HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877494Generated: October 31, 2026
Hydrogen Peroxide → 2-[2-(pyridin-3-yl)ethylamino]-4-[4-(quinolin-3-yl)-9H-carbazol-9-yl]benzamide
https://huagongshe.com/reaction/1877494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Pyridin-3-yl)ethan-1-amine | HCID 854051 | — |
| Reactant | 2-Fluoro-4-[4-(quinolin-3-yl)carbazol-9-yl]benzonitrile | HCID 67307861 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[2-(pyridin-3-yl)ethylamino]-4-[4-(quinolin-3-yl)-9H-carbazol-9-yl]benzamide | HCID 58338319 | — |
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 1 of Example 32, 166 mg of potassium carbonate and 346 mg of 3-(2-aminoethyl)pyridine 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 ethanol (95/5 by volume), 84 mg of 2-[2-(pyridin-3-yl)-ethylamino]-4-[4-(quinolin-3-yl)-9H-carbazol-9-yl]benzamide are thus obtained in the form of a white powder, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309721B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-1576d26ad50846b79a8aa2e87c37fbec |
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| Source note | uspto-grants-2012_11 |
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