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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49816Generated: October 25, 2026

Water → 4-Acetyl-n-(3-(1-acetylpiperazin-4-yl)phenyl)-2-nitroaniline

https://huagongshe.com/reaction/49816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4'-Fluoro-3'-nitroacetophenoneHCID 2734612—
Reactant1-[4-(3-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 11117539—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-Acetyl-n-(3-(1-acetylpiperazin-4-yl)phenyl)-2-nitroanilineHCID 22330226—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1b (0.75 g, 4.1 mmol) and 2d (0.9 g, 4.1 mmol) in anhydrous NMP (2 ml) was heated to 80° C. overnight under a stream of nitrogen. After cooling water (20 ml) was added and the mixture was extracted with dichloromethane. The organic extract was dried over sodium sulfate and the solvent was removed under reduced pressure. The residue was purified by column-chromatography on silica gel using ethyl acetate as the eluent to yield 4-acetyl-N-(3-(1-acetylpiperazin-4-yl)phenyl)-2-nitroaniline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710044B2
Source datasetuspto-grants-2004_03
ORD IDord-da6a3f7e113d4c7caef77cfec8bc0628
Source noteuspto-grants-2004_03