N-(6-amino-2-pyridylmethyl)-N-(2-pyridylmethyl)amine | 831195-45-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: N-(6-amino-2-pyridylmethyl)-N-(2-pyridylmethyl)amine
• 英文别名: 6-[(Pyridin-2-ylmethylamino)methyl]pyridin-2-amine
• CAS: 831195-45-0
• 化学式: C₁₂H₁₄N₄
• 分子量: 214.27
• InChiKey: NLDDGRSBHTZBLC-UHFFFAOYSA-N

物化性质

• 沸点：
  382.3±37.0 °C(Predicted)
• 密度：
  1.187±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  63.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-(6-(bromomethyl)-2-pyridyl)pivalamide 、 N-(6-amino-2-pyridylmethyl)-N-(2-pyridylmethyl)amine 在 sodium carbonate 作用下， 以 乙腈 为溶剂， 反应 3.0h， 以75%的产率得到N-(6-{[(6-Amino-pyridin-2-ylmethyl)-pyridin-2-ylmethyl-amino]-methyl}-pyridin-2-yl)-2,2-dimethyl-propionamide
  参考文献：
  名称：

  研究氢键环境对锌（II）配合物与分子内酰胺氧配位的酰胺裂解反应的影响。

  摘要：

  酰胺键与氢键合微环境周围的锌（II）离子配位是金属蛋白酶的常见结构/功能特征。我们报告了两种策略将氢键基团定位在锌（II）结合的酰胺氧附近，并且我们研究了它们对酰胺基团稳定性的影响。多齿三脚架配体（6-R1-2-吡啶甲基）-R2（R1 = NHCOtBu，R2 = N（CH2-py-6-X）2 X = H L1，X = NH2，H L2，X = NH2 L3）形式[（L）Zn] 2+阳离子（L = L1，1; L2，2; L3，3）带有分子内酰胺氧配位（1-3）和分子内NH ... O = C（酰胺）氢由配体骨架牢固固定的键（2，3）。当在50（1）摄氏度下在甲醇中添加Me4NOH.5H2O（1当量）时，1-3进行叔丁基酰胺的裂解。在这些条件下，酰胺的半衰期t（1/2）粘结时间为0.4 h，持续1 2小时9小时，3小时320小时。（6-NHCOtBu-2-吡啶基甲基）-R2（R2 = N（

  DOI：

  10.1039/b414223c
• 作为产物：
  描述：

  N-(6-甲酰基吡啶-2-基)三甲基乙酰胺 在 盐酸 、 水 作用下， 以 甲醇 为溶剂， 反应 50.5h， 生成 N-(6-amino-2-pyridylmethyl)-N-(2-pyridylmethyl)amine
  参考文献：
  名称：

  Spectroscopic Characterization of the Active Fe^IIIFe^III and Fe^IIIFe^II Forms of a Purple Acid Phosphatase Model System

  摘要：

  Two new dinucleating ligands (H3L2 and HL3), derivatives of a well-known dinucleating ligand (HL1) with two bis-picolylamine sites connected to a bridging phenolate, with hydrogen-bonding donor groups at two of the pyridine moieties were designed and synthesized. Design of these ligands suggests that they will lead to dinuclear complexes with potential to stabilize phosphoester substrates as monodentate rather than bridging ligands. We report the diferric complexes [Fe-2(III)(H2L2)(OH)(4+) and [Fe-2(III)(L-3)(OH)(OH2)(2)](4+), which have been characterized by spectrophotometric titrations, UV-vis, IR, NMR, EPR, and Mossbauer spectroscopy. The phosphatase activity of the diferric systems, in addition to the partially reduced heterovalent [(FeFeII)-Fe-III(L-3)(OH)(OH2)(2)](3+) complex, has been investigated, and the complexes are shown to catalytically hydrolyze the activated phosphodiester substrate BDNPP (bis-dinitrophenylphosphate) as well as the corresponding phosphomonoester substrate DNPP (dinitrophenylphosphate). The results indicate that indeed the secondary interactions lead to an increase of the phosphatase activity and to active phosphomonoesterase catalysts. Interestingly, the heterovalent form of the HL3-based complex is more efficient than the diferric complex, and this is also discussed.

  DOI：

  10.1021/ic301347t

文献信息

• NEAR INFRARED RAY ABSORBENT COMPOSITION, NEAR INFRARED RAY CUT FILTER, SOLID IMAGE PICKUP ELEMENT, AND CAMERA MODULE
  申请人：FUJIFILM Corporation

  公开号：US20170227690A1

  公开（公告）日：2017-08-10

  Provided are a near infrared ray absorbent composition which can form a cured film having excellent near infrared ray shielding properties, a near infrared ray cut filter, a manufacturing method of a near infrared ray cut filter, a solid image pickup element, and a camera module. The near infrared ray absorbent composition includes a copper complex that is other than a copper phthalocyanine complex and has a maximum absorption wavelength in a wavelength range of 700 to 1,200 nm and in which a molar light absorption coefficient at the maximum absorption wavelength is greater than or equal to 100 (L/mol·cm).
• NEAR INFRARED ABSORBING COMPOSITION, NEAR INFRARED CUT FILTER, METHOD OF MANUFACTURING NEAR INFRARED CUT FILTER, DEVICE, METHOD OF MANUFACTURING COPPER-CONTAINING POLYMER, AND COPPER-CONTAINING POLYMER
  申请人：FUJIFILM Corporation

  公开号：US20180094086A1

  公开（公告）日：2018-04-05

  The near infrared absorbing composition includes: a copper-containing polymer having a copper complex site at a polymer side chain; and a solvent, in which the copper complex site includes a site multidentate-coordinated to a copper atom and at least one selected from the group consisting of a site monodentate-coordinated to a copper atom and a counter ion to a copper complex skeleton, and a polymer main chain and a copper atom at the copper complex site are bonded to each other through the site monodentate-coordinated to a copper atom or the counter ion.