Pyrimidin-2-yl-[1-p-tolyl-meth-(Z)-ylidene]-amine | 164733-60-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: Pyrimidin-2-yl-[1-p-tolyl-meth-(Z)-ylidene]-amine
• 英文别名: 2-Pyrimidinamine, N-[(4-methylphenyl)methylene]-；1-(4-methylphenyl)-N-pyrimidin-2-ylmethanimine
• CAS: 164733-60-2
• 化学式: C₁₂H₁₁N₃
• 分子量: 197.239
• InChiKey: OPFHKCSNCAJGKP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  38.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Pyrimidin-2-yl-[1-p-tolyl-meth-(Z)-ylidene]-amine 在 sodium tetrahydroborate 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 以49%的产率得到N-(4-甲基苄基)-(2-嘧啶基)胺
  参考文献：
  名称：

  Research on antibacterial and antifungal agents. XI. Synthesis and antimicrobial activity of N-heteroaryl benzylamines and their Schiff bases

  摘要：

  The synthesis and antimicrobial activity of new N-heteroaryl benzylamines and their Schiff bases are reported. Antifungal data were compared with those obtained with miconazole ketoconazole, enilconazole and imazalil sulfate; which showed that some of the tested compounds possessed moderate activity against strains of Candida albicans, Candida sp and good activity against isolates of plant pathogenic fungi, In contrast the synthesized compounds showed poor antibacterial activity, except for 3j which exhibited a better activity than nalidixic acid used as positive control. The results obtained are discussed on the basis of structure-activity relationships.

  DOI：

  10.1016/0223-5234(96)88217-1
• 作为产物：
  描述：

  1,3,5-三嗪-2,4,6-三胺,N,N'''-1,2-乙二基二[N-[3-[[4,6-二[丁基(2,2,6,6-四甲基-4-哌啶基)氨基]-1,3,5-三嗪-2-基]氨基]丙基]-N,N''-二丁基-N,N''-二(2,2,6,6-四甲基-4-哌啶基)- 、 对甲基苯甲醛 反应 3.0h， 以53%的产率得到Pyrimidin-2-yl-[1-p-tolyl-meth-(Z)-ylidene]-amine
  参考文献：
  名称：

  Research on antibacterial and antifungal agents. XI. Synthesis and antimicrobial activity of N-heteroaryl benzylamines and their Schiff bases

  摘要：

  The synthesis and antimicrobial activity of new N-heteroaryl benzylamines and their Schiff bases are reported. Antifungal data were compared with those obtained with miconazole ketoconazole, enilconazole and imazalil sulfate; which showed that some of the tested compounds possessed moderate activity against strains of Candida albicans, Candida sp and good activity against isolates of plant pathogenic fungi, In contrast the synthesized compounds showed poor antibacterial activity, except for 3j which exhibited a better activity than nalidixic acid used as positive control. The results obtained are discussed on the basis of structure-activity relationships.

  DOI：

  10.1016/0223-5234(96)88217-1

文献信息

• Research on antibacterial and antifungal agents. XI. Synthesis and antimicrobial activity of N-heteroaryl benzylamines and their Schiff bases
  作者：R Fioravanti、M Biava、GC Porretta、C Landolfi、N Simonetti、A Villa、E Conte、A Porta-Puglia

  DOI：10.1016/0223-5234(96)88217-1

  日期：1995.1

  The synthesis and antimicrobial activity of new N-heteroaryl benzylamines and their Schiff bases are reported. Antifungal data were compared with those obtained with miconazole ketoconazole, enilconazole and imazalil sulfate; which showed that some of the tested compounds possessed moderate activity against strains of Candida albicans, Candida sp and good activity against isolates of plant pathogenic fungi, In contrast the synthesized compounds showed poor antibacterial activity, except for 3j which exhibited a better activity than nalidixic acid used as positive control. The results obtained are discussed on the basis of structure-activity relationships.
• The “Design, synthesis, characterization and biological evaluation of some Azetidinone derivatives containing pyrimidine moiety.”
  作者：Godhani, Dinesh R.、Mehta, Umang P.、Saiyad, Anwar H.、Parmar, Kuldip P.、Mehta, Jignasu P.

  DOI：10.56042/ijc.v62i11.4825

  日期：——