関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Ethyl bromopyruvate | HCID 66144 | — |
| 反応物 | Tryptamine hydrochloride | HCID 67652 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate | HCID 57467979 | — |
反応手順
A mixture of tryptamine hydrochloride (1.96 g, 10 mmol), ethyl 3-bromopyruvate (1.67 mL, 1.2 equiv) and decolorizing charcoal (0.5 g) in absolute ethanol was heated to reflux under nitrogen overnight. TEA was added and the reaction mixture was heated to reflux for another 7.5 hours. After cooling, charcoal was removed by filtration and washed with ethanol. The filtrate was concentrated under vacuum and diluted with water (20 mL). It was then extracted by EtOAc (3×30 mL) and the combined organic layers were washed with brine and dried over MgSO4. Evaporation of solvent and recrystallization from DCM-Hexane gave the title compound (1.17 g). 1H-NMR (CDCl3): δ 10.49 (1 H, br s), 7.79 (1H, d), 7.43 (1H, d), 7.43 (1 H, d), 7.06 (2H, m), 5.27 (1H, br s), 4.29 (2H, q) 3.58 (2H, m), 3.17 (2H, m), 1.36 (3H, t); MS (ES): 257 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524704B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-e9ef8ddee810448cb1d50790e723ab4a |
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| 出典メモ | uspto-grants-2013_09 |
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