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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507462Erstellt: 25. Oktober 2026

Hexane → 6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazoline

https://huagongshe.com/reaction/507462

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktEthyl AcetateHCID 8857—
Edukt4-(Dimethylamino)butan-1-olHCID 83350—
EduktN-(3-Bromophenyl)-7-fluoro-6-nitroquinazolin-4-amineHCID 10761182—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelMethylenechloride HexaneHCID 21226440—
LösungsmittelEthylacetate methanolHCID 21584119—
Produkt6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazolineHCID 1069391233%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a suspension of hexane prewashed sodium hydride (11.0 mmol, 440 mg of a 60% dispersion in mineral oil) in THF (20 mL) was cannulated a solution of 4-(N,N-dimethylamino)butan-1-ol (8.80 mmol, 1.03 g) in THF (30 mL). The resulting suspension was stirred at 20° C. under N2 for 2 hours and then cannulated into a solution of 4-[(3-bromophenyl)amino]-7-fluoro-6-nitroquinazoline (J Med Chem, 1996;39:918-928) (0.80 g, 2.20 mmol) in THF (30 mL) under N2. The dark red solution was then heated at reflux overnight. Identical workup as above gave, after chromatography on grade III alumina eluting with EtOAc to MeOH/EtOAc (5:95) to give 6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazoline (310 mg, 33%) as a pale brown powder, mp (CH2Cl2/hexane) 155-156° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786131B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-aaa9a787be5245399bc02482bc78573d
Quellennotizuspto-grants-2010_08