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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50860Generated: October 28, 2026

Water → HCID 22736931, compound

https://huagongshe.com/reaction/50860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-(3-Methoxyphenyl)piperidin-4-olHCID 1091076—
Reactant6-(Bromoacetyl)-5-fluoro-3,4-dihydro-2(1H)-quinolinoneHCID 22736944—
SolventDimethylformamideHCID 6228—
ProductHCID 22736931HCID 2273693128.2%

Reaction Steps

To a cooled solution of 6-(Bromoacetyl)-5-fluoro-3,4-dihydro-2(1H)-quinolinone (900 mg, 3.1 mmol) and triethylamine (0.88 ml, 6.3 mmol) in DMF (15 ml) was added dropwise a solution of 4-(3-Methoxyphenyl)-4-piperidinol (650 mg, 3.1 mmol) in DMF(15 ml) at 0° C. The mixture was stirred at room temperature for 3 h. The reaction mixture was added water and the resulting precipitate was filtered to afford 5-Fluoro-6-[[4-hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl]-3,4-dihydroquinolin-2(1H)-one (360 mg) as a brown solid. The filtrate was extracted with ethyl acetate. The extract was dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography (dichloromethane/methanol=20/1) to afford 5-Fluoro-6-[[4-hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl]-3,4-dihydroquinolin-2(1H)-one as a yellow solid (270 mg). The obtained products were combined and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713490B2
Source datasetuspto-grants-2004_03
ORD IDord-e17aa17da24e49f4bcf6d2e1943409cf
Source noteuspto-grants-2004_03