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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336721Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → 5,7-dimethoxy-2-(4-(morpholinomethyl)phenyl)quinazolin-4(3H)-one

https://huagongshe.com/de/reaction/336721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktSodium BicarbonateHCID 516892—
Edukt4-[(Morpholin-4-yl)methyl]benzaldehydeHCID 2795498—
Edukt2-Amino-4,6-dimethoxybenzamideHCID 20349016—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
Produkt5,7-dimethoxy-2-(4-(morpholinomethyl)phenyl)quinazolin-4(3H)-oneHCID 136038005—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a solution of 2-amino-4,6-dimethoxy-benzamide (150 mg, 0.76 mmol) and 4-morpholin-4-ylmethyl benzaldehyde (156 mg, 0.76 mmol) in N,N-dimethyl acetamide (10 mL), NaHSO3 (150 mg, 0.84 mmol) and p-TSA (174 mg, 0.91 mmol) were added and the reaction mixture was heated at 150° C. for 5 h. The reaction mixture was cooled to room temperature, water was added and the mixture was neutralized with NaHCO3. The solvent was removed under reduced pressure to give the crude product, which was purified by column chromatography to give 5,7-dimethoxy-2-(4-(morpholinomethyl)phenyl)quinazolin-4(3H)-one, which was converted to the hydrochloride salt (165 mg, 51%). Selected data: MS (ES) m/z: 382.07; MP 206-208° C. (at decomposition).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889698B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-6e0a664d942f43c194a3ce9759ed41eb
Quellennotizuspto-grants-2014_11