HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263129Generated: October 30, 2026
3-Chloroaniline → 6-{1-Oxo-2-[4-(3-chlorophenyl)-1-piperazinyl]-ethyl}-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/1263129
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Reactant | 6-(1-Oxo-2-morpholinoethyl)-3,4-dihydrocarbostyril monohydrochloride | HCID 20229454 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 6-{1-Oxo-2-[4-(3-chlorophenyl)-1-piperazinyl]-ethyl}-3,4-dihydrocarbostyril | HCID 13064858 | — |
Reaction Steps
5.0 Grams of 6-(1-oxo-2-morpholinoethyl)-3,4-dihydrocarbostyril monohydrochloride and 5.0 g of m-chloroaniline were mixed in 30 ml of concentrated hydrochloric acid and the mixture was heated at 200°-220° C. by removing water for 6 hours. After cooled the reaction mixture 100 ml of 5N-hydrochloric acid was added thereto and dissolved by heating and refluxed for 2 hours. Then the reaction mixture was cooled and poured into 100 ml of 8N-sodium hydroxide aqueous solution and the organic layer was extracted with chloroform. Chloroform was removed by distillation and the residue thus obtained was separated and purified by a preparative silica-gel thin layer chromatography, then recrystallized from dioxane-water to obtain 0.16 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 | US04455422 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-e950b3adc1d64702975384c6c4d6880f |
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| Source note | uspto-grants-1984_06 |
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