HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790932Generated: November 2, 2026
Hydrochloric Acid → 2-Oxo-3-[5-(3-pyrrolidin-1-yl-propyl)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-carboxylic acid
https://huagongshe.com/reaction/1790932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Oxindole-5-carboxylic acid | HCID 2773318 | — |
| Reactant | 5-(3-diethylamino-propyl)-1H-indole-2-carbaldehyde | HCID 22042114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Oxo-3-[5-(3-pyrrolidin-1-yl-propyl)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-carboxylic acid | HCID 69586864 | — |
Reaction Steps
A mixture of 5-carboxy-2-oxindole (35 mg, 0.2 mmol), 5-(3-diethylamino-propyl)-1H-indole-2-carbaldehyde (51 mg, 0.2 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 80° C. for 6 hours. The reaction was acidified with 1 N HCl and the precipitate was collected by vacuum filtration, washed with 1 N HCl, water and ethanol, dried to give the title compound.
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-0f579a24fb5e4ee5a5f70e5cfc3fa5ac |
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| Source note | uspto-grants-2006_07 |
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