反応 #43853

ord-6e5503b07a4e4e9296cb68f49fa4ee7f

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他purged with N2
  2. 2
    workup.ADDITIONPalladium on activated carbon (2.2 g, 10% by weight) was added
  3. 3
    workup.ADDITIONthe reaction mixture was charged with a balloon of H2
  4. 4
    ろ過filtered through a pad of celite
  5. 5
    洗浄The celite was washed with MeOH
  6. 6
    濃縮the filtrate was concentrated

実験手順

(4-tert-Butoxycarbonylamino-2-nitro-phenylamino)-acetic acid tert-butyl ester (10.8 g, 29.4 mmol) was dissolved in MeOH (70 mL) and purged with N2. Palladium on activated carbon (2.2 g, 10% by weight) was added, and the reaction mixture was charged with a balloon of H2. The reaction mixture was stirred for 3 h at room temperature, and then filtered through a pad of celite. The celite was washed with MeOH, and the filtrate was concentrated to afford 2.1 g (22%—two steps) of the sub-title compound. MS calculated for C17H27N3O4+H: 338, observed: 338.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07732618B2uspto-grants-2010_06