Mechanistic Investigation of a Domino N–H and C–H Borylation in the Manufacture of AMG 193
The manufacturing process of AMG193 employs iridium-catalyzed C–H borylation as a key step. In contrast to the literature precedent, irreproducibility during scale-up of this process prompted investigations that determined that N-boryl functionalization with HBpin inhibits C–H activation. An iridium-catalyzed tandem N–H/C–H borylation procedure was developed instead. Kinetic analysis indicated that N–H activation by iridium occurs at a faster rate than C–H activation. Additionally, catalyst deactivation pathways were diagnosed through these studies, which enabled a significant reduction in iridium loading. This report highlights the use of in situ reaction monitoring (ReactIR and NMR) to make rational improvements to this borylation process. Our mechanistic findings enabled a 10-fold reduction in the Ir catalyst and removed the requirement for HBpin protection of the aminopyridine substrate prior to C–H borylation.
Authors
- Maria Victoria Silva Elipe (ORCID: https://orcid.org/0000-0002-8429-9534)
- Ted Judd
- Conner V. Wilson
- Neil F. Langille
- James I. Murray (ORCID: https://orcid.org/0000-0002-8668-9261)
- Sharon Michalak
Institutions
- Amgen (United States) (US)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2026-04-21
- DOI
- https://doi.org/10.1021/acs.oprd.6c00043
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00