Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259833Generated: November 2, 2026

Ethanol → 2-[(2-Quinolinylcarbonyl)amino]butanediamide

https://huagongshe.com/reaction/2259833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantQuinaldateHCID 3538644—
Reactant2-[(Phenylmethylcarbamoyl)amino]butanediamideHCID 21610797—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
Product2-[(2-Quinolinylcarbonyl)amino]butanediamideHCID 21831133—

Reaction Steps

A solution of [1S-[1R*(R*), 2S*]]- N1[3-[[[(1,1-dimethylethyl)amino]carbonyl]n-butyl)amino]-2-hydroxy-1-(phenylmethy)propyl]-2-[(phenylmethylcarbamoyl)amino]butanediamide (1.03 g, 1.77 mmol) in 40 mL of abs. ethanol ws then deprotected by hydrogenolysis in the presence of 10% palladium on carbon catalyst to give, after filtration and concentration, the free amine (428 mg) which was coupled with N-hydroxysuccinimide ester of 2-quinoline carboxylate (270 mg, 1.0 mmol) in dichloromethane for 16 h to give 380 mg, 63% of [1S-[1R*(R*), 2S*]]-N1[3-[[[1,1-dimethylethyl)amino]carbonyl](n-butyl)amino]-2-hydroxy-1-(phenylmethyl)propyl]-2-[(2-quinolinylcarbonyl)amino]-butanediamide, mp 102.1°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475013
Source datasetuspto-grants-1995_12
ORD IDord-a6787257d8b04f41af23f7f80ab14b95
Source noteuspto-grants-1995_12