Reaktion #79720

ord-7cb721b04f754d64bf168ae69008dd51

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction was stirred overnight
  2. 2
    Extraktionextracted twice with ethyl acetate
  3. 3
    WaschenThe extracts were washed with water
  4. 4
    Trocknenwith brine, dried over magnesium sulfate
  5. 5
    Einengenconcentrated
  6. 6
    WaschenThe residue was rinsed with hexane
  7. 7
    workup.DISSOLUTIONdissolved in dichloromethane
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated

Vorschrift

A solution of 0.148 g of 5-carbamoyl-4-methoxy-1-methylcarbazole in 1.1 ml of dimethylformamide was added to 0.026 g of sodium hydride (60% in mineral oil) in 0.4 ml of dimethylformamide and stirred for 60 minutes at room temperature. Benzyl bromide (0.076 ml) was then added and the reaction was stirred overnight. The reaction mixture was poured into 20 ml of saturated ammonium chloride solution and then extracted twice with ethyl acetate. The extracts were washed with water and then with brine, dried over magnesium sulfate and concentrated. The residue was rinsed with hexane and dissolved in dichloromethane, filtered and concentrated to afford 0.21 g of the subtitle compound. FDMS m/e 344 (M+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713645B1uspto-grants-2004_03