112734-89-1Relevant articles and documents
Design, synthesis and transformation of some heteroannulated 3-aminopyridines - Purine isosteres with exocyclic nitrogen atom
Iaroshenko, Viktor O.,Vilches-Herrera, Marcelo,Gevorgyan, Ashot,Mkrtchyan, Satenik,Arakelyan, Knar,Ostrovskyi, Dmytro,Abbasi, Muhammad S.A.,Supe, Linda,Hakobyan, Ani,Villinger, Alexander,Volochnyuk, Dmitriy M.,Tolmachev, Andrei
supporting information, p. 1217 - 1228 (2013/02/23)
The synthesis of 1-deazapurines and isosteres bearing the exocyclic nitrogen atom at position-1 was developed basing on the formal [3+3]-cyclization reaction of nitro-malonaldehyde with the set of electron-excessive aminoheterocycles. Through the function
PYRIMIDINES, XXXII: SYNTHESIS AND PROPERTIES OF PYRIDOPYRIMIDINE-2,4-DIONES (5-DEAZALUMAZINES)
Pfleiderer, Mathias,Pfleiderer, Wolfgang
, p. 905 - 929 (2007/10/02)
Pyridopyrimidine-2,4-dione (8) and its N-methyl derivatives (9-11) as well as the corresponding 6-nitro analogues (12-15) have been synthesized by condensation reactions from 6-aminouracils (4-7).Reduction of compound (4-7) led to the 6-aminopyrido