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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49066Generated: October 27, 2026

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

https://huagongshe.com/reaction/49066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantOxindoleHCID 321710—
Reactant5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehydeHCID 22042109—
SolventEthanolHCID 702—
Product3-[5-(2-Morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-oneHCID 6958694695%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-oxindole (29 mg, 0.22 mmol), 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde (60 mg, 0.22 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 81 mg (95%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706709B2
Source datasetuspto-grants-2004_03
ORD IDord-6034782cbd2e46a5b16cd29f8b2cc7f1
Source noteuspto-grants-2004_03