반응 #67165

ord-714d57e088dc4977a6172e5559100308

반응 조건

온도
20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The mixture was partitioned between ethyl acetate (5 ml) and saturated ammonium chloride solution (2 ml)
  2. 2
    기타separating the layers with a hydrophilic frit
  3. 3
    기타The organic layer was evaporated to dryness under a stream of nitrogen

실험 절차

To a solution of N-(2-(methyloxy)-5-{1-(phenylsulfonyl)-4-[5-(tetrahydro-1,4-oxazepin-4(5H)-ylmethyl)-1,3,4-oxadiazol-2-yl]-1H-indazol-6-yl}-3-pyridinyl)methanesulfonamide (50 mg, 0.078 mmol) in 1,4-dioxane (1 ml) was added 2M sodium hydroxide (1 ml, 2.000 mmol) and the mixture stirred at 20° C. for 2 h. The mixture was partitioned between ethyl acetate (5 ml) and saturated ammonium chloride solution (2 ml), separating the layers with a hydrophilic frit. The organic layer was evaporated to dryness under a stream of nitrogen to give the title compound as a pale brown solid (35 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08524751B2uspto-grants-2013_09