商业化
商品化学品
过程开发
业务
产量(工程)
促炎细胞因子
工程类
反离子
再结晶(地质)
过程(计算)
纳米技术
蛋白质工程
制造工程
持续性
计算机科学
质量(理念)
生化工程
蛋白激酶C
合成生物学
化学
生物技术
比例(比率)
背景(考古学)
化学工业
生产(经济)
组合化学
蛋白激酶A
药物发现
作者
Alexander L. Ruchelman,John R. Coombs,Antonio C. Ferretti,Adam J. Freitag,Peter Galebach,Maryll E. Geherty,Jianxin Han,Bilal Hoblos,Mohit Kothare,Kevin Molter,Sujana Shifon,Eric M. Simmons,Donald Sperbeck,Hua-Chia Tai,William J. Wolf,Ryan A. Woltornist,Chengmin Zhang,Shasha Zhang,Bin Zheng
标识
DOI:10.1021/acs.oprd.5c00278
摘要
CC-99677 is an irreversible inhibitor of mitogen-activated protein kinase (MAPK)-activated protein kinase 2 (MK2) that sustainably reduces production of proinflammatory cytokines in vitro. The design and development of a concise synthetic route enabled production of multikilogram quantities for early-stage clinical trials. Continued synthesis at increasing scale required an improved route to fragment 21 to bypass the energetic chemical reactions and attendant process safety challenges posed within the enabling route. Subsequently, protecting groups and counterions were optimized and an improved API recrystallization was developed for the intended commercial route. Over the course of development, the step count was reduced from 19 to 7 (a 63% reduction), and overall yield increased from 1.3 to 37% (a nearly 30-fold improvement) while improving robustness, safety characteristics, and control overcritical quality attributes required of a commercial process.
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