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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394425Generated: November 2, 2026

2-(Tributylstannyl)pyrazine → 4-Methoxy-7-(pyrazin-2-YL)-1H-pyrrolo[2,3-C]pyridine

https://huagongshe.com/reaction/1394425

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)pyrazineHCID 2737316—
Reactant7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 20791244—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4-Methoxy-7-(pyrazin-2-YL)-1H-pyrrolo[2,3-C]pyridineHCID 2079125153%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348337B2
Source datasetuspto-grants-2008_03
ORD IDord-29ab7054e99b4fecad6a446e7a44cdff
Source noteuspto-grants-2008_03