反応 #48130

ord-cff77b2c6d6e4f489cad09671e734fa1

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 6

実験手順

In analogy to the procedure described for the synthesis of example 6, 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 2-methoxyphenylboronic acid. The title compound was obtained in 7% yield as yellow oil. MS (m/e): 512.3 (MH+, 100%).

出典

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