HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845031Generated: October 30, 2026
Acetic Anhydride → HCID 20133482, compound
https://huagongshe.com/reaction/845031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20133480 | HCID 20133480 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20133482 | HCID 20133482 | — |
Reaction Steps
6,8-Difluoro-7-(4-methyl-1-piperazinyl)-1-(4-hydroxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.14 g) is dissolved in dry pyridine (5 ml) and acetic anhydride (5 ml), and the mixture is allowed to stand at room temperature for 16 hours. Excess acetic anhydride and pyridine are distilled off under reduced pressure, and the resulting residue is dissolved in dichloromethane. The dichloromethane solution is washed with diluted hydrochloric acid, saturated aqueous sodium chloride, saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride in this order, and dried over sodium sulfate. The solvent is distilled off, and the residue is recrystallized from ethanol-chloroform to give 6,8-difluoro-7-(4-methyl-1-piperazinyl)-1-(4-acetyloxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.12 g) as pale yellowish white crystals, m.p. 247°-251° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04755513 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-c6299ec62c9c4ef7a0f3b99b1441963c |
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| Source note | uspto-grants-1988_07 |
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