Advancing Base Metal Catalysis: Development and Execution of a Ni-catalyzed Borylation/Pd-catalyzed Suzuki Telescoped Process
The development and execution of a nickel-catalyzed borylation/palladium-catalyzed Suzuki telescoped process utilizing the inexpensive NiCl2·6H2O precatalyst for the borylation step are reported. The development of the borylation reaction was guided by a preliminary mechanistic investigation to understand the origin of the dehalogenated side product. The borylation stream was telescoped into a Suzuki coupling to form a bis-heteroaryl bond in the pentacyclic core of afimetoran, an antagonist of toll-like receptors 7/8 (TLR 7/8). The optimization of the Suzuki reaction and kilogram-scale demonstration of the telescoped process showcase the viability of utilizing nickel catalysis in the development of scalable routes to clinical APIs.
Authors
- Eric M. Simmons (ORCID: https://orcid.org/0000-0002-3854-1561)
- Matthew V. Joannou (ORCID: https://orcid.org/0000-0002-0079-7107)
- Matthew J. Goldfogel (ORCID: https://orcid.org/0000-0002-6911-3068)
- Steven R. Wisniewski (ORCID: https://orcid.org/0000-0001-6035-4394)
Institutions
- Bristol-Myers Squibb (United States) (US)
- Université Bourgogne Franche-Comté (FR)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2025-02-10
- DOI
- https://doi.org/10.1021/acs.oprd.4c00498
- Citations
- 3
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 2.81