1-Cyclohexenylboronic acid → 4-amino-N-tert-butyl-3-cyclohex-1-enyl-benzenesulfonamide

Beteiligte Stoffe

Reaktionsschritte

4-Amino-N-tert-butyl-3-cyclohex-1-enyl-benzenesulfonamide was prepared according to the Suzuki coupling procedure of Example 44, step (b) using cyclohex-1-enyl boronic acid (63 mg, 0.50 mmol) and 4-amino-3-bromo-N-tert-butyl-benzenesulfonamide (123 mg, 0.400 mmol, as prepared above) to obtain 4-amino-N-tert-butyl-3-cyclohex-1-enyl-benzenesulfonamide (87 mg, 70%) after purification on silica (30% EtOAc/hexanes). Mass spectrum (ESI, m/z): Calcd. for C16H24N2O2S, 309.1 (M+H), found 309.1

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