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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228662Generated: October 31, 2026

Water → {2-[(7-{3-[4-(Hydroxymethyl)piperidino]propoxy}-6-methoxy-4-quinolyl)oxy]-5-methylphenyl}(phenyl)methanone

https://huagongshe.com/reaction/228662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-PiperidineethanolHCID 73953—
Reactant(2-{[7-(3-Chloropropoxy)-6-methoxy-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanoneHCID 57756383—
SolventDimethylformamideHCID 6228—
Product{2-[(7-{3-[4-(Hydroxymethyl)piperidino]propoxy}-6-methoxy-4-quinolyl)oxy]-5-methylphenyl}(phenyl)methanoneHCID 5775649475.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2-{[7-(3-Chloropropoxy)-6-methoxy-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanone (62 mg), 4-piperidine ethanol (25 mg), and potassium carbonate (100 mg) were suspended in N,N-dimethylformamide (4 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 (55 mg, yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-37ca9b21371c4b51996a06b95e46fcac
Source noteuspto-grants-2009_07