Reaktion #340439

ord-0c550d25001a4059a57bc31db4a502a6

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe resulting mixture was heated
  2. 2
    Temperaturat reflux for 1 hour
  3. 3
    TemperaturIt was cooled
  4. 4
    Extraktionthe mixture was extracted with ethyl acetate (3×10 mL)
  5. 5
    ExtraktionThe combined extract
  6. 6
    Waschenwas washed with aqueous sodium bicarbonate solution, brine
  7. 7
    Trocknendried over sodium sulfate
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated
  10. 10
    Sonstigeto give an oily residue which
  11. 11
    Sonstigewas purified by flash chromatography (silica gel, 5% methanol in dichloromethane)

Vorschrift

To a solution of 2-(2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrile (0.17 g, 0.65 mmol) in ethanol (5 mL) was added hydrazine dihydrochloride (99 mg, 0.94 mmol). The resulting mixture was heated at reflux for 1 hour. It was cooled, poured into a saturated sodium bicarbonate solution (10 mL), and the mixture was extracted with ethyl acetate (3×10 mL). The combined extract was washed with aqueous sodium bicarbonate solution, brine, dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (silica gel, 5% methanol in dichloromethane) to provide 3-methyl-4-(2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)-1H-pyrazol-5-amine (115 mg, 0.42 mmol, 65% yield). MS (EI) for C14H19N3O3: 278 (MH+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07872014B2uspto-grants-2011_01