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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18894Generated: October 26, 2026

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

https://huagongshe.com/reaction/18894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant3-Fluorobenzenesulfonyl ChlorideHCID 2734258—
ProductN-(2-benzoyl-4-chloro-phenyl)-3-fluoro-benzenesulfonamideHCID 11372710—

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-bf64c03c83814a838430dbdad85be7ce
Source noteuspto-grants-2010_06