2003
DOI: 10.1002/hc.10168
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Syntheses of 3,4,7‐triazaacenaphthylene and pyrido[3,4,5‐de]cinnoline derivatives

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Cited by 8 publications
(4 citation statements)
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“…Several 1,2,4-triazole derivatives show anti-inflammatory [18], vasodilatory [19] and psychotropic properties [20]. Recently, our interest in the synthesis of various substituted heterocyclic systems, which could be adapted for the preparation of small libraries, has been the subject of several publications from our laboratory [21][22][23][24][25][26][27][28][29][30][31]. During our investigation, we have found that acid hydrazides can be used as useful intermediates leading to the formation of several heterocycles of potential biological activity such as 1,2,4triazoles, 1,3,4-oxadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines [23,32].…”
Section: Introductionmentioning
confidence: 99%
“…Several 1,2,4-triazole derivatives show anti-inflammatory [18], vasodilatory [19] and psychotropic properties [20]. Recently, our interest in the synthesis of various substituted heterocyclic systems, which could be adapted for the preparation of small libraries, has been the subject of several publications from our laboratory [21][22][23][24][25][26][27][28][29][30][31]. During our investigation, we have found that acid hydrazides can be used as useful intermediates leading to the formation of several heterocycles of potential biological activity such as 1,2,4triazoles, 1,3,4-oxadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines [23,32].…”
Section: Introductionmentioning
confidence: 99%
“…The latter (107a,b) can also be prepared by treatment of (108a,b) with DMFDMA to give the corresponding enamines (109a,b) followed by coupling with diazonium salt of m-nitroaniline in sodium hydroxide to give the corresponding aldehyde derivatives (110a,b) followed by treatment with hydrazine hydrate and aromatic amines (Scheme 19) [73].…”
Section: Preparation Of Heterocyclicmentioning
confidence: 99%
“…Then, pyrido pyridazine derivatives ( 93 ) were obtained by intramolecular cyclization of enamine ( 91 ) with amines derivatives (hydrazine hydrate, aniline, 2‐aminopyridine et al.) [34] …”
Section: Formation Of Heterocycle Structures By Dmf‐dma Reactionsmentioning
confidence: 99%