HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2254302Erstellt: 26. Oktober 2026
Sodium Iodide → N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine
https://huagongshe.com/reaction/2254302
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 7-(3-Bromopropoxy)quinoline | HCID 19745014 | — |
| Edukt | 2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine | HCID 19745017 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine | HCID 9930518 | 57,6% |
Reaktionsschritte
2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine (1.3 g, 6.2 mmole), 7-(3-bromopropoxy)quinoline (1.53 g, 5.5 mmole), diisopropylethylamine 2.6 g, 20 mmole) and sodium iodide (5.5 g, 37 mmole) were combined in 200 ml of DMF and heated at 80° C. for 15 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with 500 ml of dichloromethane. The mixture was washed with 250 ml each of saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on 250 g of silica gel using 3% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue (2.25 g) recrystallized from ethanol with the addition of 6 ml of 4N isopropanolic HCl to give 1.25 g of the title compound as a yellow solid dihydrochloride salt, m.p. 224°-226° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05235055 |
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| Quelldatensatz | uspto-grants-1993_08 |
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| ORD ID | ord-1f3b8dd37368441c944a3642b06276fb |
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| Quellennotiz | uspto-grants-1993_08 |
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