180893-34-9Relevant articles and documents
Mild room-temperature palladium-catalyzed C3-arylation of 2(1H)-pyrazinones via a desulfitative kumada-type cross-coupling reaction
Mehta, Vaibhav P.,Modha, Sachin G.,Van Der Eycken, Erik
supporting information; experimental part, p. 6870 - 6873 (2009/12/30)
(Chemical Equation Presented) An efficient desulfitative Kumada-type cross-coupling protocol is reported for the C3-arylation of 5-chloro-3- (phenylsulfanyl)pyrazin-2(1H)-ones. The method has also been successfully extended to the arylation of some (heter
Synthesis of new pyrrolo[3,4-b]- and [3,4-c]pyridin(on)es and related 1,7-naphthyridinones and 2,7-naphthyridines via intramolecular Diels-Alder reactions of 2(1H)-pyrazinones
Buysens, Kris J.,Vandenberghe, Didier M.,Hoornaert, Georges J.
, p. 9161 - 9178 (2007/10/03)
2(1H)-pyrazinones 7, 10 or 12 with in 6-position a 2-propynylaminomethyl or 3-butynylaminomethyl side chain undergo intramolecular Diels-Alder reactions providing cycloadducts which can be isolated or functionalised in some cases. By further thermolysis of these compounds either pyrrolo-[3,4-b]pyridinones 15/16 and/or pyrrolo[3,4-c]pyridines 17/18 or 1,7-naphthyridinones 25 and/or 2,7-naphthyridines 26 can be generated. Loss of either cyanide or isocyanate from the respective adducts is shown to be dependent on their substitution pattern.