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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749857Generated: November 2, 2026

Piperidine → HCID 178515791, compound

https://huagongshe.com/reaction/1749857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant6-hydroxy-7-(morpholinomethyl)benzofuran-3(2H)-oneHCID 71278937—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
ProductHCID 178515791HCID 17851579163.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 6-hydroxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.125 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, and then the precipitated solid was collected by filtration to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-6-hydroxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.119 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-80068b8df9994d63a5b35ec54a00df95
Source noteuspto-grants-2015_10