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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929873Generated: October 25, 2026

Hydrochloric Acid → 3-[6-(4-Phenoxyphenylamino)-pyrimidin-4-ylamino]phenylamine

https://huagongshe.com/reaction/929873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantTert-butyl 3-(6-chloropyrimidin-4-ylamino)phenylcarbamateHCID 57708283—
Solvent1-ButanolHCID 263—
Product3-[6-(4-Phenoxyphenylamino)-pyrimidin-4-ylamino]phenylamineHCID 5770828839.3%

Reaction Steps

A solution of tert-butyl 3-(6-chloropyrimidin-4-ylamino)phenylcarbamate (200 mg, 0.6 mmol), 4-phenoxyaniline (346 mg, 1.8 mmol) and concentrated HCl (45 mg, 1.2 mmol) in n-butanol (8 mL) was subjected to microwave irradiation (160° C., 20 min). The reaction mixture was quenched with NaHCO3 solution (2 mL) and extracted with EtOAc (2×10 mL). The combined EtOAc extract was washed with water (5 mL), brine (5 mL), was dried over Na2SO4 and was concentrated under reduced pressure. The residue was further purified by column chromatography (SiO2, 60-120, Chloroform/methanol, 9/1) to give N4-(3-aminophenyl)-N6-(4-phenoxyphenyl)pyrimidine-4,6-diamine (87 mg, 37.8%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296704B2
Source datasetuspto-grants-2016_03
ORD IDord-717e3fb0b4f3489e959d50e13ae56a8d
Source noteuspto-grants-2016_03