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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913738Generated: October 26, 2026

Dimethylformamide → N-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamide

https://huagongshe.com/reaction/1913738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4-tert-butylphenolHCID 70982—
Reactant3-Fluoroisonicotinoyl chlorideHCID 23287757—
SolventWaterHCID 962—
ProductN-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamideHCID 66880592—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1.5 g of 3-fluoroisonicotinic acid, 5 ml of thionyl chloride and 50 mg of DMF was heated to reflux for two hours. The reaction mixture was cooled to room temperature, and then the reaction mixture was concentrated under reduced pressure to give 3-fluoroisonicotinic acid chloride. A mixture of the resultant 3-fluoroisonicotinic acid chloride and 5 ml of DMF was added dropwise to a mixture of 1.76 g of 2-amino-4-tert-butylphenol, 2.18 g of triethylamine and 10 ml of DMF while ice-cooling. The reaction mixture was stirred at room temperature for 1.5 hours and at 50° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then water was added. Precipitated crystals were collected by filtration. The resultant crystals were dissolved in ethyl acetate, washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, concentrated under reduced pressure to give 2.41 g of N-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-04f4c510dec845f7bfab6c01280d1f15
Source noteuspto-grants-2013_12