HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-(Bromomethyl)-2-cyanobiphenyl → 4-[(2'-cyanobiphenyl-4-yl)methyl]-(L)-valine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-(Bromomethyl)-2-cyanobiphenyl | HCID 1501912 | — |
| Reactant | L-Valine benzyl ester hydrochloride | HCID 11601206 | — |
| Product | 4-[(2'-cyanobiphenyl-4-yl)methyl]-(L)-valine benzyl ester | HCID 67408573 | — |
Reaction Steps
L-valine benzyl ester hydrochoride is N-alkylated with 4-bromomethyl-2′-cyanobiphenyl, the product 4-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine benzyl ester so formed is N-acylated with valeryl chloride to give N-[(2′-cyanobiphenyl-4-yl)methyl]-N-valeryl-(L)-valine benzyl ester. N-[(2′-cyanobiphenyl-4-yl)methyl]-N-valeryl-(L)-valine benzyl ester is treated with tributyltin azide to give valsartan benzyl ester. Valsartan benzyl ester is subjected to catalytic hydrogenation using for example palladium-charcoal as catalyst to give valsartan.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361770B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-d1b07386cb654bb890665724af349d3c |
| Source note | uspto-grants-2008_04 |