Synthesis of novel pyridazino[3,4-b]quinoxalines
β 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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β¦ Synopsis
Abstract
The pyridazino[3,4βb]quinoxaline 12 was synthesized by the cyclization of the Ξ±βarylhydrazonoacylβhydrazide 11. The reaction of compound 12 with phosphoryl chloride gave pyridazino[3,4βb]quinoxaline 13, whose reactions with sodium azide or cyclic secondary amines provided pyridazino[3,4βb]quinoxalines 14,17 and 18, respectively. The acylhydrazide 15 was also cyclized to pyridazino[3,4βb]quinoxaline 16.
π SIMILAR VOLUMES
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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