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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742875Generated: October 30, 2026

1-[3(S)-[[N-(3-benzyloxy-2-naphthoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-2(S)-piperidinecarboxamide → HCID 70041000, compound

https://huagongshe.com/reaction/742875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3(S)-[[N-(3-benzyloxy-2-naphthoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-2(S)-piperidinecarboxamideHCID 70041014—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 70041000HCID 7004100069.4%

Reaction Steps

A solution of 181 mg of 1-[3(S)-[[N-(3-benzyloxy-2-naphthoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-2(S)-piperidinecarboxamide in 5 ml of ethanol was 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. After trituration with diethyl ether there were obtained 110 mg of N-tert.butyl-1-[3(S)-[[N-(3-hydroxy-2-naphthoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-2(S)-piperidinecarboxamide as a pale yellow solid; MS: m/e 632 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554756
Source datasetuspto-grants-1996_09
ORD IDord-5e19ec65f7ed48a7a737657a3c2c58d8
Source noteuspto-grants-1996_09