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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276023Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/276023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonamideHCID 7370—
Edukt4-Acetamido-3-nitrobenzoic acidHCID 73758—
Edukt3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-benzenesulfonyl-4-acetylamino-3-nitrobenzamideHCID 1831541678,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352985B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-5431c869c2e0400b9d0d9f80ddb4dede
Quellennotizuspto-grants-2002_03