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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548429Generated: October 28, 2026

4-[(3-Chloro-4-fluorophenyl)amino]-6-nitro-3-quinolinecarbonitrile → 6-Amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrile

https://huagongshe.com/reaction/548429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(3-Chloro-4-fluorophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 11013311—
SolventEthanolHCID 702—
Product6-Amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrileHCID 1101243391.4%

Reaction Steps

A mixture of 5.360 g (15.6 mmol) 4-[(3-chloro-4-fluorophenyl)amino]-6-nitro-quinoline-3-carbonitrile, 250 ml ethanol, and 17.67 g (78.2 mmol) SnCl2 dihydrate was heated to reflux under N2. Removed heat at 1½ hours and added ice water. Made basic with sodium bicarbonate. Stirred for 2 hours extracted with chloroform. Added brine to the separatory funnel to help separate layers. Stirred organic layer with Darco and dried with sodium sulfate. Filtered, stripped solvent and dried in vacuo, giving 4.460 g of yellow-brown solid: mass spectrum (electrospray m/e): M+H=312.9, 315.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042376E1
Source datasetuspto-grants-2011_05
ORD IDord-4166f67997d74a30981bd05fc67a7bf2
Source noteuspto-grants-2011_05