Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929848Generated: November 1, 2026

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

https://huagongshe.com/reaction/929848

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 numberUS09296704B2
Source datasetuspto-grants-2016_03
ORD IDord-c2f65f5626404f91944fad2c0fde22fe
Source noteuspto-grants-2016_03