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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749855Generated: November 2, 2026

Piperidine → HCID 178480846, compound

https://huagongshe.com/reaction/1749855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 71278947HCID 71278947—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
ProductHCID 178480846HCID 17848084637.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 6-hydroxy-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.131 g, 0.500 mmol) in methanol (2 mL) was added with 1H-indazole-3-carbaldehyde (0.0731 g, 0.500 mmol), and piperidine (0.00426 g, 0.0500 mmol) at room temperature, and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to room temperature, then added with methanol (2 mL), and suspended in methanol and thereby washed to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-6-hydroxy-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.0731 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-7b5720abf5634dffafa2dc52c4788d1a
Source noteuspto-grants-2015_10