Short Scalable Route to Bis-morpholine Spiroacetals and Oxazepane Analogues: Useful 3D-Scaffolds for Compound Library Assembly

sp³-rich molecular scaffolds incorporating nitrogen heterocycles represent important starting points for assembling compound screening libraries and drug discovery. Herein, we report a four-step synthesis of a conformationally well-defined sp³-rich scaffold, incorporating two morpholine rings embedded within a spiroacetal framework. The synthesis involves the in-termediacy of a 2-chloromethyl-substituted morpholine, accessed from epichlorohydrin and readily available β-aminoalcohols. Base-mediated dehydrochlorination affords an exocyclic enol ether, from which the second morpholine ring is constructed in two steps. Scaffold synthesis is high-yielding and can be performed on large scale. The methodology al-lows ready substitution of one –or both– of the morpholine rings for 1,4-oxazepanes and the generation of 6,7- and 7,7-spiroacetal analogues, which are virtually unexplored in drug discovery. Substituted 6,6-systems can be prepared, and in some instances, undergo acid-mediated anomerization to deliver the scaffolds in high diastereoselectivity. The two amine functionalities embedded in the 6,6- and 6,7-spiroacetal scaffolds were sequentially functionalized to provide a diverse physical compound library. These library compounds occupy a similar chemical space to small-molecule drugs that have been approved for clinical application by the Food and Drug Administration yet are structurally dissimilar, and may therefore act upon novel targets, representing attractive starting materials for drug discovery.