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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367317Generated: November 2, 2026

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

https://huagongshe.com/reaction/1367317

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 numberUS07893075B2
Source datasetuspto-grants-2011_02
ORD IDord-f74179a67739439fac36211ca4662459
Source noteuspto-grants-2011_02