Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 851991Erstellt: 25. Oktober 2026

Potassium Iodide → 4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-pyrazol-1-yl-benzyl)-benzenesulfonamide

https://huagongshe.com/reaction/851991

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-PyrazoleHCID 2776479—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-pyrazol-1-yl-benzyl)-benzenesulfonamideHCID 6948924987%

Reaktionsschritte

4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamide (0.16 g, 0.52 mmol), 1-[4-(bromomethyl)phenyl]-1H-pyrazole (0.26 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/heptane (90/10 to 1/0) yielded 0.20 g (87%) 4-chloro-N-(2-oxo-azepan-3-yl)-N-(4-pyrazol-1-yl-benzyl)-benzenesulfonamide as light yellow solid, MS: m/e (%)=459.1 (MH+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253158B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-d9fd94ff77b3455fbd035414419c0093
Quellennotizuspto-grants-2007_08