Development of a Manufacturing Process for S-892216 Part I: A Novel Method for Constructing a Multi-Substituted Barbiturate Skeleton for Scalable Synthesis
S-892216, a second-generation 3CL protease inhibitor, is currently being developed as a clinical drug candidate for the treatment of SARS-CoV-2 infection. This paper outlines the development process and scaling-up of S-892216 for early-phase clinical trials. The developed synthetic route involved a condensation reaction between carboxylic acids and urea with T3P, followed by cyclization in the presence of CDI and DBU to construct a barbiturate core. This novel method facilitated the efficient production of high-quality S-892216 in six steps, with an overall yield of 41.3% from readily available starting materials.
Authors
- Yoichi Hirano
- Yuto Shimazaki (ORCID: https://orcid.org/0009-0002-1257-8881)
- Go Kato (ORCID: https://orcid.org/0000-0001-5030-5230)
- Takahiro Kawajiri (ORCID: https://orcid.org/0000-0003-1764-7102)
- Takafumi Ohara
- Satoru Shibuya
- Tadashi Oohara
- Takafumi Higuchi
- Naoto Sahara (ORCID: https://orcid.org/0000-0003-0136-9080)
- Keiichiro Hirai
- Eisaku Ohashi (ORCID: https://orcid.org/0000-0002-5935-9232)
- Katsuya Yamakawa
- Naoki Tsuno
- Kazuo Komano
- Thuyen Le
- Moriyasu Masui
Institutions
- Shionogi (Japan) (JP)
- Futaba (Japan) (JP)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2025-05-20
- DOI
- https://doi.org/10.1021/acs.oprd.5c00071
- Citations
- 1
- Primary Topic
- Innovative Microfluidic and Catalytic Techniques Innovation
- Type
- article
- Field-Weighted Citation Impact
- 0.67