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Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline**
Authors:Sarah Jane Mear  Tobias Lucas  Grace P. Ahlqvist  Dr. Juliana M. S. Robey  Dr. Jule-Philipp Dietz  Dr. Pankaj V. Khairnar  Dr. Sanjay Maity  Corshai L. Williams  Dr. David R. Snead  Dr. Ryan C. Nelson  Prof. Till Opatz  Prof. Timothy F. Jamison
Affiliation:1. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, 02139 USA;2. Department of Chemistry, Johannes Gutenberg University, Duesbergweg 10–14, 55128 Mainz, Germany;3. Medicines for All Institute, Department of Chemistry and Life Sciences Engineering, Virginia Commonwealth University, Richmond, Virginia, 23284 USA
Abstract:Bedaquiline is a crucial medicine in the global fight against tuberculosis, yet its high price places it out of reach for many patients. Herein, we describe improvements to the key industrial lithiation-addition sequence that enable a higher yielding and therefore more economical synthesis of bedaquiline. Prioritization of mechanistic understanding and multi-lab reproducibility led to optimized reaction conditions that feature an unusual base-salt pairing and afford a doubling of the yield of racemic bedaquiline. We anticipate that implementation of these improvements on manufacturing scale will be facile, thereby substantially increasing the accessibility of this essential medication.
Keywords:bedaquiline  continuous flow  diastereoselectivity  lithiation  nucleophilic addition
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