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Synthesis 2010(1): 63-66
DOI: 10.1055/s-0029-1217084
DOI: 10.1055/s-0029-1217084
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Pyridines Substituted with Five Different Elements
Further Information
Publication History
Received
22 June 2009
Publication Date:
22 October 2009 (online)


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