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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050355Generated: October 30, 2026

3-Fluorobenzaldehyde → HCID 118598772, compound

https://huagongshe.com/reaction/1050355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzaldehydeHCID 68009—
ReactantHCID 118598561HCID 118598561—
SolventAcetonitrileHCID 6342—
ProductHCID 118598772HCID 118598772—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 5-bromo-3-chloro-6-oxo-1H-pyridine-2-carboxamide (1, 0.5 g, 1.99 mmol) in acetonitrile (15 mL), 3-fluorobenzaldehyde (0.86 g, 6.96 mmol) and ferric chloride (2.25 g, 13.92 mmol) were added in a vial. The vial was sealed and heated the reaction mass to 85° C. for 16 h. After completion, the reaction mass was cooled to room temperature, filtered through celite bed, washed with 5% methanol in dichloromethane followed by concentration to get crude. The crude was then purified by column chromatography eluting with 5% methanol in dichloromethane to afford 8-chloro-3-(3-fluorophenyl)-2,3-dihydroimidazo[1,5-a]pyridine-1,5-dione as white solid. Yield: 0.45 g, 63%; MS (ESI) m/z 256.17 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382248B2
Source datasetuspto-grants-2016_07
ORD IDord-7a07ed4d22ad4bf78e766217416cbb16
Source noteuspto-grants-2016_07