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HRID 1290249作成日:2026年10月26日
Indole-3-Butyric Acid → [4-(1H-Indol-3-yl)-butyl]-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)amine
https://huagongshe.com/reaction/1290249
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 | (S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride | HCID 70200787 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | [4-(1H-Indol-3-yl)-butyl]-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)amine | HCID 18923898 | 63% |
反応手順
3-Indolebutyric acid (1.3 g, 6.5 mmole), 1-hydroxybenzotriazole hydrate (1.1 g, 7.8 mmole) and 1,3-diisopropylcarbodiimide (2.4 ml, 15.6 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 (S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.5 g, 6.5 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and replaced with dichloromethane. The mixture was then washed with H2O. The separated organic 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. Evaporation of product fractions gave 1.5 g (61%) of the desired product, (S)-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-4-(1H-indol-3-yl)-butanamide, as a foam.
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-79d3293c36994725a9b2649cf472b858 |
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| 出典メモ | uspto-grants-1998_05 |
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