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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047992Generated: October 30, 2026

Potassium Carbonate → HCID 58492597, compound

https://huagongshe.com/reaction/2047992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-oneHCID 25165678—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 58492597HCID 5849259775.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

Potassium carbonate (2.1 g, 15.2 mmol) and 4-(2-chloroethyl)morpholine hydrochloride (1.36 g, 7.31 mmol) were added to an N-methylpyrrolidone (NMP) solution (5 ml) of 5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one (1.0 g, 3.05 mmol) and then stirred at 50 to 60° C. for 45 hours. Water and ethyl acetate were added to the reaction mixture, followed by separation. The thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution twice, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane:methanol=50:1→30:1). The purified product was concentrated under reduced pressure, and the residue was recrystallized from ethyl acetate, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-1-(2-morpholin-4-ylethyl)-8-propoxy-1H-quinolin-4-one (1.01 g, yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592593B2
Source datasetuspto-grants-2013_11
ORD IDord-fe4419ff16584914a8da7102475a7be6
Source noteuspto-grants-2013_11