N, N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. V* The Preparation of some Benzimidazo-Fused [1,2,4,6]Thiatriazine Dioxides
Teresa Cablewski A , Craig L. Francis A B and Andris J. Liepa AA CSIRO Molecular and Health Technologies, Clayton VIC 3168, Australia.
B Corresponding author. Email: craig.francis@csiro.au
Australian Journal of Chemistry 61(1) 59-65 https://doi.org/10.1071/CH07336
Submitted: 21 September 2007 Accepted: 15 November 2007 Published: 18 January 2008
Abstract
N,N-dialkyl-N′-chlorosulfonyl chloroformamidines 1 were treated with 2-aminobenzimidazoles 2 to give [1,2,4,6]thiatriazino[2,3-a]benzimidazole 1,1-dioxides 3 and [1,2,4,6]thiatriazino[4,3-a]benzimidazole 2,2-dioxides 4. Some N-alkyl-, N-acyl-, and N-sulfonyl-derivatives of 3 were prepared. These products are derivatives of rare heterocycles.
Acknowledgements
We thank Roger Mulder and Jo Cosgriff for assistance with NMR spectroscopy, Carl Braybrook for assistance with mass spectrometry, and Gary Fallon, Paul Jensen, and Craig Forsyth (Monash University) for X-ray crystallography.
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