Water → HCID 22382014、化合物

HRID 895916ノート

反応式

HRID 895916 の反応式
[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]

参加物

6

実験手順

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. b) Preparation of 1,6-dimethyl-3-iodo-4-(trifluoromethyl)-2-pyridone

後処理

  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

出典と根拠

ORDレコード
ord-c7479619100a42da870923b71fe26fec
出典データセット
uspto-grants-2005_07
特許番号
US06916933B2

反応ノート

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