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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309688Generated: November 2, 2026

1-Methylpiperazine → 1,2-Dihydro-8-(4-methylpiperazinyl)-4-phenylimidazo[1,2-a]quinoxaline 5-oxide

https://huagongshe.com/reaction/2309688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant1,2-Dihydro-8-fluoro-4-phenylimidazo[1,2-a]quinoxaline 5-oxideHCID 13958607—
SolventIsopropanolHCID 3776—
Product1,2-Dihydro-8-(4-methylpiperazinyl)-4-phenylimidazo[1,2-a]quinoxaline 5-oxideHCID 1395860817.3%

Reaction Steps

1,2-Dihydro-8-fluoro-4-phenylimidazo[1,2-a]quinoxaline 5-oxide (3.5 g, 0.012 mol) and N-methylpiperazine (15 ml, 0.13 mol) were heated at 100° C. in isopropanol (5 ml) for 16 hrs. The solvent was removed in vacuo and the residue was dissolved in dichloromethane. The resulting solution was washed with saturated aqueous sodium hydrogen carbonate, dried over anhydrous magnesium sulphate and concentrated in vacuo to yield a dark oil which was chromatographed on silica gel in 2% methanol/chloroform to yield a red solid. The red solid was recrystallized from ethyl acetate to yield 1,2-dihydro-8-(4-methylpiperazinyl)-4-phenylimidazo[1,2-a]quinoxaline 5-oxide, (0.75 g), as deep red crystals m.p. 179°-183° C., (δ(CDCl3) 2.38 (3H,s) 2.58 (4H,m) 3.37 (4H,m) 3.95-4.24 (4H,m) 6.08 (1H,d,J=3.5Hz), 6.62 (1H,dd,J=9 and 3.5Hz), 7.38-7.5 (3H,m), 7.84 (2H,m), and 8.11 (1H,d,J=9 Hz)), represented by the structural formula: ##STR17##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04696928
Source datasetuspto-grants-1987_09
ORD IDord-5e3c5e28eae0487dba151cfb389db6dd
Source noteuspto-grants-1987_09