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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750436Generated: October 28, 2026

Ethyl bromopyruvate → HCID 86721278, compound

https://huagongshe.com/reaction/1750436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 86721245HCID 86721245—
SolventEthanolHCID 702—
ProductHCID 86721278HCID 8672127877%

Reaction Steps

A solution of 1-tert-butyl-5-(4-methoxyphenyl)-1H-pyrazole-4-carbothioamide (1.24 g, 4.28 mmol) and ethyl bromopyruvate (0.647 mL, 5.14 mmol) in ethanol (24 mL) was stirred at 90° C. for 14 hr. The reaction mixture was concentrated under reduced pressure, and hexane was added thereto to give ethyl 2-(1-(tert-butyl)-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazole-4-carboxylate (1.27 g, 3.29 mmol, 77%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-28d55199f5044877b14b894dfd040879
Source noteuspto-grants-2015_10