4-Chloro-4-methyl-3,5-diphenyl-4H-pyrazole | 61355-01-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-Chloro-4-methyl-3,5-diphenyl-4H-pyrazole
• 英文别名: 3,5-Diphenyl-4-methyl-4-chlor-pyrazol；4-chloro-4-methyl-3,5-diphenylpyrazole
• CAS: 61355-01-9
• 化学式: C₁₆H₁₃ClN₂
• 分子量: 268.746
• InChiKey: KWBWRMCAKNFILC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  24.7
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-Chloro-4-methyl-3,5-diphenyl-4H-pyrazole 、 环戊二烯 以82%的产率得到
  参考文献：
  名称：

  Adam Waldemar, Ammon Horst, Nau Werner M., Peters Karl, J. Org. Chem, 59 (1994) N 23, S 7067- 7071

  摘要：

  DOI：
• 作为产物：
  描述：

  4-methyl-3,5-diphenyl-1H-pyrazole 以91%的产率得到
  参考文献：
  名称：

  Adam Waldemar, Ammon Horst, Nau Werner M., Peters Karl, J. Org. Chem, 59 (1994) N 23, S 7067- 7071

  摘要：

  DOI：

文献信息

• 4-Halo-4H-pyrazoles: Cycloaddition with Cyclopentadiene to Azoalkanes of the 2,3-Diazabicyclo[2.2.1]hept-2-ene Type versus Electrophilic Addition with Cyclopentene
  作者：Waldemar Adam、Horst Ammon、Werner M. Nau、Karl Peters

  DOI：10.1021/jo00102a036

  日期：1994.11

  The acid-catalyzed reactions of the 4-halogen-substituted 4H-pyrazoles 3 with cyclopentadiene and cyclopentene in methylene chloride have been examined. The 4,4-dichloro-3,5-diphenyl-4H-pyrazole (3a) cycloadded quantitatively with cyclopentadiene to the gem-dichloro-substituted azoalkane 4a of the 2,3-diazabicyclo[2.2.1]hept-2-ene type, whose structure was established by X-ray analysis. The azoalkane 4a was catalytically hydrogenated to the azoalkane 6 with reduced C=C double bond and the relatively persistent (toward autoxidation) hydrazine 7 with reduced C=C and N=N double bonds. The cycloaddition of 4-chloro-4-methyl-3,5-diphenyl-4H-pyrazole (3b) with cyclopentadiene gave the azoalkane anti-4b in high yield and diastereoselectivity. The azoalkanes 4a,b and 6 were reluctant toward photolysis and thermolysis and the expected housanes were not produced under these conditions. The acid-catalyzed reaction of the 4-bromo-substituted 4H-pyrazoles 3c-e with cyclopentadiene gave, instead of the desired cycloadducts, complex product mixtures. In the presence of acid, the 4H-pyrazoles 3 gave with cyclopentene the 2-(alpha-halocyclopentyl)-substituted 2H-pyrazoles 5 as products of electrophilic addition.
• FREEMAN J. P.; JANIGA E. R.; LORENC J. F., J. ORG. CHEM. <JOCE-AH>, 1977, 42, NO 23, 3721-3724
  作者：FREEMAN J. P.、 JANIGA E. R.、 LORENC J. F.

  DOI：——

  日期：——