dominique Kummli, René Lebl, David Linder, Ugo Orcel, Isabelle Prévot, Jörg Sedelmeier
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引用次数: 0

Abstract

In this publication, we highlight our development efforts that resulted in the commercial manufacturing route of divarasib (1), a highly potent KRAS G12C inhibitor currently undergoing phase III clinical trials. Most prominently, our process landmarks, the first example of a highly atroposelective Negishi coupling at scale, allowing isolation of the step product (Ra)-4 as a single isomer without chromatography. The implementation of a continuous process for the metalation steps of the atroposelective Negishi coupling allowed for the elimination of the cryogenic reaction conditions from the manufacturing process. Furthermore, we detail improvements for the other chemical steps resulting in an impressive yield increase (factor of 6) and process mass intensity (PMI) reduction (factor of 39) for this sequence.

高atroopselective根岸偶联使Divarasib的商业化生产过程成为可能。
在本出版物中,我们强调了我们的开发努力,导致了divarasib(1)的商业生产路线,这是一种高效的KRAS G12C抑制剂,目前正在进行III期临床试验。最突出的是,我们的工艺标志,第一个高度atroopselective根岸偶联的例子,允许分离台阶产物(Ra)-4作为单一异构体而不需要色谱。实现一个连续过程的金属化步骤的atroposelective根岸偶联允许从制造过程中消除低温反应条件。此外,我们详细介绍了其他化学步骤的改进,从而使该序列的产率提高(6倍),工艺质量强度(PMI)降低(39倍)。
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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来源期刊
Chimia
Chimia 化学-化学综合
CiteScore
1.60
自引率
0.00%
发文量
144
审稿时长
2 months
期刊介绍: CHIMIA, a scientific journal for chemistry in the broadest sense covers the interests of a wide and diverse readership. Contributions from all fields of chemistry and related areas are considered for publication in the form of Review Articles and Notes. A characteristic feature of CHIMIA are the thematic issues, each devoted to an area of great current significance.
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