Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622717Generated: October 25, 2026

Picolinic acid → 3-(4-(4-(Trifluoromethyl)phenoxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/1622717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
Reactant4-(2-Aminopyridin-3-yl)phenolHCID 66748477—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product3-(4-(4-(Trifluoromethyl)phenoxy)phenyl)pyridin-2-amineHCID 6674772677.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

Copper(I) iodide (102 mg) was added to a mixture of picolinic acid (66.1 mg), 4-(2-aminopyridin-3-yl)phenol (500 mg), tripotassium phosphate (1710 mg), 1-bromo-4-(trifluoromethyl)benzene (725 mg) and DMSO (8 mL). The mixture was stirred at 130° C. under nitrogen for 5 hr. Activated carbon was added and the insoluble solid was removed by filtration through NH-silica gel/Celite pad (eluted with EtOAc). Water was added and the extracted organic layer was washed with brine. Silica-gel was added to the organic layer and the volatiles were removed in vacuo. The mixture supported on silica-gel was purified by column chromatography (NH-silica gel, eluted with EtOAc in hexane) to give the title compound (690.4 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778934B2
Source datasetuspto-grants-2014_07
ORD IDord-14419476a2c34e51adf3f71c398aecdd
Source noteuspto-grants-2014_07