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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287341Generated: October 26, 2026

Potassium Carbonate → 2,6-Piperidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-

https://huagongshe.com/reaction/2287341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantGlutarimideHCID 70726—
Reactant1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetoneHCID 180—
Product2,6-Piperidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-HCID 9884583—

Reaction Conditions

Temperature80 °C

Reaction Steps

Scheme-I: A mixture of 2,6-dioxopiperidine (2.60 g, 23.02 mmol), 1-[4-(2-methoxyphenyl)piperazin-1-yl]-3-chloropropane (6.18 g, 23.02 mmol), potassium carbonate (2.38 g, 17.27 mmol) and tetrabutylammonium bromide (1.48 g, 4.60 mmol) in acetone (80 ml) was refluxed for 16 hours at 80° C. with stirring. The solvent was evaporated off in vaccuo and the residue suspended in water (60 ml), extracted with chloroform (3×40 ml) and the organic layers combined, washed with water (2×40 ml), dried over anhydrous Na2SO4 and evaporated in vacuo to give the title compound. The product was purified by column chromatography over flash silica gel (230-400 mesh) using chloroform-methanol (98:1) as eluent; yield 3.58 g (45%), oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083950
Source datasetuspto-grants-2000_07
ORD IDord-40aafda72eb54d818a8ef1fdef05e4b9
Source noteuspto-grants-2000_07