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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749924Generated: October 31, 2026

HCID 71278791, compound → HCID 178480827, compound

https://huagongshe.com/reaction/1749924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71278791HCID 71278791—
ReactantHCID 178520025HCID 178520025—
CatalystPiperidineHCID 8082—
SolventMethanolHCID 887—
ProductHCID 178480827HCID 17848082724%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 5-chloro-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.12 g, 0.43 mmol) in methanol (5.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.063 g, 0.43 mmol). Then, the mixture was added with 7 drops of piperidine, and then the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and then the residue was purified by silica gel column chromatography (eluted with chloroform/methanol (99:1→90:10)) to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-5-chloro-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.042 g, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-21878bc1840843d6837a75a780cb9c0a
Source noteuspto-grants-2015_10