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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263123Generated: November 2, 2026

Water → 6-{1-Oxo-2-[4-(4-nitrophenyl)-1-piperazinyl]-butyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1263123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
Reactant6-(1-Oxo-2-piperazinylbutyl)-3,4-dihydrocarbostyrilHCID 57294315—
CatalystCopperHCID 23978—
SolventGlycol monoethyl etherHCID 8076—
Product6-{1-Oxo-2-[4-(4-nitrophenyl)-1-piperazinyl]-butyl}-3,4-dihydrocarbostyrilHCID 13064861—

Reaction Steps

1.8 Grams of 6-(1-oxo-2-piperazinylbutyl)-3,4-dihydrocarbostyril, 2.0 g of p-bromonitrobenzene, 1.2 g of potassium carbonate and 0.1 g of copper powder were dispersed in 80 ml of ethyl cellosolve and stirred at 120°-150° C. by heating for 5 hours. The reaction mixture was concentrated under a reduced pressure and the residue thus obtained was added water and extracted with chloroform. The chloroform layer was washed with water, dried and the chloroform was removed by distillation. The residue thus obtained was separated and purified by a separative thin layer chromatography and recrystallized from ethanol to obtain 0.2 g of 6-{1-oxo-2-[4-(4-nitrophenyl)-1-piperazinyl]-butyl}-3,4-dihydrocarbostyril in yellow powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04455422
Source datasetuspto-grants-1984_06
ORD IDord-ba185d5b147646969219964d50c99f68
Source noteuspto-grants-1984_06