“…27 Therefore, we adapted the previously described procedure for the preparation of the sulfamide analog 12 (Scheme 1). Initially, for their preparation, we developed a synthesis scheme starting from onitrochlorobenzene (9). Sulfochlorination of 9, followed by treatment with ammonia, yielded 4-chloro-3nitrobenzenesulfonamide (10) in high yield (Scheme 1).…”