Asymmetric Synthesis of Anti‐tuberculosis‐specific Drug TBAJ‐876 through Synergistic Li/Li Catalysis

Author:

Li Jing1,Gao Feng2,Ahmad Tanveer2,Luo Yicong2,Zhang Zhenfeng1,Yuan Qianjia2,Zhang Wanbin12

Affiliation:

1. Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmacy Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China

2. Frontiers Science Centre for Transformative Molecules, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China

Abstract

Comprehensive SummaryTBAJ‐876, developed by TB Alliance, a novel anti‐tuberculosis‐specific drug, has entered Phase II clinical trials. Herein, the first asymmetric synthesis of TBAJ‐876 has been realized using synergistic Li/Li catalysis with excellent yield of 95% and 88 : 12 er (99.6 : 0.4 er, 10 : 1 dr after simple recrystallization). Furthermore, DFT calculations and 7Li‐NMR analysis illustrated the mechanism of the synergistic reaction: a chiral Li‐complex activates the nucleophile to control the stereoselectivity, while the other achiral Li‐complex activates the electrophile to catalyze the carbonyl addition reaction. Additionally, this protocol has been successfully carried out at 5 gram‐scale, showing its industrial potential.

Publisher

Wiley

Subject

General Chemistry

Reference67 articles.

1. Global tuberculosis report 2021 World Health Organization Geneva 2021. Licence: CC BY‐NC‐SA 3.0 IGO.https://www.who.int/teams/global‐tuberculosis‐programme/tb‐reports.

2. https://www.tballiance.org/why-new-tb-drugs/inadequate-treatment.

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5. Synthetic Studies to Help Elucidate the Metabolism of the Preclinical Candidate TBAJ-876—A Less Toxic and More Potent Analogue of Bedaquiline

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