HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891044Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 67424667, compound
https://huagongshe.com/reaction/1891044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(4-Methylpiperazin-1-yl)aniline | HCID 737253 | — |
| Reactant | 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbonitrile | HCID 10678934 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | HCID 67424667 | HCID 67424667 | 72.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507505B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-1600681f245e490bb5919a589cf73e65 |
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| Source note | uspto-grants-2013_08 |
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