4.7 Article

Design, synthesis and dopamine D4 receptor binding activities of new N-heteroaromatic 5/6-ring Mannich bases

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 17, Issue 13, Pages 4448-4458

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2009.05.015

Keywords

Mannich bases; Dopamine; Heterocyclic compounds; D4 receptor

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A series of phenylpiperazine-methyl-substituted 1H-pyrrolo[2,3-c] pyridine, imidazo[1,2-c]-, pyrrolo[2,3-d]- and pyrrolo[3,2-d] pyrimidines were prepared as selective dopamine D4-ligands. The pyrrolo[2,3-d] pyrimidine derivatives 12d (K-i = 1,9 nM) and 34d (K-i = 2,4 nM) as well as the pyrrolo[3,2-d] pyrimidine Mannich base 49f (K-i = 2,8 nM) showed high dopamine D4 receptor activity superior to the atypical antipsychotic agent clozapine. (C) 2009 Elsevier Ltd. All rights reserved.

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