化学
双金属片
组合化学
对映体
基岩
药品
产量(工程)
再结晶(地质)
立体化学
药理学
有机化学
肺结核
结核分枝杆菌
催化作用
冶金
材料科学
古生物学
病理
生物
医学
作者
Tanveer Ahmad,Feng Gao,Jing Li,Zhenfeng Zhang,Tao Song,Qianjia Yuan,Wanbin Zhang
标识
DOI:10.1021/acs.joc.3c00705
摘要
TBAJ-587, an analogue of the antituberculosis drug bedaquiline (BDQ), bearing a diarylquinoline skeleton retains the high bacterial potency, is less toxic, and has a better pharmacokinetic profile than the parent molecule, which has entered phase I clinical trials. In contrast to its fascinating bioactivity, however, the highly efficient synthesis of this molecule is still an unsolved challenge. Herein, the first asymmetric synthesis of TBAJ-587 based on a synergistic Li/Li bimetallic system is reported. The product could be obtained in an excellent yield of 90% and an enantiomeric ratio (er) of 80:20. Furthermore, the reaction could be conducted on a 5 g scale, and the product was obtained with 99.9:0.1 er after a simple recrystallization. The realization of this protocol will greatly aid the demand for clinical drug production.
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