Development of Suzuki–Miyaura Coupling between 4-Pyridine Boronate Derivatives and Aryl Halide to Suppress Phenylated Impurities Derived from Phosphorus Ligands
A method has been developed to suppress the formation of impurities derived from the aryl group on the phosphorus atom of the ligand used in the Suzuki-Miyaura coupling of 4-pyridineboronic acid derivatives. 4-Arylpyridine, a key substructure in several active pharmaceutical ingredients (API), is typically synthesized using this coupling reaction. However, in API synthesis, the generation of impurities derived from the aryl group on the phosphorus atom of the ligand has posed a significant challenge. In previously reported Suzuki-Miyaura coupling of 4-pyridineboronic acid derivatives, both the desired product and the aforementioned impurities were obtained. Here, we present a method to address and resolve this problem.
Authors
- Mitsuhiro Arisawa (ORCID: https://orcid.org/0000-0002-7937-670X)
- Yoshitaka Kitano
Institutions
- The University of Osaka (JP)
Publication Details
- Journal
- Chemical and Pharmaceutical Bulletin
- Published
- 2025-04-07
- DOI
- https://doi.org/10.1248/cpb.c24-00874
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Agency for Medical Research and Development
- Japan Society for the Promotion of Science
- Core Research for Evolutional Science and Technology