NEW[G]-FUSED [1,2,4]TRIAZOLO[1,5-C]PYRIMIDINES - SYNTHESIS OF PYRIDO[3,2-E] AND [4,3-E][1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE, PYRIMIDO[5,4-E][1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE AND [1,2,4]TRIAZOLO[1,5-C]PTERIDINE DERIVATIVES

Authors
DELGIUDICE MR BORIONI A MUSTAZZA C GATTA F
Citation
Mr. Delgiudice et al., NEW[G]-FUSED [1,2,4]TRIAZOLO[1,5-C]PYRIMIDINES - SYNTHESIS OF PYRIDO[3,2-E] AND [4,3-E][1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE, PYRIMIDO[5,4-E][1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE AND [1,2,4]TRIAZOLO[1,5-C]PTERIDINE DERIVATIVES, Journal of heterocyclic chemistry, 31(6), 1994, pp. 1503-1507
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
31
Issue
6
Year of publication
1994
Pages
1503 - 1507
Database
ISI
SICI code
0022-152X(1994)31:6<1503:N[-SOP>2.0.ZU;2-P
Abstract
A number of 2-aryl-substituted pyrido[3,2-e] and [4,3-e][1,2,4]triazol o[1,5-c]pyrimidines and [1,2,4]triazolo[1,5-c]pteridines 11,12a,b,e, t heir corresponding 5-carbonyl derivatives 7,8a,b,e and some imido[5,4- e][1,2,4]triazolo[1,5-c]pyrimidin-5-ones 7,8c,d, have been synthesized , according to different pathways. The new tricyclic heterocycles were prepared with the aim of studying their possible benzodiazepine recep tors affinity.