Abstract
1-Azaspiro[3.3]heptanes were synthesized, characterized, and validated biologically as bioisosteres of piperidine. The key synthesis step was thermal [2+2] cycloaddition between endocyclic alkenes and Graf's isocyanate, ClO2S-NCO, into spirocyclic β-lactams. Reduction of the β-lactam ring with alane produced 1-azaspiro[3.3]heptanes. Incorporation of this core into the anesthetic drug Bupivacaine instead of the piperidine fragment resulted in the new patent-free analogue with high activity.
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