QSAR & Combinatorial Science · 2004 · 15 citations · 14 references
PharmacyChemistryMedicinal ChemistryCombinatorial ChemistryOrganic ChemistrySynthetic Medicinal ChemistryCombinatorial SynthesisCross-coupling ReactionsDiversity-oriented SynthesisMacrocycle SynthesisMicrowave-assisted SynthesisOrganic SynthesisDerivatizationDerivatization TechniquesDiversity-oriented Heterocycle SynthesisMicrowave Irradiation EffectsMicrowave-assisted Condensation ReactionsMicrowave-assisted Heterocycle SynthesisMicrowave-assisted Organic Synthesis
Abstract A microwave‐assisted protocol for the synthesis of 4‐oxo and 4‐chloropyrido[2,3‐ d ]pyrimidin‐7(8 H )‐ones, 13 and 9 respectively, bearing a carbon substituent at C2 and a chlorine atom at C4 is reported. The introduction of a wide range of substituents at C2 renders this methodology easily amenable to combinatorial chemistry applications. Two examples of further derivatization of compounds 9 , substitution by amine and Suzuki coupling, under microwave irradiation are also described.
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Diane H. Boschelli, Zhipei Wu, S. KLUTCHKO et al. · Journal of Medicinal Chemistry · 1998 · 84 citations · Full text
A three-component synthesis of pyrido[2,3-d]pyrimidines
Núria Mont, Jordi Teixidó, José I. Borrell et al. · Tetrahedron Letters · 2003 · 82 citations