反应详情

The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate (step 1 of Example 22) and 3-chloro-2-pyridinesulfonamide (U.S. Pat. No. 4,490,380): 1H-NMR (DMSO-d6) δ 8.62 (1H, d, J=4.3 Hz), 8.20 (1H, d, J=7.9 Hz), 7.71-7.67 (1H, m), 7.49-7.31 (9H, m), 6.57 (1H, br.s), 3.37-3.28 (2H, m), 2.79-2.74 (2H, m), 2.27 (3H, s), 2.23 (3H, s).