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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877458Generated: October 23, 2026

Hydrogen Peroxide → 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[3(R,S)hydroxybutylamino)benzamide

https://huagongshe.com/en/reaction/1877458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant2-Butanol, 4-amino-HCID 170254—
Reactant2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
Product4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[3(R,S)hydroxybutylamino)benzamideHCID 58338280—

Reaction Steps

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)-9H-carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 296 mg of potassium carbonate and 1.273 g of 4-aminobutan-2(R,S)-ol 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 (95/5 by volume), 270 mg of 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-[3(R,S)-hydroxybutylamino]benzamide are thus obtained in the form of a beige solid, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309721B2
Source datasetuspto-grants-2012_11
ORD IDord-17c94908b430454d833ae98b77d7c3ac
Source noteuspto-grants-2012_11