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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521805Generated: October 30, 2026

4-Aminophenol → 4-(4-Aminophenoxy)-6-chloropyridin-2-amine

https://huagongshe.com/reaction/521805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Amino-4,6-dichloropyridineHCID 5316649—
SolventDimethyl SulfoxideHCID 679—
Product4-(4-Aminophenoxy)-6-chloropyridin-2-amineHCID 58167806—

Reaction Steps

A stirred solution of 4-aminophenol (335 mg, 3.1 mmol) in anhydrous DMSO (8 ml) was flushed with nitrogen and treated with 1M KOBut/THF solution (3.1 ml, 3.1 mmol). The mixture was stirred at room temperature under nitrogen for 10 minutes. 4,6-dichloropyridin-2-ylamine (500 mg, 3.1 mmol) was added and the mixture was heated at 88° C. for 16 hours, cooled to room temperature and poured into 100 ml of water. The resulting precipitates were filtered, washed with water and dried to give the crude product, which was purified by silica gel chromatography with 2˜5% MeOH/CHCl3 to give 4-(4-aminophenoxy)-6-chloropyridin-2-amine as light brown solid. Yield: 350 mg, 49%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328103B2
Source datasetuspto-grants-2016_05
ORD IDord-5b01820ef9cf4c3db15ae197be043e7f
Source noteuspto-grants-2016_05