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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742854Generated: November 1, 2026

Benzyloxycarbonyl-asparagine → N-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-(4-methoxyphenyl)butyl]-L-proline tert.butyl ester

https://huagongshe.com/reaction/742854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonyl-asparagineHCID 75314—
ReactantHCID 70042910HCID 70042910—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-(4-methoxyphenyl)butyl]-L-proline tert.butyl esterHCID 7004111310.5%

Reaction Steps

A solution of 730 mg of N-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(4-methoxyphenyl)butyl]-L-proline tert.butyl ester in 20 ml of ethanol was hydrogenated over 50 mg of 10% palladium-on-carbon for 2 hours. The catalyst was removed by filtration and the filtrate was evaporated to give an oil which was coupled with 340 mg of N-(benzyloxycarbonyl)-L-asparagine in a manner analogous to that described in Example 1. The crude product was chromatographed on a column of silica gel using 10% methanol in dichloromethane for the elution. There were obtained 82 mg of N-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-(4-methoxyphenyl)butyl]-L-proline tert.butyl ester as a white solid; MS: m/e 613 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554756
Source datasetuspto-grants-1996_09
ORD IDord-a44b0e5442a44478a1b7975081398fae
Source noteuspto-grants-1996_09