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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397548Generated: October 25, 2026

Ethyl bromoacetate → 6-chloro-2-ethyl-1-ethoxycarbonylmethyl-1H-imidazo[4,5-b]quinoxaline

https://huagongshe.com/reaction/2397548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxalineHCID 178437541—
SolventDimethylformamideHCID 6228—
Product6-chloro-2-ethyl-1-ethoxycarbonylmethyl-1H-imidazo[4,5-b]quinoxalineHCID 21435966—

Reaction Steps

A mixture of 100 parts of 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline, 70 parts of anhydrous potassium carbonate, 75 parts of ethyl bromoacetate, and 600 parts of anhydrous dimethylformamide was heated at 100° for 2.5 hours. The mixture was filtered and the crude product was precipitated from the filtrate by addition of 1200 parts of water, collected by filtration, washed with water, ethanol, and ether, and airdried. Recrystallization from 95% ethanol afforded 63 parts of 6-chloro-2-ethyl-1-ethoxycarbonylmethyl-1H-imidazo[4,5-b]quinoxaline, m.p. 174°-175°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022777
Source datasetuspto-grants-1977_05
ORD IDord-2d02fb0618364871867ce677d5505903
Source noteuspto-grants-1977_05