二氮卓
三环
化学
过程(计算)
药理学
立体化学
组合化学
计算机科学
有机化学
医学
戒指(化学)
操作系统
作者
Matthew L. Maddess,Ed Cleator,Mariko Morimoto,Adrian Goodyear,A. Dieguez-Vazquez,Andrew Gibb,Andy Kirtley,Melodie Christensen,Chaohui Song,Feng Peng,Mahbub Alam,Stephen P. Keen,Steven F. Oliver
标识
DOI:10.1021/acs.oprd.4c00171
摘要
Process development to improve synthetic access to a potent, selective, and brain-penetrant tricyclic diazepine clinical candidate that inhibits mutant IDH1 is described. A variety of disconnections were evaluated to determine the preferred sequence of fragment coupling. The optimized route involves a metal-catalyzed C–N coupling/reductive cascade to form the central diazepine core, improved entries to both the zigzag morpholine and cyclohexyl acid peripheral pieces, and an efficient end-game sequence of acylation, C–N coupling, and deprotection. In addition, a dynamic acylation process that enables selective acylation at N6 of an unprotected diazepine core is described.
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