With favorable colour purity, multi-resonance thermally activated delayed fluorescence (MR-TADF) molecules exhibit enormous potential in high-definition displays. Due to the relatively small chemical space of MR-TADF molecules, it is challenging to improve molecular performance through domain-specific expertise alone. To address this problem, we focused on optimizing the classic molecule, DABNA-1, using machine learning (ML). Molecular morphing operations were initially employed to generate the adjacent chemical space of DABNA-1. Subsequently, a machine learning model was trained with a limited database and used to predict the properties throughout the generated chemical space. It was confirmed that the top 100 molecules suggested by machine learning present excellent electronic structures, characterized by small reorganization energy and singlet-triplet energy gaps. Our results indicate that the improvement in electronic structures can be elucidated through the view of the molecular orbital (MO). The results also reveal that the top 5 molecules present weaker vibronic peaks of the emission spectrum, demonstrating higher colour purity when compared to DABNA-1. Notably, the M2 molecule presents a high RISC rate, indicating its promising future as a high-efficiency MR-TADF molecule. Our machine-learning-assisted approach facilitates the rapid optimization of classical molecules, addressing a crucial requirement within the organic optoelectronic materials community.