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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934988Generated: November 2, 2026

4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrile → 6-Amino-4-(3-chlorophenylamino)quinoline-3-carbonitrile

https://huagongshe.com/reaction/1934988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 22466674—
SolventEthanolHCID 702—
Product6-Amino-4-(3-chlorophenylamino)quinoline-3-carbonitrileHCID 22466692100.4%

Reaction Steps

A mixture of 6.30 g (19.4 mmol) 4-[(3-chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrile, 300 ml ethanol, and 21.9 g (97 mmol) SnCl2 dihydrate were heated to reflux under N2. Removed heat at 2.5 hours, added ice water and made basic with sodium bicarbonate. Stirred for 2 hours and extracted with chloroform. Dried organic layer with sodium sulfate, filtered, stripped solvent and dried residue in vacuo, giving 5.74 g of yellow-brown solid: mass spectrum (electrospray m/e): M+H=295.1, 297.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-1e989240626f40388b6d74998603f2f5
Source noteuspto-grants-2002_05