HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49067Generated: October 27, 2026
Piperidine → 5-Bromo-3-[5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/49067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-Bromo-2-oxindole | HCID 611193 | — |
| Reactant | 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde | HCID 22042109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-3-[5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-1,3-dihydro-indol-2-one | HCID 69586546 | 64% |
Reaction Steps
A mixture of 5-bromo-2-oxindole (46 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 65 mg (64%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706709B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-711fa2fb9e39407f9567267629567b3b |
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| Source note | uspto-grants-2004_03 |
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