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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277969Generated: November 1, 2026

Propylene Oxide → Ethyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylate

https://huagongshe.com/reaction/1277969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
ReactantEthyl bromopyruvateHCID 66144—
Reactant4-Bromoquinolin-2-amineHCID 14067419—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylateHCID 12763980—

Reaction Steps

1 g of 2-amino-4-bromoquinoline was dissolved in 20 ml of dimethoxyethane and a mixture of 1.5 g of ethyl bromopyruvate and 0.5 g of propylene oxide was added thereto. The solution was allowed to stand at room temperature for 1 hour and the quaternary salt thus precipitated was filtered off, was washed with ether and then was dissolved in 20 ml of ethanol. The solution was refluxed for 1 hour, cooled and then was evaporated to dryness under vacuum. The residue was partitioned between 50 ml of chloroform and 50 ml of 2 N sodium carbonate and the organic extract was washed with 50 ml of water, was dried over MgSO4, and was reduced in volume under vacuum. Then, ether was added thereto to give cream needles of ethyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylate melting at 205°-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279912
Source datasetuspto-grants-1981_07
ORD IDord-d5aba955bfc34ba0b11ccd5bb94f10c6
Source noteuspto-grants-1981_07