Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Ethyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 800521 | — |
| Reactant | 2-{[(Propan-2-yl)oxy]methyl}piperazine | HCID 19763542 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14839388 | HCID 14839388 | 107% |
Reaction Steps
A mixture of 2 g of 2-[(1-methylethoxy)methyl]piperazine, 1.27 g of 1-ethyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid and 5 ml of pyridine was heated at 80° C. for 3 hours, then evaporated in vacuo. The residue was reevaporated three times from toluene, giving a gum. Ether was added to the gum which solidified. The solid was triturated with ether containing methanol and then dried giving 2.1 g of solid. A 1 g portion was purified by chromatography, giving 650 mg of the desired product, mp 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05210193 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-9dac272b2a7743059d996daba7a7bb51 |
|---|
| Source note | uspto-grants-1993_05 |
|---|