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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837378Generated: November 1, 2026

(4-Aminophenoxy)benzene → HCID 23498106, compound

https://huagongshe.com/reaction/1837378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 23498077HCID 23498077—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 23498106HCID 2349810662.2%

Reaction Conditions

Temperature115 °C

Reaction Steps

A reaction mixture of 0.12 g (0.38 mmol) of 4-chloro-6-methoxy-7-(4-methylpiperazin-1-yl)-quinoline-3-carbonitrile, 0.077 g (0.42 mmol) of 4-phenoxyaniline and 0.044 g (0.38 mmol) of pyridine hydrochloride in 2 ml of 2-ethoxyethanol is heated at 115° C. for 45 minutes. After cooling, the mixture is filtered, washed with cold 2-ethoxyethanol, then ethyl acetate. After drying in vacuo, the solid is suspended in a saturated solution of sodium carbonate, stirred for 45 minutes and collected by filtration. The reaction product is washed with water and dried in vacuo, to provide 0.11 g of 6-methoxy-7-(4-methylpiperazin-1-yl)-4-(4-phenoxyphenylamino)-quinoline-3-carbonitrile as a yellow solid, mp softens at 93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780996B2
Source datasetuspto-grants-2004_08
ORD IDord-50f203e540f746af9187eebe592864a9
Source noteuspto-grants-2004_08