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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757767Generated: October 28, 2026

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

https://huagongshe.com/reaction/1757767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert.butyl-L-prolinamideHCID 86746290—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert-butyl-L-ProlinamideHCID 8674628899%

Reaction Steps

0.22 g of N2 -[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide was dissolved in 10 ml of ethanol and hydrogenated over 0.05 g of 10% palladium-on-carbon at room temperature and under atmospheric pressure for 2 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.17 g of N2 -[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide as a gum which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446161
Source datasetuspto-grants-1995_08
ORD IDord-087284a098e94b49abfa22d85aed7be2
Source noteuspto-grants-1995_08