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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120164Generated: October 31, 2026

HCID 54100165, compound → HCID 22956155, compound

https://huagongshe.com/reaction/2120164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54100165HCID 54100165—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 22956155HCID 22956155—

Reaction Steps

A suspension of 2-{[1-(2-acetylthio-3-methyl-butanoylamino)-cyclopentanecarbonyl]-amino}-3-[6-(3-nitro-phenyl)-pyridin-3-yl]-propanoic acid ethyl ester (110 mg) and 25 mg of 10% Pd/C in 10 mL of EtOH is stirred under a H2 atmosphere for 18 h. The catalyst is filtered off, and the reaction mixture is concentrated in vacuo. The residue is purified by chromatography on silica gel (50% EtOAc/hexane) to produce yellow product; 1H NMR (250 MHz, CDCl3) δ8.39 (d, 1H), 7.60 (s, 2H), 7.10-7.36 (m, 3H), 6.71 (d, 1H), 6.34 (d, 1H), 4.76 (app q, 1H), 4.15 (q, 2H), 3.62 (dd, 1H), 3.05-3.25 (m, 2H), 2.35, 2.32 (two s, 3H), 1.55-2.40 (m, 9H), 1.19 (t, 3H), 0.92-1.06 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689801B2
Source datasetuspto-grants-2004_02
ORD IDord-41ffc7ee9cf6470482c03ec380dff4d2
Source noteuspto-grants-2004_02