참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Indole-3-Butyric Acid | HCID 8617 | — |
| 반응물 | N,N-dimethylhydroxylamine hydrochloride | HCID 27969 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-Methyl-N-Methoxy-4-(3-indolyl)butyramide | HCID 11107631 | 94.3% |
반응 단계
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-yloxytris(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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05620971 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-335b9dd89de54030898409aded9b82d1 |
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| 출처 메모 | uspto-grants-1997_04 |
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