Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758852Generated: October 31, 2026

L-Alanyl-L-proline → HCID 6321214, compound

https://huagongshe.com/reaction/1758852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Alanyl-L-prolineHCID 83525—
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 6321214HCID 632121459.6%

Reaction Steps

A mixture of 0.814 g of L-alanyl-L-proline, 0.206 g of ethyl 2-oxo-4-phenylbutyrate, and 1.6 g of molecular sieves in 10 ml ethanol is hydrogenated at room temperature under 40 pounds pressure with 0.1 g of 10% Pd on carbon as catalyst. After uptake of hydrogen ceases the crude product obtained by filtration and concentration is absorbed on ion exchange resin, (Dowex 50, H+) and eluted with 2% pyridine in water to yield 0.224 g of N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-L-proline. HPLC indicates a 55:45 isomer ratio.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374829
Source datasetuspto-grants-1983_02
ORD IDord-0d7f5d3a05a646bf80659b296ce95570
Source noteuspto-grants-1983_02