N-Benzyl-6-aminohexanamide hydrochloride

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: N-Benzyl-6-aminohexanamide hydrochloride
• 英文别名: 6-amino-N-benzylhexanamide;hydrochloride
• 化学式: C₁₃H₂₀N₂O*ClH
• 分子量: 256.776
• InChiKey: DICMMETWRPQSOC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.24
• 重原子数：
  17
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  55.1
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2'-O-acetyl-4''-O-acylimidazolylclarithromycin 、 N-Benzyl-6-aminohexanamide hydrochloride 在 甲醇 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 48.0h， 生成 4''-O-(((benzyl)amino)-6-oxo-hexyl)carbamoylclarithromycin
  参考文献：
  名称：

  Synthesis and antibacterial evaluation of novel clarithromycin derivatives with C-4″ elongated arylalkyl groups against macrolide-resistant strains

  摘要：

  Novel clarithromycin derivatives with C-4 '' elongated arylalkyl groups were designed, synthesized and evaluated to probe the effect of different lengths of their C-4 '' side chains on the activity against resistant bacterial strains. These derivatives had excellent activity against erythromycin-susceptible Streptococcus pneumoniae, Streptococcus aureus or Streptococcus pyogenes and some of them exhibited greatly improved activity against erythromycin-resistant strains. Compounds 18 and 16, which had the C-4 '' elongated arylalkyl groups with eight atoms from the 4 ''-oxygen atom to the terminal benzene ring, were the most effective against S. pneumoniae expressing the erm gene and the erm and me! genes. In contrast, the most potent compounds 3, 5, 9,17 and 18 against S. pneumoniae expressing the mef gene had C-4 '' elongated arylalkyl groups with three to eight atoms between the 4 ''-oxygen atom and the terminal aromatic ring. (C) 2010 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2010.11.035
• 作为产物：
  描述：

  2-苄基氨基乙酰胺 在 盐酸 、 溴 、 sodium 、 一水合肼 、 三乙胺 作用下， 以 甲醇 、 乙醇 、 氯仿 、 乙酸乙酯 为溶剂， 反应 5.33h， 生成 N-Benzyl-6-aminohexanamide hydrochloride
  参考文献：
  名称：

  An Approach to Simple Aminal Synthesis: Preparation ofN-(6-Aminohexyl)-N-benzyl-N′-methylmethylenediamine

  摘要：

  DOI：

  10.1055/s-1983-30329

文献信息

• Synthesis and antibacterial activity of 4″-O-carbamoyl analogs of clarithromycin
  作者：Xue Cui Shen、Bo Jiao、Shu Tao Ma

  DOI：10.1016/j.cclet.2009.11.023

  日期：2010.3

  Abstract A series of novel 4″- O -carbamoyl analogs of clarithromycin were synthesized and evaluated for their in vitro antibacterial activity. All of the desired compounds showed excellent activity against erythromycin-susceptible S. pneumoniae . Particularly, 4-fluorobenzyl carbamate 7a demonstrated potent activity against erythromycin-resistant S. pneumoniae encoded by the mef gene, and remarkably

  摘要合成了一系列新颖的克拉霉素4” -O-氨基甲酰基类似物，并对其体外抗菌活性进行了评价。所有所需化合物均显示出对易患红霉素的肺炎链球菌的优异活性。特别地，4-氟苄基氨基甲酸酯7a显示出对由mef基因编码的抗红霉素的肺炎链球菌的有效活性，并显着提高了对由erm基因以及erm和mef基因编码的抗红霉素的肺炎链球菌的活性。
• GRANADOS, R.;ALVAREZ, M.;LOPEZ-CALAHORRA, F.;SALAS, M., SYNTHESIS, BRD, 1983, N 4, 329-330
  作者：GRANADOS, R.、ALVAREZ, M.、LOPEZ-CALAHORRA, F.、SALAS, M.

  DOI：——

  日期：——
• Synthesis and antibacterial evaluation of novel clarithromycin derivatives with C-4″ elongated arylalkyl groups against macrolide-resistant strains
  作者：Shutao Ma、Bo Jiao、Yongjing Ju、Manjie Zheng、Ruixin Ma、Lin Liu、Ling Zhang、Xuecui Shen、Chenchen Ma、Ya Meng、Hui Wang、Yunkun Qi、Xiaodong Ma、Wenping Cui

  DOI：10.1016/j.ejmech.2010.11.035

  日期：2011.2

  Novel clarithromycin derivatives with C-4 '' elongated arylalkyl groups were designed, synthesized and evaluated to probe the effect of different lengths of their C-4 '' side chains on the activity against resistant bacterial strains. These derivatives had excellent activity against erythromycin-susceptible Streptococcus pneumoniae, Streptococcus aureus or Streptococcus pyogenes and some of them exhibited greatly improved activity against erythromycin-resistant strains. Compounds 18 and 16, which had the C-4 '' elongated arylalkyl groups with eight atoms from the 4 ''-oxygen atom to the terminal benzene ring, were the most effective against S. pneumoniae expressing the erm gene and the erm and me! genes. In contrast, the most potent compounds 3, 5, 9,17 and 18 against S. pneumoniae expressing the mef gene had C-4 '' elongated arylalkyl groups with three to eight atoms between the 4 ''-oxygen atom and the terminal aromatic ring. (C) 2010 Elsevier Masson SAS. All rights reserved.
• An Approach to Simple Aminal Synthesis: Preparation of<i>N</i>-(6-Aminohexyl)-<i>N</i>-benzyl-<i>N</i>′-methylmethylenediamine
  作者：R. Granados、M. Alvarez、F. Lopez-Calahorra、M. Salas

  DOI：10.1055/s-1983-30329

  日期：——