1. Start with a saturated six-membered ring (piperidine) that contains one nitrogen and five carbons.
2. At the nitrogen of this piperidine, attach a three-carbon chain. The second carbon bears a substituent described below.
3. This substituent begins with a methylene linker that connects to an oxamide group (-NH-C(=O)-C(=O)-NH-), which further leads to a fused bicyclic aromatic system.
4. The fused ring system is a quinoline ring system featuring a benzene ring fused to a pyridine ring.
    - Label the pyridine ring sequentially as N1, C2, C3, C4, C5, and C6, and label the benzene ring sequentially as C5, C6, C7, C8, C9, and C10 (with C5 and C6 shared with the pyridine ring).
    - The oxamide group attaches to the fused system via C10, and both C7 and C8 each carry a methyl substituent.
