还原胺化
胺气处理
胺化
酮
小学(天文学)
化学
有机化学
组合化学
高分子化学
催化作用
物理
天文
作者
Xiangyu Liu,Ensheng Zhan,Zhi Wang,Guo-Liang Dong,Gaochao Dong,Shuai Wu,Yunlin Zhang,Jingrui Chen,Jialin Wen,Lei Zhang
标识
DOI:10.1021/acs.oprd.4c00095
摘要
Direct asymmetric reductive amination provides a straightforward approach to preparing α-chiral amine synthons. We herein disclose a chemical process to produce α-chiral secondary amine from alkyl (hetero)aryl ketone, primary amine, and molecular hydrogen. By using high-throughput screening technology, an iridium/bisphosphine catalyst was selected that gives a turnover number of ∼1000 and a ee value of 91–92% in the production of (R)-2-((1-(2-(bis(4-methoxybenzyl)amino)pyridin-3-yl)ethyl)amino)ethan-1-ol (1). The formation of diastereomeric salt from the crude chiral amine with L-tartaric acid and crystallization upgrade the ee value to >99% and the purity to >99%. The multikilogram production of an enantiopure chiral secondary amine was realized with good reproducibility with this process.
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