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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264882Generated: October 26, 2026

2-[3(S)-(tert-butoxycarbonyl)amino-5(S)-(p-tert-butyl-benzyl)-2(S)-hydroxy-6-methyl-heptyl]-N-butyl-acrylamide → HCID 53839344, compound

https://huagongshe.com/reaction/264882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3(S)-(tert-butoxycarbonyl)amino-5(S)-(p-tert-butyl-benzyl)-2(S)-hydroxy-6-methyl-heptyl]-N-butyl-acrylamideHCID 54501741—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53839344HCID 53839344—

Reaction Steps

150 mg of N-tert-butoxycarbonyl-2-methylene-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(p-tert-butyl-phenyl)-octanoic acid (N-butyl)amide (diastereoisomer I) are hydrogenated in the presence of 150 mg of 10% Pd/C in 20 ml of tetrahydrofuran for 2 hours at room temperature and under normal pressure. The reaction mixture is filtered and concentrated by evaporation. The residue is purified by means of FC (50 g of silica gel, dichloromethane/diethyl ether=8:2). The title compound is obtained in the form of a diastereoisomeric mixture: Rf (dichloromethane/diethyl ether=8:2)=0.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646143
Source datasetuspto-grants-1997_07
ORD IDord-e8739cafc62e46d6b5e7a4d851bc92ed
Source noteuspto-grants-1997_07