Synthesis of Substituted 1H-Indazoles by Pyrazole Annelation to an Arene

被引:4
作者
Garkushenko, A. K. [1 ]
Sorokina, O. P. [1 ]
Kryuchkova, G. A. [1 ]
Zmeev, A. A. [1 ]
Makarova, M. A. [1 ]
Vorontsova, M. A. [1 ]
Sagitullina, G. P. [1 ]
机构
[1] FM Dostoevskii Omsk State Univ, Omsk 644077, Russia
关键词
5-aroyl-3-aryl-1,6-dimethyl-1H-indazoles; 5-amino-1,3,6-trimethyl-1H-indazole; 3,5-bis(cyclopropylcarbonyl)-2,6-dimethyl-1,4-dihydropyridine; 3,5-bis(cyclopropylcarbonyl)-2,6-dimethylpyridine; substituted ortho-aroyl-N-methylanilines; substituted N-methyl-N-nitrosobenzenes; Hantzsch synthesis; PHARMACOLOGICAL-PROPERTIES; 3-SUBSTITUTED INDAZOLES; EFFICIENT SYNTHESIS; CHEMISTRY; BENDAZAC; RING;
D O I
10.1007/s10593-013-1244-y
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Substituted 1H-indazoles have been synthesized by reductive intramolecular heterocyclization of 2,4-di-aroyl-N-nitrosomethylanilines and 2,4-diacetyl-N-nitrosomethylaniline. The N-nitrosoanilines were obtained by nitrosation of N-methyl-2,4-diaroyl- and 2,4-diacetylanilines, the products of quaternary 3,5-diaroyl- and 3,5-diacetylpyridinium salt recyclization.
引用
收藏
页码:273 / 280
页数:8
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