HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877479Generated: October 25, 2026
Hydrogen Peroxide → 4-{4-[5-(benzyloxy)pyridin-3-yl]-9H-carbazol-9-yl}-2-[(3-hydroxypropyl)amino]benzamide
https://huagongshe.com/reaction/1877479
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-{4-[5-(benzyloxy)pyridin-3-yl]-9H-carbazol-9-yl}-2-fluorobenzonitrile | HCID 67309196 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-{4-[5-(benzyloxy)pyridin-3-yl]-9H-carbazol-9-yl}-2-[(3-hydroxypropyl)amino]benzamide | HCID 58338224 | 45.6% |
Reaction Steps
0.47 g of potassium carbonate and 1.7 g of 3-amino-1-propanol are successively added to a solution of 0.55 g of 4-{4-[5-(benzyloxy)pyridin-3-yl]-9H-carbazol-9-yl}-2-fluorobenzonitrile, obtained in stage 3 of Example 67, in 6 ml of dimethyl sulphoxide. The reaction mixture is heated at 90° C. for 1 hour 20 minutes in a microwave, and then 11.5 ml of ethanol are added, followed by 2.2 ml of a 1N solution of sodium hydroxide and 2.2 ml of 30% aqueous hydrogen peroxide. The reaction mixture is stirred at ambient temperature for 1 hour and then diluted with distilled water. The aqueous phase is extracted twice with ethyl acetate and the combined organic phases are washed with water and a saturated solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure, and the residue is triturated with dichloromethane and diisopropyl ether, so as to give 0.29 g of 4-{4-[5-(benzyloxy)pyridin-3-yl]-9H-carbazol-9-yl}-2-[(3-hydroxypropyl)amino]benzamide in the form of a white solid, 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-e9e1eae0b13b40e7a5bfaae3ec3566bf |
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| Source note | uspto-grants-2012_11 |
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