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A clinical candidate for treating COVID-19, Ensitrelvir (a nonproprietary name for S-217622), which was discovered through a research collaboration between Shionogi & Co., Ltd. and Hokkaido university, as the first nonpeptidic, noncovalent CLpro inhibitor. Ensitrelvir exhibited significant potent antiviral activity and high bioavailability arising from a favorable drug metabolism and pharmacokinetic (DMPK) profile as a once-daily oral medicine to treat COVID-19.

Like Paxlovid, Ensitrelvir also targets the 3CL protease (3CLpro). These two oral drugs are designed to block the activity of the SARS-CoV-2-3CL protease, thereby blocking the replication of the novel coronavirus.  It became the first Japanese domestic pill to treat COVID-19 and the third to be regulatorally approved in February 2022 in Japan.

The clinical trial results also showed that after taking Ensiprevir, symptoms such as runny nose, nasal congestion, sore throat, cough, and dyspnea were greatly improved, with minimal side effects. And it has a significant inhibitory effect on the proliferation of the novel coronavirus strain of Omicron.

A practical route to Ensitrelvir: The unprecedented strategy utilizing a meta-cresolyl moiety enhanced the stability of intermediate compounds and enabled scalable manufacturing of 1. The 6-step longest linear sequence (from 26) delivers the target molecule in 35.1% yield. This overall yield was improved by approximately 7-fold compared to the earlier process used in the early research and development stage (4.8%). Our convergent approach to the synthesis of 1 made the manufacturing process concise, streamlined, and short. Direct crystallization was achieved in 9 out of the 12 steps, thus establishing a greener process without silica-gel column chromatographic purification. In addition, the present practical process settled all the issues that made large-scale synthesis difficult, i.e., removal of corrosive acid by evaporation and the generation of noxious odors from thiol derivatives.

[1] YOTSUYANAGI H, OHMAGARI N, DOI Y, et al. Efficacy and Safety of 5-Day Oral Ensitrelvir for Patients With Mild-to-Moderate COVID-19: The SCORPIO-SR Randomized Clinical Trial[C]. 2023: 0. DOI:10.1101/2023.07.11.23292264.
[2] TAKAHIRO KAWAJIRI*, TAKAYUKI TSURITANI    Development of a Manufacturing Process toward the Convergent Synthesis of the COVID-19 Antiviral Ensitrelvir[J]. ACS Central Science, 2023, 9 4: 836-843. DOI:10.1021/acscentsci.2c01203.