Efficient microwave combinatorial synthesis of novel indolic arylpiperazine derivatives as serotoninergic ligands

Eur J Med Chem. 2010 Feb;45(2):752-9. doi: 10.1016/j.ejmech.2009.11.023. Epub 2009 Dec 1.

Abstract

An easy and convenient microwave-assisted synthesis of a small library of indolic arylpiperazine derivatives is described. Parallel and mixed pool combinatorial methods are reported and compared. The described reactions are nucleophilic substitutions of several aromatic piperazines in presence of K(2)CO(3). Good yields and short reaction times are the main aspect of these procedures. Binding assays shed additional light on the influence of the LCAPs on the 5-HT(1A), 5-HT(2A) and 5-HT(2C) receptors affinity and allowed to disclose three interesting compounds as 5-HT(2C), mixed 5-HT(2A)/5-HT(2C) and 5-HT(1A)/5-HT(2C) ligands (4i, 4l and 4d, respectively), with potential antiepileptic, anxiolytic or atypical antipsychotic agent therapeutical profiles.

MeSH terms

  • Animals
  • Combinatorial Chemistry Techniques*
  • Drug Evaluation, Preclinical
  • Indoles / chemistry*
  • Ligands
  • Male
  • Microwaves*
  • Piperazine
  • Piperazines / chemistry*
  • Piperazines / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Serotonin / metabolism
  • Serotonin / metabolism*

Substances

  • Indoles
  • Ligands
  • Piperazines
  • Receptors, Serotonin
  • Piperazine
  • Serotonin
  • indole