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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765517Generated: October 25, 2026

4-Methoxybenzenesulfonyl chloride → N-(2-benzoyl-4-bromo-phenyl)-4-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/1765517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
Reactant2-Amino-5-bromobenzophenoneHCID 99677—
ProductN-(2-benzoyl-4-bromo-phenyl)-4-methoxy-benzenesulfonamideHCID 9955192—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 138 mg of (2-Amino-5-bromo-phenyl)-phenyl-methanone and 103 mg of 4-Methoxy-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 3.78 (s, 3H), 6.83 (d, 2H, J=9.2 Hz), 7.39 (b, 1H), 7.49 (d, 2H, J=6.4 Hz), 7.68 (m, 4H), 8.85 (d, 2H, J=6.0 Hz), 9.96 (b, 1H). MS: m/z 447.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07227035B2
Source datasetuspto-grants-2007_06
ORD IDord-709f7f613e534fdfa30244654eb7f27f
Source noteuspto-grants-2007_06