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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228521Generated: October 26, 2026

6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinoline → 4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/228521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinolineHCID 23078402—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
Solventtriethylamine N,N-dimethylformamideHCID 22056947—
Product4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinolineHCID 2307858755%

Reaction Steps

6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinoline (480 mg) was dissolved in triethylamine/N,N-dimethylformamide (2 ml/10 ml), and palladium hydroxide (1.2 g) was added to the solution. The mixture was stirred at room temperature in a hydrogen gas atmosphere overnight. The reaction solution was filtered through Celite, and the solvent was removed therefrom by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give 4-(2-amino-4-methylphenoxy)-6,7-dimethoxyquinoline (240 mg, yield 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-930b457f96284836a2aa31352c709973
Source noteuspto-grants-2009_07