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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346417Erstellt: 25. Oktober 2026

3-Morpholino-1-propanol → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline

https://huagongshe.com/reaction/346417

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Morpholino-1-propanolHCID 199576—
EduktSodiumHCID 5360545—
Edukt4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazolineHCID 11176185—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazolineHCID 2108000172%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Sodium metal (5 equivalents) was added, under nitrogen atmosphere, to a solution of 3-(4-morpholinyl)-1-propanol (4 equivalents) in THF. The obtained suspension was stirred at 20° C. for two hours and was thereafter cannulated, under nitrogen atmosphere, into a solution of 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline. The reaction mixture was refluxed for 18 hours, the solvent was thereafter partially removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate. Drying the combined organic extracts, evaporation and silica gel chromatography (using a mixture of 20% MeOH/30% CH2Cl2/50% EtOAc as elute) gave 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline in 72% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07172749B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-44f5507bc07f4cd99812ba644cbcabc3
Quellennotizuspto-grants-2007_02