반응 #47946

ord-7355567d588f487aa754fd38b156d94d

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the resulting mixture was heated
  2. 2
    온도at reflux for 4 hours
  3. 3
    세척washed with water
  4. 4
    건조dried over anhydrous Na2SO4
  5. 5
    농축concentrated under reduced pressure
  6. 6
    기타The crude product was purified by a silica SPE cartridge (10 g)
  7. 7
    세척eluting with dichloromethane/methanol from 99/1 to 97/3

실험 절차

To a solution of (1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (151 mg, prepared following the procedure reported in WO 2005080382) in dry tetrahydrofuran (3.3 mL), triethylamine (0.112 mL), 3-bromo-1-propanol (0.073 mL) and NaI were added and the resulting mixture was heated at reflux for 4 hours. After cooling at room temperature it was diluted with ethyl acetate (20 mL), washed with water, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product was purified by a silica SPE cartridge (10 g) eluting with dichloromethane/methanol from 99/1 to 97/3 to give the title compound as a colourless oil (144 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745458B2uspto-grants-2010_06