首页> 外文期刊>Molecules >Synthesis and Crystal Structures of N-Substituted Pyrazolines
【24h】

Synthesis and Crystal Structures of N-Substituted Pyrazolines

机译:N-取代的吡唑啉的合成与晶体结构

获取原文
       

摘要

Four pyrazole compounds, 3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazole-1-carbaldehyde (1), 5-(4-bromophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbaldehyde (2), 1-[5-(4-chlorophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone (3) and 1-[3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl]propan-1-one (4), have been prepared by condensing chalcones with hydrazine hydrate in the presence of aliphatic acids, namely formic acid, acetic acid and propionic acid. The structures were characterized by X-ray single crystal structure determination. The dihedral angles formed between the pyrazole and the fluoro-substituted rings are 4.64(7)° in 1, 5.3(4)° in 2 and 4.89(6)° in 3. In 4, the corresponding angles for molecules A and molecules B are 10.53(10)° and 9.78(10)°, respectively.
机译:四种吡唑化合物,3-(4-氟苯基)-5-苯基-4,5-二氢-1H-吡唑-1-甲醛(1),5-(4-溴苯基)-3-(4-氟苯基)-4 ,5-二氢-1H-吡唑-1-甲醛(2),1- [5-(4-氯苯基)-3-(4-氟苯基)-4,5-二氢-1H-吡唑-1-基]乙酮(3)和1- [3-(4-氟苯基)-5-苯基-4,5-二氢-1H-吡唑-1-基]丙-1-酮(4)是通过将查耳酮与肼缩合而制备的在脂肪酸,即甲酸,乙酸和丙酸的存在下水合。通过X射线单晶结构测定来表征结构。吡唑与氟取代的环之间形成的二面角为1中的4.64(7)°,2中的5.3(4)°和3中的4.89(6)°。在4中,分子A和分子B的对应角分别为10.53(10)°和9.78(10)°。

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