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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877506Generated: November 1, 2026

Hydrogen Peroxide → HCID 58338299, compound

https://huagongshe.com/reaction/1877506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant1-(Aminomethyl)cyclopropan-1-olHCID 12609623—
Reactant2-Fluoro-4-[4-(quinolin-3-yl)carbazol-9-yl]benzonitrileHCID 67307861—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductHCID 58338299HCID 58338299—

Reaction Steps

The process is carried out as in stage 3 of Example 3, but using 165.4 mg of 2-fluoro-4-[4-(quinolin-3-yl)-9H-carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 165.8 mg of potassium carbonate and 279 mg of 1-(aminomethyl)cyclopropan-1-ol in 1.7 ml of dimethyl sulphoxide, in a microwave for 1 hour and 30 minutes at 115° C. 0.76 ml of a 1M aqueous solution of sodium hydroxide, 0.735 ml of a 30% aqueous solution of hydrogen peroxide and 4 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 methanol (95/5 by volume), 11 mg of 4-[4-(quinolin-3-yl)-9H-carbazol-9-yl]-2-[(1-hydroxycyclopropan-1-yl)methylamino]benzamide are thus obtained in the form of a pale yellow powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309721B2
Source datasetuspto-grants-2012_11
ORD IDord-bf15cb8127414df2800c9be90c7601f0
Source noteuspto-grants-2012_11