반응 #48126

ord-89edaa65bc104e0c882285743a42b47b

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타In analogy to the procedure described for the synthesis of example 6

실험 절차

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 3-trifluoromethoxybenzene boronic acid. The title compound was obtained in 73% yield as light green foam. MS (m/e): 566.4 (MH+, 100%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745479B2uspto-grants-2010_06