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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 71278800HCID 71278800—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
Product(2Z)-6-hydroxy-2-(2H-indazol-3-ylmethylidene)-7-[(4-methylsulfonylpiperazin-1-yl)methyl]-1-benzofuran-3-oneHCID 17850495753%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-55a8ebbf4853469ead8bd3f8b44e5609
Source noteuspto-grants-2015_10