A facile synthesis of novel 1-aryl-1 H -pyrazolo[3,4- b ]quinoxalines
暂无分享,去创建一个
The reactions of 3-methyl-2-oxo-1,2-dihydroquinoxaline 3 with chlorophenyl diazonium salts afforded the hydrazones 4a-c, whose chlorinations with phosphoryl chloride gave the dichlorides 5a-c. Refluxing of the dichlorides 5a-c and base in N,N-dimethylformamide provided the 1-aryl-1H-pyrazolo[3,4-b]quinoxalines 6a-c.
[1] E. Ashry,et al. Synthesis of nitrogen-heterocyclic analogs of L-ascorbic acid: a triazolyl analog and its reactions , 1980 .
[2] A. Amer,et al. Transformation of the hydrazones of 6-chloro-3-(l-threo-2,3,4-trihydroxy-1-oxobutyl)-2-quinoxalinone into other heterocyclic compounds , 1978 .
[3] E. Ashry,et al. Dehydrative ring-closure of 3-substituted 2-quinoxalinones to give fused and nonfused pyrazoloquinoxalines , 1978 .