A new dendritic oligoarylamine, N,N,N',N',N",N"-hexakis[4-(di-4-anisylamino)phenyl]-1,3,5-benzenetriamine (BTA) 2, which contains a 1,3,5-benzenetriamiiie molecular unit as an potential precursor of a high-spin molecule and three oligoarylamine moieties as spin-carrying units surrounding the core BTA, has been prepared by the sequential palladium-catalyzed amination reactions. The redox property has been investigated by cyclic voltammetry, and the highly charged states up to the hexacation are accessible to 2. The polycationic high-spin species have been generated by stepwise chemical oxidation, and the electronic structures have been examined in detail by the continuous wave (CW) and pulsed ESR spectroscopy in comparison with the previously studied 1. The pulsed ESR technique enabled us to determine the definite spin multiplicity of the generated polycationic species of 2. It was confirmed that the dominant oxidized species observed by the two- and three-electron oxidations were assigned to the spin triplet 2 21 and the spin quartet 2(3+), respectively. Moreover, these high-spin polycationic species turned out to be far more stable as compared to 1, and the isolation of 2(3+) as the SbCl6- salt has been accomplished. The temperature dependence of the magnetic susceptibility for the 2(3+) (SbCl6-)(3) salt revealed that the intramolecular ferromagnetic interaction exists in 2(3+), and moreover, the trication 2(3+) was found to be deformed in the solid state.