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Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline**

Author(s)
Mear, Sarah Jane; Lucas, Tobias; Ahlqvist, Grace P; Robey, Juliana MS; Dietz, Jule‐Philipp; Khairnar, Pankaj V; Maity, Sanjay; Williams, Corshai L; Snead, David R; Nelson, Ryan C; Opatz, Till; Jamison, Timothy F; ... Show more Show less
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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.
Date issued
2022-08-22
URI
https://hdl.handle.net/1721.1/145710
Department
Massachusetts Institute of Technology. Department of Chemistry
Journal
Chemistry – A European Journal
Publisher
Wiley
Citation
Mear, Sarah Jane, Lucas, Tobias, Ahlqvist, Grace P, Robey, Juliana MS, Dietz, Jule‐Philipp et al. 2022. "Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline**." Chemistry – A European Journal, 28 (47).
Version: Final published version

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