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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402646Generated: October 30, 2026

1H-Pyrrolo[2,3-b]pyridine-3-carbaldehyde → HCID 178469527, compound

https://huagongshe.com/reaction/402646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
ReactantHCID 86708338HCID 86708338—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178469527HCID 17846952743.2%

Reaction Steps

To a solution of ethyl 2-{[2-(2-methoxyethoxy)-4-methylphenyl]amino}-4-oxo-4,5-dihydrofuran-3-carboxylate (0.015 g, 0.045 mmol) which similarly prepared according to the procedure described in the Example 29, First step and 7-azaindole-3-carboxaldehyde (0.0067 g, 0.046 mmol) in ethanol (0.2 mL), 2M hydrochloric acid in ethanol (0.023 mL, 0.045 mmol) was added at ambient temperature. The mixture was refluxed for 4 h. Cooled to ambient temperature, the solvent was removed under reduced pressure. The residue was purified by preparative HPLC to afford the titled compound as solid (0.0090 g, y. 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-c27bafa3d3b54841926c7dd13453a962
Source noteuspto-grants-2014_06