反应详情

The titled compound was prepared using the experimental protocol described for Preparation 43B employing N-(6-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)-5-phenyl-4-(trifluoromethyl)isoxazole-3-carboxamide (Preparation 49A). 1H NMR (400 MHz, CDCl3) δ ppm 7.73 (2H, d, J=7.26 Hz), 7.51-7.60 (3H, m), 7.48 (1H, d, J=9.02 Hz), 6.78-6.84 (2H, m), 3.82 (3H, s), 3.08-3.17 (2H, m), 2.95-3.03 (2H, m).