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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50854Generated: October 26, 2026

Water → 6-{[4-Hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl}-3,4-dihydroquinolin-2(1h)-one

https://huagongshe.com/reaction/50854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-(3-Methoxyphenyl)piperidin-4-olHCID 1091076—
Reactant6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-oneHCID 4961790—
SolventDimethylformamideHCID 6228—
Product6-{[4-Hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl}-3,4-dihydroquinolin-2(1h)-oneHCID 2273694046%

Reaction Steps

To a stirred solution of 6-(Chloroacetyl)-3,4-dihydroquinolin-2(1H)-one (7.30 g, 32.7 mmol) in DMF (32 ml) were added 4-(3-methoxyphenyl)-4-piperidinol (J. Labelled Compd. Radiopharm., 41, p464, 1998). (8.12 g, 39.2 mmol) and triethylamine (13.7 ml, 98.0 mmol) at room temperature under nitrogen. The reaction mixture was stirred for 4 hours at room temperature and poured into water (80 ml). The precipitate was collected by filtration and washed with dichloromethane (20 ml). The solid was stirred in 0.5N NaOH (65 ml) for 1 hour at room temperature and the suspension was filtered to afford the title compound (5.98 g, 46%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713490B2
Source datasetuspto-grants-2004_03
ORD IDord-d86044666d9546f3a6c6ddc2f0319d7b
Source noteuspto-grants-2004_03