Реакция #48156

ord-4c2aa5e56d35437cacdc1e4643f999ef

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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-morpholino-5-pyridine boronic acid. The title compound was obtained in 7% yield as yellow solid. MS (m/e): 568.4 (MH+, 100%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745479B2uspto-grants-2010_06