Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290262생성일: 2026년 10월 26일
Diisopropylcarbodiimide → (2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-fluoro-1H-indol-3-yl)-butyl]-amine
https://huagongshe.com/reaction/1290262
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 반응물 | 1,4-Benzodioxan, 2-(aminomethyl)-, hydrochloride | HCID 2849836 | — |
| 반응물 | 4-(5-Fluoro-1H-indol-3-yl)butanoic acid | HCID 15047268 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-fluoro-1H-indol-3-yl)-butyl]-amine | HCID 18923897 | 62.2% |
반응 단계
5-Fluoroindole-3-butyric acid (1.5 g, 6.8 mmole), 1-hydroxybenzotriazole hydrate (1.1 g, 8.2 mmole) and 1,3-diisopropylcarbodiimide (2.6 ml, 16.3 mmole) were combined in 150 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-2-methanamine hydrochloride (1.4 g, 6.8 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 of the products were concentrated and washed with a minimum amount of THF to remove a by-product and to give 1.5 g (60%) of the desired product, (2,3-dihydrobenzo[1,4]dioxin-2-ylmethyl)-4-(5-fluoro-1H-indole-3yl)-butanamide, as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05750724 |
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| 출처 데이터셋 | uspto-grants-1998_05 |
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| ORD ID | ord-b751c17837eb4944b4c7098d9437aded |
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| 출처 메모 | uspto-grants-1998_05 |
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