An Efficient Chemoenzymatic Process for Preparation of Ribavirin

Author:

Sakharov Vladimir1,Baykov Sergey1,Konstantinova Irina2,Esipov Roman2,Dorogov Mikhail1

Affiliation:

1. Ushinsky Yaroslavl State Pedagogical University, Yaroslavl 150000, Russia

2. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow 117997, Russia

Abstract

Ribavirin is an important antiviral drug, which is used for treatment of many diseases. The pilot-scale chemoenzymatic process for synthesis of the active pharmaceutical ingredient Ribavirin was developed with 32% overall yield and more than 99.5% purity. The described method includes the chemical synthesis of 1,2,4-triazole-3-carboxamide, which is a key intermediate and enzyme-catalyzed transglycosylation reaction for preparation of the desired product. 1,2,4-Triazole-3-carboxamide was synthesized from 5-amino-1,2,4-triazole-3-carboxylic acid by classical Chipen-Grinshtein method. Isolated fromE. сoliBL21(DE3)/pERPUPHHO1 strain the purine nucleoside phosphorylase was used as a biocatalytical system. All steps of this process were optimized and scaled.

Funder

Russian Federation Government

Publisher

Hindawi Limited

Subject

General Chemical Engineering

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