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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277953Generated: November 1, 2026

Ethyl bromopyruvate → Ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylate

https://huagongshe.com/reaction/1277953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant4-methoxyquinolin-2-amineHCID 9855604—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylateHCID 13055756—

Reaction Steps

350 mg of 2-amino-4-methoxyquinoline [Grout et al., J. C. S. Perkin I, (1973), p. 1314] were dissolved in 10 ml dimethoxyethane and 390 mg of ethyl bromopyruvate were added thereto. The crystalline intermediate thus formed was filtered off, washed with ether and then was dissolved in ethanol. The solution obtained was refluxed for 1 hour and then the solvent was removed under vacuum. The residue was purified by column chromatography (silica gel--chloroform as eluant) and was crystallized from chloroform/ether to give colorless needles of ethyl 5-methoxyimidazo-[1,2-a]-quinoline-2-carboxylate melting at 178°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279912
Source datasetuspto-grants-1981_07
ORD IDord-c770da7f72e547628346220c8bfdebcf
Source noteuspto-grants-1981_07