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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857214Generated: November 2, 2026

4-Chloro-6,7-dimethoxyquinoline → (2-Trifluoromethylphenyl){4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}methanone

https://huagongshe.com/reaction/1857214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant2-Trifluoromethylphenyl 4-hydroxyphenyl ketoneHCID 22132619—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventO-XyleneHCID 7237—
Product(2-Trifluoromethylphenyl){4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}methanoneHCID 2213272555.1%

Reaction Steps

Under argon, 2-trifluoromethylphenyl 4-hydroxyphenyl ketone (959 mg) obtained in Example 145 and 4-dimethylaminopyridine (484 mg) were added to xylene (7 ml), and the admixture was stirred at room temperature for 1 hour. 4-Chloro-6,7-dimethoxyquinoline (805 mg) was added, and the admixture was then refluxed with heat overnight. The reaction mixture was treated in the same manner as described in Example 130 to obtain 899 mg of the title compound (yield: 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143764
Source datasetuspto-grants-2000_11
ORD IDord-847e6bd1312f481ca9e706ea76f11346
Source noteuspto-grants-2000_11