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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376083Generated: October 25, 2026

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

https://huagongshe.com/reaction/2376083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamineHCID 68963176—
ReactantEthyl (2E)-3-(5-chloro-2-pyrazinyl)acrylateHCID 86603667—
SolventDimethylformamideHCID 6228—
Productethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylateHCID 8660370763.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of ethyl (2E)-3-(5-chloro-2-pyrazinyl)acrylate (500 mg) in DMF (5 mL) was added (3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamine (951 mg) and Et3N (1.15 mL). After stirring for 3 hours at 120° 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-chlorobenzoyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate (601 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465731B2
Source datasetuspto-grants-2008_12
ORD IDord-e0eeefb523a141e0b10cb6fd924da15b
Source noteuspto-grants-2008_12