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 | N,N-dimethylhydroxylamine hydrochloride | HCID 27969 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-Methyl-N-Methoxy-4-(3-indolyl)butyramide | HCID 11107631 | 94.3% |
反応手順
To a slurry of 1.75 g (8.61 mmol) of 3-indolebutyric acid (Aldrich Chemical Co.) in acetonitrile at room temperature was added 7.0 mL (40.2 mmol) of N,N-diisopropylethylamine, 1.0 g (10.3 mmol) of N,N-dimethylhydroxylamine hydrochloride and 4.19 g (9.5 mmol) of benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent) and the resulting mixture was allowed to stir at room temperature overnight and was then concentrated to dryness. The residue was dissolved into ethyl acetate and washed with water, 0.5N HCl, saturated NaHCO3 and brine and then dried over MgSO4 and concentrated. Flash chromatography (elution with a gradient of 2-10% ether in methylene chloride) provided 2.0 g of the amide 139. 1H NMR consistent with structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05723459 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-5ab94114d8b645e082906ef9a74075cf |
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| 出典メモ | uspto-grants-1998_03 |
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