HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ciprofloxacin → HCID 13337926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ciprofloxacin | HCID 2764 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13337926 | HCID 13337926 | 59.9% |
Reaction Steps
3.3 g (0.01 mol) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid in 50 ml of dimethylformamide are heated at 90° C. with 2.5 g (0.015 mole) of ethyl bromoacetate, 1.2 g (0.02 mole) of triethylamine and 2.5 g of potassium iodide for 5 hours. The reaction mixture is poured into 30 ml of water and the precipitate is filtered off with suction, washed with water and recrystallized from methanol. 2.5 g of 1-cyclopropyl-6-fluoro-7-[4-(ethoxycarbonylmethyl)-1-piperazinyl]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid of melting point 192° to 194° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563448 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-864e331b9ddc4017af38532f4a0b1951 |
| Source note | uspto-grants-1986_01 |