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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272368Generated: November 2, 2026

Triethylamine → Ethyl 6-((3-bromophenyl)amino)-5-cyclopropyl-2-(4-fluorophenyl)benzofuran-3-carboxylate

https://huagongshe.com/reaction/2272368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3-Bromophenyl)boronic acidHCID 2734318—
ReactantEthyl 6-amino-5-cyclopropyl-2-(4-fluorophenyl)benzofuran-3-carboxylateHCID 67353798—
CatalystCupric acetateHCID 8895—
SolventEthyl AcetateHCID 8857—
ProductEthyl 6-((3-bromophenyl)amino)-5-cyclopropyl-2-(4-fluorophenyl)benzofuran-3-carboxylateHCID 7125835951%

Reaction Steps

A mixture of ethyl 6-amino-5-cyclopropyl-2-(4-fluorophenyl)benzofuran-3-carboxylate (1.00 g, 2.95 mmol), (3-bromophenyl)boronic acid (1.184 g, 5.89 mmol), copper(II) acetate (0.803 g, 4.42 mmol), triethylamine (1.232 mL, 8.84 mmol) and 4 A molecular sieves (2 g) was stirred at room temperature for 24 hours. The reaction mixture was diluted with EtOAc and filtered through Celite. The solvent was evaporated and the residue was purified by chromatography on silica gel (hexane:EtOAc) to give ethyl 6-((3-bromophenyl)amino)-5-cyclopropyl-2-(4-fluorophenyl)benzofuran-3-carboxylate (740 mg, 51%). LCMS (m/z, ES+)=494, 496 (M+H, M+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119868B2
Source datasetuspto-grants-2015_09
ORD IDord-7e9bf8f60e84413a8445b41a1bf6dc39
Source noteuspto-grants-2015_09