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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1044269생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1044269

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4,6-Dichloro-5-nitropyrimidineHCID 20312—
반응물4-[(1-methyl-1H-benzimidazol-2-yl)oxy]anilineHCID 21563677—
용매TetrahydrofuranHCID 8028—
생성물6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amineHCID 5857767148.9%

반응 단계

To a solution of 4-[(1-methyl-1H-benzimidazol-2-yl)oxy]aniline (0.30 g) and TEA (0.26 ml) in THF (15 mL) was added 4,6-dichloro-5-nitropyrimidine (0.24 g) at room temperature, and the mixture was stirred at room temperature for 2 h. The mixture was poured into water, and the mixture was extracted with AcOEt. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography (dry charge, silica gel, eluted with 5%-50% AcOEt in hexane) to give 6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amine (0.24 g) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563575B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-9890c5be30c342cca09d6c8496f57d85
출처 메모uspto-grants-2013_10