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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1420963Erstellt: 27. Oktober 2026

Potassium Iodide → 4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-((1-methylbenzimidazol-2-yl)methoxy)quinazoline

https://huagongshe.com/reaction/1420963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt2-(Chloromethyl)-1-methylbenzimidazoleHCID 248044—
Edukt4-(3-Acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochlorideHCID 135671180—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-((1-methylbenzimidazol-2-yl)methoxy)quinazolineHCID 2262497295%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A mixture of 4 -(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride (240 mg, 0.64 mmol), (prepared as described for the starting material in Example 1), potassium carbonate (310 mg, 2.25 mmol), potassium iodide (10 mg, 0.064 mmol) and 2-chloromethyl-1-methylbenzimidazole (153 mg, 0.7 mmol) in DMF (12 ml) was heated at 65° C. for 3 hours. Further 2-chloromethyl-1-methylbenzimidazole (90 mg, 0.41 mmol) and potassium carbonate (165 mg, 1.2 mmol) were added and heating continued for 2 hours. The solvent was removed by evaporation and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, dried (MgSO4) and the solvent removed by evaporation. The residue was triturated with water and the solid product collected by filtration, washed with ether and dried under vacuum to give 4-(3-acetoxy-4-methylanilino)-6-methoxy-7-((1-methylbenzoimidazol-2-yl)methoxy)quinazoline (292 mg, 95%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06071921
Quelldatensatzuspto-grants-2000_06
ORD IDord-8a7fdee4fcd64ef7a133df40604019ce
Quellennotizuspto-grants-2000_06