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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244995Generated: October 31, 2026

Potassium Carbonate → HCID 10223348, compound

https://huagongshe.com/reaction/1244995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21922745HCID 21922745—
Reactant3-(4-Fluorophenyl)-2-propenalHCID 53384379—
SolventWaterHCID 962—
ProductHCID 10223348HCID 1022334849%

Reaction Steps

14.25 g (46.51 mmol) of α-(1-benzylpiperidin-4-yl)amino-α-(pyridin-4-yl)acetonitrile [prepared as described in step 12(ii) above] and 6.98 g (46.51 mmol) of 3-(4-fluorophenyl)acrolein were dissolved in 145 ml of N,N-dimethylacetamide, 1.29 g (9.30 mmol) of potassium carbonate were added to the solution, and then this was stirred at room temperature for 5 hours. At the end of this time, water was added to the reaction mixture and then this was extracted with ethyl acetate. The organic extract was washed with water and then concentrated by evaporation under reduced pressure. 150 ml of ethylene glycol were added to the residue thus obtained and the resulting mixture was stirred at 180° C. for 1 hour. After cooling to room temperature, a saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture which was then extracted with ethyl acetate. The organic extract was washed with water and then concentrated by evaporation under reduced pressure. The residue thus obtained was purified by chromatography on a silica gel column using a 1:3 by volume mixture of hexane and ethyl acetate as the eluant to give 10.31 g (yield 49%) of the title compound as a pale brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122666B2
Source datasetuspto-grants-2006_10
ORD IDord-ee9e3feb7a8d429793a83dbf5855012c
Source noteuspto-grants-2006_10