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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934929Generated: November 1, 2026

3-Aminobenzonitrile → HCID 5328845, compound

https://huagongshe.com/reaction/1934929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminobenzonitrileHCID 16702—
Reactant1-EthoxyethanolHCID 10129898—
Reactant4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrileHCID 10586676—
SolventPyridineHCID 1049—
ProductHCID 5328845HCID 532884588.8%

Reaction Steps

A mixture of 0.5 g of 4-chloro-6,7-dimethoxy-3-quinolinecarbonitrile, 0.47 g of 3-aminobenzonitrile, 0.16 ml of pyridine, and 12 ml of ethoxyethanol was stirred, under nitrogen, at reflux temperature for 22 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-hexanes to give 0.59 g of 4-[(3-cyanophenyl)amino]-6,7-dimethoxy-3-quinolinecarbonitrile as a solid, mp 285-288° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-7830f8288cee444ca32ac73899ba8e8c
Source noteuspto-grants-2002_05