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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884978Generated: October 25, 2026

Triethylamine → 3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamide

https://huagongshe.com/reaction/884978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant3-Chloropyridine-4-carboxylic acidHCID 2735816—
Reactant2-Amino-4-(trifluoromethoxy)phenolHCID 2737729—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamideHCID 6688003371.3%

Reaction Steps

A mixture of 0.35 g of 2-amino-4-trifluoromethoxy phenol, 0.29 g of 3-chloroisonicotinic acid, 1.04 g of (benzotriazole-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (hereinafter, referred to as a BOP reagent), 0.24 g of triethylamine and 5 ml of DMF was stirred at room temperature for two hours. Water was added to the reaction mixture, precipitated solid was collected by filtration. The resultant solid was dissolved in ethyl acetate. Then, the organic layer was 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 0.43 g of 3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242133B2
Source datasetuspto-grants-2012_08
ORD IDord-6b396ef73cef4d3fab5bf1f3fc422a28
Source noteuspto-grants-2012_08