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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496971Generated: October 30, 2026

1-(4-(4-aMino-3-Methoxyphenyl)piperazin-1-yl)ethanone → HCID 72546716, compound

https://huagongshe.com/reaction/1496971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(4-aMino-3-Methoxyphenyl)piperazin-1-yl)ethanoneHCID 55232737—
ReactantHCID 118105738HCID 118105738—
SolventHCID 19698338HCID 19698338—
ProductHCID 72546716HCID 72546716—

Reaction Steps

1-(4-(4-amino-3-methoxyphenyl)piperazin-1-yl)ethanone (40 mg) prepared in Preparation Example 1 and 1-(4-(4-(2,5-dichloropyrimidine-4-ylamino)-3-ethoxyphenyl)piperazin-1-yl)ethanone (50 mg) prepared in Preparation Example 15 were dissolved in 0.08M HCl ethoxyethanol solution (1.2 mL), and allowed to react at 115° C. overnight. Upon completion of the reaction, the solvent of the mixture was removed under reduced pressure, diluted with ethyl acetate, neutralized with an aqueous saturated sodium carbonate solution, water was removed from the organic layer with sodium sulfate, and the solvent was removed under reduced pressure. The mixture was purified by column chromatography to obtain a target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199944B2
Source datasetuspto-grants-2015_12
ORD IDord-38dfc35b5e5d4bbeacce2517d28a0079
Source noteuspto-grants-2015_12