反応 #48124

ord-21a9012f47474bc9855922e663dfd827

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他In analogy to the procedure described for the synthesis of Example 1

実験手順

In analogy to the procedure described for the synthesis of Example 1, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and bromoacetonitrile. The title compound was obtained in 38% yield as light green foam. MS (m/e): 445.2 (MH+, 100%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07745479B2uspto-grants-2010_06