Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290249생성일: 2026년 10월 26일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Indole-3-Butyric Acid | HCID 8617 | — |
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 반응물 | (S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride | HCID 70200787 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [4-(1H-Indol-3-yl)-butyl]-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)amine | HCID 18923898 | 63% |
반응 단계
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.
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-79d3293c36994725a9b2649cf472b858 |
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| 출처 메모 | uspto-grants-1998_05 |
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