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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 851992Erstellt: 25. Oktober 2026

Potassium Iodide → 4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-[1,2,4]triazol-1-yl-benzyl)-benzenesulfonamide

https://huagongshe.com/reaction/851992

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamideHCID 2738683—
Edukt1-(4-(bromomethyl)phenyl)-1H-1,2,4-triazoleHCID 2776489—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-[1,2,4]triazol-1-yl-benzyl)-benzenesulfonamideHCID 1845539564%

Reaktionsschritte

4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamide (0.16 g, 0.52 mmol), 1-[4-(bromomethyl)phenyl]-1H-1,2,4-triazol (0.25 g, 1.03 mmol), potassium carbonate (0.72 g, 5.17 mmol) and potassium iodide (0.02 g, 0.10 mmol) in 5 ml dimethylformamide were stirred at 65° C. for 5 hours. Extraction with water/ethylacetate and chromatography on silicagel with ethylacetate yielded 0.15 g (64%) 4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-[1,2,4]triazol-1-yl-benzyl)-benzenesulfonamide as white solid, MS: m/e (%)=460.1 (MH+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253158B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-ba4aa8c69cfc44c6ac5421bf27243573
Quellennotizuspto-grants-2007_08