113686-04-7Relevant articles and documents
Synthesis of diverse azolo[c]quinazolines by palladium(II)- catalyzed aerobic oxidative insertion of isocyanides
Vlaar, Tjostil,Bensch, Lisa,Kraakman, Jasper,Vande Velde, Christophe M. L.,Maes, Bert U. W.,Orru, Romano V. A.,Ruijter, Eelco
supporting information, p. 1205 - 1209 (2014/05/06)
We report the palladium(II)-catalyzed aerobic oxidative coupling of isocyanides with various (2-aminophenyl)azoles using air as the stoichiometric oxidant. A diverse range of medicinally valuable azolo[c]quinazolines was obtained by this new approach.
Synthesis of Triazoloquinazoline and Triazolo-1,4-benzodiazepine Derivatives
Gatta, Franco,Giudice, Del, Maria Rosaria,Borioni, Maria
, p. 11 - 16 (2007/10/02)
Some triazoloquinazolin-5(6H)-ones 7, the corresponding isomers triazoloquinazolin-5(6H)-ones and the 5-amino derivatives 8,9 and 11 have been synthesized starting from the acylamidrazones 5.The preparation of 5H-triazol
Structure-Activity Profile of a Series of Novel Triazoloquinazoline Adenosine Antagonists
Francis, John E.,Cash, William D.,Psychoyos, Stacy,Ghai, Geetha,Wenk, Paul,et al.
, p. 1014 - 1020 (2007/10/02)
During a search for benzodiazepine receptor modulators, a highly potent adenosine antagonist (CGS 15943) was discovered.The compound was defined as resonance-stabilized hybrid of the canonical structures 9-chloro-2-(2-furyl)triazoloquinazoli