Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 454879Erstellt: 24. Oktober 2026

Cesium carbonate → 2-(3-((3-Bromopyridin-4-YL)oxy)azetidin-1-YL) quinoline

https://huagongshe.com/de/reaction/454879

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt3-Bromo-4-chloropyridineHCID 817696—
EduktHCID 58547721HCID 58547721—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(3-((3-Bromopyridin-4-YL)oxy)azetidin-1-YL) quinolineHCID 5854768461,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 1-(quinolin-2-yl)azetidin-3-ol (see PREPARATION P1.2, step 1; 320 mg, 1.60 mmol) in DMF (10 mL) was added Cs2CO3 (1.04 g, 3.2 mmol) and 3-bromo-4-chloropyridine (307 mg, 1.60 mmol). The mixture was stirred at 90° C. overnight and then diluted with water (20 mL) and extracted with EtOAc (2×30 mL). The combined organic extracts were washed with water (30 mL) and brine (30 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (5% to 30% EtOAc in petroleum ether) to give the title product (350 mg, 0.98 mmol, 61% yield) as white solid. ESI-MS (M+1): 356 calc. for C17H14BrN3O 355.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08497265B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-19efdbaebc044124addd1d073d33e0e3
Quellennotizuspto-grants-2013_07