Decagram scale synthesis of favipiravir was performed in 9 steps using diethyl malonate as cheap starting material. Hydrogenation and bromination steps were achieved by employing a continuous flow reactor. The synthetic process provided a total of 16% yield and it is suitable for larger-scale synthesis and production.
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Thanat Tiyasakulchaia
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Netnapa Charoensetakula
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Thitiphong Khamkhenshorngphanuchb
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Chawanee Thongpanchangaa
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Onsiri Srikunc
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Yongyuth Yuthavonga
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Nitipol Srimongkolpithaka
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aNational Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani, Thailand
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bDepartment of General Education, Faculty of Science and Health Technology, Navamindradhiraj University, Bangkok, Thailand
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cGovernment Pharmaceutical Organization (GPO), Bangkok, Thailand
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