HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988204Generated: October 27, 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/988204
Participants
| Role | Name | HCID | Charge |
|---|
| 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 |
|---|
| Patent number | US06635640B2 |
|---|
| Source dataset | uspto-grants-2003_10 |
|---|
| ORD ID | ord-5b1eb36fdcc9425986b040cfbde5138e |
|---|
| Source note | uspto-grants-2003_10 |
|---|