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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878460Generated: November 1, 2026

Ethyl bromopyruvate → HCID 68780924, compound

https://huagongshe.com/reaction/1878460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant5-Iodo-6-methylpyridin-2-amineHCID 959613—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 68780924HCID 68780924—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of 2 g of 5-iodo-6-methylpyridine-2-amine in 15 mL of dimethoxyethane are added 1.3 mL of ethyl bromopyruvate. The reaction mixture is stirred at 20° C. for 16 hours and then concentrated to dryness, taken up in 15 mL of ethanol, refluxed for 2.5 hours and finally concentrated under reduced pressure. The residue is taken up in a mixture of dichloromethane and saturated sodium bicarbonate solution. The organic phase is dried over magnesium sulfate and concentrated to dryness under reduced pressure to give 2.77 g of ethyl 6-iodo-5-methyl(pyrid-2-yl)imidazo[1,2-a]pyridine-2-carboxylate in the form of a beige-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314109B2
Source datasetuspto-grants-2012_11
ORD IDord-514273dccb134c478054a75931c48c86
Source noteuspto-grants-2012_11