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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857202Generated: November 1, 2026

4-Chloro-6,7-dimethoxyquinoline → {4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}(3-methylphenyl)methanone

https://huagongshe.com/reaction/1857202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant(4-Hydroxyphenyl)(3-methylphenyl)methanoneHCID 22132621—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventO-XyleneHCID 7237—
Product{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}(3-methylphenyl)methanoneHCID 2213275345.3%

Reaction Steps

Under argon, 4-hydroxyphenyl 3-methylphenyl ketone (307 mg) obtained in Example 132 and 4-dimethylaminopyridine (194 mg) were added to xylene (5 ml), and the admixture was stirred at room temperature for 1 hour. 4-Chloro-6,7-dimethoxyquinoline (324 mg) was added, and the admixture was then refluxed with heat for 23 hours. The reaction mixture was treated in the same manner as described in Example 122 to obtain 262 mg of the title compound (yield: 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143764
Source datasetuspto-grants-2000_11
ORD IDord-c1850388ecb6446b89fcabf56ebe3d03
Source noteuspto-grants-2000_11