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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014136Generated: October 29, 2026

3-Methoxyphenol → N2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine

https://huagongshe.com/reaction/1014136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyphenolHCID 9007—
ReactantPotassium CarbonateHCID 11430—
ReactantN2-(6-chloropyrimidin-4-yl)pyridine-2,6-diamineHCID 57708264—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamineHCID 5770823140.7%

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 3-methoxyphenol (112 mg, 0.90 mmol) and anhydrous K2CO3 (186 mg, 1.353 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). It was washed with water (5 mL), brine (5 mL), dried over Na2SO4 and then concentrated under reduced pressure to give a crude product. This was further purified by column chromatography (SiO2, 60-120, hexane/EtOAc, 5/5) to give N2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine (110 mg, 40.7%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-5e63e4ffff354ac4a6fde60ca07f29c7
Source noteuspto-grants-2011_07