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.

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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
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Development of a Manufacturing Process for S-892216 Part I: A Novel Method for Constructing a Multi-Substituted Barbiturate Skeleton for Scalable Synthesis

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1 citations
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Innovative Microfluidic and Catalytic Techniques Innovation
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article

Development of a Manufacturing Process for S-892216 Part I: A Novel Method for Constructing a Multi-Substituted Barbiturate Skeleton for Scalable Synthesis

Yoichi Hirano, Yuto Shimazaki, Go Kato, Takahiro Kawajiri, Takafumi Ohara, Satoru Shibuya, Tadashi Oohara, Takafumi Higuchi, Naoto Sahara, Keiichiro Hirai, Eisaku Ohashi, Katsuya Yamakawa, Naoki Tsuno, Kazuo Komano, Thuyen Le, Moriyasu Masui
article en
1 citations

Abstract

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.

Organic Process Research & DevelopmentVol. 29(6)
Shionogi (Japan) (JP), Futaba (Japan) (JP)
Openalex Percentile: Top 31%
Innovative Microfluidic and Catalytic Techniques Innovation
0.67
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