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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473981Generated: November 1, 2026

Ethyl bromopyruvate → Ethyl 2-(3-hydroxy-4-methoxyanilino)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1473981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 55276262HCID 55276262—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-hydroxy-4-methoxyanilino)-1,3-thiazole-4-carboxylateHCID 5343856863%

Reaction Steps

Following the general procedure for the synthesis of derivatives 6 and 7, a solution of 1-(3-hydroxy-4-methoxyphenyl)thiourea (150 mg, 0.76 mmol) and ethyl 3-bromopyruvate (0.095 mL, 0.76 mmol) in dry DMF (3.0 mL) was heated at 60° C. for 6 h. The title compound was obtained after purification by flash chromatography on silica gel (hexane:EtOAc 6/4) in 63% yield (139 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018209B2
Source datasetuspto-grants-2015_04
ORD IDord-4d91efbfd2c3430589f6bd4a878bd3b6
Source noteuspto-grants-2015_04