HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1290255Erstellt: 25. Oktober 2026
Diisopropylcarbodiimide → HCID 18923868, Verbindung
https://huagongshe.com/reaction/1290255
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylcarbodiimide | HCID 12734 | — |
| Edukt | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Edukt | 5-Methoxyindole-3-butyric acid | HCID 11241777 | — |
| Edukt | 2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine hydrochloride | HCID 18923890 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 18923868 | HCID 18923868 | 65,4% |
Reaktionsschritte
5-Methoxyindole-3-butyric acid (1.5 g, 6.4 mmole), 1-hydroxybenzotriazole hydrate (1.0 g, 7.7 mmole) and 1,3-diisopropylcarbodiimide (2.4 ml, 15.4 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 (1.4 g, 6.4 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 first ethyl acetate and then 5% methanol in ethyl acetate as eluants. Evaporation of product-containing fractions gave 1.6 g (63%) of the desired product, (7-hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-4-(5-methoxy-1H-indol-3-yl)-butanamide, as an oily solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05750724 |
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| Quelldatensatz | uspto-grants-1998_05 |
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| ORD ID | ord-c882b072f41e44a080ce475d587f4cc2 |
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| Quellennotiz | uspto-grants-1998_05 |
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