戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1163909作成日:2026年10月26日

N-Ethyltryptamine → N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine

https://huagongshe.com/reaction/1163909

反応式

関与物質

役割名称HCID仕込み量
反応物N-EthyltryptamineHCID 6092—
反応物TriethylamineHCID 8471—
反応物BenzyloxycarbonylglycineHCID 14349—
反応物Isobutyl chloroformateHCID 62365—
溶媒TetrahydrofuranHCID 8028—
生成物N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamineHCID 20513176101.6%

反応条件

温度-15 °C

反応手順

30 ml of anhydrous tetrahydrofuran and 1.05 g of triethylamine are added to 2.17 g of N-benzyloxycarbonyl-glycine, and 1.43 g of isobutyl chloroformate are added dropwise thereto at -15° C. under stirring. A solution of 1.96 g of N-ethyl-tryptamin (i.e., 3-(2-ethylamino)ethylindole) in 40 ml of anhydrous tetrahydrofuran is added dropwise to the mixture at the same temperature, and said mixture is stirred at 0° C. for one hour and further stirred at room temperature for 16 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (oil) is purified by silica gel chromatography (Solvent: ethyl acetate-chloroform (1:1). 4.0 g of N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine are thereby obtained as a colorless oil. Yield: 100%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04367230
出典データセットuspto-grants-1983_01
ORD IDord-c07ad14976464c3099faf93d61d2dd8f
出典メモuspto-grants-1983_01