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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987542Generated: October 30, 2026

Hydrazine → 4-Methoxy-1H-pyrrolo(2,3-c)pyridine

https://huagongshe.com/reaction/987542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant5,7-Dibromo-4-methoxy-6-azaindoleHCID 22476267—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Methoxy-1H-pyrrolo(2,3-c)pyridineHCID 2247623788%

Reaction Steps

A solution of 5,7-Dibromo-4-methoxy-6-azaindole 36 (680 mg, 2.22 mmol), 5% Pd/C (350 mg, 0.17 mmol) and hydrazine (2.5 mL, 80 mmol) in EtOH was heated at reflux for 1 h. The reaction mixture was allowed to cool to rt, filtered through celite and the filtrate concentrated. Aqueous NH4OH (11% in H2O, 45 mL) was added to the residue and the solution was extracted with CH2Cl2 (3×30 mL). The combined organics were dried (MgSO4), filtered and concentrated to yield 4-methoxy-6-azaindole 37 (290 mg, 1.95 mmol, 88%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632819B1
Source datasetuspto-grants-2003_10
ORD IDord-936d3f1a1f804cb3b7a652cf16e150df
Source noteuspto-grants-2003_10