氢甲酰化
区域选择性
钥匙(锁)
对映选择合成
氰化
计算机科学
过程(计算)
序列(生物学)
过程开发
组合化学
开发(拓扑)
化学
亲核细胞
四氢呋喃
联营
生化工程
选择(遗传算法)
作者
Jacob C. Timmerman,Allen Y. Hong,Kurt Püntener,Anna-Lena Glass,Sandro Tonazzi,Katarzyna A. Piechowicz,Maud Guillemot-Plass,José G. Napolitano,Breanna Conklin,Haiming Zhang,Francis Gosselin
标识
DOI:10.1021/acs.oprd.6c00017
摘要
We report the development of a second-generation manufacturing process for a key N -hydroxyamidine intermediate ( 3 ) en route to GDC-6599 ( 1 ). To obviate the safety hazards associated with a decakilogram-scale nucleophilic cyanation used in the first-generation route, we developed a sequence leveraging an enantioselective Pd-catalyzed Hayashi-Heck arylation followed by a stereo- and regioselective Rh-catalyzed hydroformylation reaction. This new route utilizes a synergistic high-throughput experimentation (HTE)/multivariate linear regression (MLR)-driven catalyst selection to establish the key stereochemical dyad of the tetrahydrofuran core. A detailed mechanistic understanding of the regioselective hydroformylation step was established and allowed for implementation on the manufacturing scale. The optimized 5-step sequence proceeds in 38% overall yield, avoiding the use of cyanide reagents and providing a robust control strategy for regio- and stereoisomeric impurities.
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