1. Pyrazole-3/5-carboxylic acids from 3/5-trifluoromethyl NH-pyrazoles
- Author
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Sandrine Guillou, Mikhail S. Ermolenko, Yves L. Janin, Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Chimie organique (CNR - UMR3523), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris], Region Ile de France I 06-222/R I 09-1739/R, Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Chimie organique (CNRS - UMR3523), and Institut Pasteur [Paris] (IP)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Trifluoromethyl ,010405 organic chemistry ,Negishi coupling ,[CHIM.ORGA]Chemical Sciences/Organic chemistry ,Organic Chemistry ,Pyrazole ,010402 general chemistry ,01 natural sciences ,Biochemistry ,0104 chemical sciences ,chemistry.chemical_compound ,Hydrolysis ,chemistry ,Drug Discovery ,Organic chemistry ,Derivative (chemistry) ,Building blocks 3/5-Trifluoromethylpyrazoles Pyrazole-3/5-carboxylic acids Cross-coupling Palladium catalysis - Abstract
International audience; We report here the transformation of 3/5-trifluoromethylpyrazoles derivative into the corresponding NH-pyrazole-3/5-carboxylic acids. Moreover, from 4- or 5-iodinated-3/5-trifluoromethylpyrazoles building blocks and the use of SuzukieMiyaura or Negishi reactions followed by the trifluoromethyl hydrolysis, we illustrate short and original accesses to many series of NH-pyrazole-3/5-carboxylic acids otherwise difficult to prepare.
- Published
- 2013
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