2-Amino-5-chlorobenzophenone → N-(2-benzoyl-4-chloro-phenyl)-3-fluoro-benzenesulfonamide

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Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-amino-5-chloro-phenyl)-phenyl-methanone and 3-fluoro-benzenesulfonyl chloride. 1H NMR (CDCl3): δ (ppm): 7.00–7.05 (m, 1H), 7.35 (m, 1H), 7.37 (m, 1H), 7.39–7.44 (m, 4H), 7.37–7.43 (m, 4H), 7.45–7.46 (m, 1H), 7.49–7.50 (m, 1H), 7.51–7.52 (m, 2H), 7.58–7.62 (m, 1H), 9.80 (s, 1H). MS: m/z 390.0 (M++1).

Provenance & Evidence