Process Development to Synthesize SGD-11275 Utilizing a Pd-Catalyzed Acetamide Arylation and Gallium-Mediated Friedel–Crafts Acylation
An improved synthesis of SGD-11275 was developed to address inefficiencies in cost, time, and safety associated with the previous supply route. The new route features a Buchwald-Hartwig amination with acetamide optimized by high-throughput experimentation as well as a GaCl3-mediated Friedel–Crafts acylation. Subsequent amide hydrolysis was demonstrated from the isolated Friedel–Crafts product and as a through-process with equal effectiveness. The new route reduced the commercial synthesis by three steps and increased the overall yield by 18.6%.
Authors
- Aaron M. Whittaker (ORCID: https://orcid.org/0000-0002-8348-5490)
- Tristan M. McGinnis (ORCID: https://orcid.org/0000-0002-1273-8833)
- Srinath Thirumalai Rajan
- Apparao Bokka (ORCID: https://orcid.org/0000-0003-3138-8178)
- Noah Porter
- Kun‐Liang Wu
- Brooke Gill
- Jared Abbruzzese
Institutions
- Pfizer (United States) (US)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2024-11-26
- DOI
- https://doi.org/10.1021/acs.oprd.4c00375
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00