微分器
过程(计算)
相(物质)
化学
过程开发
少突胶质细胞
组合化学
神经科学
计算机科学
生物
工程类
工艺工程
有机化学
髓鞘
中枢神经系统
电信
操作系统
带宽(计算)
作者
Donald G. Walker,Steven Ferguson,Michael Humora,Erwin Irdam,William F. Kiesman,Daw-Iong Albert Kwok,Wenli Liang,Suzanne M. Opalka
标识
DOI:10.1021/acs.oprd.3c00293
摘要
Herein are described improvements in a discovery synthesis to enable a rapid scale up of 1 to support early phase clinical trials and formulation development studies. Process modifications included route redesign, simplifying a Mitsunobu reaction product's isolation, improving yields and impurity profiles for isolated intermediates, and removal of a chromatographic purification. Particle engineering studies identified a recrystallization protocol to produce 1 with enhanced solid-state properties. This improved process was scaled up to generate multikilogram quantities of drug substance with >99.8% area purity.
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