Scalable Synthesis of a Nucleoside Phosphoramidate Prodrug Inhibitor of HCV NS5B RdRp: Challenges in the Production of a Diastereomeric Mixture
| Autor: | Roberta Glynn, Steven Mathieu, David Bauer, Jeevanandam Arumugasamy, Jie Li, Jingyang Wang, Alistair Stewart, Alan Becker, Jinsoo Lim, Elodie Rosinovsky, F. Patrick McGarry, Narayan Chaudhuri, G. Mark Latham, Erkan Baloglu, Adrien F. Soret, Kannan Arunachalam, Jia Liu, Adel Moussa, Benjamin Alexander Mayes |
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| Rok vydání: | 2015 |
| Předmět: | |
| Zdroj: | Organic Process Research & Development. 19:520-530 |
| ISSN: | 1520-586X 1083-6160 |
| Popis: | A scalable process is described for the synthesis of 2′-C-methylguanosine-5′-[2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)thio]ethyl-N-benzylphosphoramidate], a nucleotide prodrug inhibitor of hepatitis C virus NS5B polymerase. The route features the use of phenylboronic acid to transiently protect the 2′,3′-hydroxyls of 2′-C-methylguanosine under mild conditions. The requirement to produce a 1:1 phosphorus diastereomeric mixture precluded the use of traditional crystallization techniques. High sensitivity of the drug substance to acidic and basic conditions and its preferred solubility in mixed aqueous–organic solvents presented additional processing challenges. The use of reverse phase chromatography for the final purification was eliminated by the development of a dual liquid–liquid extraction protocol, which removed both non-polar and polar impurities whilst maintaining the 1:1 diastereomeric ratio. Ethylene sulfide, a potential genotoxic impurity that was observed at significant levels in the original pro... |
| Databáze: | OpenAIRE |
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