Reaktion #156194

ord-00cc7d72754a4c8b8cae090396375e20

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled to room temperature
  2. 2
    workup.ADDITIONAfter adding aqueous
  3. 3
    Extraktionammonia, extraction
  4. 4
    WaschenThe organic layer was washed with saturated saline
  5. 5
    Trocknendried with sodium sulfate
  6. 6
    Sonstigecondensed under reduced pressure
  7. 7
    Sonstigethe residue was purified by silica gel column chromatography (ethyl acetate:methanol=100:0,70:30)
  8. 8
    Sonstigecondensed under reduced pressure
  9. 9
    Sonstigefollowed by condensation under reduced pressure
  10. 10
    SonstigeThe residue was recrystallized from isopropyl alcohol/water

Vorschrift

2-(2-{[3-(4-Bromophenoxy)propyl]pyridin-4-ylmethylamino}ethyl)-2H-isoquinolin-1-one (500 mg), 2-pyrrolidone (0.228 ml), potassium carbonate (415 mg), copper iodide (I)(190 mg), and N,N′-dimethyl ethylenediamine (0.39 ml) were added to toluene (5 ml). The mixture was stirred at 100° C. for 12 hours under nitrogen atmosphere. The reaction mixture was cooled to room temperature. After adding aqueous ammonia, extraction was performed using ethyl acetate. The organic layer was washed with saturated saline, and dried with sodium sulfate. After the organic layer was condensed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate:methanol=100:0,70:30). The purified product was condensed under reduced pressure. A condensed hydrochloric acid (0.3 ml) was added to an ethanol solution of the residue, followed by condensation under reduced pressure. The residue was recrystallized from isopropyl alcohol/water to give the title compound (350 mg) as a white powder. mp: 210 to 214° C. (dec.)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822453B2uspto-grants-2014_09