HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171285Generated: November 1, 2026
Hydrogen Peroxide → HCID 117643709, compound
https://huagongshe.com/reaction/2171285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethylsulfoxide ethanol | HCID 22338741 | — |
| Reactant | HCID 117644363 | HCID 117644363 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 117643709 | HCID 117643709 | — |
Reaction Steps
A 5M sodium hydroxide aqueous solution (0.038 ml) and a 30% hydrogen peroxide solution (0.008 ml) were added to a DMSO/EtOH (0.1 ml/0.1 ml) solution containing 6-((1-acetyl-3-aminopiperidin-4-yl)amino)-5-fluoro-2-((5-methylpyridin-3-yl)amino)nicotinonitrile hydrochloride (6 mg), followed by stirring at room temperature for 30 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layers were washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure. Ethyl acetate (0.5 ml) and 4M hydrochloric acid/1,4-dioxane (0.004 ml) were added to the obtained residue, followed by stirring at room temperature for 0.5 hours. The solvent was removed under reduced pressure. The obtained residue was washed with ethyl acetate. A yellow solid of 6-((1-acetyl-3-aminopiperidin-4-yl)amino)-5-fluoro-2-((5-methylpyridin-3-yl)amino)nicotinamide hydrochloride (3.2 mg) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051310B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3f82ee0c994b4c28a6ac9f140e8074c9 |
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| Source note | uspto-grants-2015_06 |
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