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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405739Generated: October 26, 2026

2-Methylpyridine → 3-(4-(3-Chlorophenoxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/1405739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpyridineHCID 7975—
Reactant1-Chloro-3-iodobenzeneHCID 12269—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-(2-Aminopyridin-3-yl)phenolHCID 66748477—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-(4-(3-Chlorophenoxy)phenyl)pyridin-2-amineHCID 6682416448.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 4-(2-aminopyridin-3-yl)phenol (400 mg), 1-chloro-3-iodobenzene (615 mg), picoline acid (52.9 mg) and tripotassium phosphate (1368 mg) in DMSO (6 mL) was added copper (I) iodide (82.0 mg). The reaction mixture was stirred under a nitrogen atmosphere at 120° C. for 4 hr. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) and concentrated under reduced pressure to give the title compound (307 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916551B2
Source datasetuspto-grants-2014_12
ORD IDord-bcc77ad560204b39a60895ec6cd9aae8
Source noteuspto-grants-2014_12