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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633598Generated: October 26, 2026

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

https://huagongshe.com/reaction/1633598

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 numberUS06503925B1
Source datasetuspto-grants-2003_01
ORD IDord-0ee5d9a713b94eb8a0f32b69f69c26e9
Source noteuspto-grants-2003_01