4-Chlorobenzenesulfonamide → N-[({2-[4-(3,5-Dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethyl}amino)carbonyl]-4-chlorobenzenesulfonamide

関与物質

反応手順

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-chlorobenzenesulfonamide: 1H-NMR (CDCl3) δ 7.84-7.79 (2H, m), 7.48-7.21 (11H, m), 6.24 (1H, br.s), 3.48-3.42 (2H, m), 2.83 (2H, t, J=7.1 Hz), 2.32 (3H, s), 2.24 (3H, s).

情報源と証拠