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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktDiisopropylethylamineHCID 81531—
Edukt7-(3-Bromopropoxy)quinolineHCID 19745014—
Edukt2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 19745017—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 993051857,6%

Reaktionsbedingungen

Temperatur80 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05235055
Quelldatensatzuspto-grants-1993_08
ORD IDord-1f3b8dd37368441c944a3642b06276fb
Quellennotizuspto-grants-1993_08