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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-bromo-1H-pyrrolo[2,3-b]pyridine | HCID 10307932 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-methoxy-1H-pyrrolo[2,3-b]pyridine | HCID 10307871 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722702B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b723d3e724e0431fac65976f94221972 |
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| Source note | uspto-grants-2014_05 |
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