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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749843Generated: November 2, 2026

Piperidine → HCID 86682014, compound

https://huagongshe.com/reaction/1749843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantHCID 71278683HCID 71278683—
SolventMethanolHCID 887—
ProductHCID 86682014HCID 8668201474.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl 4-[(6-ethoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.138 g, 0.367 mmol) in methanol (1.5 mL) was added with indole-3-carboxaldehyde (0.0553 g, 0.367 mmol) and piperidine (0.0250 g, 0.294 mmol), 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 tert-butyl (Z)-4-({2-[(1H-indol-3-yl)methylene]-6-ethoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate (0.137 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-1e6acccd3b0d432e858170dd3d1c1596
Source noteuspto-grants-2015_10