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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440873생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/440873

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물(3-Nitro-phenyl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amineHCID 9860872—
용매DichloromethaneHCID 6344—
생성물N-(3-nitro-phenyl)-4-(N-oxido-3-pyridyl)-2-pyrimidine-amineHCID 22405644—

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05521184
출처 데이터셋uspto-grants-1996_05
ORD IDord-c3431567551c499387cdf45b4c7175ae
출처 메모uspto-grants-1996_05