反応 #43865

ord-6730698d80b343098f5ffc7e550a1de5

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮concentrated
  2. 2
    その他purified by preparative LCMS

実験手順

[5-(Benzyl-cyclohexanecarbonyl-amino)-2-propyl-benzoimidazol-1-yl]-acetic acid tert-butyl ester (0.12 mmol) was treated with TFA (2 mL) for 2 hours, concentrated, and purified by preparative LCMS to give the title compound. 1H NMR (d6-DMSO) δ7.50 (d, 1H), 7.21 (m, 6H), 6.95 (m, 1H), 5.09 (s, 2H), 4.86 (s, 2H), 2.72 (t, 2H), 2.18 (m, 1H), 1.60 (m, 9H), 1.10 (m, 1H), 0.99 (t, 3H), 0.85 (m, 2H). MS calculated for C26H31N3O3+H: 434, observed: 434.

出典

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