Реакция #10195

ord-61f22df1abf941a0bb796b93e209b430

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другое(reaction becomes dark red)
  2. 2
    ДругоеThe reaction was quenched with NaHSO3 and water (pH 2.5)
  3. 3
    Экстракцияthen extracted with ethyl acetate (4×30 mL)
  4. 4
    СушкаAfter drying (Na2SO4)
  5. 5
    Фильтрацияthe solution was filtered
  6. 6
    Концентрированиеconcentrated to a yellow oil which
  7. 7
    Другоеwas chromatographed on Silica gel
  8. 8
    Другоеto provide a yellow oil
  9. 9
    Другоеabove yielded 5 g, 67%)

Методика

1-(4-Amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (500 mg, 1.85 mmol) was dissolved in H2O (5 mL) and concentrated H2SO4 solution (0.5 mL) then cooled to 0° C. and treated with a solution of sodium nitrite (NaNO2) (140 mg, 2.04 mmol) in H2O (2 mL) dropwise. Potassium iodide (460 mg, 2.78 mmol) in 1N H2SO4 solution (0.5 mL) was added over 10 minutes (reaction becomes dark red). The resulting solution was warmed to room temperature and stirred 18 hours. The reaction was quenched with NaHSO3 and water (pH 2.5) then extracted with ethyl acetate (4×30 mL). After drying (Na2SO4), the solution was filtered and concentrated to a yellow oil which was chromatographed on Silica gel to provide a yellow oil. (260 mg, 37%). (TLC 30% ethyl acetate/hexanes Rf 0.70). (A 5.4 g scale performed as above yielded 5 g, 67%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091372B2uspto-grants-2006_08