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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374212Erstellt: 26. Oktober 2026

Sodium Iodide → HCID 19778665, Verbindung

https://huagongshe.com/reaction/374212

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktDiisopropylethylamineHCID 81531—
Edukt2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
EduktHCID 18923891HCID 18923891—
EduktIsopropanol hydrochlorideHCID 21912024—
LösungsmittelMethanolHCID 887—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 19778665HCID 1977866516%

Reaktionsschritte

2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine (3.00 g, 16.6 mmole), 7-(3-chloropropoxy)coumarin (2.95 g, 12.4 mmole), diisopropylethylamine (8.0 ml, 46.0 mmole) and sodium iodide (2.58 g, 17.2 mmole) were combined in 150 ml of DMF and heated at 80°-100° C. for 2 days under a nitrogen atmosphere. The solvent was then removed and replaced with dichloromethane. The mixture was washed with an equal volume of saturated aqueous sodium bicarbonate, with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on silica gel using first dichloromethane and then 0.25% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the pure free base (1.0 g, an additional 2.0 g were obtained of lower purity) redissolved in methanol and boiled on a hot plate, the methanol gradually being replaced with isopropanol. 4N HCl/IPA was added and the title compound was collected by filtration and dried in vacuum at 80° C. The procedure yielded 0.76 g of beige solid, monohydrochloride, m.p. 252° C. (d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166367
Quelldatensatzuspto-grants-1992_11
ORD IDord-37ea97c2bcb44e0db0b441e64c640a41
Quellennotizuspto-grants-1992_11