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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586408Generated: October 25, 2026

Water → Ethyl 4-(3-(4-acetyl-1-piperazinyl)-phenyl)-amino-6-fluoro-3-nitrobenzoate

https://huagongshe.com/reaction/586408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-[4-(3-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 11117539—
ReactantEthyl 2,4-difluoro-5-nitrobenzoateHCID 22330120—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 4-(3-(4-acetyl-1-piperazinyl)-phenyl)-amino-6-fluoro-3-nitrobenzoateHCID 86592319—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 2,4-difluoro-5-nitrobenzoate (22) (1.0 g; 4.33 mmol), 4f (0.95 g; 4.33 mmol) and triethylamine (0.6 ml; 0.33 mmol) in anhydrous NMP (10 ml) was heated to 80° C. for one hour. The cooled mixture was poured into water and extracted with ethyl acetate. The organic extract was dried over magnesium sulphate, concentrated under reduced pressure and purified by column-chromatography on silica gel using ethyl acetate as the eluent. Yield: 1.53 g (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936613B2
Source datasetuspto-grants-2005_08
ORD IDord-8cdcfc701a2143938457e41a3dc09192
Source noteuspto-grants-2005_08