戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 370061作成日:2026年10月27日

Melatonin → N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide

https://huagongshe.com/reaction/370061

反応式

関与物質

役割名称HCID仕込み量
反応物MelatoninHCID 896—
反応物BoraneHCID 6331—
反応物Acetic AnhydrideHCID 7918—
反応物Potassium HydroxideHCID 14797—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒Trifluoroacetic acidHCID 6422—
生成物N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamideHCID 23283701—

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140372
出典データセットuspto-grants-2000_10
ORD IDord-b487646d24224174922936a970b2bb5f
出典メモuspto-grants-2000_10