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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405793Generated: November 1, 2026

Picolinic acid → 3-(4-(3,4-Dimethylphenoxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/1405793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-o-xyleneHCID 68504—
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-(3,4-Dimethylphenoxy)phenyl)pyridin-2-amineHCID 6674858618.5%

Reaction Conditions

Temperature110 °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), 4-bromo-1,2-dimethylbenzene (596 mg) and DMSO (8 mL). The mixture was stirred at 130° C. under nitrogen for 3 hr and at 110° C. under nitrogen overnight. Activated carbon was added and the insoluble solid was removed by filtration through NH-silica gel/Celite pad (eluted with EtOAc). Water and EtOAc were 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 (144 mg) as a pale yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916551B2
Source datasetuspto-grants-2014_12
ORD IDord-aa533d8b34b4448aa7956d638b9940ad
Source noteuspto-grants-2014_12