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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 517443Erstellt: 25. Oktober 2026

Dimethylformamide → 4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholine

https://huagongshe.com/reaction/517443

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium CarbonateHCID 10340—
Edukt3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
Edukt4-(7-Bromo-2-chloroquinazolin-4-yl)morpholineHCID 86665758—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
Produkt4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholineHCID 8666576080%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

To a 50 mL round bottom flask, 7-bromo-2-chloro-4-morpholin-4-yl-quinazoline (0.65 g, 0.0019 mol), 3-methylsulfonylphenylboronic acid (0.35 g, 0.0018 mol), sodium carbonate (0.314 g, 0.0029 mol), DMF (25 mL) and water (6 mL) were added and degassed the reaction vessel with nitrogen for 5-10 min. To the same reaction mixture, Pd(PPh3)2Cl2 (0.069 g, 0.00099 mol) was added and again degassed with nitrogen for 5-10 min. The reaction mixture was stirred at 95° C. for 2 h. The reaction mixture was cooled and diluted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulfate. The solvent was removed under reduced pressure to afford the crude product. The crude product was purified; using column chromatography (60-120 silica gel, 50% ethyl acetate in hexane) to yield the desired product [400 mg, 80%]. LC-MS (ESI): Calculated mass: 403.1; Observed mass: 404.0 [M+H]+ (RT: 1.36 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115092B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-46992e6d80c4486e82692d33cf54a5d9
Quellennotizuspto-grants-2015_08