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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750026Generated: November 2, 2026

Piperidine → HCID 178487052, compound

https://huagongshe.com/reaction/1750026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 71278717HCID 71278717—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
ProductHCID 178487052HCID 17848705261.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 7-[(3,5-dimethyl-1H-pyrazol-4-yl)methyl]-6-methoxybenzofuran-3(2H)-one (0.0427 g, 0.157 mmol) in methanol (0.6 mL) was added with 1H-indazole-3-carboxaldehyde (0.0229 g, 0.157 mmol) and piperidine (0.0107 g, 0.126 mmol), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to room temperature, and the precipitated solid was collected by filtration to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-7-[(3,5-dimethyl-1H-pyrazol-4-yl)methyl]-6-methoxybenzofuran-3(2H)-one (0.0388 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-f49031e182cb48e6b3dc654a1ba4ec6f
Source noteuspto-grants-2015_10