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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651805Generated: November 3, 2026

2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2'-[N-(benzyloxycarbonyl)-glycinyl]-4-methylvalerohydrazide → 2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2'-glycinyl-4-methylvalerohydrazide

https://huagongshe.com/reaction/651805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2'-[N-(benzyloxycarbonyl)-glycinyl]-4-methylvalerohydrazideHCID 70239547—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2'-glycinyl-4-methylvalerohydrazideHCID 8675731198.4%

Reaction Steps

A solution of 2.95 g of 2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2′-[N-(benzyloxycarbonyl)-glycinyl]-4-methylvalerohydrazide in 30 ml of methanol was hydrogenated in the presence of 0.300 g of 5% palladium-on-carbon for 0.5 hours. The mixture was filtered and evaporated to give 2.2 g of 2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-2′-glycinyl-4-methylvalerohydrazide in the form of a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281363B1
Source datasetuspto-grants-2001_08
ORD IDord-de776090e824496c884bd04b95d6a22f
Source noteuspto-grants-2001_08