Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376034Generated: October 25, 2026

Cesium carbonate → ethyl (2E)-3-(6-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate

https://huagongshe.com/reaction/2376034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-(6-Chloro-pyridin-3-yl)-acrylic acid ethyl esterHCID 10846187—
Reactant(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamineHCID 68963176—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Productethyl (2E)-3-(6-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-3-pyridyl)acrylateHCID 8660365932.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of ethyl (2E)-3-(6-chloro-3-pyridyl)acrylate (3.5 g) in dioxane (70 mL) was added palladium(II) acetate (371 mg) and 2′-(dicyclohexylphosphino)-N,N-dimethyl-2-biphenylamine (110 mg) and cesium carbonate (583 mg), and (3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamine (4.09 g). The mixture was heated at 90° C. for 3 hours. The resulting mixture was diluted with AcOEt, and the precipitate was removed by filtration. The filtrate was concentrated and residual brown oil was purified by purified by silica gel column chromatography eluted with AcOEt and hexane (1:4)-AcOEt to give ethyl (2E)-3-(6-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate (2.16 g) as dark yellow form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465731B2
Source datasetuspto-grants-2008_12
ORD IDord-095b240c2a4d4283ac372fc039136bbf
Source noteuspto-grants-2008_12