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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577779Generated: October 23, 2026

Potassium Carbonate → 2-[4-(Cyclohexylmethyl)piperazin-1-yl]quinoline-3-carbaldehyde

https://huagongshe.com/en/reaction/577779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-quinolinecarboxaldehydeHCID 690958—
Reactant1-(Cyclohexylmethyl)piperazineHCID 2735885—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[4-(Cyclohexylmethyl)piperazin-1-yl]quinoline-3-carbaldehydeHCID 5748681786%

Reaction Conditions

Temperature110 °C

Reaction Steps

1-(Cyclohexylmethyl)piperazine (0.42 mL, 2.2 mmol) was added to a mixture of 2-chloro-3-quinolinecarboxaldehyde (0.383 g, 2.0 mmol) and potassium carbonate (0.7 g, 5.0 mmol) in anhydrous DMF (4 mL) at ambient temperature under a nitrogen atmosphere. After being stirred for 20 minutes, the reaction mixture was heated at 110° C. for 4.5 h. After cooling to room temperature this mixture was diluted with water (40 mL) and extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and then concentrated under vacuum to give a pale brown crude product. Purification by silica gel column chromatography and eluting with 2.5% methanol in dichloromethane afforded the title compound (0.56 g), yield: 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-596641ef58e540a4a5d550a7168db462
Source noteuspto-grants-2015_05