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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236315Generated: October 30, 2026

2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide → Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate

https://huagongshe.com/reaction/236315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromideHCID 20217059—
SolventEthanolHCID 702—
ProductEthyl imidazo[1,2-a]quinoxaline-2-carboxylateHCID 1322832588.1%

Reaction Steps

A suspension of 0.4 g of the product of Step A in 15 ml of ethanol was refluxed for 2 hours and the resulting clear orange solution was concentrated to half its volume. The mixture was filtered to obtain 0.25 g of ethyl imidazo-[1,2-a]-quinoxaline-2-carboxylate as a pale yellow solid which were crystallized from an ether-methanol mixture to obtain the product in the form of soft-white needles melting at 184°-187° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04644002
Source datasetuspto-grants-1987_02
ORD IDord-c28d37fa37cc449898444505ef17aa18
Source noteuspto-grants-1987_02