Process for preparing acyclic HCV protease inhibitors
US8101765B2 · kind B2 · utility
11Cited by
6References
6Claims
0Family size
Assignee
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Key dates
| Filing date | Jan 16, 2009 |
| Grant date | Jan 24, 2012 |
| Priority date | — |
| Expiry date | Apr 4, 2030 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07D417/14
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
Disclosed are highly convergent processes for preparing compounds of formula (I), which compounds are potent active agents for the treatment of hepatitis C virus (HCV) infection:The disclosed processes use SNAr-type coupling reactions between peptidic compounds having a hydroxyproline moiety of the following formula:and halogenated or sulfonated bromoquinoline compounds.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.