HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745659Generated: October 31, 2026
Hydrochloric Acid → HCID 13377054, compound
https://huagongshe.com/reaction/745659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | HCID 15571787 | HCID 15571787 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13377054 | HCID 13377054 | 60% |
Reaction Steps
A mixture of 9-fluoro-6,7-dihydro-5-methyl-8-(1-piperazinyl)-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid (Compound [III]), hydrochloride (1.1 g), p-nitrobenzyl bromide (Compound [IV]) (1.87 g) and triethylamine (1.46 g) in N,N-dimethylformamide (50 ml) was heated with stirring at 80°-90° C. for 10 hr. After evaporation of the solvent, water was added to the residue, and the aqueous mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate and evaporated to dryness. The residue was recrystallized from a mixture of N,N-dimethylformamide and ethanol (2:1) to give 0.83 g (yield: 60%) of 8-[4-(4-nitrobenzyl)-1-piperazinyl]-9-fluoro-6,7-dihydro-5-methyl-1-oxo-1H, 5H-benzo[ij]quinolizine-2-carboxylic acid (Compound [II]) as pale yellow needles, m.p. 230°-233° C. (decompd.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599418 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-0208913166824fd3b3cff771bf82c585 |
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| Source note | uspto-grants-1986_07 |
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