1-phenyl-2-[5-phenyl-2-(trifluoromethyl)-3H-1,3,4-thiadiazol-2-yl]ethanone | 392668-04-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-phenyl-2-[5-phenyl-2-(trifluoromethyl)-3H-1,3,4-thiadiazol-2-yl]ethanone
• CAS: 392668-04-1
• 化学式: C₁₇H₁₃F₃N₂OS
• 分子量: 350.364
• InChiKey: MMNPEYNZEWXNRC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  66.8
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  苯乙酮 在 sodium hydride 作用下， 以 甲醇 为溶剂， 生成 1-phenyl-2-[5-phenyl-2-(trifluoromethyl)-3H-1,3,4-thiadiazol-2-yl]ethanone 、 3-Phenyl-1-(phenylthioxomethyl)-5-(trifluoromethyl)-2-pyrazolin-5-ol
  参考文献：
  名称：

  Interactions of aroyl-and heteroaroyltrifluoroacetones with thiobenzoylhydrazine

  摘要：

  The interaction of aroyl( heteroaroyl) trifluoroacetones with thiobenzoylhydrazine may occur at both carbonyl groups. Reaction at the trifluoroacetyl group is facilitated by terminal substituents in the 1,3-dicarbonyl part, which leads can effectively conjugate with the adjacent carbonyl group. The products of condensation at the trifluoroacetyl group are 2-[2-aryl(heteroaroyl)-2-oxoethyl]-5-phenyl-2-trifluoromethyl-2,3-dihydro-1,3,4-thiadiazoles, while condensation at the aroyl(heteroaroyl) group gave 3-aryl(heteroaryl)-5-hydroxy-1-thiobenzoyl-5-trifluoromethyl-4,5-dihydro-1H-pyrazoles, which are not prone to tautomeric transformations in solution.

  DOI：

  10.1007/s10593-008-0081-x

文献信息

• [EN] ANTIFUNGAL AGENTS<br/>[FR] AGENTS ANTIFONGIQUES
  申请人：F2G LTD

  公开号：WO2005092304A2

  公开（公告）日：2005-10-06

  Compounds of formula (I), and pharmaceutically acceptable salts thereof, may be used in therapy, for example as antifungal agents, wherein: R1, R2 and R3 are as defined herein. Certain compounds of formula (I) are also provided. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.
• Interactions of aroyl-and heteroaroyltrifluoroacetones with thiobenzoylhydrazine
  作者：V. V. Pakalnis、I. V. Zerova、S. I. Yakimovitch、V. V. Alekseyev

  DOI：10.1007/s10593-008-0081-x

  日期：2008.5

  The interaction of aroyl( heteroaroyl) trifluoroacetones with thiobenzoylhydrazine may occur at both carbonyl groups. Reaction at the trifluoroacetyl group is facilitated by terminal substituents in the 1,3-dicarbonyl part, which leads can effectively conjugate with the adjacent carbonyl group. The products of condensation at the trifluoroacetyl group are 2-[2-aryl(heteroaroyl)-2-oxoethyl]-5-phenyl-2-trifluoromethyl-2,3-dihydro-1,3,4-thiadiazoles, while condensation at the aroyl(heteroaroyl) group gave 3-aryl(heteroaryl)-5-hydroxy-1-thiobenzoyl-5-trifluoromethyl-4,5-dihydro-1H-pyrazoles, which are not prone to tautomeric transformations in solution.