Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1877469Erstellt: 26. Oktober 2026

Hydrogen Peroxide → 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[(furan-3-ylmethyl)amino]benzamide

https://huagongshe.com/reaction/1877469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
Edukt1-(Furan-3-yl)methanamineHCID 2776197—
Edukt2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthanolHCID 702—
Produkt4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[(furan-3-ylmethyl)amino]benzamideHCID 58338302—

Reaktionsschritte

The process is carried out as in stage 3 of Example 3, but using 300 mg of 2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 296 mg of potassium carbonate and 1.387 g of 3-furylmethylamine in 3 ml of dimethyl sulphoxide. 1.357 ml of a 1M aqueous solution of sodium hydroxide, 1.313 ml of a 30% aqueous solution of hydrogen peroxide and 7 ml of ethanol are then added to the reaction medium. After treatment as in stage 3 of Example 3, and then purification by flash chromatography on silica gel, elution being carried out with a mixture of dichloromethane and ethanol (96/4 by volume), followed by crystallization from 5 ml of ethyl acetate, 220 mg of 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[(furan-3-ylmethyl)amino]benzamide are thus obtained in the form of a beige solid, the characteristics of which are the following:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08309721B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-d58e60af69264206a6fa1b9f8af3aa83
Quellennotizuspto-grants-2012_11