The triphenylimidazolyl radical (TPIR) is generated by the irradiation of the photochromic molecule hexaarylbiimidazole (1,2'-HABI). Usually, the unsubstituted TPIRs form 1,2'-HABI thermally at room temperature. In this study, we report the thermal reaction behavior of TPIR with a tBu group (tBu-TPIR) under N2 atmosphere and the novel reactivities of TPIRs. Under N2 atmosphere at room temperature, tBu-TPIRs form SpI with a spiro carbon and a novel HABI isomer tBu-1,4'-HABI, whose bonding pattern is different from that of the original unsubstituted HABI (1,2'-HABI). The results of 1H NMR spectroscopy, EPR measurements, and DFT calculations revealed that SpI is generated via three steps: (1) intramolecular hydrogen transfer from the tBu group to the nitrogen atom of the imidazole ring, (2) intramolecular cyclization of alkyl radicals, and (3) intermolecular hydrogen transfer with another tBu-TPIR. Furthermore, we found that the thermal reaction of tBu-TPIR at a low temperature affords the diastereomers of other isomers (tBu-4,4'-HABI_RS and tBu-4,4'-HABI_RR); in other words, the thermal reaction of tBu-TPIR depends on temperature.