化工社化工社 化学情報印刷レポート · 研究参考用
1-Methylimidazole → (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Methylimidazole | HCID 1390 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 3-Benzoylpropionic acid | HCID 72871 | — |
| 反応物 | (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine | HCID 57943187 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide | HCID 59464671 | — |
反応手順
3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of thionyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09440963B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-f1df7ed542cf4c39a393af7f90a4d2ef |
| 出典メモ | uspto-grants-2016_09 |