HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056893Generated: October 25, 2026
Dimethyl Sulfoxide → 3'-fluoro-4'-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2'-bipyridin-4-one
https://huagongshe.com/reaction/1056893
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-DIFLUORO-4-IODOPYRIDINE | HCID 11447837 | — |
| Reactant | 3-[(4-methoxybenzyl)oxy]pyridin-4(1H)-one | HCID 67405695 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3'-fluoro-4'-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2'-bipyridin-4-one | HCID 67418473 | — |
Reaction Steps
To a 20 mL microwave vial (Biotage) was added 0.70 g (3.03 mmol) 3-[(4-methoxybenzyl)oxy]pyridin-4(1H)-one, 1.26 g (9.08 mmol) potassium carbonate, 1.10 g (4.54 mmol) 2,3-difluoro-4-iodopyridine and 15 mL DMSO, A yellow suspension formed and the vial was sealed and heated at 85° C. for 48 h on a heat block. The suspension was cooled, diluted with ethyl acetate, and washed twice with 10 mL brine. The organic layer was dried over sodium sulfate, filtered, and evaporated onto silica gel. Purification by flash chromatography (silica gel 0-100% hexanes/EtOAc gradient, followed by 10% MeOH in EtOAc) afforded 3′-fluoro-4′-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2′-bipyridin-4-one as a yellow solid. LCMS (M+H)+ 453.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09399651B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-fddb9030d44b4f3a9472ed4e70b53494 |
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| Source note | uspto-grants-2016_07 |
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