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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1500204Erstellt: 26. Oktober 2026

2-Aminophenol → 4-(Aminophenoxy)quinazoline

https://huagongshe.com/reaction/1500204

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminophenolHCID 5801—
EduktSodium hydrideHCID 24758—
Edukt4-ChloroquinolineHCID 69140—
Edukt4-(Aminophenoxy)quinolineHCID 21890324—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt4-(Aminophenoxy)quinazolineHCID 22637147—

Reaktionsschritte

Alternatively, the 4-(aminophenoxy)quinoline derivative can be produced by reacting an aminophenol derivative with the 4-chloroquinoline derivative in a suitable solvent, for example, dimethyl sulfoxide, in the presence of a base, for example, sodium hydride. Alternatively, the 4-(aminophenoxy)quinazoline derivative can also be produced by dissolving an aminophenol derivative in an aqueous sodium hydroxide solution and subjecting the solution to a two-phase reaction with a solution of the 4-chloroquinazoline derivative in a suitable organic solvent, for example, ethyl methyl ketone, in the presence of a phase transfer catalyst, for example, tetra-n-butylammonium chloride, or in the absence of a catalyst (Scheme 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206130B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-14a81141ea904ce4a5132d609f55a4e6
Quellennotizuspto-grants-2015_12