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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440873Generated: October 27, 2026

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

https://huagongshe.com/reaction/440873

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant(3-Nitro-phenyl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amineHCID 9860872—
SolventDichloromethaneHCID 6344—
ProductN-(3-nitro-phenyl)-4-(N-oxido-3-pyridyl)-2-pyrimidine-amineHCID 22405644—

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521184
Source datasetuspto-grants-1996_05
ORD IDord-c3431567551c499387cdf45b4c7175ae
Source noteuspto-grants-1996_05