Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228871Generated: October 30, 2026

Water → 6,7-Dimethoxy-4-(7-methoxy-quinolin-6-yloxy)-quinoline

https://huagongshe.com/reaction/228871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant6-Hydroxy-7-methoxyquinolineHCID 23078429—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
Product6,7-Dimethoxy-4-(7-methoxy-quinolin-6-yloxy)-quinolineHCID 23078554100%

Reaction Conditions

Temperature155 °C

Reaction Steps

6-Hydroxy-7-methoxyquinoline (65 mg), 4-chloro-6,7-dimethoxyquinoline (100 mg), and 4-dimethylaminopyridine (148 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 155° C. overnight. The reaction solution was cooled to room temperature. Water was then added thereto, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give the title compound (134 mg, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-6b8e2cf01bb04fc8a9e7e4d33214cc27
Source noteuspto-grants-2009_07