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Synthesis of novel pyridazino[3,4-b]quinoxalines

✍ Scribed by Ho Sik Kim; Eun Kyoung Kim; Sung Sik Kim; Yong Tae Park; Young Seuk Hong; Yoshihisa Kurasawa


Publisher
Journal of Heterocyclic Chemistry
Year
1997
Tongue
English
Weight
225 KB
Volume
34
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

The pyridazino[3,4‐b]quinoxaline 12 was synthesized by the cyclization of the α‐arylhydrazonoacyl‐hydrazide 11. The reaction of compound 12 with phosphoryl chloride gave pyridazino[3,4‐b]quinoxaline 13, whose reactions with sodium azide or cyclic secondary amines provided pyridazino[3,4‐b]quinoxalines 14,17 and 18, respectively. The acylhydrazide 15 was also cyclized to pyridazino[3,4‐b]quinoxaline 16.


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Quinolone analogues I -VI with pyridazino [3,4-b]quinoxaline ring system were synthesized from the (1-alkylhydrazino)quinoxaline N-oxides 1 via oxidation of pyridazino [3,4-b] quinoxalines 2,3,5,7, quinoxalino[2,3-c]cinnolines 4, and1,2-diazepino[3,4-b]quinoxalines 6. The biological activities of qu

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## Abstract For Abstract see ChemInform Abstract in Full Text.