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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267153Generated: October 30, 2026

N2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide → N2 [3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide

https://huagongshe.com/reaction/267153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamideHCID 86746265—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN2 [3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamideHCID 8674626498.8%

Reaction Steps

A solution of 0.725 g of N2 -[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1 -tert.butyl-L-prolinamide was dissolved in 25 ml of ethanol and hydrogenated at room temperature and under atmospheric pressure over 0.5 g of 10% palladium-on-carbon for 20 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.54 g of N2 -[3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1 -tert.butyl-L-prolinamide as a white foam which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652369
Source datasetuspto-grants-1997_07
ORD IDord-c218a31d73d74f4f8ebc991cd2b74d0a
Source noteuspto-grants-1997_07