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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913731Generated: November 2, 2026

Pyridine → 3-fluoro-N-[4-chloro-2-hydroxy-5-trifluoromethylphenyl]isonicotinamide

https://huagongshe.com/reaction/1913731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-Fluoropyridine-4-carboxylic acidHCID 345361—
Reactant2-Amino-5-chloro-4-(trifluoromethyl)phenolHCID 14011736—
SolventWaterHCID 962—
Product3-fluoro-N-[4-chloro-2-hydroxy-5-trifluoromethylphenyl]isonicotinamideHCID 6688004865.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.0 g of 2-amino-5-chloro-4-trifluoromethylphenol, 1.33 g of 3-fluoroisonicotinic acid, 2.36 g of WSC and 15 ml of pyridine was stirred while heating at 80° C. for 3.5 hours. The reaction mixture was cooled to room temperature, and then water was added, followed by extraction with ethyl acetate three times. The combined organic layers were washed with water and a saturated sodium chloride solution, then dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2.08 g of 3-fluoro-N-[4-chloro-2-hydroxy-5-trifluoromethylphenyl]isonicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-96dd4a4885d746169bec5a493b9cbd61
Source noteuspto-grants-2013_12