Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 13385162 | HCID 13385162 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 4594465 | HCID 4594465 | 54% |
Reaction Steps
A mixture of 9.3 g (0.03 mole) of 7-chloro-1-cyclopropyl-1,4-dihydro-6-nitro-4-oxo-3-quinolinecarboxylic acid and 12.9 g (0.15 mole) of piperazine in 60 ml of dimethylsulphoxide is warmed at 120° C. for 15 minutes. After a short time, a precipitate separates out of the hot solution. The mixture is concentrated under a high vacuum, the residue is stirred with 30 ml of water and the mixture is heated again at 95° C. for 30 minutes. The mixture is adjusted to pH 8 with 2N hydrochloric acid and the precipitate is filtered off with suction and washed with water and methanol. 5.8 g (54% of theory) of 1-cyclopropyl-1,4-dihydro-6-nitro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid of decomposition point 296° to 298° C. are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04563448 |
|---|
| Source dataset | uspto-grants-1986_01 |
|---|
| ORD ID | ord-8030a2fcaddc434f87b8b3287c7c4422 |
|---|
| Source note | uspto-grants-1986_01 |
|---|