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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972594Generated: November 2, 2026

Potassium Carbonate → 4-(((2R)-1,4-dibenzyl-2-piperazinyl)methyl)-3,3-dimethyl-2-piperazinone

https://huagongshe.com/reaction/1972594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Piperazinone, 3,3-dimethyl-HCID 211157—
ReactantAmmonium chloride monohydrateHCID 57429219—
Reactant((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonateHCID 86670397—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
Product4-(((2R)-1,4-dibenzyl-2-piperazinyl)methyl)-3,3-dimethyl-2-piperazinoneHCID 6658353559.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

A 20 ml, microwave vial was charged with ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate (0.817 g, 2.18 mmol, Example 184, Step 1), 3,3-dimethylpiperazin-2-one (0.297 g, 2.32 mmol, ChemBridge, San Diego, Calif.), potassium carbonate (0.910 g, 6.58 mmol) and acetonitrile (10 mL). The vial was sealed and the reaction mixture was stirred at 130° C. for 30 min. The reaction was allowed to cool to room temperature then saturated aqueous NH4Cl/water (1:1) (100 mL) and 10% iPrOH in chloroform (100 mL) were added. The aqueous phase was extracted with 10% iPrOH in chloroform (2×50 mL). The combined organic phases were washed with saturated aqueous NaCl (200 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by column chromatography (50 g of silica gel, 0 to 10% iPrOH (with 10% NH4OH) in CHCl3) to afford 4-(((2R)-1,4-dibenzyl-2-piperazinyl)methyl)-3,3-dimethyl-2-piperazinone (0.53 g) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-0b59e959963c457f80777cd3e296d2f1
Source noteuspto-grants-2013_04