HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383835Generated: October 25, 2026
Potassium Carbonate → 7-(4-(2-(6-Methoxypyridin-2-yl)ethyl)piperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamide
https://huagongshe.com/reaction/383835
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N,N-dimethyl-7-(piperazin-1-yl)benzofuran-2-carboxamide | HCID 59636743 | — |
| Reactant | 2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate | HCID 59636776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(4-(2-(6-Methoxypyridin-2-yl)ethyl)piperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamide | HCID 59636781 | — |
Reaction Steps
A reaction mixture of N,N-dimethyl-7-(piperazin-1-yl)benzofuran-2-carboxamide (0.090 g, 0.33 mmol) (Example 39d), 2-(6-methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate (0.10 g, 0.33 mmol) and potassium carbonate (0.046 g, 0.33 mmol) in dry acetonitrile (10 mL) was heated at 80° C. for over night. After cooling, the mixture was filtered and the solvent removed in vacuo. The product was purified by preparative HPLC to give the title compound. Yield: 0.048 g (36%).
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-2d069d98923d4027ae5fde24d9917ef9 |
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| Source note | uspto-grants-2013_02 |
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