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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014138Generated: October 30, 2026

4-Methoxyphenol → N2-(6-(4-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine

https://huagongshe.com/reaction/1014138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantPotassium CarbonateHCID 11430—
ReactantN2-(6-chloropyrimidin-4-yl)pyridine-2,6-diamineHCID 57708264—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN2-(6-(4-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamineHCID 5770832959.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N2-(6-chloropyrimidin-4-yl)pyridine-2,6-diamine (200 mg, 0.90 mmol) in dry DMF (2 mL) was added 4-methoxyphenol (168 mg, 1.3 mmol) and anhydrous K2CO3 (179 mg, 1.3 mmol). The reaction mixture was heated at 100° C. for 16 h under N2 atmosphere. It was then cooled and DMF removed under reduced pressure to give a yellowish gummy residue that was taken in EtOAc (10 mL). The solution was washed with water (5 mL) and brine (5 mL), was dried over Na2SO4 and was then concentrated under reduced pressure to get crude product. This was further purified by column chromatography (SiO2, 60-120, hexane/EtOAc, 5/5) to give N2-(6-(4-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine (160 mg, 59.2%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-f0c723bc201348f2a70a6ac783aa12af
Source noteuspto-grants-2011_07