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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383842Generated: October 25, 2026

Potassium Carbonate → 1-(5-(2-(4-(2-(Azetidine-1-carbonyl)benzofuran-7-yl)piperazin-1-yl)ethyl)indolin-1-yl)ethanone

https://huagongshe.com/reaction/383842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(5-(2-Bromoethyl)indolin-1-yl)ethanoneHCID 51713236—
ReactantAzetidin-1-yl(7-(piperazin-1-yl)benzofuran-2-yl)methanoneHCID 59636763—
SolventAcetonitrileHCID 6342—
Product1-(5-(2-(4-(2-(Azetidine-1-carbonyl)benzofuran-7-yl)piperazin-1-yl)ethyl)indolin-1-yl)ethanoneHCID 59636721—

Reaction Conditions

Temperature120 °C

Reaction Steps

The reaction mixture of azetidin-1-yl(7-(piperazin-1-yl)benzofuran-2-yl)methanone (0.070 g, 0.25 mmol) (Example 45c), 1-(5-(2-bromoethyl)indolin-1-yl)ethanone (0.099 g, 0.37 mmol) and potassium carbonate (0.068 g, 0.49 mmol) in acetonitrile (1 mL) was heated by microwave irradiation at 120° C. for 15 min. The mixture was cooled and the solvent was removed in vacuo. The product was purified by flash chromatography (SiO2; DCM/MeOH; gradient 0-5%) to give the title compound. Yield: 0.056 g (48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367676B2
Source datasetuspto-grants-2013_02
ORD IDord-d54033741b7a45acbf37b5802ee1ee1f
Source noteuspto-grants-2013_02