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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612089Generated: October 30, 2026

4-[(4-Bromophenyl)amino]-6-nitro-3-quinolinecarbonitrile → 6-Amino-4-[(4-bromophenyl)amino]-3-quinolinecarbonitrile

https://huagongshe.com/reaction/612089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(4-Bromophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 22466762—
SolventEthanolHCID 702—
Product6-Amino-4-[(4-bromophenyl)amino]-3-quinolinecarbonitrileHCID 2246659779.5%

Reaction Steps

A mixture of 3.10 g (8.40 mmol) 4-[(4-bromophenyl)amino]-6-nitro-3-quinolinecarbonitrile, 155 ml ethanol, and 9.47 g (42.0 mmol) SnCl2 dihydrate was heated to reflux under N2. After 4 hours, removed heat and added ice water. Made basic with sodium bicarbonate and stirred for 2 hours. With mixture still basic, extracted with chloroform, stirred organic layer with Darco and dried with sodium sulfate. Filtered, stripped solvent and dried in vacuo, giving 2.265 g of brown-yellow solid: mass spectrum (electrospray m/e): M+H=339.0, 341.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-8b6c547541b14b05919e8c384c60ef10
Source noteuspto-grants-1999_12