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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649247Generated: October 25, 2026

Sodium Bicarbonate → 6-[4-(4-Acetyloxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1649247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Acetoxybenzoyl chlorideHCID 2756254—
Reactant6-(piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-oneHCID 11117896—
Reactant6-(1-Piperazinyl)-3,4-dihydrocarbostyril hydrobromideHCID 13236308—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product6-[4-(4-Acetyloxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyrilHCID 20480597—

Reaction Steps

A suspension of 1.0 g of 6-(1-piperazinyl)-3,4-dihydrocarbostyril monohydrobromide in 10 ml of DMF was added 296 mg of sodium hydrogencarbonate and stirred at room temperature for 30 minutes to convert the compound to 6-piperazinyl-3,4-dihydrocarbostyril, to which was added 0.62 ml of triethylamine. Then, a solution of 605 mg of 4-acetyloxybenzoyl chloride in 5 ml of DMF was slowly added dropwise to the mixture. After completion of addition, the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into a large amount of water and extracted with chloroform. The extract was washed serially with saturated aqueous sodium hydrogencarbonate solution and with water and then dried over anhydrous sodium sulfate. Chloroform was distilled off to give 6-[4-(4-acetyloxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415572
Source datasetuspto-grants-1983_11
ORD IDord-5ce33e036acc4c32a542b76e163be5b9
Source noteuspto-grants-1983_11