Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone

被引：0
|
作者：
Jasouri, S. [1 ,2 ]
Khalafy, J. [1 ]
Badali, M. [2 ]
Prager, R. H. [3 ]
机构：
[1] Urmia Univ, Dept Chem, Orumiyeh 57154, Iran
[2] Daana Pharmaceut Co, Tabriz 51575, Iran
[3] Flinders Univ S Australia, Sch Chem & Phys Sci, Adelaide, SA 5001, Australia
来源：
SOUTH AFRICAN JOURNAL OF CHEMISTRY-SUID-AFRIKAANSE TYDSKRIF VIR CHEMIE | 2011年 / 64卷
关键词：
2-bromo-4-chloro-1-indanone; diaminopyridine; indeno[1,2-b]quinoxaline; indeno[1,2-b]pyrazine; debromination; BIOLOGICAL EVALUATION; ANTITUMOR; DESIGN;
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The reaction of 2-bromo-4-chloro-1-indanone with 2,3-diaminomaleonitrile, benzene-1,2-diamine and 4-methylbenzene-1,2-diamine in glacial acetic acid gave 8-chloro-9H-indeno[1,2-b] pyrazine-2,3-dicarbonitrile, 1-chloro-11H-indeno[1,2-b] quinoxaline and 1-chloro-7-methyl-11H-indeno[1,2-b] quinoxaline, respectively, in good yield.
引用
收藏
页码：105 / 107
页数：3
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