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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171285Generated: November 1, 2026

Hydrogen Peroxide → HCID 117643709, compound

https://huagongshe.com/reaction/2171285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantDimethylsulfoxide ethanolHCID 22338741—
ReactantHCID 117644363HCID 117644363—
SolventWaterHCID 962—
ProductHCID 117643709HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051310B2
Source datasetuspto-grants-2015_06
ORD IDord-3f82ee0c994b4c28a6ac9f140e8074c9
Source noteuspto-grants-2015_06