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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(5-(2-Bromoethyl)indolin-1-yl)ethanone | HCID 51713236 | — |
| Reactant | Azetidin-1-yl(7-(piperazin-1-yl)benzofuran-2-yl)methanone | HCID 59636763 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(5-(2-(4-(2-(Azetidine-1-carbonyl)benzofuran-7-yl)piperazin-1-yl)ethyl)indolin-1-yl)ethanone | HCID 59636721 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367676B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d54033741b7a45acbf37b5802ee1ee1f |
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| Source note | uspto-grants-2013_02 |
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