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MAOS ls for the general synthesis and lead optimization of 3,6-disubstituted-[1,2,4]triazolo[4,3-b]pyridazines
Authors:Aldrich Leslie N  Lebois Evan P  Lewis L Michelle  Nalywajko Natalia T  Niswender Colleen M  Weaver C David  Conn P Jeffrey  Lindsley Craig W
Institution:Department of Chemistry, Vanderbilt University and Medical Center, Nashville, TN 37232, USA.
Abstract:General, high-yielding MAOS protocols for the expedient synthesis of functionalized 3,6-disubstituted-1,2,4]triazolo4,3-b]pyridazines are described amenable to an iterative analog library synthesis strategy for the lead optimization of an M1 antagonist screening hit. Optimized compounds proved to be highly selective M1 antagonists.
Keywords:
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