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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1913671Erstellt: 25. Oktober 2026

Dimethylformamide → 2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913671

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktBromocyclopentaneHCID 8728—
EduktPotassium CarbonateHCID 11430—
Edukt4-[5-(Trifluoromethyl)benzoxazole-2-yl]pyridin-3-olHCID 136331268—
LösungsmittelWaterHCID 962—
Produkt2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688022083,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a mixture of 0.28 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 0.28 g of potassium carbonate and 2 ml of DMF, a mixture of 0.29 g of cyclopentyl bromide and 2 ml of DMF was added at room temperature. The reaction mixture was stirred while heating at 60° C. for four hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.29 g of 2-(3-cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 115”).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08609705B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-6ba03f1821ac4b9aa8bc2a75d6dac585
Quellennotizuspto-grants-2013_12