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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309691Generated: November 3, 2026

1-Benzylpiperazine → HCID 135838364, compound

https://huagongshe.com/reaction/2309691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
ReactantHCID 135838365HCID 135838365—
SolventIsopropanolHCID 3776—
ProductHCID 135838364HCID 13583836484.4%

Reaction Steps

8-Chloro-1,2-dihydro-4-phenylimidazo[1,2-a]pyrido[3,2-e]pyrazine 5-oxide (3 g, 0.01 mol) and benzylpiperazine (3.6 g, 0.02 mol) were heated at 80° C., in isopropanol (100 ml) under an atmosphere of nitrogen for 16 hrs. As the reaction mixture cooled to room temperature, a yellow solid precipitated. The yellow solid was collected by filtration, washed with cold isopropanol and recrystallized from isopropanol to yield 1,2-dihydro-4-phenyl-8-(4-phenylmethylpiperazinyl)imidazo [1,2-a]pyrido[3,2-e]pyrazine 5-oxide (3.7 g), as orange needles, m.p. 184°-187° C. (Found: C,71.03; H,6.02; N,19.30%; C26H24N6O.O.1H2O requires C,70.92; H,6.00; N,19.09%), represented by the structural formula: ##STR30##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04696928
Source datasetuspto-grants-1987_09
ORD IDord-789e5f6aae6d432e87df6317cbcb1ef3
Source noteuspto-grants-1987_09