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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787563Generated: October 30, 2026

Ethyl 3-oxo-3-(thiophen-2-yl)propanoate → HCID 136044398, compound

https://huagongshe.com/reaction/1787563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-oxo-3-(thiophen-2-yl)propanoateHCID 255159—
Reactant2-(1H-Imidazol-2-yl)anilineHCID 15620500—
SolventTolueneHCID 1140—
ProductHCID 136044398HCID 13604439833.2%

Reaction Steps

A mixture of 2-(1H-imidazol-2-yl)aniline (60.0 mg, 0.38 mmol), ethyl3-oxo-3-(2-thienyl)propanoate (74.7 mg, 0.38 mmol) and p-tolenesulfonicacid monohydrate (36.1 mg, 0.19 mmol) in toluene (30 ml) was heated at reflux for 2 hours. After cooling to room temperature, the reaction mixture was poured into aqueous saturate NaHCO3 solution, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica-gel (ethyl acetate/hexane, 2/3-1/1) to give (Z)-2-imidazo[1,2-c]quinazolin-5-yl-1-(2-thienyl)ethenol (37.0 mg, 33% yeild) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511041B2
Source datasetuspto-grants-2009_03
ORD IDord-e1a974e612b7416093fa8922a5458776
Source noteuspto-grants-2009_03