Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290254생성일: 2026년 10월 27일
Diisopropylcarbodiimide → (7-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-methoxy-1 H-indol-3-yl)-butyl]-amine
https://huagongshe.com/reaction/1290254
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 반응물 | 5-Methoxyindole-3-butyric acid | HCID 11241777 | — |
| 반응물 | 7-Methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride | HCID 18923873 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (7-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-methoxy-1 H-indol-3-yl)-butyl]-amine | HCID 18923902 | 76.3% |
반응 단계
5-Methoxyindole-3-butyric acid (1.0 g, 4.3 mmole), 1-hydroxybenzotriazole hydrate (0.7 g, 5.2 mmole) and 1,3-diisopropylcarbodiimide (1.6 ml, 10.3 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 7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.0 g, 4.3 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 eluant. Evaporation of product-containing fractions gave 1.3 g (74%) of the desired product, (7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-4-(5-methoxy-1H-indol-3-as an off-white solid.
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-57ac7f372d1141ed8f33c4cf7fbe130c |
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| 출처 메모 | uspto-grants-1998_05 |
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