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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860010Erstellt: 25. Oktober 2026

6-Bromoquipazine → (2S)-2-{[4-(6-Bromoquinolin-2-yl)piperazin-1-yl]methyl}-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinoline

https://huagongshe.com/reaction/860010

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-BromoquipazineHCID 130261—
EduktSodium BicarbonateHCID 516892—
Edukt[(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl4-bromobenzenesulfonateHCID 20624762—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(2S)-2-{[4-(6-Bromoquinolin-2-yl)piperazin-1-yl]methyl}-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolineHCID 4421992239,3%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

To a solution of [(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl 4 bromobenzene sulfonate (2.31 g, 5.13 mmol) in dimethylsulfoxide (123 mL) is added the 6-bromo-2-piperazin-1-yl-quinoline of Step B (1.5 g, 5.13 mmol) and the mixture is heated at 75° C. under nitrogen overnight. The mixture is poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The extracts are dried over anhydrous magnesium sulfate and evaporated to dryness. The residue is flash chromatographed on silica gel Merck-60 using a gradient of methanol (0.5–2%) in ethyl acetate-hexane (55:45) to provide the title compound as an off-white solid (1.02 g), m.p. 153–154° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07153849B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-bb354057eb944558a4c9fedc147cdf05
Quellennotizuspto-grants-2006_12