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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068054Erstellt: 27. Oktober 2026

Sodium Hydroxide → N-[(4-bromophenyl)methyl]-1-morpholino-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1068054

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt4-Bromobenzylamine hydrochlorideHCID 2724096—
EduktEthyl 1-(4-morpholinyl)-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylateHCID 21192510—
LösungsmittelWaterHCID 962—
ProduktN-[(4-bromophenyl)methyl]-1-morpholino-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamideHCID 49048968%

Reaktionsbedingungen

Temperatur190 °C

Reaktionsschritte

4-Bromobenzylamine hydrochloride (2.22 g) is suspended in water (5 mL) and neutralized with 2N aqueous NaOH (5 mL). The free amine is extracted with dichloromethane (2×25 mL). The organic layers are combined, washed with brine (5 mL), and dried with Na2SO4. The solution is concentrated in vacuo to afford 1.48 g of a clear, colorless oil which is then combined with ethyl 1-(4-morpholinyl)-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylate (0.48 g) from Preparation No. 56 and heated to 190° C. for 3 hours. The reaction mixture is allowed to cool to room temperature, and the resulting solid is recrystallized in ethyl acetate to afford 0.44 g of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06248739B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-e40cb64c7f374a5ea9db5bbe926592f0
Quellennotizuspto-grants-2001_06