片段(逻辑)
吡唑
过程开发
组合化学
比例(比率)
化学
立体化学
生化工程
工艺工程
计算机科学
工程类
算法
物理
量子力学
作者
Nathaniel T. Kadunce,Olivier St‐Jean,Amy M. Cagulada,Wen‐Tau T. Chang,Alexander F. G. Goldberg,Zilin Huang,Jihun Kang,Jinsik Kim,K. M. KWON,Olga B. Lapina,Lennie Lin,Trevor J. Rainey,Lyubov Roever,Nisha P. Shah,Scott A. Wolckenhauer
标识
DOI:10.1021/acs.oprd.4c00235
摘要
We describe herein the process development and scale-up of a complex cyclopropyl pyrazole fragment of lenacapavir, a drug recently approved for long-acting treatment of HIV (Sunlenca). A ten-step asymmetric synthesis was developed utilizing simple starting materials capable of supporting the commercial supply chain of lenacapavir. Key aspects of this development effort were the oxidation strategy to elaborate the core and optimization of the fluorination reaction to afford the final product.
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