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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094420Generated: October 31, 2026

Dimethylformamide → 6-Chloro-2-[3-(2,2,2-trifluoroethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/2094420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880110—
SolventWaterHCID 962—
Product6-Chloro-2-[3-(2,2,2-trifluoroethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazoleHCID 8665105774.1%

Reaction Steps

A mixture of 46 mg of 60% sodium hydride (in oil) and 2 ml of DMF was stirred at room temperature, to which a mixture solution of 0.12 g of 2,2,2-trifluoroethanol and 0.5 ml of DMF was added. After 15 minutes, 0.28 g of 6-chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole was added and stirred at room temperature for one hour. Water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.26 g of 6-chloro-2-[3-(2,2,2-trifluoroethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 92”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445522B2
Source datasetuspto-grants-2013_05
ORD IDord-07d50df87dfb478ab4ba747b47e9889e
Source noteuspto-grants-2013_05