Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4,6-Dichloro-5-nitropyrimidine | HCID 20312 | — |
| 반응물 | 4-[(1-methyl-1H-benzimidazol-2-yl)oxy]aniline | HCID 21563677 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-chloro-N-{4-[(1-methyl-1H-benzimidazol-2-yl)oxy]phenyl}-5-nitropyrimidin-4-amine | HCID 58577671 | 48.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09226921B2 |
| 출처 데이터셋 | uspto-grants-2016_01 |
| ORD ID | ord-f538561b6d944626a90efd7831685d94 |
| 출처 메모 | uspto-grants-2016_01 |