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  4. Recommendable routes to trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids
 
research article

Recommendable routes to trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids

Cottet, Fabrice  
•
Marull, Marc  
•
Lefebvre, Olivier
Show more
2003
European Journal of Organic Chemistry

As part of a case study, rational strategies for the prepn. of all ten 2-, 3-, or 4-pyridinecarboxylic acids and all nine 2-, 3-, 4-, or 8-quinolinecarboxylic acids bearing trifluoromethyl substituents at the 2-, 3-, or 4-position were elaborated. The trifluoromethyl group, if not already present in the precursor, was introduced either by the deoxygenative fluorination of suitable carboxylic acids with sulfur tetrafluoride or by the displacement of ring-bound bromine or iodine by trifluoromethylcopper generated in situ. The carboxy function was produced by treatment of organolithium or organomagnesium intermediates, products of halogen/metal or hydrogen/metal permutation, with carbon dioxide. [on SciFinder (R)]

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Type
research article
DOI
10.1002/ejoc.200390215
Web of Science ID

WOS:000182357500023

Author(s)
Cottet, Fabrice  
•
Marull, Marc  
•
Lefebvre, Olivier
•
Schlosser, Manfred  
Date Issued

2003

Published in
European Journal of Organic Chemistry
Issue

8

Start page

1559

End page

1568

Subjects

trifluoromethyl pyridinecarboxylic acid quinolinecarboxylic acid prepn

Note

CAN 139:214305 27-17 Heterocyclic Compounds (One Hetero Atom) Institut de Chimie moleculaire et Biologique,Ecole Polytechnique Federale,Lausanne,Switz. Journal 1434-193X written in English. 102-92-1 (Cinnamoyl chloride); 368-48-9 (2-Trifluoromethylpyridine); 615-36-1 (2-Bromoaniline); 624-28-2 (2,5-Dibromopyridine); 18706-25-7; 52334-81-3; 65753-47-1; 77332-76-4; 81290-20-2 ((Trifluoromethyl)trimethylsilane); 81565-18-6; 128676-85-7 (2-Chloro-3-iodoquinoline); 189278-27-1; 587885-93-6; 587886-11-1; 590371-90-7; 590372-06-8; 590372-17-1; 590372-20-6 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids); 13534-89-9P (2,3-Dibromopyridine); 25199-86-4P; 30766-11-1P; 50488-42-1P; 52200-48-3P; 67805-67-8P; 71910-51-5P; 100366-75-4P; 163485-86-7P; 175205-81-9P; 175205-82-0P; 176722-63-7P; 223463-13-6P (5-Bromo-2-iodopyridine); 408502-43-2P; 436799-32-5P; 505084-55-9P; 505084-56-0P; 505084-58-2P; 505084-59-3P; 590371-58-7P; 590371-71-4P; 590371-73-6P; 590371-81-6P; 590371-88-3P; 590371-93-0P; 590371-95-2P; 590371-97-4P; 590372-03-5P; 590372-08-0P; 590372-14-8P; 590372-23-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids); 18706-39-3P; 80194-69-0P; 87407-12-3P; 131747-40-5P; 131747-41-6P; 131747-42-7P; 131747-43-8P; 155495-82-2P; 158063-66-2P; 231291-22-8P; 587886-26-8P; 588702-62-9P; 588702-63-0P; 588702-64-1P; 588702-65-2P; 588702-66-3P; 588702-67-4P; 590371-38-3P; 590371-53-2P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids)

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REVIEWED

Written at

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EPFL units
LSCO  
Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/227007
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