반응 #48167

ord-96e7a180dc8e4421bce134f73e5a6610

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 [6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4,4-difluoro-piperidin-1-yl)-methanone (example 42, step 1) and 2-chloropyridine-4-boronic acid. The title compound was obtained in 20% yield as light yellow oil. MS (m/e): 595.1 (MH+, 100%).

출처

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