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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874062Generated: November 1, 2026

1-(2-Pyridyl)piperazine → HCID 58492583, compound

https://huagongshe.com/reaction/1874062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58492476HCID 58492476—
SolventDichloromethaneHCID 6344—
ProductHCID 58492583HCID 5849258335.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304546B2
Source datasetuspto-grants-2012_11
ORD IDord-a468e7320b9743f182fb664aa72edaab
Source noteuspto-grants-2012_11