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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877462Generated: November 1, 2026

Ethanolamine → HCID 58338263, compound

https://huagongshe.com/reaction/1877462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)carbazol-9-yl]benzonitrileHCID 58338358—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductHCID 58338263HCID 58338263—

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 0.872 g of 2-aminoethanol 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 mixtures of dichloromethane and ethanol (from 95/5 to 90/10 by volume), followed by crystallization from 10 ml of diisopropyl ether, 180 mg of 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(2-hydroxyethylamino)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-79a670d630994ab391eccfa3cab9e59a
Source noteuspto-grants-2012_11