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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822238Generated: October 26, 2026

1-(1H-Imidazol-1-yl)ethanone → HCID 178475390, compound

https://huagongshe.com/reaction/1822238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1H-Imidazol-1-yl)ethanoneHCID 17174—
ReactantHCID 178514896HCID 178514896—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178475390HCID 17847539060%

Reaction Steps

To a solution of 3-(4-hydroxybenzyl)-5-phenyl-1H-pyrazolo [4,3-c][1,8]naphthyridin-4 (5H)-one (192 mg, 0.52 mmol, prepared in Example 41) in DMF (2 ml) was added a solution of 1-acetylimidazole (114 mg, 1.04 mmol, 2 eq.) in DMF (2 ml) while ice-cooling, and the mixture was stirred overnight at room temperature, and then diluted with aqueous sodium hydrogen carbonate. Precipitates were filtered off, and the mixture was dried and purified by flash column chromatography to afford 3-(4-acetoxybenzyl)-5-phenyl-1H-pyrazolo[4,3-c][1,8]naphthyridin-4 (5H)-one (128 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608716B2
Source datasetuspto-grants-2009_10
ORD IDord-754f6ecfd952413fb8b93cc2cfe0ae65
Source noteuspto-grants-2009_10