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-oxoquinoline-3-carboxylic acid, 30.1 g of anhydrous piperazine and 100 ml of dimethyl sulphoxide is heated at 135°-140° C. for 2 hours. The solvent is distilled out under high 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 with 100 ml of water, filtered with suction at room temperature, the solid is washed with H2O and dried to constant weight over CaCl2 in a vacuum oven at 100° C. 19.6 g of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic acid, of decomposition point 255°-257° C., are obtained; RF value: 0.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547503 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-a44e77e3fe6b4197b805ca7494468061 |
| Source note | uspto-grants-1985_10 |