反应详情

The title compound was prepared according to the procedure described in step 2 of Example 22 from phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate (step 1 of Example 22) and 4-pyridinesulfonamide (J. Chem. Soc., 1958, 3514: 1H-NMR (CDCl3) δ 8.81 (2H, d, J=5.4 Hz), 7.77 (2H, d, J=5.9 Hz), 7.46-7.18 (9H, m), 6.11 (1H, br.s), 3.44-3.41 (2H, m), 2.84-2.79 (2H, m), 2.31 (3H, s), 2.21 (3H, s).