Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035903Generated: October 26, 2026

Picolinic acid → 3-(4-(3-(1,1-Difluoroethyl)phenoxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/2035903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Bromo-3-(1,1-difluoroethyl)benzeneHCID 22240121—
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-(3-(1,1-Difluoroethyl)phenoxy)phenyl)pyridin-2-amineHCID 6674805256.9%

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-3-(1,1-difluoroethyl)benzene (712 mg) and DMSO (8 mL). The mixture was stirred at 130° C. under nitrogen for 10 hr. Activated carbon was added and the insoluble solid was removed by filtration through NH-silica gel/Celite pad (eluted with EtOAc). Silica-gel was added to the filtrate 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) and concentrated. The residue was purified by column chromatography (silica gel, eluted with EtOAc in hexane) to give the title compound (499 mg) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575154B2
Source datasetuspto-grants-2013_11
ORD IDord-68e6add1ef124d1b9539505a989a1de7
Source noteuspto-grants-2013_11