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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578071Generated: October 30, 2026

Ethanol → Ethyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylate

https://huagongshe.com/reaction/1578071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromideHCID 14067523—
ProductEthyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylateHCID 13770479—

Reaction Steps

A suspension of 6.5 g of the product of Step A in 500 ml of ethanol was refluxed with stirring for 2 hours and the resulting clear yellow solution was concentrated and cooled in a refrigerator. The mixture was filtered and then 3.70 g of white crystalline product was crystallized from ethanol to obtain ethyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylate in the form of shiny crystals melting at 292°-293° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04291033
Source datasetuspto-grants-1981_09
ORD IDord-5f8decd4314c4126852b17f6599f5377
Source noteuspto-grants-1981_09