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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913673Generated: October 25, 2026

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

https://huagongshe.com/reaction/1913673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChlorodifluoromethaneHCID 6372—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[5-(Trifluoromethyl)benzoxazole-2-yl]pyridin-3-olHCID 136331268—
SolventWaterHCID 962—
Product2-(3-Difluoromethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880475—

Reaction Steps

A mixture of 0.50 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 1.23 g of potassium carbonate and 14 ml of DMF was stirred while heating at 70° C. for three hours with chlorodifluoromethane gas injected. By stopping injection of gas, the mixture was cooled to room temperature and allowed to stand overnight. 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 0.11 g of 2-(3-difluoromethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 126”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-74df6f667add46f188820196f37c26df
Source noteuspto-grants-2013_12