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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328131Erstellt: 25. Oktober 2026

Benzene, 1-chloro-3-isocyanato- → 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione

https://huagongshe.com/reaction/328131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-chloro-3-isocyanato-HCID 17968—
EduktSodium hydrideHCID 24758—
Edukt2-(m-nitroanilino)-N-allylbenzamideHCID 21444004—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dioneHCID 1327234470,5%

Reaktionsschritte

3.0 g of 2-(m-nitroanilino)-N-allylbenzamide was dissolved in 20 ml of tetrahydrofuran. To the solution was added 1.0 g of approximately 50 % sodium hydride and stirring was performed for 30 minutes. To this was added dropwise under cooling 4.6 g of m-chlorophenyl isocyanate, and the mixture was stirred for one hour, and then refluxed for 5 hours. After the reaction was complete, the solvent was distilled off from the resulting mixture. The residue thus obtained was recrystallized from methanol to give 2.3 g of 1-(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione as colorless needles, melting at 165°-166° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04016166
Quelldatensatzuspto-grants-1977_04
ORD IDord-519dbbb3c2ea4057b55b69026901ce1e
Quellennotizuspto-grants-1977_04