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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226950Erstellt: 24. Oktober 2026

Dimethylformamide → HCID 16730933, Verbindung

https://huagongshe.com/de/reaction/226950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktAcetonitrileHCID 6342—
EduktSodium hydrideHCID 24758—
Edukt3-(Chloromethyl)-1,2,4-oxadiazoleHCID 2735765—
Edukt3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-oneHCID 57754515—
ProduktHCID 16730933HCID 16730933—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

26 mg (0.65 mmol) of sodium hydride (60%) was suspended in 3 mL of anhydrous dimethylformamide and to it was added 138.7 mg (0.50 mmol) of 3-(3,4-dimethyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one 3a and the resultant mixture was stirred at rt for 30 min. Then 77.4 mg (0.65 mmol) of 3-chloromethyl-1,2,4-oxadiazole was added to the reaction solution and the mixture was stirred at 80° C. for 1 h. The reaction solution was quenched by the addition of 10 mL of water. The crude product precipitated out of solution and was isolated by filtration. Purification of the crude product by flash chromatography provided 55 mg of 4cc as a colorless solid: LC-MSD, m/z for C23H20N2O3, [M+H]+=373.4, [M+2H]+=374.4; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time =2.639 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.30 (d, 6H), 2.36 (s, 3H), 5.38 (s, 2H), 5.90 (s, 1H), 7.15 (d, 1H), 7.42 (t, 1H), 7.50-7.68 (m, 4H), 8.27 (s, 1H), 8.44 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557213B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-b1b7d3dc6c0d410b90c1fceaad4c1d8e
Quellennotizuspto-grants-2009_07