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Microwave-assisted sequential one-pot protocol to benzothiadiazin-3-one-1,1-dioxides via a copper-catalyzed N-arylation strategy

Rolfe, Alan
Hanson, Paul R.
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Abstract
A microwave-assisted, sequential, one-pot protocol has been developed for the synthesis of a variety of benzothiadiazin-3-one-1,1-dioxides. This protocol utilizes a copper-catalyzed N-arylation of α-bromo-benzenesulfonamides with a number of amines to generate the corresponding 2-aminobenzenesulfonamides, which undergo cyclization to the desired sultams using carbonyl diimidazole (CDI). A range of conditions was evaluated for the key C–N bond formation step with tolerance toward functionalized amines.
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2009-12-16
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Elsevier
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Rolfe, Alan, and Paul R. Hanson. “Microwave-Assisted Sequential One-Pot Protocol to Benzothiadiazin-3-One-1,1-Dioxides via a Copper-Catalyzed N-Arylation Strategy.” Tetrahedron letters 50.50 (2009): 6935–6937.
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