Reaction Steps
5-(Pent-4-ynyloxy)-2-(3-(piperidin-4-ylidenemethyl)phenoxy)pyridine (0.26 g, 0.746 mmol) and phenyl pyridin-3-ylcarbamate (0.159 g, 0.746 mmol) were dissolved in DMSO (3 mL) and triethylamine (0.3 mL) was added dropwise. The reaction was stirred for 12 h at RT. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water, dried over sodium sulfate and evaporated to dryness. The residue was purified by silica gel column chromatography (acetone:hexane, 2:5) to give the title compound (0.23 g, 65%). 1H NMR (500 MHz, CDCl3): δ 8.60 (s, 1H), 8.24 (s, 1H), 8.16 (d, J=7.5 Hz, 1H), 7.88 (s, 1H), 7.29 (m, 3H), 6.98 (d, J=7.5 Hz 2H), 6.93 (d, J=11 Hz, 2H), 6.86 (d, J=9 Hz, 1H), 6.38 (s, 1H), 4.07 (t, J=6 Hz, 2H), 3.64 (m, 2H), 3.53 (m, 2H), 2.59 (m, 2H), 2.46 (m, 2H), 2.40 (d, J=7 Hz, 2H), 1.98 (t, J=7 Hz, 3H); 13C NMR (125 MHz, CDCl3): δ 157.51, 155.22, 154.49, 151.84, 143.19, 140.58, 138.81, 137.68, 136.57, 133.71, 129.44, 127.90, 126.87, 124.84, 124.63, 123.78, 120.59, 118.35, 112.56, 83.15, 69.15, 67.28, 45.74, 44.74, 35.76, 29.17, 28.09, 15.08; m/z (469.2, MH+); HPLC: 97.8%.
