Molecular hybridization-guided one-pot multicomponent synthesis of chromanone-fused 3,3′-pyrrolidinyl-dispirooxindoles through a 1,3-dipolar cycloaddition reaction.

A new methodology was developed for the synthesis of 3,3′-pyrrolidinyl-dispirooxindoles <bold>3</bold> through a 1,3-dipolar cycloaddition event of isatylidenyl-chromanones <bold>2</bold> with azomethine ylides (thermally generated <italic>in situ</italic> from isatins and sarcosine). The method gives an easy access to a series of highly functionalized products containing three consecutive stereocenters and vicinal spiroquaternary stereocenters fused in one ring structure with 15 examples in high yields (up to 82% yield) and good diastereoselectivity (up to >20:1), which makes possible the synthesis of libraries under similar circumstances. Moreover, the current method provides a convenient approach for the efficient incorporation of two biologically important scaffolds (chromanone and 3,3′-pyrrolidinyl-dispirooxindoles). X-ray diffraction studies of one of the cycloadducts proved the structure and regiochemistry of the cycloaddition. In particular, their biological activity against human leukemia cells K562 and normal L929 cells has been evaluated. These results suggested that 3,3′-pyrrolidinyl-dispirooxindoles <bold>3</bold> may be potential leads for further biological screenings. [ABSTRACT FROM AUTHOR]