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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54076Generated: October 29, 2026

HCID 70041394, compound → HCID 70043572, compound

https://huagongshe.com/reaction/54076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70041394HCID 70041394—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 70043572HCID 70043572100.2%

Reaction Steps

A solution of 397 mg of 1-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-octahydro-(3aS,6aS)-cyclopenta[b]pyrrole-2(S)-carboxamide in 20 ml of ethanol was hydrogenated over 10% palladium-on-carbon at 20° C. and under atmospheric pressure for 4 hours, The catalyst was removed by filtration and the filtrate was evaporated to give 312 mg of 1-[3(S)-[[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-octahydro-(3aS,6aS)-cyclopenta[b]pyrrole-2(S)-carboxamide as a pale yellow gum; m/e 488 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620987
Source datasetuspto-grants-1997_04
ORD IDord-afa4d2581520430c8e3553f0efdc6c5c
Source noteuspto-grants-1997_04