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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609196Generated: October 30, 2026

HCID 178418361, compound → HCID 178447302, compound

https://huagongshe.com/reaction/1609196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178447301HCID 178447301—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178447302HCID 178447302—

Reaction Steps

A solution of 21.1 g (40 mmol) of N-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-N-valeryl-(L)-valine benzyl ester in 210 ml of methanol is hydrogenated at room temperature with the addition of 4 g of Pd/C (10% ) until the calculated amount of hydrogen has been absorbed (24 hours). The crude acid is obtained by filtration and evaporation of the solution. It is partitioned between 80 ml of 2N potassium hydroxide solution and 50 ml of ether. The aqueous phase is separated off and rendered acidic, and the title compound is isolated by extraction with ethyl acetate. It is obtained from ethyl acetate in crystalline form and has a melting interval of 105°-1150° and an optical rotation [α]D20 of -69.95°±0.05° (c=1% in methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399578
Source datasetuspto-grants-1995_03
ORD IDord-591f4a7763f4428e98e4233c1bfa5da7
Source noteuspto-grants-1995_03