HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477176Generated: October 26, 2026
Dimethylformamide → 6-[4-(2-Phenyl-2-hydroxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride
https://huagongshe.com/reaction/477176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3-Chlorophenyl)(piperazin-1-yl)methanone | HCID 1074765 | — |
| Reactant | 6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-one | HCID 4961790 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-[4-(2-Phenyl-2-hydroxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride | HCID 131716209 | — |
Reaction Steps
To 60 ml of anhydrous dimethylformamide solution containing 6.7 g of 6-(α-chloroacetyl)-3,4-dihydrocarbostyril was added 11.5 g of 4-(3-chlorobenzoyl)piperazine and 5 ml of triethylamine and the whole mixture was stirred at 50 to 60° C. for 1 hour. The reaction mixture was poured into a large amount of water, and the organic layer was extracted with chloroform. The chloroform layer was washed with water, dried, then chloroform was removed by evaporation. The residue thus obtained was recrystallized from methanol-chloroform to yield 5.5 g of 6-[-4-(3-chlorobenzoyl)-1-piperazinylacetyl]-3,4-dihydrocarbostyril 1/2-hydrate in the form of colorless powdery substance. Melting point: 231°-234° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886809 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-9a6a6ea73ee74987b7d27f19eae57234 |
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| Source note | uspto-grants-1989_12 |
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