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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460680Generated: November 1, 2026

Ethanol → 6-{4-[3-(4-Chlorobenzoyl)-3-hydroxyliminopropyl]-1-piperazinylcarbonyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1460680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactant2-(4-Chlorobenzoyl)ethyl[-1-piperazinylcarbonyl}-3,4-dihydrocarbostyrilHCID 131717095—
SolventWaterHCID 962—
Product6-{4-[3-(4-Chlorobenzoyl)-3-hydroxyliminopropyl]-1-piperazinylcarbonyl}-3,4-dihydrocarbostyrilHCID 88124386—

Reaction Steps

1.7 Grams of 6-{4-[2-(4-chlorobenzoyl)ethyl[-1-piperazinylcarbonyl}-3,4-dihydrocarbostyril, 0.83 g of hydroxylamine hydrochloride and 2.29 g of sodium acetate were dissolved in 40 ml of ethanol and 20 ml of water, and the solution was stirred overnight at room temperature. Then the reaction mixture was concentrated under reduced pressure, then the residue thus obtained was extracted with chloroform, the extract was dried with anhydrous sodium carbonate, then the solvent was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: dichloromethane:methanol =50:1), then recrystallized from ethanol to yield 1.2 g of 6-{4[-3-(4-chlorobenzoyl)-3-hydroxyliminopropyl]-1-piperazinylcarbonyl}-3,4-dihydrocarbostyril. White powdery substance. Melting point: 207° C.-209° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071856
Source datasetuspto-grants-1991_12
ORD IDord-8cf757d0714b4a5aa2e8e9b21c6197bc
Source noteuspto-grants-1991_12