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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913727Generated: November 2, 2026

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

https://huagongshe.com/reaction/1913727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsonicotinic AcidHCID 5922—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-Amino-5-chloro-4-(trifluoromethyl)phenolHCID 14011736—
SolventWaterHCID 962—
ProductN-[4-chloro-2-hydroxy-5-trifluoromethylphenyl]isonicotinamideHCID 6688003858.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.2 g of 2-amino-5-chloro-4-trifluoromethylphenol, 1.35 g of WSC, 0.67 g of isonicotinic acid and 10 ml of pyridine was stirred while heating at 80° C. for three 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, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 1.01 g of 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-8f8e37e72b7b4c93b91e3a354cc87be7
Source noteuspto-grants-2013_12