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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 96Generated: October 23, 2026

Ethyl 7-bromobenzofuran-2-carboxylate → Ethyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate

https://huagongshe.com/en/reaction/96

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-bromobenzofuran-2-carboxylateHCID 46738833—
Reactant1-(5-(2-(Piperazin-1-yl)ethyl)indolin-1-yl)ethanoneHCID 59636747—
ReagentCesium carbonateHCID 10796—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 5963675661.47%

Reaction Conditions

Temperature95 °C

Reaction Steps

06/05 2009 14:53:56 +0200 To ethyl 7-bromobenzofuran-2-carboxylate (0.460 g, 1.71 mmol) and 1-(5-(2-(piperazin-1-yl)ethyl)indolin-1-yl)ethanone (0.491 g, 1.79 mmol) (from EN02198-74) in dry degassed dioxane (8 mL) were added Cesium carbonate (0.724 g, 2.22 mmol), 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (0.081 g, 0.17 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (0.078 g, 0.09 mmol) under argon and the reaction heated at 95°C overnight. After cooling to rt, 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 0.485 g (61%) of the product as a yellow solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-90e612e9a6744ee3af3c528f17e1b1ce
Source note750 AstraZeneca ELN dataset