Synthesis of Enantiomerically Pure 3‑Substituted Piperazine-2-acetic Acid Esters as Intermediates for Library Production
journal contributionposted on 05.09.2018, 00:00 by Shiva Krishna Reddy Guduru, Srinivas Chamakuri, Idris O. Raji, Kevin R. MacKenzie, Conrad Santini, Damian W. Young
The piperazine heterocycle is broadly exploited in FDA-approved drugs and biologically active compounds, but its chemical diversity is usually limited to ring nitrogen substitutions, leaving the four carbon atoms underutilized. Using an efficient six-step synthesis, chiral amino acids were transformed into 3-substituted piperazine-2-acetic acid esters as diastereomeric mixtures whose cis and trans products (dr 0.56 → 2.2:1, respectively) could be chromatographically separated. From five amino acids (both antipodes) was obtained a complete matrix of 20 monoprotected chiral 2,3-disubstituted piperazines, each as a single absolute stereoisomer, all but one in multigram quantities. In keeping with our overall purpose of constructing more Csp3-enriched compound libraries for drug discovery, these diverse and versatile piperazines can be functionalized on either nitrogen atom, allowing them to be used as scaffolds for parallel library synthesis and as intermediates for the production of novel piperazine compounds.
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diastereomeric mixturesnovel piperazine compoundstrans productsmultigram quantitiespiperazine -2-acetic acid esterspiperazine heterocycledrug discoverynitrogen atomFDA-approved drugsCsp 3library synthesiscarbon atomssix-step synthesischiralchemical diversitycompound librariesLibrary Productionring nitrogen substitutions