吗啉
小分子
组合化学
化学
过程开发
药物发现
纳米技术
药物开发
候选药物
药品
治疗窗口
药理学
过程(计算)
分子
进程窗口
前药
化学合成
作者
A. Arunachalampillai,Prashantha Chandrappa,Richard Crockett,Colin S. Gaines,Kanghong Hu,Ted Judd,Venkata Chandrasekhar Kommuri,James I. Murray,John Nidhiry,Adrian Ortiz,Jo Anna Robinson,Andreas R. Rötheli,Robert B. Vernon,Carolyn S. Wei,Shane Wells,Conner V. Wilson,Shu Xu,Kumiko Yamamoto,Lara E. Zetzsche
标识
DOI:10.1021/acs.oprd.5c00310
摘要
AMG 193 is an MTA-cooperative PRMT5 inhibitor that has shown promising antitumor activity in the clinic. Despite a five-month development window from molecule identification to multi-kg manufacture of this small molecule drug substance, a robust process was developed, featuring multiple bio- and chemocatalytic steps. In particular, two wild-type enzymes were applied to the synthesis of key building blocks, including the formation of a chiral morpholine fragment, which was further improved through directed evolution. Additionally, a selective Ir-catalyzed C–H borylation, followed by a Pd-catalyzed Suzuki coupling and cyclization, was executed in a single pot, enabling rapid access to the naphthyridine core. Altogether, the development of this convergent synthesis has enabled a continued supply of AMG 193 for clinical studies.
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