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Synthesis and characterization of the atropisomeric relationships of a substituted N-phenyl-bipyrazole derivative with anti-inflammatory properties
Authors:Veloso Marcia P  Romeiro Nelilma C  Silva Gilberto M S  Alves Hélio De M  Doriguetto Antonio C  Ellena Javier  Miranda Ana L P  Barreiro Eliezer J  Fraga Carlos A M
Affiliation:1. Laboratório de Avalia??o e Síntese de Substancias Bioativas (LASSBio), Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, , Rio de Janeiro, RJ, Brazil;2. Programa de Pós‐Gradua??o em Química, Instituto de Química, Universidade Federal do Rio de Janeiro, , RJ, Brazil;3. Faculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, , Alfenas, MG, Brazil;4. Universidade Federal do Rio de Janeiro, , Macaé, RJ, Brazil;5. Programa de Pós‐Gradua??o em Farmacologia e Química Medicinal, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, , RJ, Brazil;6. Instituto de Pesquisa Clínica Evandro Chagas, FIOCRUZ, , Rio de Janeiro, RJ, Brazil;7. Instituto de Ciências Exatas, Universidade Federal de Alfenas, , Alfenas, MG, Brazil;8. Instituto de Física de S?o Carlos, Universidade de S?o Paulo, , S?o Carlos, SP, Brazil;9. +55 21 25626503
Abstract:This work describes the atropisomeric relationships of 3-methyl-5-(3-methyl-5-phenyl-1H-pyrazol-1-yl)-1-phenyl-1H-pyrazol-4-amine (2d), which belongs to series 4-aminobipyrazole derivatives designed as anti-inflammatory agents. The (1)H nuclear magnetic resonance spectra obtained in the presence of a chiral lanthanide shift salt associated to chiral high-performance liquid chromatography analysis, X-ray diffraction, and molecular modeling tools confirmed that ortho bis-functionalized bipyrazole 2d exists as a mixture of aR,aS-atropisomers. These results provide useful information to understand the pharmacological profile of this derivative and of other 4-aminobipyrazole analogs.
Keywords:bipyrazole  atropisomerism  axial chirality  nonsteroidal anti‐inflammatory drugs  celecoxib  COX inhibitors
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