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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587563생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/587563

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 번호US09226921B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-f538561b6d944626a90efd7831685d94
출처 메모uspto-grants-2016_01