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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54078Generated: October 28, 2026

N2 [3(S)-[[N-[4-(benzyloxycarbonyl)benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-L-prolinamide → HCID 86746240, compound

https://huagongshe.com/reaction/54078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2 [3(S)-[[N-[4-(benzyloxycarbonyl)benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-L-prolinamideHCID 86746242—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
ProductHCID 86746240HCID 8674624080.6%

Reaction Steps

274 mg of N2 -[3(S)-[[N-[4-(benzyloxycarbonyl)benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide in 100 ml of isopropanol were hydrogenated over 10% palladium-on-carbon at 20° C. and under atmospheric pressure for 16 hours. The catalyst was removed by filtration and the filtrate was evaporated to give 193 mg of N2 -[3(S)-[[N-(4-carboxybenzoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as a white solid from methanol/ethyl acetate; MS: m/e 596 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620987
Source datasetuspto-grants-1997_04
ORD IDord-18bb88a983bf4187bf82e8ecc9b13575
Source noteuspto-grants-1997_04