HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68169Generated: October 29, 2026
1-(2-Pyridyl)piperazine → HCID 58492583, compound
https://huagongshe.com/reaction/68169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 58492476 | HCID 58492476 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58492583 | HCID 58492583 | 35.4% |
Reaction Steps
1-(2-Pyridyl)piperazine (551 mg, 3.38 mmol) was added to a 1,2-dichloromethane solution (20 ml) of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydroquinoline-2-carbaldehyde (800 mg, 2.25 mmol) and stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (670 mg, 3.16 mmol) was added to the resulting mixture and stirred at room temperature for 4 hours. Dichloromethane was added to the resulting reaction mixture, washed with water, and then the mixture was dried over sodium sulfate. Thereafter, the solvent was removed under reduced pressure. The residue was then purified using NH silica gel column chromatography (dichloromethane:ethyl acetate=1:1). The solvent was removed under reduced pressure and the residue was recrystallized from ethyl acetate-n-hexane, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-8-propoxy-2-(4-pyridin-2-yl-piperazin-1-ylmethyl)-1H-quinolin-4-one (400 mg, yield: 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE045108E1 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-80709b10b6264e958f909b444dc362c2 |
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| Source note | uspto-grants-2014_09 |
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