HuagongsheHuagongshe Chemistry Print Report · For research reference only
Valeryl chloride → Valeryl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | N-((2'-Cyano(1,1'-biphenyl)-4-yl)methyl)-L-valine methyl ester | HCID 16744794 | — |
| Product | Valeryl chloride | HCID 61186 | — |
| Product | N-((2'-Cyano(1,1'-biphenyl)-4-yl)methyl)-N-(1-oxopentyl)-L-valine methyl ester | HCID 16744795 | — |
Reaction Steps
According to US 2006/0149079 A1 N-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine methylester is acylated with valerylchloride in the presence of inorganic base to give N-[(2′-cyanobiphenyl-4-yl)methyl]-N-valeryl-(L)-valine methylester with valerylchloride, followed by the conversion of cyano to tetrazole and hydrolyzing the tetrazole derivative to obtain valsartan.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492577B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-8a943008a0814b1da97cc487f2d9b617 |
| Source note | uspto-grants-2013_07 |