化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrate | HCID 215415 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide | HCID 22754838 | 105.7% |
反応手順
To 3-[2-(4-Amino-1-piperidyl)ethyl]indole (1.307 g.) suspended in a solution of triethylamine (2 mls.) in dichloromethane (10 mls.) at room temperature with stirring was added methane sulphonyl chloride (0.570 g.) in dichloromethane (5 mls.). After stirring for 18 hours the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.690 g.) as an oil. This was recrystallized from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04131680 |
| 出典データセット | uspto-grants-1978_12 |
| ORD ID | ord-945371300be648fc962154efaeb99079 |
| 出典メモ | uspto-grants-1978_12 |