Introduction:
Pyrazine derivatives are widely recognized as important building blocks in heterocyclic and medicinal chemistry, with numerous applications in pharmaceuticals, agrochemicals, and advanced materials. Among them, 2-chloropyrazine is a synthetically versatile substrate due to the electron-withdrawing chlorine substituent, which directs lithiation to the 3-position. Although selective monolithiation at this site is well documented, achieving multiple metalations on the pyrazine ring has remained a significant synthetic challenge because of its electron-deficient nature and the instability of potential poly-lithiated intermediates.

Methods:
In this study, we developed a new strategy for the regioselective 3,6-dilithiation of 2-chloropyrazine by employing lithium 2,2,6,6-tetramethylpiperidide (LiTMP) as a strong, hindered base. Careful control of stoichiometry and reaction temperature was essential to generate the dilithiated intermediate efficiently, which was then trapped in situ with ethyl benzoate to introduce carbonyl functionality.

Results:
Under optimized conditions, the reaction provided the novel symmetrical 3,6-dicarbonyl derivative in good isolated yield. The structure was confirmed by a subsequent Sonogashira coupling with 1-hexyne, followed by detailed ¹H and ¹³C NMR spectroscopy, which unambiguously established substitution at both the 3- and 6-positions of the pyrazine core.

Conclusions:
These findings demonstrate for the first time that regioselective 3,6-dilithiation of 2-chloropyrazine is feasible under mild, practical conditions. This approach provides a straightforward and scalable route to novel polyfunctionalized pyrazine frameworks, expanding the scope of directed ortho-lithiation strategies for nitrogen-containing heterocycles with promising potential in synthetic and medicinal chemistry.