1. Begin with a benzene ring bearing three substituents:
   - A fluoro group at carbon 1.
   - A methoxy group (-OCH3) at carbon 3.
   - A five-membered ring (see below) that is fused to the benzene by sharing carbons 4 and 5.

2. The five-membered ring is constructed in sequence from carbon 4 of the benzene, a nitrogen atom, another carbon atom (which bears the substituent described below and is double bonded to the nitrogen), a sulfur atom, and finally carbon 5 of the benzene.

3. On the five-membered ring, the carbon situated between the nitrogen and sulfur atoms bears a substituent. This substituent comprises a nitrogen atom, which is directly connected to the ring carbon, and is double-bonded to a carbon. This carbon atom is also single-bonded to a hydroxyl group and linked to an additional aromatic ring.

4. The additional aromatic ring, attached through this imine-like linkage, is a second benzene ring substituted with three fluorines at positions 2, 4, and 5 (with the attachment is at carbon 1).

No chiral centers or double-bond stereochemistry are present.