HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Cyclopropyl-7-fluoro-8-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 14853346 | HCID 14853346 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-Cyclopropyl-7-fluoro-8-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid | HCID 14700574 | 50.4% |
Reaction Steps
A suspension of 0.85 g of 1-cyclopropyl-3-ethoxycarbonyl-7-fluoro-8-(4-methyl-1-pip-erazinyl)-4 -oxo-1,4-dihydro-benzo[b][1,8]naphthyridine in 12 cm3 of ethanol, 5 cm3 of 2 N aqueous potassium hydroxide solution and 7 cm3 of water is heated at a temperature close to 80° C. for 1 hour. After adding 5.8 cm3 of a 10% aqueous solution of acetic acid, the precipitate obtained is drained and washed with 3 times 5 cm3 of water. After recrystallizing twice from a mixture of 7.5 cm3 of ethanol and 7.5 cm3 of dimethylformamide each time, 0.4 g of 1-cyclopropyl-7-fluoro-8-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid is obtained in the form of a yellow solid melting at 250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05004745 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-948a5d8083b94684b71cbf9f710c02e5 |
| Source note | uspto-grants-1991_04 |