Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine | HCID 136335844 | — |
| 반응물 | HCID 178506173 | HCID 178506173 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine | HCID 66835968 | — |
반응 단계
To a solution of (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine (70 mg) in tetrahydrofurane (3 mL) is added a 1.5M solution of 3-trifluoromethylphenylmagnesium bromide in tetrahydrofurane (0.77 mL) at room temperature. The mixture is then stirred at 40° C. for 1 h, hydrolyzed with water and extracted with ethyl acetate. The pooled organic extracts are washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography (gradient dichloromethane/methanol/ammonia from 95/5/0.5 to 90/10/0.5) to give [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine as a yellow solid melting at 90° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09029357B2 |
| 출처 데이터셋 | uspto-grants-2015_05 |
| ORD ID | ord-1307a4a9dfd7453aaf605f302d87ff9d |
| 출처 메모 | uspto-grants-2015_05 |