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The invention discloses a method for synthesizing amino – (N – alkyl) benzenesulfonamide method. Comprises the following steps: in the reaction container, adding amino sulfonamide, iridium complex catalyst, alkali, the compound is mellow, tertiary amyl alcohol solvent, the reaction mixture is 120 – 150o C lower reaction after several hours, cooling to room temperature, the solvent is removed by rotary evaporation, then through the column separation, to obtain the target compound. This invention uses the commercial amino sulfonamide and almost non-toxic compound alcohol starting material; only generates water as a by-product of the reaction, environmental hazard; reaction the atom economy is high. (by machine translation)

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion