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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276023Generated: October 25, 2026

Benzenesulfonamide → N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide

https://huagongshe.com/reaction/276023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamideHCID 7370—
Reactant4-Acetamido-3-nitrobenzoic acidHCID 73758—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventDimethylformamideHCID 6228—
ProductN-benzenesulfonyl-4-acetylamino-3-nitrobenzamideHCID 1831541678.2%

Reaction Steps

N,N′-carbonyldiimidazole (14.45 g) was added to a solution of 10.00 g of 4-acetylamino-3-nitrobenzoic acid in 300 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for 1 hour. Subsequently, 14.03 g of benzenesulfonamide and 13.58 g of diazabicycloundecene were added thereto, and the mixture was stirred at 100° C. for 72 hours. The reaction mixture was separated with the addition of chloroform and water. The organic layer was then concentrated, and the resulting residue was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and methanol at a ratio of 4:1) to give 12.67 g of N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-5431c869c2e0400b9d0d9f80ddb4dede
Source noteuspto-grants-2002_03