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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790921Generated: October 31, 2026

Piperidine → 5-Bromo-3-[5-(2-dimethylamino-ethoxy)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1790921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-Bromo-2-oxindoleHCID 611193—
Reactant5-(2-dimethylamino-ethoxy)-1H-indole-2-carbaldehydeHCID 22042141—
SolventEthanolHCID 702—
Product5-Bromo-3-[5-(2-dimethylamino-ethoxy)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-oneHCID 6958679280.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-2-oxindole (46 mg, 0.215 mmol), 5-(2-dimethylamino-ethoxy)-1H-indole-2-carbaldehyde (50 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 72 mg (78%) of the title compound as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071332B2
Source datasetuspto-grants-2006_07
ORD IDord-3515eaf7aaae4663a11dd8cca09db1cc
Source noteuspto-grants-2006_07