HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095851Generated: November 2, 2026
Dabco → 1-(2,4-Difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
https://huagongshe.com/reaction/2095851
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dabco | HCID 9237 | — |
| Reactant | (3E)-4-Methoxy-3-buten-2-one | HCID 639675 | — |
| Reactant | 2-cyano-N-(2,4-difluorophenyl)acetamide | HCID 737512 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2,4-Difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile | HCID 58158462 | 9.4% |
Reaction Steps
To a solution of 2-cyano-N-(2,4-difluorophenyl)acetamide (5.5 g, 28 mmol) and (3E)-4-methoxybut-3-en-2-one (3.65 g, 36.5 mmol) in dimethyleneglycol monomethylether (50 mL) was added 1,4-diazabicyclo[2.2.2]octane (3.14 g, 28 mmol), and the mixture was stirred at 120° C. for 12 hr. The reaction mixture was diluted with 2N hydrochloric acid, tetrahydrofuran and ethyl acetate, and extracted 3 times with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure. The obtained residue was washed with ethyl acetate to give a slightly yellow solid. The slightly yellow solid was suspended in tetrahydrofuran at 80° C., and the suspension was stirred for 30 min. The suspension was filtrated, and the obtained solid was washed with tetrahydrofuran to give the title compound (650 mg, 9.4%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445509B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-93b22f8105d94c18b026de6b677b93d2 |
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| Source note | uspto-grants-2013_05 |
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