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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014140Generated: October 25, 2026

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

https://huagongshe.com/reaction/1014140

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 numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-6f14348b6ac645e2a988498f7628cdaa
Source noteuspto-grants-2011_07