HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → Ciprofloxacin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Fluoroquinolonic acid | HCID 483180 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ciprofloxacin | HCID 2764 | 84.6% |
Reaction Steps
A mixture of 19.7 g of 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 30.1 g of anhydrous piperazine and 100 ml of dimethylsulphoxide is heated at 135° to 140° C. for 2 hours. The solvent is distilled off under a fine vacuum and the residue is suspended in H2O, filtered off with suction and washed with water. For further purification, the moist crude product is boiled up with 100 ml of water, filtered off with suction at room temperature, washed with H2O and dried to constant weight at 100° C. over CaCl2 in a vacuum drying cabinet. 19.6 g of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid of decomposition point 255° to 257° C. are obtained;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563448 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-578bf11210854b14a8074da8ad48a930 |
| Source note | uspto-grants-1986_01 |