HRID891106
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
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 3-methoxybenzenesulfonamide: 1H-NMR (CDCl3) δ 7.47-7.09 (13H, m), 6.36 (1H, br.s), 3.81 (3H, s), 3.49-3.43 (2H, m), 2.83 (2H, t, J=6.6 Hz), 2.32 (3H, s), 2.24 (3H, s).