A General and Practical Synthesis of N‐Aryl‐3‐[4‐(imidazol‐4‐yl)‐1,2,3‐triazol‐1‐yl]benzamide Anti‐Inflammatory Cytokine Inhibitors

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Abstract
A practical, safe, and efficient synthesis of anti‐inflammatory cytokine inhibitors was developed and implemented for a number of analogues. A key aspect of the process is an efficient, one‐pot, tandem copper‐catalyzed azidonation and Huisgen 1,3‐dipolar cycloaddition using silyl protected alkynes.

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