HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745660Generated: November 1, 2026
HCID 13377054, compound → HCID 13377055, compound
https://huagongshe.com/reaction/745660
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13377054 | HCID 13377054 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13377055 | HCID 13377055 | 37.1% |
Reaction Steps
The Compound [II] (0.71 g), mixed with 10% palladium on charcoal (0.2 g) and acetic acid (25 ml), was hydrogenated with the calculated volume of hydrogen under normal pressure at room temperature. After the calculated volume of hydrogen was taken up, palladium on charcoal was filtered, and the filtrate was concentrated to dryness. The residue was dissolved in a small amount of water, and neutralized with 10% sodium hydroxide solution. The resulting precipitate was collected, dried, and purified by column chromatography on silicagel using a mixture of chloroform and ethanol (10:1) as the developing solvent. The purified product was recrystallized from ethanol to give 0.25 g (yield: 37.1%) of 8-[4-(4-aminobenzyl)-1-piperazinyl]-9-fluoro-6,7-dihydro-5-methyl-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid (Compound [I]) as pale yellow needles, m.p. 215.5°-217.5° 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-14c9097ef855485c9f119b87b0d54aab |
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| Source note | uspto-grants-1986_07 |
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