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Synthesis of functionalized 4-fluoropyridazines

Asian J. Org. Chem. 2017, in press

DOI: 10.1002/ajoc.201700216

Feraldi-Xypolia A.; Fredj G.; Tran G.; Tsuchiya T.; Vors J.-P.; Mykhailiuk P.; Gomez Pardo D.; Cossy J.

A route to novel 4-fluoropyridazines by a [2+1]/[3+2]-cycloaddition sequence between acetylenic derivatives, a difluorocarbene source and diazo compounds is reported. This sequence features high modularity, broad functional group compatibility, and does not require the isolation of any reactive intermediates, thus allowing access to a wide range of 4-fluoropyridazines in a single synthetic step from simple alkynes. Furthermore, these fluorinated compounds can be easily diversified by an aromatic nucleophilic substitution (SNAr) of the fluorine atom, to give a wider range of 3,4,6-trisubstituted pyridazines. Given the increasing interest in functionalized pyridazines as well as fluorinated derivatives, this efficient and concise approach to 4-fluoropyridazines, should be of interest for medicinal chemists.

Synthesis of functionalized 4-fluoropyridazines

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