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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790912Generated: November 3, 2026

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

https://huagongshe.com/reaction/1790912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-Bromo-2-oxindoleHCID 611193—
Reactant5-(3-diethylamino-propyl)-1H-indole-2-carbaldehydeHCID 22042114—
SolventEthanolHCID 702—
Product5-Bromo-3-[5-(3-diethylamino-propyl)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-oneHCID 6958667860.5%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 5-bromo-2-oxindole (41 mg, 0.19 mmol), 5-(3-diethylamino-propyl)-1H-indole-2-carbaldehyde (50 mg, 0.19 mmol) and piperidine(0.1 mL) in ethanol (1 mL) was heated in a sealed tube at 95° C. for 20 hours. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give 52 mg (59%) of the title compound as a red-orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071332B2
Source datasetuspto-grants-2006_07
ORD IDord-3f636c0e24cc43d8915a9f71c967d359
Source noteuspto-grants-2006_07