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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749794Generated: November 1, 2026

Piperidine → (Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one

https://huagongshe.com/reaction/1749794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantIndole-3-CarboxaldehydeHCID 10256—
Reactant6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-oneHCID 71278987—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product(Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-oneHCID 7127854710.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.079 g, 0.300 mmol) in methanol (1.2 mL) was added with 1H-indole-3-carboxaldehyde (0.0523 g, 0.300 mmol) and piperidine (0.00255 g, 0.0300 mmol), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (chloroform/methanol) to obtain an orange crude product as a solid. This solid was suspended in ethyl acetate and thereby washed to obtain the objective (Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.0128 g, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-fb352bceaaf24093a8c13178293993ec
Source noteuspto-grants-2015_10