期刊
ACS CATALYSIS
卷 4, 期 1, 页码 40-43出版社
AMER CHEMICAL SOC
DOI: 10.1021/cs400926z
关键词
palladium; isocyanides; heterocycles; insertion reactions; homogeneous catalysis; cross-coupling
资金
- Netherlands Organization for Scientific Research
- Hercules Foundation
A new synthetic approach to 4-aminopyrido-[2,3-d]pyrimidines and 4-aminopyrido[3,2-d]pyrimidines based on palladium-catalyzed reaction of isocyanides with readily available N-(bromopyridyl)amidines is reported. The target heterocycles were obtained in generally good to excellent yield. For the two regioisomeric pyrimidopyrimidines, we compared our approach involving oxidative addition with the analogous C H activation protocol because both methods have been reported for the synthesis of 4-aminoquinazolines. We found that the C H activation protocol does not allow one to obtain the target pyridopyrimidines, but the imidoylative cross-coupling protocol provided a new entry to the synthesis of these medicinally important scaffolds.
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