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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934994Generated: November 1, 2026

3-Methoxyaniline → HCID 22466687, compound

https://huagongshe.com/reaction/1934994

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
ProductHCID 22466687HCID 2246668772.6%

Reaction Steps

A mixture of 5.00 g (21.5 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile, 200 ml ethanol, and 3.0 ml (26.0 mmol) m-anisidine was heated to reflux under N2. Removed heat at 4.5 hours and made basic with saturated sodium bicarbonate. Stripped solvents and azeotroped with ethanol. Slurried with hexane and collected crystals. Washed with water, dried in vacuo. Dissolved 5.94 g of crude product in 320 ml boiling ethyl acetate, stirred with Darco, filtered, stripped solvent, and dried in vacuo, giving about 5 g of yellow-orange solid: mass spectrum (electrospray m/e): M+H=291.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-41c37aa61f684d8b9ff642b38f4673d2
Source noteuspto-grants-2002_05