HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291173Generated: October 31, 2026
1-(3-Chlorophenyl)piperazine → 6-{1-Oxo-2-[4-(3-chlorophenyl)-1-piperazinyl]-ethyl}-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/2291173
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(3-Chlorophenyl)piperazine | HCID 1355 | — |
| Reactant | 6-(Bromoacetyl)-3,4-dihydroquinolin-2(1H)-one | HCID 2756837 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-{1-Oxo-2-[4-(3-chlorophenyl)-1-piperazinyl]-ethyl}-3,4-dihydrocarbostyril | HCID 13064858 | — |
Reaction Steps
3.0 of 6-(1-oxo-2-bromoethyl)-3,4-dihydrocarbostyril and 5.5 g of 4-(3-chlorophenyl)piperazine were dispersed in 50 ml of dioxane and the dispersion was stirred at 50° C. for 5 hours. Then the reaction mixture was cooled and the insoluble matters formed in the reaction mixture were removed and the dioxane mother liquor was concentrated under a reduced pressure to dryness. 80 Milliliter of ether was added to the dried matter to effect the crystallization. Crude crystals thus obtained were recrystallized from dioxane-water to obtain 3.1 g of 6-{1-oxo-2-[4-(3-chlorophenyl)-1-piperazinyl]ethyl}-3,4-dihydrocarbostyril in light yellow needle-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04619932 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-1311461e0381405da1fa136402c1980e |
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| Source note | uspto-grants-1986_10 |
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