4-Chlorobenzenesulfonamide → HCID 22244564, compound

Participants

Reaction Steps

The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-{4-[5-amino-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamate (step 4 of Example 80) and 4-chlorobenzenesulfonamide: 1H-NMR (CDCl3) δ 7.85-7.80 (2H, m), 7.51-7.27 (11H, m), 6.08-6.03 (1H, m), 3.99 (2H, br.s), 3.50-3.44 (2H, m), 2.88-2.84 (2H, m).

Provenance & Evidence