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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913616Generated: October 30, 2026

Water → 2-(3-Cyanopyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-(3-Iodopyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880597—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
Product2-(3-Cyanopyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688031438%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 0.39 g of 2-(3-iodopyridin-4-yl)-5-(trifluoromethyl)benzoxazole, 0.18 g of copper (I) cyanide and 2 ml of 1-methyl-2-pyrrolidinone was stirred while heating at 80° C. for 2 hours. Water and ethyl acetate were poured into the reaction mixture, which was filtered through Celite™. The resultant filtrate was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.11 g of 2-(3-cyanopyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 31”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-9df1e391bf494c98878291b2c5d3b11e
Source noteuspto-grants-2013_12