A tandem strategy for the synthesis of 2‐aminobenzothiazoles from 2‐bromophenylisothiocyanate and amines is reported. The reaction occurred efficiently in presence of Ni(acac)2 as the catalyst precursor and ethanol as the solvent. A wide range of aliphatic amines including linear, branched, and cyclic primary and secondary amines proved potential substrates to construct diverse 2‐aminobenzothiazole derivatives in good yields. The reaction is thought to proceed via the formation of a thiourea intermediate and a sequential nickel‐catalyzed C−S bond formation.