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HRID 394738Erstellt: 25. Oktober 2026

3-Morpholino-1-propanol → HCID 10526285, Verbindung

https://huagongshe.com/reaction/394738

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Morpholino-1-propanolHCID 199576—
EduktSodiumHCID 5360545—
Edukt7-Fluoro-4-[(3-methylphenyl)-amino]-6-nitroquinazolineHCID 10542070—
EduktDichloromethane ethyl acetate methanolHCID 21901258—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelMethylenechloride HexaneHCID 21226440—
ProduktHCID 10526285HCID 1052628588%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a solution of 3-morpholinopropan-1-ol (8.40 mmol, 1.22 g) in THF (40 mL) under N2 was added sodium metal (11.8 mmol, 0.27 g). The resulting suspension was stirred at 20° C. for 2 hours and then cannulated into a solution of 7-fluoro-4-[(3-methyl-phenyl)amino]-6-nitroquinazoline (0.70 g, 2.35 mmol) in THF (30 mL) under N2. The reaction procedure and workup above were followed to give after chromatography on silica gel eluting with MeOH/CH2Cl2/EtOAc (5:45:50) to MeOH/CH2C0.50/EtOAc (3:7:10) 4-[(3-methylphenyl)-amino]-7-[(3-morpholino)propyloxy]-6-nitroquinazoline (0.87 g, 88%) as a yellow powder, mp (CH2Cl2/hexane) 169-170° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06602863B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-4ea7868d374341998b12f231bd3ca726
Quellennotizuspto-grants-2003_08