HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 20399356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-one | HCID 4961790 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 20399356 | HCID 20399356 | — |
Reaction Steps
In to a solution consisting of 6.7 g of 6-(α-chloroacetyl)-3,4-dihydrocarbostyril and 60 ml of anhydrous dimethylformamide was added 4.4 g of piperazine and 5 ml of triethylamine and the reaction mixture was stirred at 50° to 60° C. for 1 hour. The reaction mixture thus obtained was poured into a large amount of water and was extracted with chloroform. The chloroform layer was washed with water, dried and chloroform was removed by distillation. The residue obtained was suspended in a mixture of methanol-chloroform and by adding hydrochloric acid/methanol to obtain 3.5 g of 6-(1-piperazinyl)acetyl-3,4-dihydrocarbostyril monohydrochloride trihydrate in the form of colorless needle-like crystals. Melting point: 265°-267° C. (decomposed).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514401 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-e73af9f2d5e14216afdf90a542758a1d |
| Source note | uspto-grants-1985_04 |