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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1008340Erstellt: 24. Oktober 2026

Chloroform → 4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline

https://huagongshe.com/de/reaction/1008340

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktSodium HydroxideHCID 14798—
Edukt7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
Edukt4-Amino-3-chlorophenol hydrochlorideHCID 12598190—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroanilineHCID 2266723290%

Reaktionsschritte

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline (30.0 g) and tetrabutylammonium chloride (13.9 g) were dissolved in acetone (400 ml), and the solution was stirred at room temperature. A solution of 4-amino-3-chlorophenol hydrochloride (36.0 g) in a 20% aqueous sodium hydroxide solution (64 ml) was added thereto. The mixture was then heated under reflux for 3 hr. The reaction solution was cooled to room temperature, and chloroform and water were added to the cooled reaction solution, followed by extraction with chloroform. The extract was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was then dried over anhydrous sodium sulfate. Next, sodium sulfate was removed, and the solvent was then removed by distillation. The residue was washed with methanol, and the washed solid was subjected to evaporation to dryness in vacuo through a vacuum pump to give 36.6 g (yield 90%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06797823B1
Quelldatensatzuspto-grants-2004_09
ORD IDord-2f79078892f0406ba85cbcd90b3c5a14
Quellennotizuspto-grants-2004_09