Реакция #44469

ord-bac32aa16a0143ae82d270190b816ba0

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияAfter filtration through dicalite
  2. 2
    Промывкаwashing with CH2Cl2
  3. 3
    Другоеthe volatiles were removed in vacuo
  4. 4
    workup.DISSOLUTIONThe crude product was dissolved in ethanol (250 mL) wherafter 2N (aq) NaOH (20 mL)
  5. 5
    workup.ADDITIONwas added
  6. 6
    workup.STIRRINGThis mixture was stirred at room temperature for 2.5 h
  7. 7
    ФильтрацияThe reaction mixture was filtrated through dicalite
  8. 8
    Промывкаwashed with CH2Cl2
  9. 9
    ДругоеAfter removal of the solvent under reduced pressure
  10. 10
    workup.DISSOLUTIONthe residu was dissolved in ethanol (350 mL)
  11. 11
    workup.ADDITIONNaOH (2N, 20 mL) was added
  12. 12
    workup.STIRRINGthe mixture was stirred for 3 h
  13. 13
    workup.ADDITIONWater was added
  14. 14
    Экстракцияthe mixture was extracted with ethyl acetate (3×)
  15. 15
    ПромывкаThe combined organic layers were washed with brine
  16. 16
    Другоеdried
  17. 17
    Другоеevaporated

Методика

To a solution of 8-chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepine (8.75 g, 37.9 mmol) in CH2Cl2 (375 mL) was added MnO2 (14.5 g, 166 mmol). The reaction mixture was stirred at room temperature for 1.5 h. After filtration through dicalite, washing with CH2Cl2, the volatiles were removed in vacuo. The crude product was dissolved in ethanol (250 mL) wherafter 2N (aq) NaOH (20 mL) was added. This mixture was stirred at room temperature for 2.5 h. The reaction mixture was filtrated through dicalite and washed with CH2Cl2. After removal of the solvent under reduced pressure, the residu was dissolved in ethanol (350 mL). NaOH (2N, 20 mL) was added and the mixture was stirred for 3 h. Water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried and evaporated to afford the title compound (8.9 g, 38.9 mmol).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07737136B2uspto-grants-2010_06