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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226367Generated: October 29, 2026

Potassium Carbonate → ethyl (2E)-3-(5-{[(3R)-1-benzyl-3-piperidinyl]amino}2-pyrazinyl)acrylate

https://huagongshe.com/reaction/226367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-1-benzyl-3-Aminopiperidine DihydrochlorideHCID 22831369—
ReactantEthyl (2E)-3-(5-chloro-2-pyrazinyl)acrylateHCID 86603667—
SolventDimethylformamideHCID 6228—
Productethyl (2E)-3-(5-{[(3R)-1-benzyl-3-piperidinyl]amino}2-pyrazinyl)acrylateHCID 8660367224.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of ethyl (2E)-3-(5-chloro-2-pyrazinyl)acrylate (300 mg) and potassium carbonate (4.94 mg) in DMF (15 mL) was added (3R)-1-benzyl-3-piperidinamine dihydrochloride (668 mg) under nitrogen at ambient temperature and the mixture was stirred at 85° C. for 18 hrs. The reaction mixture was evaporated in vacuo and the residue was partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform-MeOH=97-3) to give ethyl (2E)-3-(5-{[(3R)-1-benzyl-3-piperidinyl]amino}2-pyrazinyl)acrylate (125 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-a1cd390e29ec4101b5ede8d540346e4d
Source noteuspto-grants-2009_07