Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744771Generated: October 27, 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/744771

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 m g 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 numberUS05559111
Source datasetuspto-grants-1996_09
ORD IDord-7af0d93a2d2f484a8a0e371ad414f349
Source noteuspto-grants-1996_09