Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024203Generated: October 29, 2026

5-bromo-1H-pyrrolo[2,3-b]pyridine → 5-methoxy-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1024203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
ReactantSodium MethoxideHCID 10942334—
Catalystcopper(I) bromideHCID 24593—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 1030787154%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 5-bromo-7-azaindole (1 g, 0.005 mol) in N,N-Dimethylformamide (20 mL) and methanol (20 mL) were added sodium methoxide (13 g, 0.24 mol) and Copper (I) bromide (0.7 g, 0.0048 mol) at room temperature. The reaction mixture was stirred at 120° C. under nitrogen for 3 hours. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate and water. The organic layer was collected, washed with a solution of ammonium chloride and ammonium hydroxide (4:1), brine, and dried over magnesium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with ethyl acetate in hexane to provide the compound as a white solid (81, 0.4 g, 50%). MS (ESI) [M+H+]+=149.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722702B2
Source datasetuspto-grants-2014_05
ORD IDord-b723d3e724e0431fac65976f94221972
Source noteuspto-grants-2014_05