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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228522Generated: October 26, 2026

Phenylboronic Acid → N-[2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl]-N-phenylamine

https://huagongshe.com/reaction/228522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinolineHCID 23078587—
CatalystCupric acetateHCID 8895—
Solventtriethylamine N,N-dimethylformamideHCID 22056947—
ProductN-[2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl]-N-phenylamineHCID 2315662477.2%

Reaction Steps

4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline (52 mg) was dissolved in triethylamine/N,N-dimethylformamide (0.5 ml/2.5 ml), and phenylboronic acid (100 mg) and copper acetate (250 mg) were added to the solution which was then stirred at room temperature overnight. The reaction solution was filtered, 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. Next, 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 thin layer chromatography using acetone-chloroform to give the title compound (50 mg, yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-cb2c590698844012b3e2a9628d8f6546
Source noteuspto-grants-2009_07