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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227236Generated: October 30, 2026

Ethyl bromopyruvate → 4-Methyl-2-nitro-phenyl-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/227236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant4-Methyl-2-nitro-thiobenzamideHCID 54168808—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4-Methyl-2-nitro-phenyl-thiazole-4-carboxylic acid ethyl esterHCID 86622912—

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Methyl-2-nitro-thio benzamide (60 mgs, 0.30 mmol, prepared as described in compound 5, Step 2, was stirred in 1 mL absolute EtOH at room temperature under N2. Ethyl bromo pyruvate (65 mgs, 0.33 mmol) was added, and the resulting solution was heated to 70° C. for 3 h. The reaction was diluted to 30 mL with EtOAc and washed with saturated NaHCO3, and saturated NaCl. The organic layer was dried over MgSO4, filtered and concentrated to a yellow oil, which was used as is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560462B2
Source datasetuspto-grants-2009_07
ORD IDord-0071cf80c814424a9604bf2d5f427a1a
Source noteuspto-grants-2009_07