Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612086Generated: November 1, 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/612086

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-3-quinolinecarbonitrile, 250 ml ethanol, and 17.67 g (78.2 mmol) SnCl2 dihydrate was heated to reflux under N2. Removed heat at 1.5 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 numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-7c08c5b8a9c4478e8c178a752cbf0caf
Source noteuspto-grants-1999_12