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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 433970Erstellt: 24. Oktober 2026

Dimethylformamide → HCID 12114211, Verbindung

https://huagongshe.com/de/reaction/433970

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTrifluoroacetic acidHCID 6422—
EduktPotassium CarbonateHCID 11430—
Edukt1-[2-(2-propynyloxy)ethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 9856610—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelAcetonitrile--water (1/1)HCID 18373917—
ProduktHCID 12114211HCID 12114211—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

Under a nitrogen atmosphere, a mixture of 1-[2-(2-propynyloxy)ethyl]-1H-imidazo[4,5-c]quinolin-4-amine (10 g, 37.6 mmol), anhydrous N,N-dimethylformamide (150 mL) and potassium carbonate (6.23 g, 45.1 mmol) was heated to 70° C. lodobenzene (4.43 mL, 39.5 mmol), dichlorobis(triphenylphosphine)palladium(II) (0.53 g, 0.75 mol), and copper(I) iodide (0.29 g, 1.50 mmol) were added and the mixture was allowed to stir for 0.5 hour. The temperature was raised to about 85° C. After 1.5 hours analysis by HPLC (reverse phase, acetonitrile/water with 0.1% trifluoroacetic acid) indicated that the reaction was complete. The mixture was allowed to cool to ambient temperature and then it was filtered. The filtrate was concentrated under reduced pressure. The residue was purified twice by flash chromatography (95/5 dichloromethane/methanol) to provide 2.7 g of 1-{2-[(3-phenyl-2-propynyl)oxy]ethyl}-1H-imidazo[4,5-c]quinolin-4-amine as a white solid, m.p. 196-197° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06670372B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-d5a4024a39d344898ec0b79911be0166
Quellennotizuspto-grants-2003_12