関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Ethyltryptamine | HCID 6092 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Benzyloxycarbonylglycine | HCID 14349 | — |
| 反応物 | Isobutyl chloroformate | HCID 62365 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine | HCID 20513176 | 101.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04367230 |
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| 出典データセット | uspto-grants-1983_01 |
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| ORD ID | ord-c07ad14976464c3099faf93d61d2dd8f |
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| 出典メモ | uspto-grants-1983_01 |
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