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

页码：105 / 107

页数：3

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