Реакция #2013601

ord-8f17390d279e45f38f3148c7cd543e4a

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеat 80° C.
  2. 2
    Другоеfor 3 h

Методика

Following the procedure for 3-(7-fluoro-4-trifluoromethylbenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine, using 2-chloro-4,5-difluoro-1,3-benzothiazole and conducting the Suzuki coupling at 80° C. for 3 h, the title compound was obtained as a yellow solid. MS (ES+): m/z=413.13 [MH+]. HPLC: tR=2.46 min (ZQ3, polar—5 min).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08178668B2uspto-grants-2012_05