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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891044Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 67424667, compound

https://huagongshe.com/reaction/1891044

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
Reactant4-(Methylamino)-2-(methylthio)pyrimidine-5-carbonitrileHCID 10678934—
SolventTetrahydrofuran tolueneHCID 22635083—
ProductHCID 67424667HCID 6742466772.9%

Reaction Steps

248 mg of mCPBA was added to a 3:1 toluene-tetrahydrofuran (30 mL) solution containing 130 mg of 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carbonitrile, and the mixture was stirred at room temperature for 15 minutes. Then, 138 mg of 4-(4-methylpiperazin-1-yl)aniline, and 280 mg of DIPEA were added to the mixture, which was then stirred at 80° C. for 8 hours. The solvent was distilled away after cooling the reaction mixture. Then, water was added, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated saline, and the solution was concentrated after drying with anhydrous magnesium sulfate. The resulting crude product was purified by basic silica gel column chromatography, and 170 mg of a white solid was obtained as a subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507505B2
Source datasetuspto-grants-2013_08
ORD IDord-1600681f245e490bb5919a589cf73e65
Source noteuspto-grants-2013_08