Publication | Closed Access
I<sub>2</sub>/CHP‐Mediated Oxidative Coupling of 2‐Aminobenzamides and Isocyanides: Access to 2‐Aminoquinazolinones
15
Citations
41
References
2016
Year
Cross-coupling ReactionBiochemistryNatural SciencesOrganic ChemistryOxidative CouplingIsocyanides 2ChemistryHeterocycle ChemistryPharmacologyHigh Atom EconomySynthetic Chemistry
An oxidative coupling of 2‐aminobenzamides 1 and isocyanides 2 mediated by I 2 and cumyl hydroperoxide (CHP) leads to the formation of 2‐aminoquinazolinones 3 in moderate to excellent yields. This method provides an efficient approach to 2‐aminoquinazolinones with high atom economy under metal‐free conditions through two C–N bond‐formation reactions. The products can be further transformed to give benzo[4,5]imidazo[2,1‐ b ]quinazolin‐12(6 H )‐one ( 4 ).
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