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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402627Generated: November 2, 2026

1H-Pyrrolo[2,3-b]pyridine-3-carbaldehyde → HCID 178469790, compound

https://huagongshe.com/reaction/402627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
ReactantHCID 86708320HCID 86708320—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178469790HCID 178469790—

Reaction Steps

To a solution of ethyl 2-[(2-methoxyethyl)amino]-4-oxo-4,5-dihydrofuran-3-carboxylate (0.50 g, 2.2 mmol) which similarly prepared according to the procedure described in the Example 4, First step and 7-azaindole-3-carboxaldehyde (0.32 g, 2.2 mmol) in ethanol (3.0 mL), piperidine (5 drops) was added at ambient temperature. The mixture was refluxed for 16 h. Cooled to ambient temperature, the precipitate was collected by filtration, washed with ethanol then dried to afford the titled compound as solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-24bac71b87c54a259e0d76c5694b0e92
Source noteuspto-grants-2014_06