We describe an efficient method for the direct preparation of -substituted aryl amidines from nitriles and primary amines. The protocol employs activation of amines by a strong base and provides greater access to a pharmaceutically relevant functional group. This synthetic approach tolerates deactivated nitriles, nitriles with competing substitution sites, and aryl amines.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470429 | PMC |
http://dx.doi.org/10.1016/j.tetlet.2015.05.029 | DOI Listing |
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