Development of an Inherently Safe and Scalable Nickel-Catalyzed Borylation Process of an Aryl Sulfamate
A safe and scalable synthesis of A, a key aryl boronate ester intermediate toward an immunology asset udifitimod, via a Ni-catalyzed Miyaura borylation is reported. High-throughput experimentation, design of experiment, and reagent stability/compatibility studies were used to optimize the reaction conditions and furnish the borylation of aryl sulfamate B in 80–85% yield and >98% purity/potency. Significant hydrogen off-gassing was observed during the reaction, metal remediation, and crystallization steps of the first-generation process, and efforts were made to quantify, understand, and mitigate this off-gassing to ensure a safe and reliable scale-up. Two multikilogram batches of the process were successfully run to afford A in an average 85% yield, >99% potency, and ≤28 ppm residual Ni. Using the mechanistic learnings from this work, a second-generation process was developed which significantly reduced hydrogen off-gassing at all steps of the process, as well as increasing final yield and reducing process mass intensity. This second-generation process was demonstrated on a 1 kg scale to afford the product in 90% yield, >99% purity/potency, and 50 ppm residual Ni.
Authors
- Sharla Wood
- Rebecca A. Green (ORCID: https://orcid.org/0000-0002-8492-3122)
- Jeffrey Nye
- Christopher Y. Bemis
- Matthew V. Joannou (ORCID: https://orcid.org/0000-0002-0079-7107)
- Candice L. Joe (ORCID: https://orcid.org/0000-0002-7167-2416)
- Geoffrey E. Purdum
- Amy A. Sarjeant (ORCID: https://orcid.org/0000-0002-1993-0406)
- Kyle W. Eckenroad
- Shasha Zhang (ORCID: https://orcid.org/0000-0001-7602-3055)
- Steven R. Wisniewski (ORCID: https://orcid.org/0000-0001-6035-4394)
- Scott Savage (ORCID: https://orcid.org/0000-0002-7823-0696)
Institutions
- Bristol-Myers Squibb (United States) (US)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2024-12-12
- DOI
- https://doi.org/10.1021/acs.oprd.4c00454
- Citations
- 5
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.25