HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → N-Methylciprofloxacin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Fluoroquinolonic acid | HCID 483180 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-Methylciprofloxacin | HCID 465907 | 59.1% |
Reaction Steps
A mixture of 20 g of 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 28.5 g of N-methylpiperazine and 120 ml of anhydrous dimethylsulphoxide is heated at 135°-140° C. for 2.5 hours. The solvent is distilled off under a fine vacuum and the residue is suspended in about 50 ml of water. The solid is filtered off with suction, rinsed with water, dried over calcium chloride in a vacuum drying cabinet at 80° C. and recrystallized from glycol monomethyl ether. 14.5 g of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-methyl-1-piperazinyl)-3-quinolinecarboxylic acid of decomposition point 248°-250° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563459 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-1724f4b515014d9f893eb661a686b58d |
| Source note | uspto-grants-1986_01 |