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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228677Generated: October 30, 2026

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

https://huagongshe.com/reaction/228677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-PiperidineethanolHCID 73953—
Reactant(2-{[6-Methoxy-7-(2-oxiranylmethoxy)-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanoneHCID 57756552—
SolventDimethylformamideHCID 6228—
Product{2-[(7-{2-Hydroxy-3-[4-(hydroxymethyl)piperidino]-propoxy}-6-methoxy-4-quinolyl)oxy]-5-methylphenyl}(phenyl)methanoneHCID 5775650193%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2-{[6-Methoxy-7-(2-oxiranylmethoxy)-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanone (41 mg) and 4-piperidine ethanol (32 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 (48 mg, yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-7c913fd176044eda962bfcf17f766896
Source noteuspto-grants-2009_07