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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871032Generated: October 27, 2026

Ethyl bromopyruvate → Ethyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1871032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantPyridine-2-carbothioamideHCID 1549499—
SolventEthanolHCID 702—
ProductEthyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylateHCID 10082761—

Reaction Steps

16.3 ml of ethyl bromopyruvate were added dropwise to 15.9 g of the product of Stage B in 250 ml of ethanol and the mixture was refluxed for 5 hours. The solvent was evaporated under reduced pressure and the residue was chromatographed on silica (eluant: hexane-AcOEt 1-1) to obtain 10.2 g of the expected product melting at 69.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100404
Source datasetuspto-grants-2000_08
ORD IDord-49f8b9933fcf4a94af540d1776f1b1b1
Source noteuspto-grants-2000_08