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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577344Generated: October 28, 2026

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

https://huagongshe.com/reaction/577344

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 numberUS09040541B2
Source datasetuspto-grants-2015_05
ORD IDord-b55897edc0ff487594a09c2fc0fd83f9
Source noteuspto-grants-2015_05