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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890811Generated: November 1, 2026

Acetic Acid → 1-{[2-(2-Fluorophenyl)-3-oxo-2,3-dihydropyrazolo[4,3-c]quinolizin-5-yl]methyl}-4-(4-methylpyridin-2-yl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1890811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-Methylpyridin-2-yl)piperidine-4-carbonitrileHCID 53363276—
Reactant2-(2-Fluorophenyl)-3-oxo-2,3-dihydropyrazolo[4,3-c]quinolizine-5-carbaldehydeHCID 86762007—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetonitrileHCID 6342—
Product1-{[2-(2-Fluorophenyl)-3-oxo-2,3-dihydropyrazolo[4,3-c]quinolizin-5-yl]methyl}-4-(4-methylpyridin-2-yl)piperidine-4-carbonitrileHCID 53482142—

Reaction Steps

2-(2-Fluorophenyl)-3-oxo-2,3-dihydropyrazolo[4,3-c]quinolizine-5-carbaldehyde (0.025 g, 0.081 mmol) was suspended in a mixture of 1,2-dichloroethane (2 mL) and acetonitrile (4 mL) containing powdered 4 Å molecular sieves and treated with 4-(4-methylpyridin-2-yl)piperidine-4-carbonitrile (0.018 g, 0.094 mmol. 1.2 equiv), acetic acid (0.028 mL, 0.49 mmol, 6.0 equiv), and sodium triacetoxyborohydride (0.034 g, 0.16 mmol, 2.0 equiv). After stirring at ambient temperature for 60 hours, the mixture was poured into saturated aqueous sodium bicarbonate and extracted with dichloromethane (2×).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507494B2
Source datasetuspto-grants-2013_08
ORD IDord-36e57b1be5924defb92d4a4661c87b0e
Source noteuspto-grants-2013_08