HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606743Generated: October 26, 2026
2-(Tributylstannyl)pyrazine → 4-Methoxy-7-(pyrazin-2-YL)-1H-pyrrolo[2,3-C]pyridine
https://huagongshe.com/reaction/606743
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)pyrazine | HCID 2737316 | — |
| Reactant | 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine | HCID 20791244 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Methoxy-7-(pyrazin-2-YL)-1H-pyrrolo[2,3-C]pyridine | HCID 20791251 | 53% |
Reaction Steps
A mixture of 7-bromo-4-methoxy-6-azaindole (1.160 g, 5.11 mmol) and 2-(tri-n-butylstannyl)pyrazine (2.07 g, 5.62 mmol) in 25 mL of dry DMF was degassed with a stream of Ar bubbles for 10 min. To this solution was added tetrakis(triphenylphosphine)palladium (0.590 g, 0.511 mmol) and CuI (0.097 g, 0.511 mmol) and the mixture was heated in a sealed tube at 90° C. for 4 h. The cooled mixture was filtered through methanesulfonic acid SCX cartridges (7×3 g) with MeOH, to remove triphenylphosphine oxide. The filtrate was evaporated and the residue triturated with MeOH to give the title compound (0.612 g, 53%) as a light yellow solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915283B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-a07fc0e66b1347be8aafff7f8c297070 |
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| Source note | uspto-grants-2011_03 |
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