HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050355Generated: October 30, 2026
3-Fluorobenzaldehyde → HCID 118598772, compound
https://huagongshe.com/reaction/1050355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorobenzaldehyde | HCID 68009 | — |
| Reactant | HCID 118598561 | HCID 118598561 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118598772 | HCID 118598772 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382248B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-7a07ed4d22ad4bf78e766217416cbb16 |
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| Source note | uspto-grants-2016_07 |
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