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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 412025Erstellt: 25. Oktober 2026

Water → 8-Carbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-one

https://huagongshe.com/reaction/412025

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Edukt2-Aminobenzene-1,3-dicarboxamideHCID 10241384—
Edukt2-Propoxybenzoyl chlorideHCID 15921913—
LösungsmittelEthanolHCID 702—
LösungsmittelPyridineHCID 1049—
Produkt8-Carbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-oneHCID 13598515640%

Reaktionsschritte

2-n-Propoxybenzoyl chloride (7.27 g, 0.366 mol) was added dropwise to a stirred suspension of 2-amino-3-carbamoylbenzamide (Preparation 17; 2.63 g, 0.0147 mol) in pyridine (50 ml) at 0° C. The mixture was stirred at room temperature for 3 days, then the solvent evaporated under vacuum. The residue was treated with water (100 ml) and, on chilling the solution, colorless crystals formed. The product was collected by filtration and then suspended in a stirred mixture of sodium hydroxide (1.73 g, 0.043 mol), water (90 ml) and ethanol (20 ml). The mixture was heated under reflux for 3 hours, allowed to cool and filtered. The filtrate was acidified to pH 2 with concentrated hydrochloric acid and extracted with a methanol-dichloromethane mixture (2:98, 3×100 ml). The organic extracts were combined, washed sequentially with saturated aqueous sodium carbonate solution (3×100 ml) and brine (3×50 ml), dried (Na2SO4) and evaporated under vacuum. Crystallization of the residue from ethyl acetate-methanol gave the title compound as a white solid (1 g, 40%), m.p. 226-227° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06562830B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-9647eecc6d814232a5ed24039f001f77
Quellennotizuspto-grants-2003_05