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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267082Generated: November 3, 2026

Sodium Bicarbonate → 1-[1-(3-Chloro-2-pyridyl)-5-methyl-4-pyrazolyl]-3-[4-(3,5-difluorophenyl)-1-piperazinyl]-1-trans-propene Hydrochloride

https://huagongshe.com/reaction/1267082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3,5-Difluorophenyl)piperazineHCID 10987219—
Reactant4-Acetyl-1-(3-chloro-2-pyridyl)-5-methylpyrazoleHCID 11817206—
ReactantEthanol hydrochlorideHCID 21887872—
SolventEthanolHCID 702—
Product1-[1-(3-Chloro-2-pyridyl)-5-methyl-4-pyrazolyl]-3-[4-(3,5-difluorophenyl)-1-piperazinyl]-1-trans-propene HydrochlorideHCID 18545293—

Reaction Steps

In 40 ml of absolute ethanol was dissolved 0.72 g of 4-acetyl-1-(3-chloro-2-pyridyl)-5-methylpyrazole, and 1.38 g of 1-(3,5-difluorophenyl)piperazine, 7 ml of a 1N hydrochloric acid/ethanol solution, and 0.917 g of p-formaldehyde were added thereto, followed by refluxing for 20 hours. To the reaction mixture was further added 0.917 g of p-formaldehyde, followed by refluxing for 50 hours. After the reaction mixture was allowed to stand at room temperature for 21 hours, a saturated aqeous solution of sodium hydrogencarbonate was added thereto, and the mixture was extracted with chloroform three times. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by evaporation. The residue was subjected to silica gel column chromatography using a mixture of chloroform-methanol (50:1 by volume) as a developing solvent. The fraction containing the desired compound was concentrated to yield 0.72 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552018B1
Source datasetuspto-grants-2003_04
ORD IDord-67de3da8c3a64c8cab544c1c7abf8956
Source noteuspto-grants-2003_04