HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826786Generated: October 31, 2026
Piperidine → 3-[3,5-Dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-pyridin-2-yl-1,3-dihydroindol-2-one
https://huagongshe.com/reaction/1826786
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde | HCID 12111582 | — |
| Reactant | 4-Pyridin-2-yl-1,3-dihydroindol-2-one | HCID 22135431 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[3,5-Dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-pyridin-2-yl-1,3-dihydroindol-2-one | HCID 24942411 | — |
Reaction Steps
A mixture of 4-pyridin-2-yl-1,3-dihydroindol-2-one (31.5 mg, 0.15 mmol), 3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde (37.4 mg, 0.15 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated in a sealed tube at 70° C. for 6 hours. The reaction was concentrated and the residue was re-crystallized from ethyl acetate and hexane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053086B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-c9690b2e1c7e4317b388ac33e15ab61a |
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| Source note | uspto-grants-2006_05 |
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