반응 #1779405

ord-c87ad40eb8d0435d9dcdc90dfcf4262c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.STIRRINGthe solution stirred for 2 hours
  3. 3
    기타the solution evaporated
  4. 4
    추출extracted with ethyl acetate (1×20 mL)
  5. 5
    기타The organic layer was separated
  6. 6
    세척washed with brine (2×20 mL)
  7. 7
    기타The organic layer was separated
  8. 8
    건조dried over anhydrous sodium sulphate
  9. 9
    여과filtered
  10. 10
    기타evaporated
  11. 11
    기타to give a foam
  12. 12
    기타The foam was purified
  13. 13
    세척an ISCO™ Companion (4 g. silica gel, eluting with dichloromethane:acetic acid 99.5:0.5 to dichloromethane:methanol:acetic acid 95:5:0.5)
  14. 14
    기타The appropriate fractions were evaporated
  15. 15
    기타to give a film
  16. 16
    기타The film was triturated with diethyl ether

실험 절차

2-[1-(1-Methylazetidin-3-yl)-1H-pyrazol-5-yl]-4-(trifluoromethyl)phenol, (Preparation 855, 137 mg, 0.00046 mol) was dissolved in acetonitrile (10 mL) and treated with potassium tert-butoxide (57 mg, 0.0005 mol) and stirred under nitrogen for 30 minutes. Tert-butyl 1,3-thiazol-4-yl[(2,4,5-trifluorophenyl)sulfonyl]carbamate, (Preparation 297, 182 mg, 0.00046 mol) was added and the solution stirred for 2 hours. Water (0.2 mL) was added and the solution evaporated. The residue was suspended in water and extracted with ethyl acetate (1×20 mL). The organic layer was separated and washed with brine (2×20 mL). The organic layer was separated, dried over anhydrous sodium sulphate, filtered and evaporated to give a foam. The foam was purified using an ISCO™ Companion (4 g. silica gel, eluting with dichloromethane:acetic acid 99.5:0.5 to dichloromethane:methanol:acetic acid 95:5:0.5). The appropriate fractions were evaporated to give a film. The film was triturated with diethyl ether to give the title compound as a white solid (11 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08153814B2uspto-grants-2012_04