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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363712Generated: October 29, 2026

Ethyl bromopyruvate → HCID 68780924, compound

https://huagongshe.com/reaction/2363712

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 numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-ace58320a9594ae8a6188a4f94215da4
Source noteuspto-grants-2014_04