(Pyrimidin-5-yl)boronic acid → 5-(Pyrimidin-5-yl)-6-(pyrrolidin-1-yl)-N-(4-(trifluoromethoxy)phenyl)nicotinamide

Participants

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Example 66 using 5-bromo-6-(pyrrolidin-1-yl)-N-(4-(trifluoromethoxy)phenyl)nicotinamide (Stage 67.1) and pyrimidin-5-ylboronic acid to afford a white solid. UPLC-MS (Condition 3) tR=1.07 min, m/z=430.4 [M+H]+, m/z=428.3 [M−H]−; 1H-NMR (400 MHz, DMSO-d6) δ ppm 1.68-1.94 (m, 4H) 3.15 (t, J=6.15 Hz, 4H) 7.37 (d, J=8.78 Hz, 2H) 7.86 (d, J=8.91 Hz, 2H) 8.11 (d, J=2.01 Hz, 1H) 8.80 (d, J=1.88 Hz, 1H) 8.90 (s, 2H) 9.20 (s, 1H) 10.19 (s, 1H).

Provenance & Evidence