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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1452318Erstellt: 25. Oktober 2026

Water → 8-{3-[4-(2-Methoxyphenyl)-1-piperazinyl]-propoxycarbonyl}-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran dihydrochloride

https://huagongshe.com/reaction/1452318

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt3-Methylflavone-8-carboxylic acidHCID 77016—
Edukt1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-{3-[4-(2-Methoxyphenyl)-1-piperazinyl]-propoxycarbonyl}-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran dihydrochlorideHCID 19972518—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 4.24 g of 8-carboxy-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran and 6.3 g of anhydrous potassium carbonate in 60 ml of dimethylformamide was stirred at 80° C. for 30 minutes. 5.23 g of 1-(3-chloropropyl)-4-(2-methoxyphenyl)-piperazine was then added and stirring was continued at 80° C. for 3.5 hours. The reaction mixture was cooled to ambient temperature, poured on to iced water and extracted with ethyl acetate. The organic extracts were washed with aqueous sodium chloride solution, dried on anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residue was taken up in ethanol and excess ethanolic hydrogen chloride was added to the solution. Yield: 8.16 g of the title compound, m.p. 198°-203° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05605896
Quelldatensatzuspto-grants-1997_02
ORD IDord-2e4fa8d28f9d4926887f7aec3539bd5e
Quellennotizuspto-grants-1997_02