Reaction #48143

ord-0d499b5b7dad4b6cb3176cc455c46b1c

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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 4-cyanophenylboronic acid. The title compound was obtained in 45% yield as yellow foam. MS (m/e): 507.4 (MH+, 100%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745479B2uspto-grants-2010_06