Journal of Combinatorial Chemistry · 2003 · 16 citations · 7 references
PharmacyChemistryMedicinal ChemistryDrug DesignDrug DiscoveryOrganic ChemistryChemical Library DesignCombinatorial SynthesisHeterocyclic ChemistryLead Compound DesignNatural Product Drug DiscoveryBioactive Compound LibrariesBiological Activity FeaturesChemical Synthesis Of AnaloguesDiversity-oriented Heterocycle SynthesisMedicinal Chemistry ApplicationsMedicinal HeterocyclesMild Reaction Conditions
The design and synthesis of a library of novel families of 3-oxopiperazinium and perhydro-3-oxo-1,4-diazepinium derivatives is reported. The library was composed of 44 3-oxopiperazinium derivatives (11 of these compounds had a spiranic skeleton) and 22 perhydro-3-oxo-1,4-diazepinium compounds. The synthetic procedure involved a 6-step sequence carried out in solution, along with the use of solid-phase linked scavengers and microwave activation for the rapid removal of the excess of amine reagents. A final cyclization step performed under mild conditions led to the charged heterocyclic moiety. Screening of this library in two biological assays identified active compounds that inhibit the activity of the vanilloid receptor TRPV1 and modulators of the multidrug resistance phenomenon. Thus, this synthetic sequence represents a facile and convenient entry to unprecedented libraries of this sort of tetraalkylammonium derivatives that may be of use for identification of novel scaffolds of diverse biological activity.
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