Abstract
Scalable Synthesis of C5aR1 Antagonist ACT-1014-6470 via <i>N</i><sup>7</sup>-Selective Reductive Amination of an Unprotected Pyrazole Starting Material and Intramolecular Urea Formation with 1,1′-Carbonyl-di(1,2,4-triazol) (CDT)
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