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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13331Erstellt: 23. Oktober 2026

Cesium carbonate → 5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-trifluoromethyl-pyridin-3-yloxy)-1H-benzimidazole

https://huagongshe.com/de/reaction/13331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
Edukt5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazoleHCID 135697984—
KatalysatorCopper oxideHCID 14829—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-trifluoromethyl-pyridin-3-yloxy)-1H-benzimidazoleHCID 23145778—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

16 mg of 5-bromo-2-trifluoromethyl-pyridine, 50 mg of cesium carbonate and 10 mg of copper(II) oxide were added to an N-methylpyrrolidinone (1 ml) solution of 21 mg of 5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazole obtained in Example 251 (step 1), and the reaction liquid was stirred at 130° C. for 5 hours. The deposit was separated through filtration, and the solution was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]. The resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728025B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a8cabb912c264e1fb37b38fd8adc589b
Quellennotizuspto-grants-2010_06