Journal of Combinatorial Chemistry · 2003 · 21 citations · 11 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryAmino Acid ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisSolid-phase SynthesisAmino AcidsNitro CompoundsNitro ReductionSolid-phase Organic Synthesis
A versatile method for the solid-phase synthesis of 2-aminoquinazoline-based derivatives, 3-substituted-3,4-dihydroquinazolin-2-amines and imidazoquinazolines, has been developed. They were obtained by treating the amino group of polymer-linked amino acids with 2-nitrobenzaldehyde followed by reduction of the nitro group to an amine. Cyclization of the resulting immobilized intermediates with cyanogen bromide followed by acidic/basic cleavage yielded the desired quinazoline-based compounds in high yields and purities.
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Michael R. Myers, Natalie N. Setzer, Alfred P. Spada et al. · Bioorganic & Medicinal Chemistry Letters · 1997 · 45 citations