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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-Bromo-2-oxindole | HCID 611193 | — |
| Reactant | 5-(3-diethylamino-propyl)-1H-indole-2-carbaldehyde | HCID 22042114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-3-[5-(3-diethylamino-propyl)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-one | HCID 69586678 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071332B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-3f636c0e24cc43d8915a9f71c967d359 |
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| Source note | uspto-grants-2006_07 |
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