Reaktion #617949

ord-6cbb5b4bfd664254a9e8b69ce020987c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added
  2. 2
    Temperaturrefluxed under nitrogen for 6 h
  3. 3
    SonstigeThe reaction was quenched with water
  4. 4
    Sonstigethe toluene layer was removed
  5. 5
    Sonstigeevaporated in a rotary evaporator under vacuum

Vorschrift

Following the above procedure, Suzuki coupling of 3.8 g of 7-acetyl-12-bromo-7H-dibenzo [a,g]carbazole and 2.7 g of (4-benzo[d]thiazol-2-yl) phenylboronic acid were stirred together in 30 ml of toluene. To this was added 0.02 g of tetrakis(triphenylphosphine)palladium, 2.1 g of potassium carbonate and 10 ml of aqueous ethanol were added and refluxed under nitrogen for 6 h. The reaction was quenched with water and the toluene layer was removed and passed through a celite column. The organic layers were combined and then evaporated in a rotary evaporator under vacuum to yield 4.1 g of 7-acetyl-12-[4-benzo[d]thiazol-2-yl) phenyl]-7H-dibenzo[a,g]carbazole as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09353085B2uspto-grants-2016_05