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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49068Generated: October 26, 2026

Piperidine → 3-[5-(2-Morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-6-phenyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/49068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant6-Phenyl-1,3-dihydro-indol-2-oneHCID 10536384—
Reactant5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehydeHCID 22042109—
SolventEthanolHCID 702—
Product3-[5-(2-Morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-6-phenyl-1,3-dihydro-indol-2-oneHCID 6958699871.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-phenyl-2-oxindole (44 mg, 0.21 mmol), 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde (58 mg, 0.21 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 100° C. for 2 hours. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give 70 mg (71%) of the title compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706709B2
Source datasetuspto-grants-2004_03
ORD IDord-96b2f85123af4623a8d7be6ca8d1fb88
Source noteuspto-grants-2004_03