Development of a Synthetic Route to Vonoprazan via Atom Transfer Radical Cyclization
In this Note, a new synthetic route to vonoprazan via atom transfer radical cyclization (ATRC) is described. The pivotal 1,3,5-trisubstituted pyrrole ring of vonoprazan has been accomplished by ATRC, the subsequent aromatization which simultaneously occurred with the introduction of <i>N</i>-methylamine moiety into the cyclic imine, and the sulfonylation at the 1-position of pyrrole. Furthermore, our approach enabled the synthesis of vonoprazan on a 0.7 kg scale without the isolation of intermediates throughout the process.
Authors
- Shigenobu Nishiguchi (ORCID: https://orcid.org/0009-0001-3819-116X)
- Nobuyoshi Doi
- Ken-ichi Ojima
- Toru Nishikawa (ORCID: https://orcid.org/0000-0001-6636-7540)
- Tatsuya Komori
- Ryoya Imaizumi
Institutions
- Towa Pharmaceutical (Japan) (JP)
- Automated Precision (United States) (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-02-26
- DOI
- https://doi.org/10.1021/acs.joc.4c02368
- Citations
- 3
- Primary Topic
- Oxidative Organic Chemistry Reactions
- Type
- article
- Field-Weighted Citation Impact
- 2.81