709-06-8Relevant academic research and scientific papers
2-Aminoquinazolines by Chan-Evans-Lam Coupling of Guanidines with (2-Formylphenyl)boronic Acids
Solomin, Vitalii V.,Seins, Alberts,Jirgensons, Aigars
supporting information, p. 1507 - 1510 (2020/07/24)
A new method is presented for the synthesis of 2-aminoquinazolines, which is based on a Chan-Evans-Lam coupling of (2-formylphenyl)boronic acids with guanidines. Relatively mild conditions involving the use of inexpensive CuI as a catalyst and methanol as a solvent permit the application of the method to a wide range of substrates. Nonsubstituted, N-monosubstituted, and N,N-disubstituted guanidines can be used as reactants to give the corresponding 2-aminoquinazolines in moderate yields from readily available (2-formylphenyl)boronic acids.
Copper-catalyzed sequential N-Arylation and aerobic oxidation: Synthesis of quinazoline derivatives
Liu, Qing,Zhao, Yufen,Fu, Hua,Cheng, Changmei
supporting information, p. 2089 - 2094 (2013/10/21)
A novel and efficient copper-catalyzed cascade method for the synthesis of quinazoline derivatives has been developed. The protocol uses readily available substituted (2-bromophenyl)methylamines and amidine hydrochlorides as the starting materials, inexpensive CuBr as the catalyst, and economical and environment friendly air as the oxidant, and the corresponding quinazoline derivatives were obtained in moderate to good yields. The procedure underwent sequential intermolecular N-arylation, intramolecular nucleophilic substitution and aerobic oxidation. Georg Thieme Verlag Stuttgart, New York.
