Abstract
By stepwise and regioselective installation of functional groups,
we have synthesized and characterized two pyridines, 3-fluoro-5-iodo-2-(methylthio)-6-(trimethylsilyl)isonicotinonitrile
and
3-fluoro-5-iodo-2-methoxy-6-(trimethylsilyl)isonicotinonitrile,
substituted with five different elements, not including hydrogen,
using known and newly developed methods. Novel methodology for dehalocyanation
of iodopyridines and rapid, high-yielding microwave-assisted acidic
hydrolysis of 2-fluoropyridines to their corresponding 2-pyridones
are disclosed.
Key words
pyridines - regioselectivity - lithiation - hydrolyses - nucleophilic aromatic substitutions
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