Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935002Generated: October 29, 2026

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

https://huagongshe.com/reaction/1935002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-fluoroanilineHCID 9708—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
Product4-[(3-Chloro-4-fluorophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 1101331181.9%

Reaction Steps

A mixture of 5.00 g (21.5 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile, 200 ml ethanol, and 3.75 g (25.8 mmol) 3-chloro-4-fluoroaniline was heated to reflux under N2. Removed heat at 3.5 hours and added a solution of saturated sodium bicarbonate until mixture was basic. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane, collected solids, washed with water and dried in vacuo. Dissolved solids in 250 ml boiling ethyl acetate, stirred with Darco, and filtered. Stripped solvent and dried in vacuo, giving 6.036 g of yellow solid: mass spectrum (electrospray m/e): M+H=343.1, 345.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-47b52b704e9845bf935efc1f3e0b911c
Source noteuspto-grants-2002_05