반응 #46476

ord-5273fb302fec4087ac4dbb737e7d1db6

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척eluted with 1/1 ethyl acetate/hexane
  2. 2
    기타further purified on two analytical thin layer chromatography plates (1/1 ethyl acetate/hexane)
  3. 3
    기타additionally purified on two more analytical plates (35/65 ethyl acetate/hexane)

실험 절차

4-[2-Carbamoyl-1-(4-fluoro-benzyl)-1H-indol-4-yl]-piperazine-1-carboxylic acid tert-butyl ester (0.0155 gm, 0.034 mmol) was dissolved in dichloromethane and 1-fluoro-2,4,6-trimethylpyridinium triflate (85%, 0.012 gm, 0.035 mmol) was added and the reaction mixture was stirred at room temperature overnight. The mixture was transferred onto two preparative thin layer chromatography plates and eluted with 1/1 ethyl acetate/hexane, then further purified on two analytical thin layer chromatography plates (1/1 ethyl acetate/hexane), and then additionally purified on two more analytical plates (35/65 ethyl acetate/hexane) to give 4-[2-carbamoyl-3-fluoro-1-(4-fluoro-benzyl)-1H-indol-4-yl]-piperazine-1-carboxylic acid tert-butyl ester (0.009 gm, 56% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741326B2uspto-grants-2010_06