Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity

Our thesis works concern the development of new methods of synthesis allowing a rapid and effective access to variously functionalized pyrazolo [1,5-a] pyrimidines derivatives.First, we were explored the study and the application of the condensation of the pyran-2 one with 5(3)-amino-3 (5)-arylpyrazoles whether it is by classic heating or under microwaves. Indeed, we have described the first example of the direct and regioselective palladium-catalyzed (hetero)arylation of 5,7-dimethylpyrazolo[1,5-a]pyrimidine, the reaction may be inducted to occur at either an sp2 or an sp3 carbon atom.The last part of this report was dedicated to the preparation of some 7-substituted pyrazolo[1,5-a]pyrimidines via a one-pot two steps palladium-catalyzed direct CH-arylation followed by a saponification-decarboxylation.

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Source https://theses.hal.science/tel-00789954
Author Bassoude, Ibtissam
Maintainer CCSD
Last Updated May 14, 2026, 09:46 (UTC)
Created May 14, 2026, 09:46 (UTC)
Identifier NNT: 2012ORLE2025
Language fr
Rights https://about.hal.science/hal-authorisation-v1/
contributor Institut de Chimie Organique et Analytique (ICOA) ; Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université d'Orléans (UO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
creator Bassoude, Ibtissam
date 2012-07-09T00:00:00
harvest_object_id aedae09a-0d2d-43b3-8f51-8253b53d91d8
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2026-03-30T00:00:00
set_spec type:THESE