Synthetic Development and Scale-Up of the Aminoindazole Fragment of Lenacapavir
Abstract We describe herein the development and scale-up of the aminoindazole fragment of lenacapavir, a drug recently approved for long-acting treatment of HIV (Sunlenca) and pre-exposure prophylaxis (as Yeztugo and Yeytuo). This five-step route to fragment 1 was developed from the initial “fit-for-purpose” large-scale synthesis to a commercially viable process. Key improvements include an alternative condition to hydroxylamine-O-sulfonic acid-mediated nitrile formation and a significant overhaul of the key Miyaura borylation process. The culmination of all development efforts improved the final product quality and process safety, resulting in a more efficient and higher-yielding process.
Authors
- 孙宏伟
- Alexander F. G. Goldberg (ORCID: https://orcid.org/0000-0002-3198-5688)
- Scott A. Wolckenhauer
- Lennie Lin
- B. Michael O’Keefe (ORCID: https://orcid.org/0009-0002-8355-8597)
- Wen‐Tau T. Chang
- Anna M. Wagner (ORCID: https://orcid.org/0009-0001-6258-3024)
- Chloe Y. Wong
- Wei Wang
- Huy Van Huynh
- Jason Davy
Institutions
- Pharmaron (United Kingdom) (GB)
- Gilead Sciences (United States) (US)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2026-09-30
- DOI
- https://doi.org/10.1021/acs.oprd.6c00302
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00