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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376788Generated: November 1, 2026

Piperidine → HCID 54168434, compound

https://huagongshe.com/reaction/1376788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
Reactant2-Oxoindoline-5-sulfonamideHCID 10198232—
SolventEthanolHCID 702—
ProductHCID 54168434HCID 5416843470%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663346
Source datasetuspto-grants-1997_09
ORD IDord-994831b2ad6542b4870c9feec76c9c99
Source noteuspto-grants-1997_09