HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466993Generated: November 1, 2026
1-Piperonylpiperazine → HCID 178419743, compound
https://huagongshe.com/reaction/466993
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Piperonylpiperazine | HCID 94426 | — |
| Reactant | HCID 178517109 | HCID 178517109 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178419743 | HCID 178419743 | 67% |
| Product | HCID 178429828 | HCID 178429828 | 22% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158953 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-4dfeb3a9e7a04fab833fe6c2b1ff162b |
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| Source note | uspto-grants-1992_10 |
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