1,3,5-Trisubstituted and 5-Acyl-1,3-Disubstituted Hydantoin Derivatives via Novel Sequential Three-Component Reaction
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文摘
1,2-Diaza-1,3-dienes (DDs) react as Michael acceptors with primary amines to afford 伪-aminohydrazone derivatives that were in situ coupled with isocyanates. Intramolecular ring closure of the asymmetric urea derivatives so formed allows for a selectively substituted hydantoin ring to be obtained. The hydrazone side chain introduced by the conjugated heterodiene system at the 5-position of the heterocycle represents a valuable functionality for accessing novel 5-acyl derivatives difficult to obtain by other methods.

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