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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461737Generated: November 1, 2026

Hydrochloric Acid → 1-{3-[4-(4-Fluorobenzoyl)piperidino]propyl}-4-(2-pyridylmethyl) piperazine 2,6-dione hydrochloride

https://huagongshe.com/reaction/1461737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant[1-(3-Chloropropyl)piperidin-4-yl](4-fluorophenyl)methanoneHCID 12404419—
Reactant4-(2-Pyridylmethyl)-2,6-piperazinedioneHCID 14882692—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product1-{3-[4-(4-Fluorobenzoyl)piperidino]propyl}-4-(2-pyridylmethyl) piperazine 2,6-dione hydrochlorideHCID 14882694—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 1.86 g of 4-(2-pyridylmethyl)piperazine 2,6-dione in 30 ml of dimethylformamide is added at 20° C. to a suspension of 0.36 g of sodium hydride. The mixture is brought to 60° C. for 30 minutes and 2.7 g of 1-(3-chloropropyl)-4-(4-fluorobenzoyl)piperidine, dissolved in 30 ml of dimethylformamide, are then added, again at 20° C. The mixture is kept stirring at 20° C. for approximately 15 hours and the reaction is completed by bringing to 70° C. for 2 hours. After concentration, the residue is taken up in water and the product is extracted with benzene. The oil obtained is purified by chromatography under pressure on 280 g of b 230-400 mesh silica, eluting with a mixture of dichloromethane and methanol (93.5:6.5 V/V). The base obtained is converted to the hydrochloride in ethanol. The precipitate obtained is then filtered off.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077288
Source datasetuspto-grants-1991_12
ORD IDord-f9fc9fc4a1d34e958e3ec71fbbd0d3cc
Source noteuspto-grants-1991_12