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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884903Generated: October 31, 2026

Methanol → 6-Chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/884903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880110—
SolventWaterHCID 962—
Product6-Chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688055844.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.28 g of 6-chloro-2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole, 0.24 g of potassium carbonate and 3 ml of methanol was stirred while heating at 60° C. for two hours. 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 concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.13 g of 6-chloro-2-(3-methoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 91”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242133B2
Source datasetuspto-grants-2012_08
ORD IDord-787c4d2d3e204d7595b661d9c96421a0
Source noteuspto-grants-2012_08