Importance of a Fluorine Substituent for the Preparation of meta‐ and para‐Pentafluoro‐λ6‐sulfanyl‐Substituted Pyridines |
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| Authors: | Dr. Mikhail Kosobokov Benqiang Cui Dr. Andrii Balia Kohei Matsuzaki Etsuko Tokunaga Norimichi Saito Prof. Dr. Norio Shibata |
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| Affiliation: | 1. Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya, Japan;2. Pharmaceutical Division, Ube Industries, Ltd., Minato-ku, Tokyo, Japan |
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| Abstract: | Although there are ways to synthesize ortho‐pentafluoro‐λ6‐sulfanyl (SF5) pyridines, meta‐ and para‐SF5‐substituted pyridines are rare. We disclose herein a general route for their synthesis. The fundamental synthetic approach is the same as reported methods for ortho‐SF5‐substituted pyridines and SF5‐substituted arenes, that is, oxidative chlorotetrafluorination of the corresponding disulfides to give pyridylsulfur chlorotetrafluorides (SF4Cl‐pyridines), followed by chloride/fluoride exchange with fluorides. However, the trick in this case is the presence on the pyridine ring of at least one fluorine atom, which is essential for the successful transformation of the disulfides into m‐and p‐SF5‐pyridines. After enabling the synthesis of an SF5‐substituted pyridine, ortho‐F groups can be efficiently substituted by C, N, S, and O nucleophiles through an SNAr pathway. This methodology provides access to a variety of previously unavailable SF5‐substituted pyridine building blocks. |
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| Keywords: | chlorination fluorination fluorine nitrogen heterocycles pentafluorosulfanyl substitution |
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