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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
| Reactant | 6-(piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-one | HCID 11117896 | — |
| Reactant | 6-(1-Piperazinyl)-3,4-dihydrocarbostyril hydrobromide | HCID 13236308 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-[4-(4-Acetyloxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04415572 |
|---|
| Source dataset | uspto-grants-1983_11 |
|---|
| ORD ID | ord-5ce33e036acc4c32a542b76e163be5b9 |
|---|
| Source note | uspto-grants-1983_11 |
|---|