Azido(N)-nucleosides are known for their antiviral and anticancer properties. Recently, N-nucleosides have attracted attention for augmenting radiation damage in tumor cells via dissociative electron attachment (DEA) reactions mediated by the simplest and the most potent reducing species (the electron). To investigate the effect of N group substitution at specific sites of the pyrimidine base-ring (C4, C5, and C6) on the DEA reaction, we employed both commercially available and in-house-synthesized N-nucleosides. We conducted a comprehensive study combining electron paramagnetic resonance (EPR) spectroscopy at a low temperature, picosecond pulse radiolysis in an aqueous solution under ambient conditions, and DFT calculations. For N substitution at C4, EPR studies and DFT calculations established a stable azide anion radical (R-N) formation, after the addition of radiation-produced electrons. For N substitution at C5, the DEA leads to a π-type aminyl radical (R-NH) formation. For N substitution at C6, a conjugated iminyl σ-radical (R═N) is formed via DEA. R═N is in equilibrium with R-NH. Thus, this work reports a significant finding: the stabilization and reactivity of each type of nitrogen-centered radical (RN, RNH, R═N) are determined by the position of N substitution on the pyrimidine base-ring.