Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877471Generated: November 2, 2026

Hydrogen Peroxide → HCID 58338332, compound

https://huagongshe.com/reaction/1877471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant4-AminotetrahydropyranHCID 419223—
Reactant2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductHCID 58338332HCID 58338332—

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)carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 296 mg of potassium carbonate and 1.444 g of 4-aminotetrahydropyran 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 (97/3 by volume), followed by crystallization from 2 ml of ethyl acetate, 150 mg of 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(tetrahydropyran-4-ylamino)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-326af91c33a7472387c989b8616fce7e
Source noteuspto-grants-2012_11