HuagongsheHuagongshe Chemistry Print Report · For research reference only
Valeryl chloride → HCID 57823153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | benzyl (2S)-2-amino-3-methylbutanoate | HCID 6950584 | — |
| Product | HCID 57823153 | HCID 57823153 | — |
Reaction Steps
According to EP 1714963 4-Bromomethyl-2′-cyanobiphenyl is condensed with L-valinebenzylester tosylate to give (S)-N-[(2′-cyanobiphenyl-4-yl]methyl]-(L)-valine benzylester hydrochloride. (S)-N-cyanobiphenyl-4-yl]methyl]-(L)-valine benzylester on reaction with valerylchloride yields (S)-N-cyanobiphenyl-4-yl]methyl]-N-valeryl-(L)-valine benzylester further by the reaction of tributyltin chloride and sodiumazide gives benzyl valsartan and debenzylation with Pd/C to give valsartan. Also discloses the process for the recovery of benzyl valsartan substantially free of organo tin impurity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492577B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-f897accd59864cd0b0d8f47a866dca81 |
| Source note | uspto-grants-2013_07 |