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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309693Generated: November 1, 2026

Iodoacetamide → 2-[4-(1,2-Dihydro-5-oxido-4-phenylimidazo[1,2-a]-quinoxalin-8-yl)piperazinyl]acetamide

https://huagongshe.com/reaction/2309693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantTriethylamineHCID 8471—
Reactant1,2-Dihydro-4-phenyl-8-piperazinylimidazo[1,2-a]quinoxaline 5-oxideHCID 9950158—
SolventEthanolHCID 702—
Product2-[4-(1,2-Dihydro-5-oxido-4-phenylimidazo[1,2-a]-quinoxalin-8-yl)piperazinyl]acetamideHCID 1395861953.7%

Reaction Steps

Triethylamine (0.75 g, 0.0072 mol.) was added to a solution of iodoacetamide (0.59 g, 0.0032 mol.) and 1,2-dihydro-4-phenyl-8-piperazinylimidazo[1,2-a]quinoxaline 5-oxide (1.0 g, 0.0029 mol.) in ethanol (50 ml) and the reaction mixture stirred overnight at room temperature. The resulting precipitate was removed by filtration, washed with ethanol and then ether. Recrystallization from ethanol yielded 2-[4-(1,2-dihydro-5-oxido-4-phenylimidazo[1,2-a]-quinoxalin-8-yl)piperazinyl]acetamide, (0.63 g) as bright yellow crystals, m.p. 225°-227° C. (Found: C, 63.50; H, 5.89; N, 19.72%; C22H24N6O6.O.75H2O requires C, 63.23; H, 6.11; N, 20.12%) represented by the structural formula: ##STR32##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04696928
Source datasetuspto-grants-1987_09
ORD IDord-634ecd35dbcb45ec9f7f39ce41cd0a7e
Source noteuspto-grants-1987_09