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Synthesis 2011(10): 1638-1648  
DOI: 10.1055/s-0030-1260011
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© Georg Thieme Verlag Stuttgart ˙ New York

Comprehensive and Facile Entry into Substituted Amidines via the Condensation of N-Pmc-Substituted Thioamides with Amines Using Mukaiyama Reagent as a Thiophile

Stevenson Flemer, José S. Madalengoitia*
Department of Chemistry, 232 Cook Physical Sciences Building, University of Vermont, Burlington, VT 05405, USA
Fax: +1(802)6568705; e-Mail: jose.madalengoitia@uvm.edu;
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Publication History

Received 18 February 2011
Publication Date:
20 April 2011 (online)

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Abstract

A convenient approach is presented for the preparation of substituted amidines through the fusion of N-Pmc-substituted thioamides with amines, facilitated by a variety of thiophilic reagents. Assorted thiophiles were evaluated for their effectiveness as condensation reagents between the two partners, with the Mukaiyama reagent emerging as the optimal candidate for this process. The scope and limitations of this method were explored, revealing interesting synthetic challenges and constraints. Many of these limitations were overcome through the application of alternative reaction pathways in the construction of troublesome products. Treatment of the resultant Pmc-amidines with trifluoroacetic acid and trimethylsilyl trifluoromethanesulfonate cleanly afforded the deprotected substituted amidines.

Key words

amidine - thioamide - Mukaiyama reagent - thiophile - N-sulfonyl