HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578259Generated: November 3, 2026
1-(2-Hydroxyethyl)piperazine → HCID 12944895, compound
https://huagongshe.com/reaction/1578259
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | 6,7-Dichloro-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 12733886 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 12944895 | HCID 12944895 | 61.3% |
Reaction Steps
As described in Example 1, 4.3 g of 6,7-dichloro-1-ethyl-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid and 10.6 g of 1-(β-hydroxyethyl)-piperazine in 45 cm3 of DMSO (dimethylsulphoxide) were heated for 3 hours at 110° C. After evaporation of the solvent under a good vacuum, the viscous residue was taken up in 20 cm3 of isopropanol; the mixture was stirred and heated under reflux for 20 minutes. After standing for one night at 4° C., the solid was filtered off, washed with ethanol and recrystallised from methyl cellosolve (15 cm3). 3.5 g of 6-chloro-1-ethyl-7-[4-(β-hydroxyethyl)-piperazinyl]-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid, m.p. 215° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04292317 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-14dc1bb9bbf240e489859cd6de7d945d |
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| Source note | uspto-grants-1981_09 |
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