HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649211Generated: October 31, 2026
Water → 5-[4-(4-Methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/1649211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(1-Piperazinyl)-3,4-dihydrocarbostyril monohydrobromide | HCID 20480591 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[4-(4-Methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril | HCID 13236342 | 36.1% |
Reaction Steps
5-(1-Piperazinyl)-3,4-dihydrocarbostyril monohydrobromide (2.6 g) and 2.34 ml of triethylamine were dissolved in 40 ml of DMF. The mixture was stirred at room temperature while slowly adding dropwise 10 ml of DMF solution containing 2.5 g of 4-methoxybenzoyl chloride. After completion of addition the reaction mixture was stirred for 30 minutes. The reaction mixture was poured into a large amount of water and extracted with chloroform. The extract was washed with saturated sodium hydrogencarbonate solution and subsequently with water and dried over anhydrous sodium sulfate. Chloroform was distilled off and residual crystals were recrystallized from methanol-chloroform to give 1.1 g of 5-[4-(4-methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril, m.p. 219°-220° C., colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04415572 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-b96a25f375e547de96f3ce2f53ef1fdd |
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| Source note | uspto-grants-1983_11 |
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