Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1703387Erstellt: 25. Oktober 2026

Dimethylformamide → 7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline

https://huagongshe.com/reaction/1703387

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt2-Amino-3,4-dimethoxybenzonitrileHCID 18778990—
EduktEthyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochlorideHCID 20506452—
LösungsmittelWaterHCID 962—
Produkt7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazolineHCID 12920014—

Reaktionsschritte

To a stirred solution of 1.78 g. (0.01 mole) 3,4-dimethoxy-2-aminobenzonitrile in 30 ml. of N,N-dimethylformamide is added 2.88 g. (0.01 mole) ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochloride followed by 855 mg. (0.02 mole) of a 56.1% dispersion of sodium hydride in mineral oil. The reaction mixture is stirred at ambient temperature for 30 minutes, and then it is heated to ca. 100° C. and maintained at that temperature for 12 hours. The reaction mixture is cooled to ambient temperature, diluted with an excess of water, and then extracted with chloroform. The chloroform extract is washed several times with water, dried using anhydrous magnesium sulfate, and then evaporated to dryness in vacuo. This affords crude 7,8-dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline, which is purified further by recrystallization from aqueous ethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04351940
Quelldatensatzuspto-grants-1982_09
ORD IDord-662e012e42b440e49cc52795ac9bde36
Quellennotizuspto-grants-1982_09