Start this molecule from a central carbonyl carbon. It forms a double bond with an oxygen atom and carries two distinct substituents:
1. An aminoalkyl-pyrrolidine chain: Starting from the carbonyl carbon, a nitrogen atom is directly attached, followed by two methylene groups. This chain terminates with a pyrrolidine ring, a saturated five-membered ring containing one nitrogen and four carbons, connected via its nitrogen atom.
2. A para-substituted phenyl ring: Attached to the carbonyl carbon, the phenyl ring bears an amide group (-NH-C(=O)-) at the position opposite the attachment point. The carbonyl carbon of this amide is linked to a methylene group, which is further connected to an unsubstituted indane ring (a fused bicyclic structure consisting of a benzene ring and a cyclopentane ring). The methylene group attaches exclusively to one benzene carbon that is at the beta position relative to one of the shared carbons of the benzene-cyclopentane junction.