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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471671Generated: October 25, 2026

Cesium carbonate → Ethyl 4-(4-benzylpiperazin-1-yl)benzofuran-2-carboxylate

https://huagongshe.com/reaction/1471671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantEthyl 4-chlorobenzofuran-2-carboxylateHCID 67983046—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-(4-benzylpiperazin-1-yl)benzofuran-2-carboxylateHCID 67982691—

Reaction Steps

X-Phos (1.1 g, 2.2 mmol.), Pd2(dba)3 (1.0 g, 1.1 mmol) and cesium carbonate (14.5 g, 44 mmol) were added to a degassed solution of ethyl 4-chlorobenzofuran-2-carboxylate (Example 1b), 5.0 g, 22 mmol) and benzylpiperazine (5.8 ml, 33 mmol) in dioxane (100 mL). The reaction mixture was heated to +110° C. for 3 h, cooled to room temperature, filtered through a short pad of Celite and the filtrate was concentrated under reduced pressure. The crude residue was purified by silica gel column chromatography by using hexane/ethyl acetate (3/1) as eluant to give the title compound. Yield: 7.0 g (86%). 1H NMR (400 MHz, CDCl3) δ ppm 1.43 (t, 3H) 2.69 (m, 4H) 3.28 (m, 4H) 4.46 (q, 2H) 6.68 (d, 1H) 7.20-7.43 (m, 7H) 7.59 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012457B2
Source datasetuspto-grants-2015_04
ORD IDord-dacc73c9c5b74f2390d103ed9a1ee9ba
Source noteuspto-grants-2015_04