化工社化工社 化学情報印刷レポート · 研究参考用
Water → [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine | HCID 136335844 | — |
| 反応物 | HCID 178506173 | HCID 178506173 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine | HCID 66835968 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09029357B2 |
| 出典データセット | uspto-grants-2015_05 |
| ORD ID | ord-1307a4a9dfd7453aaf605f302d87ff9d |
| 出典メモ | uspto-grants-2015_05 |