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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 440873Erstellt: 23. Oktober 2026

m-Chloroperbenzoic acid → N-(3-nitro-phenyl)-4-(N-oxido-3-pyridyl)-2-pyrimidine-amine

https://huagongshe.com/de/reaction/440873

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt(3-Nitro-phenyl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amineHCID 9860872—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-nitro-phenyl)-4-(N-oxido-3-pyridyl)-2-pyrimidine-amineHCID 22405644—

Reaktionsschritte

200 mg (0.68 mmol) of N-(3-nitrophenyl)-4-(3-pyridyl)-2-pyrimidine-amine are suspended in 5 ml of methylene chloride, and 225 mg (0.71 mmol) of 3-chloroperbenzoic acid are added. After 2 hours a further 10 ml of methylene chloride are added. The suspension is stirred for a further 20 hours at room temperature. Filtration and flash chromatography of the residue (methylene chloride:methanol:25% aqueous ammonia solution=90:10:1) yield N-(3-nitro-phenyl)-4-(N-oxido-3-pyridyl)-2-pyrimidine-amine; Rf =0.4 (methylene chloride:methanol:25% aqueous ammonia solution=90: 10:1), m.p. 252°-258°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05521184
Quelldatensatzuspto-grants-1996_05
ORD IDord-c3431567551c499387cdf45b4c7175ae
Quellennotizuspto-grants-1996_05