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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466993Generated: November 1, 2026

1-Piperonylpiperazine → HCID 178419743, compound

https://huagongshe.com/reaction/466993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperonylpiperazineHCID 94426—
ReactantHCID 178517109HCID 178517109—
SolventAcetonitrileHCID 6342—
ProductHCID 178419743HCID 17841974367%
ProductHCID 178429828HCID 17842982822%

Reaction Steps

A mixture of 2-bromomethyl-2,3-dihydroimidazo[1,2-c]-quinazolin-5(6H)-one (0.5 g, 1.78 mmol), 1-piperonylpiperazine (0.78 g, 3.56 mmol) in acetonitrile (25 mL) was refluxed for 17 hours. The solvent was then removed in vacuo to the oily residue. The residue was purified by column chromatography [silica gel: 25 g, column diameter: 2.5 cm, solvent system: chloroform/ethylacetate (9/1)] to furnish 2-[4-piperonyl-1-piperazinyl]methyl-2,3-dihydroimidazo[1,2-c]-quinazolin-5(6H)-one hydrobromide (620 mg, 67%) and 2-methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-one (90 mg, 22%). 2-[4-piperonyl-1-piperazinyl]methyl-2,3-dihydroimidazo[1,2-c]-quinazolin-5(6H)-one hydrobromide: mp 236°-238° C. Anal. Calcd for C23H23N5O3 /H2O/HBr: C, 53.29; H, 5.44; N, 13.50. Found: C, 53.45; H, 5.46 ; N, 13.54.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158953
Source datasetuspto-grants-1992_10
ORD IDord-4dfeb3a9e7a04fab833fe6c2b1ff162b
Source noteuspto-grants-1992_10