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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228669Generated: October 30, 2026

Water → [2-({7-[4-(Diethylamino)butoxy]-6-methoxy-4-quinolyl}oxy)-5-methylphenyl](phenyl)methanone

https://huagongshe.com/reaction/228669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethylamineHCID 8021—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-{[7-(4-Chlorobutoxy)-6-methoxy-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanoneHCID 57756358—
SolventDimethylformamideHCID 6228—
Product[2-({7-[4-(Diethylamino)butoxy]-6-methoxy-4-quinolyl}oxy)-5-methylphenyl](phenyl)methanoneHCID 5775646041.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2-{[7-(4-Chlorobutoxy)-6-methoxy-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanone (60 mg), diethylamine (29 mg), and potassium carbonate (90 mg) were suspended in N,N-dimethylformamide (2 ml), and the suspension was stirred at 80° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with ethyl acetate. 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 methanol-chloroform to give the title compound (27 mg, yield 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-12d512249242407bbf2b7408616606e6
Source noteuspto-grants-2009_07