関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Indole-3-Butyric Acid | HCID 8617 | — |
| 反応物 | Diisopropylcarbodiimide | HCID 12734 | — |
| 反応物 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 反応物 | 1,4-Benzodioxan, 2-(aminomethyl)-, hydrochloride | HCID 2849836 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(1H-indol-3-yl)-butyl]-amine | HCID 18923886 | 59.4% |
反応手順
3-Indolebutyric acid (1.2 g, 6.0 mmole), 1-hydroxybenzotriazole hydrate (0.97 g, 7.2 mmole) and 1,3-diisopropylcarbodiimide (2.3 ml, 14.4 mmole) were combined in 100 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise 2,3-dihydro-1,4-benzodioxin-2methanamine hydrochloride (1.2 g, 6.0 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and the residue partitioned between dichloromethane and water. The separated dichloromethane layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was chromatographed on a silica gel column using ethyl acetate as the eluant. Fractions were concentrated and washed with a minimum amount of THF to remove a by-product and to give 1.2 g (57%) of the desired product, (2,3-dihydro-benzo [1,4]dioxin-2-ylmethyl)-4-(1H-indol-3-yl)-butanamide, as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05750724 |
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| 出典データセット | uspto-grants-1998_05 |
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| ORD ID | ord-6126f80f08954d2a87a485f198927309 |
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| 出典メモ | uspto-grants-1998_05 |
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