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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70841Generated: October 29, 2026

Ethyl bromopyruvate → Ethyl oxazole-4-carboxylate

https://huagongshe.com/reaction/70841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 59607699HCID 59607699—
SolventEthanolHCID 702—
ProductEthyl oxazole-4-carboxylateHCID 2763217—

Reaction Steps

To a suspension of (R)-4-biphenyl-4-yl-3-ureido-butyric acid ethyl ester (169 mg, 0.518 mmol) in EtOH (5 ml) at ice bath is added ethyl bromopyruvate (0.098 ml, 0.777 mmol). The reaction is warmed up slowly to room temperature and stirred at reflux overnight. The reaction is concentrated and the residue is taken up in EtOAc and H2O. The combined organic layer is washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-(R)-1-biphenyl-4-ylmethyl-2-ethoxycarbonyl-ethylamino)-oxazole-4-carboxylic acid ethyl ester. HPLC retention time=1.42 minutes (condition B); MS (m+1)=423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822534B2
Source datasetuspto-grants-2014_09
ORD IDord-dbce352a00364816a63b1e7008a8ba72
Source noteuspto-grants-2014_09