[1-(3,5-Dichloro-phenyl)-meth-(E)-ylidene]-ethyl-amine | 75692-67-0

• 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: [1-(3,5-Dichloro-phenyl)-meth-(E)-ylidene]-ethyl-amine
• CAS: 75692-67-0
• 化学式: C₉H₉Cl₂N
• 分子量: 202.083
• InChiKey: XYVFYIPBUDFTIJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.43
• 重原子数：
  12.0
• 可旋转键数：
  2.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  12.36
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  [1-(3,5-Dichloro-phenyl)-meth-(E)-ylidene]-ethyl-amine 在 lithium aluminium tetrahydride 作用下， 以 乙醚 为溶剂， 反应 2.0h， 生成 (3,5-Dichloro-benzyl)-ethyl-amine
  参考文献：
  名称：

  Benzylamines: synthesis and evaluation of antimycobacterial properties

  摘要：

  The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (19, MIC 10.2 micrograms/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 micrograms/mL), and N-butyl-3,5-difluorobenzylamine (103, MIC 6.4 micrograms/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combinations of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

  DOI：

  10.1021/jm00375a005
• 作为产物：
  描述：

  3,5-二氯苯甲醛 、 乙胺 反应 1.0h， 生成 [1-(3,5-Dichloro-phenyl)-meth-(E)-ylidene]-ethyl-amine
  参考文献：
  名称：

  Benzylamines: synthesis and evaluation of antimycobacterial properties

  摘要：

  The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (19, MIC 10.2 micrograms/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 micrograms/mL), and N-butyl-3,5-difluorobenzylamine (103, MIC 6.4 micrograms/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combinations of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

  DOI：

  10.1021/jm00375a005

文献信息

• N,N'-Dialkylbis(dichlorophenyl)ethylenediamines and -imidazolidines: relationship between structure and estradiol receptor affinity
  作者：Erwin Von Angerer、Gerhard Kranzfelder、Ashok K. Taneja、Helmut Schoenenberger

  DOI：10.1021/jm00186a012

  日期：1980.12

  6-dichloro-substituted compounds exhibit for N-CH3 (2e, 3e), N-C2H5 (2f, 3f), and N-C3H7 (2g, 3g) an affinity to the estradiol receptor (Ka values ranging from 9.1 X 10(4) to 9.1 X 10(6)), because the nitrogen atoms are shielded by the ortho-located chlorine atoms; therefore, a binding interaction with hydrophobic receptor areas is possible. These substances show weak uterotrophic activity and no significant effect

  合成了具有2,4,2,6,3,4和3,5位氯的非对映异构N，N'-二烷基双（二氯苯基）乙二胺和相应的咪唑烷。仅2,6-二氯取代的化合物的立体异构体对N-CH3（2e，3e），N-C2H5（2f，3f）和N-C3H7（2g，3g）表现出对雌二醇受体（Ka值范围从9.1 X 10（4）到9.1 X 10（6）），因为氮原子被邻位氯原子屏蔽；因此，与疏水性受体区域的结合相互作用是可能的。这些物质具有弱的子宫营养能力，并且对DMBA诱导的激素依赖性大鼠乳腺腺癌的生长没有明显影响。