HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101637Generated: October 30, 2026
Oxindole → N-[2-(Diethylamino)ethyl]-5-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
https://huagongshe.com/reaction/2101637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxindole | HCID 321710 | — |
| Reactant | N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamide | HCID 20761785 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[2-(Diethylamino)ethyl]-5-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide | HCID 72816604 | 55.5% |
Reaction Steps
A mixture of 1,3-dihydro-indol-2-one (266 mg, 2 mmol), 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylamino-ethyl)-amide (530 mg, 2 mmol) and piperidine (1 drop) in ethanol was heated at 90° C. for 2 hours. The reaction was cooled to room temperature, the resulting precipitate was collected by vacuum filtration, washed with ethanol and dried to give 422 mg (55%) of the title compound as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572924B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-95d306084e9341fd950fc67227a384e6 |
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| Source note | uspto-grants-2009_08 |
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