...
首页> 外文期刊>Open Chemistry >New 1H-1-alkyl-6-methyl-3-phenyl-7-phenylazo-pyrazolo[5,1-c][1,2,4]triazoles through regioselective alkylation of 1H-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles
【24h】

New 1H-1-alkyl-6-methyl-3-phenyl-7-phenylazo-pyrazolo[5,1-c][1,2,4]triazoles through regioselective alkylation of 1H-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles

机译:通过1H-6-甲基-3-苯基-7的区域选择性烷基化制备新的1H-1-烷基-6-甲基-3-苯基-7-苯基偶氮-吡唑并[5,1-c] [1,2,4]三唑-苯基偶氮吡唑[5,1-c] [1,2,4]三唑

获取原文

摘要

1H-1-Alkyl-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles (2aa-ad) were obtained by regioselective alkylation of 1H-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles (2a). 1H-1-Alkyl-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles 2aa and 2ab were also prepared by coupling phenyldiazonium chloride with 1H-1-alkyl-6-methyl-3-phenyl-pyrazolo[5,1-c][1,2,4]triazoles 1aa and 1ab. The new compounds were characterized by IR, UV-VIS, 1H-NMR, 13C-NMR, and 15N-NMR spectroscopy and their structures and actual tautomeric forms were established unequivocally.
机译:通过1H-6-甲基-3的区域选择性烷基化反应获得1H-1-烷基-6-甲基-3-苯基-7-苯基偶氮吡唑[5,1-c] [1,2,4]三唑(2aa-ad) -苯基-7-苯基偶氮吡唑并[5,1-c] [1,2,4]三唑(2a)。 1H-1-烷基-6-甲基-3-苯基-7-苯基偶氮吡唑并[5,1-c] [1,2,4]三唑2aa和2ab也可以通过将氯化苯基重氮与1H-1-烷基-6偶联而制得。 -甲基-3-苯基-吡唑并[5,1-c] [1,2,4]三唑1aa和1ab。通过IR,UV-VIS,1H-NMR,13C-NMR和15N-NMR光谱对这些新化合物进行了表征,并明确确定了它们的结构和实际的互变异构形式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号