Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290253생성일: 2026년 10월 27일
Diisopropylcarbodiimide → 3-{3-[(7-Hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-amino]-propyl}-1H-indol-5-ol
https://huagongshe.com/reaction/1290253
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 반응물 | 2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine hydrochloride | HCID 18923890 | — |
| 반응물 | 3-[5-(Benzyloxy)-3-indolyl]propanoic Acid | HCID 18923892 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-{3-[(7-Hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-amino]-propyl}-1H-indol-5-ol | HCID 18923895 | 90.3% |
반응 단계
5-Benzyloxyindole-3-propionic acid (1.5 g, 5.0 mmole), 1-hydroxybenzotriazole hydrate (0.8 g, 6.0 mmole) and 1,3-diisopropylcarbodiimide (1.9 ml, 12.0 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-hydroxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.1 g, 5.0 mmole) in 50 ml of DMF and the mixture was further stirred for 48 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 silica gel using ethyl acetate as eluant. Fractions containing product were concentrated and recrystallized from ethyl acetate to give 1.6 g (68%) of the desired product, (7-hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-3-(5-hydroxy-1H-indol-3-yl)-propanamide, as a 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-8778b93efd1b4216936f3ad614e754e3 |
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| 출처 메모 | uspto-grants-1998_05 |
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