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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379123Generated: November 1, 2026

3-Chloroaniline → 4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrile

https://huagongshe.com/reaction/379123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
Product4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 22466674—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 10.0 g (42.9 mmol) ) 4-chloro-6-nitro-quinoline-3-carbonitrile, 260 ml ethanol, and 5.40 ml 3-chloroaniline was heated to reflux under N2. Removed heat at 4 hours, cooled to 25° C. and added saturated sodium bicarbonate until the pH was basic. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane, collected solid, and air dried. Washed solids with water and dried in vacuo. Dissolved in boiling ethyl acetate, stirred with Darco, and filtered. Stripped solvent and dried residue in vacuo, giving 6.5 g of yellow solid: mass spectrum (electrospray m/e): M+H=325.0, 327.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297258B1
Source datasetuspto-grants-2001_10
ORD IDord-bb2b8a59169c430d8fe4da28640ea656
Source noteuspto-grants-2001_10