Water → HCID 22382014, compound

HRID 1936479Notes

Reaction equation

HRID 1936479 reaction equation
[CH3:1][C:2]1[NH:7][C:6](=[O:8])[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:3]=1.[C:13](=O)([O-])[O-].[K+].[K+].IC.O>COCCOC>[CH3:13][N:7]1[C:2]([CH3:1])=[CH:3][C:4]([C:9]([F:12])([F:10])[F:11])=[CH:5][C:6]1=[O:8]

Participants

6

Procedure

To a suspension of 6-methyl-4-(trifluoromethyl)-1H-2-pyridone (2 g, 11.25 mmol) and potassium carbonate (4.68 g, 33.9 mmol) in DME (25 mL) was added iodomethane (9.62 g, 67.8 mmol) at room temperature and the reaction mixture was heated to reflux overnight. The reaction mixture was cooled to room temperature, poured into water (100 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with brine solution (200 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration of the solvent gave the crude product which was purified by silica gel chromatography on a Biotage (40 m) column to obtain 2.1 g (97% yield) of 1,6-dimethyl-4-(trifluoromethyl)-2-pyridone as a white solid: mp 80-82° C. EI-HRMS m/e calcd for C8H8F3NO (M+) 191.0558, found 191.0559.

Workup

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux overnight
  3. extractionextracted with ethyl acetate (3×100 mL)
  4. washThe combined extracts were washed with brine solution (200 mL)
  5. dry with materialwere dried over anhydrous magnesium sulfate
  6. filtrationFiltration of the drying agent and concentration of the solvent
  7. customgave the crude product which
  8. customwas purified by silica gel chromatography on a Biotage (40 m) column

Sources & evidence

ORD record
ord-c4f3431211d645ab96ff05c87428cabd
Source dataset
uspto-grants-2002_05
Patent number
US06388084B1

Reaction notes

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