HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 12733892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 6-Bromo-7-chloro-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 12733873 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12733892 | HCID 12733892 | 33% |
Reaction Steps
3.3 g of 6-bromo-7-chloro-1-ethyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (0.01 mol) and 4.5 cm3 of 1-methylpiperazine (0.04 mol) in solution in 30 cm3 of dimethylsulphoxide, were heated at 110° C. for 4 hours. After cooling, the solution was diluted with 250 cm3 of water. The precipitate formed was filtered off, washed with water and recrystallised from 50 cm3 of methyl cellosolve. 1.3 g of 6-bromo-1-ethyl-7-(4-methylpiperazinyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid, m.p. 209C (decomposition), were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04292317 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-3d53d407a21149c7b6f73674428e541f |
| Source note | uspto-grants-1981_09 |