関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Melatonin | HCID 896 | — |
| 反応物 | Borane | HCID 6331 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide | HCID 23283701 | — |
反応手順
To a solution, cooled to 0° C., of melatonin (1 mmol) in trifluoroacetic acid (2 ml) is added dropwise borane (2 eq, 1M solution in THF). The mixture is stirred for 30 min at 0° C. followed by dropwise addition of water (1.5 ml), and the medium is left stirring for 1 h at room temperature. The mixture is then brought to pH=10 using 2N potassium hydroxide solution and is then extracted with dichloromethane. The crude product is separated on a column of flash silica (25/75/5 acetone/dichloromethane/methanol) and 110 mg of N-[2-(5-methoxyindolin-3-yl)ethyl]acetamide are obtained, which product is then acetylated with acetic anhydride in pyridine to give N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06140372 |
|---|
| 出典データセット | uspto-grants-2000_10 |
|---|
| ORD ID | ord-b487646d24224174922936a970b2bb5f |
|---|
| 出典メモ | uspto-grants-2000_10 |
|---|