HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 54168434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridine-3-carbaldehyde | HCID 5372812 | — |
| Reactant | 2-Oxoindoline-5-sulfonamide | HCID 10198232 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54168434 | HCID 54168434 | 70% |
Reaction Steps
A solution of 3-formyl-7-azaindole (1.46 g, 10 mmol), 5-sulfamoyl-2-oxindole (2,122 g, 10 mmol) and piperidine (0,255 g, 3 mmol) in absolute ethanol (50 ml) was treated for 3 h at reflux. The reaction mixture was chilled to room temperature, the precipitate filtered, the residue washed with ice-cold ethanol and dried under vacuum. Almost pure title compound was so obtained in about 70% yield. Compounds of higher purity were obtained by crystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663346 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-994831b2ad6542b4870c9feec76c9c99 |
| Source note | uspto-grants-1997_09 |