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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857124Generated: November 1, 2026

4-Chloro-6,7-dimethoxyquinoline → HCID 22132715, compound

https://huagongshe.com/reaction/1857124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
ReactantHCID 15640646HCID 15640646—
ProductHCID 22132715HCID 2213271523%

Reaction Conditions

Temperature180 °C

Reaction Steps

4-Chloro-6,7-dimethoxyquinoline (112 mg) and 4-hydroxyphenyl 2-naphthyl ketone (124 mg) obtained in Example 36 were mixed and stirred at 180° C. for 30 minutes. The reaction mixture was partitioned between saturated aqueous sodium hydrogen carbonate and chloroform, and then the chloroform layer was dried with anhydrous magnesium sulfate. After removing the solvent by reduced-pressure distillation, a portion (50 mg) of the resulting residue (227 mg) was purified by thin layer chromatography on silica gel eluting with chloroform/ethyl acetate (5/1) to obtain 11 mg of the title compound (yield: 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143764
Source datasetuspto-grants-2000_11
ORD IDord-11442cdf0a4e4bae8d3eeab06a566ca6
Source noteuspto-grants-2000_11