HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749926Generated: October 31, 2026
Piperidine → (2Z)-6-hydroxy-2-(2H-indazol-3-ylmethylidene)-7-[(4-methylsulfonylpiperazin-1-yl)methyl]-1-benzofuran-3-one
https://huagongshe.com/reaction/1749926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 71278800 | HCID 71278800 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2Z)-6-hydroxy-2-(2H-indazol-3-ylmethylidene)-7-[(4-methylsulfonylpiperazin-1-yl)methyl]-1-benzofuran-3-one | HCID 178504957 | 53% |
Reaction Steps
A solution of 6-hydroxy-7-{[4-(methylsulfonyl)piperazin-1-yl]methyl}benzofuran-3(2H)-one (0.0681 g, 0.209 mmol) in methanol (0.8 mL) was added with 1H-indazole-3-carboxaldehyde (0.0305 g, 0.209 mmol) and piperidine (0.00178 g, 0.0209 mmol), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to room temperature, and then added with methanol (2 mL), and the precipitated solid was suspended in methanol and thereby washed to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-6-hydroxy-7-{[4-(methylsulfonyl)piperazin-1-yl]methyl}benzofuran-3(2H)-one (0.0503 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156827B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-55a8ebbf4853469ead8bd3f8b44e5609 |
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| Source note | uspto-grants-2015_10 |
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