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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 100Generated: October 25, 2026

Piperazine, 2-pyridylethyl- → Ethyl 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate

https://huagongshe.com/reaction/100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazine, 2-pyridylethyl-HCID 566605—
ReactantEthyl 7-bromobenzofuran-2-carboxylateHCID 46738833—
ReagentCesium carbonateHCID 10796—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 5963675146.88%

Reaction Conditions

Temperature95 °C

Reaction Steps

07/01 2009 12:44:11 +0100 To ethyl 7-bromobenzofuran-2-carboxylate (0.100 g, 0.37 mmol) and 1-(2-(pyridin-2-yl)ethyl)piperazine (0.075 g, 0.39 mmol) in dry degassed dioxane (1.5 mL) were added Cesium carbonate (0.157 g, 0.48 mmol), 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (0.018 g, 0.04 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (0.017 g, 0.02 mmol) under argon and the reaction heated at 95°C o/n. All starting material consumed. Water and DCM were added and the layers separated. The aq phase was extracted with DCM (3x). The combined org phases were washed with water, dried (MgSO4), filtered and evaporated. The crude was purified by flash (SiO2; DCM/MeOH 95/5) to give 0.0661 g of the product as a pale yellow semisolid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-ca59850458054174b55daef8c9f3b978
Source note750 AstraZeneca ELN dataset