Organic electrode materials (OEMs) have garnered significant attention in the field of sodium‐ion batteries (SIBs) due to their sustainability and structural tunability. However, many OEMs suffer from low specific capacity and poor cycling stability. In this study, we have successfully designed and synthesized a heteroaromatic molecule called 2,3,8,9,14,15‐hexanol hexaazatrinaphthalene (HATN‐6OH) with catechol/ortho‐quinone coupling functional groups and HATN conjugated core structures. Through extensive analysis using density functional theory (DFT) calculation, ATR‐FTIR, and Raman techniques, we have determined that the abundant coupling function groups and imine redox‐active moieties on HATN‐6OH enable a nine‐electron transfer mechanism, resulting in a high specific capacity for sodium ion storage. Furthermore, the π‐π coupling interactions and intermolecular hydrogen bond forces among HATN‐6OH molecules contribute to its resilient structural and chemical stability during cycling. As a result, our HATN‐6OH electrode exhibits remarkable specific capacity (554 mA h g‐1 at 0.1 A g‐1), excellent rate capability (202 mA h g‐1 at 10 A g‐1), and stable long‐term cycling performance (73% capacity retention after 3000 cycles at 10 A g‐1) in SIBs. This study highlights the importance of synergistic coupling of redox‐active sites on OEMs in simultaneously enhancing capacity and stability.