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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521667Erstellt: 25. Oktober 2026

2-Amino-4-(trifluoromethyl)benzamide → 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one

https://huagongshe.com/reaction/521667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-(trifluoromethyl)benzamideHCID 69739—
EduktSodium BicarbonateHCID 516892—
EduktSodium BisulfiteHCID 23665763—
Edukt4-Chloro-2-ethylsulfanylbenzaldehydeHCID 114863540—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-oneHCID 13696875080,7%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 1.0 g of 2-amino-4-trifluromethylbenzamide, 944 mg of 4-chloro-2-ethylsulfanylbenzaldehyde, 765 mg of sodium bisulfite and 4 ml of DMA was stirred at 150° C. for 15 hours. A saturated aqueous sodium bicarbonate solution and water were added to the cooled reaction mixture, and the precipitated solid was filtered. The resulting solid was washed with water and n-hexane and then dried to obtain 1.46 g of 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328121B1
Quelldatensatzuspto-grants-2016_05
ORD IDord-8f4b80ef8cfc4a818ce6750c2e33ca20
Quellennotizuspto-grants-2016_05