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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093503Generated: October 31, 2026

(4-Aminophenoxy)benzene → N4-(6-(methylamino)pyridine-2-yl)-N6-(4-phenoxyphenyl)pyrimidine-4,6-diamine

https://huagongshe.com/reaction/2093503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
Reactantn2-(6-Chloropyrimidin-4-yl)-n6-methylpyridine-2,6,diamineHCID 57708344—
CatalystHydrochloric AcidHCID 313—
Solvent1-ButanolHCID 263—
ProductN4-(6-(methylamino)pyridine-2-yl)-N6-(4-phenoxyphenyl)pyrimidine-4,6-diamineHCID 5770827141%

Reaction Steps

A solution of N2-(6-chloropyrimidin-4-yl)-N6-methylpyridine-2,6,diamine (0.3 g 1.27 mmol), 4-phenoxy aniline (0.28 g, 1.52 mmol) and conc. HCl (2 drops) in n-butanol (2 mL) was subjected to microwave irradiation (120° C., 1 h). The reaction mixture was cooled, was concentrated under reduced pressure, and the residue was diluted with CH2Cl2 (5 mL). The dichloromethane solution was washed with NaHCO3 (2 mL), water (2 mL), and brine (2 mL), and was dried over Na2SO4. Filtration followed by concentration under reduced pressure gave a residue which was purified by column chromatography (SiO2, 60-120, chloroform/methanol, 9/1) to give N4-(6-(methylamino)pyridine-2-yl)-N6-(4-phenoxyphenyl)pyrimidine-4,6-diamine (0.2 g, 41%) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445498B2
Source datasetuspto-grants-2013_05
ORD IDord-6148ad5106054ba5bf3a15d98b9cbd6a
Source noteuspto-grants-2013_05