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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1877442Erstellt: 26. Oktober 2026

Hydrogen Peroxide → 2-cyclohexylamino-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]benzamide

https://huagongshe.com/reaction/1877442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktCyclohexylamineHCID 7965—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
Edukt2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthanolHCID 702—
Produkt2-cyclohexylamino-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]benzamideHCID 44223734—

Reaktionsschritte

The process is carried out as in stage 3 of Example 3, but using 100 mg of 2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 263 mg of potassium carbonate and 94 mg of cyclohexylamine in 0.8 ml of dimethyl sulphoxide. 0.4 ml of a 1M aqueous solution of sodium hydroxide, 0.4 ml of a 30% aqueous solution of hydrogen peroxide and 2 ml of ethanol are then added to the reaction medium. After treatment and purification as in stage 3 of Example 3, 40 mg of 2-cyclohexylamino-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]benzamide are thus obtained in the form of a white solid, the characteristics of which are the following:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08309721B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-26725bbae2b44aba84b559bff6d73e75
Quellennotizuspto-grants-2012_11