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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934930Generated: November 2, 2026

4-Fluoroaniline → 4-[(4-Fluorophenyl)amino]-6,7-dimethoxyquinoline-3-carbonitrile

https://huagongshe.com/reaction/1934930

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
Reactant1-EthoxyethanolHCID 10129898—
Reactant4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrileHCID 10586676—
SolventPyridineHCID 1049—
Product4-[(4-Fluorophenyl)amino]-6,7-dimethoxyquinoline-3-carbonitrileHCID 532884690.8%

Reaction Steps

A mixture of 0.5 g of 4-chloro-6,7-dimethoxy-3-quinolinecarbonitrile, 0.44 g of 4-fluoroaniline, 0.16 ml of pyridine, and 6 ml of ethoxyethanol was stirred, under nitrogen, at reflux temperature for 4 h. The mixture was cooled and partitioned with dichloromethane and aqueous sodium bicarbonate. The organic layer was washed with water, dried and evaporated. The residue was recrystallized from ethyl acetate to give 0.59 g of 4-[(4-fluorophenyl)amino]-6,7-dimethoxy-3-quinolinecarbonitrile as a solid, mp 282-285° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-59ab4fc4352748c0ba810bad1bb7d7d7
Source noteuspto-grants-2002_05