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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1817383Erstellt: 25. Oktober 2026

2-Nitrophenol → Quinazoline

https://huagongshe.com/reaction/1817383

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-NitrophenolHCID 6947—
EduktQuinazolineHCID 9210—
Edukt4-ChloroquinolineHCID 69140—
Edukt4-(Nitrophenoxy)quinolineHCID 21890535—
KatalysatorHCID 178418390HCID 178418390—
KatalysatorHCID 178502593HCID 178502593—
LösungsmittelDimethylformamideHCID 6228—
ProduktQuinazolineHCID 9210—
Produkt4-(Aminophenoxy)quinolineHCID 21890324—

Reaktionsschritte

Next, a 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative is produced by reacting nitrophenol with the 4-chloroquinoline derivative or corresponding quinazoline derivative in the presence or absence of a suitable solvent to synthesize a 4-(nitrophenoxy)quinoline derivative or a corresponding quinazoline derivative, then conducting stirring in a suitable solvent, for example, N,N-dimethyl formamide, in the presence of a catalyst, for example, palladium hydroxide-carbon or palladium-carbon, under a hydrogen atmosphere. Alternatively, the 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative may also be produced by reacting amino phenol with a 4-chloroquinoline derivative or a corresponding quinazoline derivative in the presence of a base, for example, sodium hydride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07598258B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-84c2fb696c4a42c8b8fd59fb00e33e09
Quellennotizuspto-grants-2009_10