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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226371Generated: October 31, 2026

Potassium Carbonate → ethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate

https://huagongshe.com/reaction/226371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-3-amino-1-(4-chlorobenzyl)pyrrolidineHCID 24904911—
ReactantEthyl (2E)-3-(5-chloro-2-pyrazinyl)acrylateHCID 86603667—
SolventDimethylformamideHCID 6228—
Productethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylateHCID 8660367748.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl (2E)-3-(5-chloro-2-pyrazinyl)acrylate (1.78 g) and (3R)-1-(4-chlorobenzyl)-3-pyrrolidinamine (2.65 g) in DMF (25 mL) was added K2CO3 (5.79 g). After stirring for 3 hours at 100° C., the reaction mixture was partitioned between ethyl acetate and H2O. The organic layer was washed with H2O, dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give ethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate (1.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-fb9f8dd917704d4e88c889b8ba9b4561
Source noteuspto-grants-2009_07