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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82651생성일: 2026년 10월 26일

6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amine → N4-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}pyrimidine-4,5-diamine

https://huagongshe.com/reaction/82651

반응식

참여 물질

역할이름HCID투입량
반응물6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amineHCID 58577671—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N4-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}pyrimidine-4,5-diamineHCID 5857732539.8%

반응 단계

A mixture of 6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amine (240 mg) and 10% palladium on carbon (160 mg) in MeOH (10 mL) and THF (10 mL) was hydrogenated under balloon pressure at room temperature overnight. To the mixture was added TEA (0.50 mL). The catalyst was removed by filtration and the filtrate was concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with 0%-5% MeOH in AcOEt) to give N4-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}pyrimidine-4,5-diamine (80 mg) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846713B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6fbeaca5d6f84c4382fbc1401bbf4c03
출처 메모uspto-grants-2014_09