N-苄基-3-氟-N-甲基苯胺 | 113734-42-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: N-苄基-3-氟-N-甲基苯胺
• 英文名称: 3-fluoro-N-methyl-N-benzylaniline
• 英文别名: N-benzyl-3-fluoro-N-methylaniline；meta-fluoro-N-methyl-N-benzylaniline
• CAS: 113734-42-2
• 化学式: C₁₄H₁₄FN
• 分子量: 215.27
• InChiKey: LHEXQSNVSDFVSB-UHFFFAOYSA-N

物化性质

• 沸点：
  135 °C(Press: 0.05 Torr)
• 密度：
  1.119±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  3.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-苄基-3-氟-N-甲基苯胺 在 lithium aluminium tetrahydride 、 ammonium acetate 、 三氯氧磷 作用下， 以 四氢呋喃 、 乙醚 、 乙醇 为溶剂， 反应 9.0h， 生成 [4-(2-Amino-propyl)-3-fluoro-phenyl]-benzyl-methyl-amine
  参考文献：
  名称：

  Prodrugs of neuron-selective monoamine oxidase inhibitors: amino acid derivatives of 1-(4-aminophenyl)-2-aminopropanes

  摘要：

  Six amino acid derivatives of 1-(4-aminophenyl)-2-aminopropanes and their parent amines were synthezised and tested for their potency and selectivity in inhibiting monoamine oxidase (MAO) in vitro and in vivo. The amino acid derivatives were 300-1000 times less potent than the parent amines in inhibiting the MAO-A activity in a rat brain mitochondrial preparation in vitro. All compounds, except the (R)-valinamide derivative (22), were potent inhibitors of MAO in the rat brain in vivo and were, like the parent amines markedly more potent within the monoaminergic neurons than in other neurons. The glycinamide derivative 7 showed the largest difference between intra- and extra-neuronal inhibition in serotonergic neurons. The time course of the inhibitory effect of 7 in vivo showed that it is a reversible inhibitor with a long duration. (C) Elsevier, Paris.

  DOI：

  10.1016/s0223-5234(99)80047-6
• 作为产物：
  描述：

  N-(3-fluorophenyl)formamide 在 lithium aluminium tetrahydride 、 potassium carbonate 、 potassium iodide 作用下， 以 四氢呋喃 、 乙醚 、 N,N-二甲基甲酰胺 为溶剂， 反应 4.0h， 生成 N-苄基-3-氟-N-甲基苯胺
  参考文献：
  名称：

  Prodrugs of neuron-selective monoamine oxidase inhibitors: amino acid derivatives of 1-(4-aminophenyl)-2-aminopropanes

  摘要：

  Six amino acid derivatives of 1-(4-aminophenyl)-2-aminopropanes and their parent amines were synthezised and tested for their potency and selectivity in inhibiting monoamine oxidase (MAO) in vitro and in vivo. The amino acid derivatives were 300-1000 times less potent than the parent amines in inhibiting the MAO-A activity in a rat brain mitochondrial preparation in vitro. All compounds, except the (R)-valinamide derivative (22), were potent inhibitors of MAO in the rat brain in vivo and were, like the parent amines markedly more potent within the monoaminergic neurons than in other neurons. The glycinamide derivative 7 showed the largest difference between intra- and extra-neuronal inhibition in serotonergic neurons. The time course of the inhibitory effect of 7 in vivo showed that it is a reversible inhibitor with a long duration. (C) Elsevier, Paris.

  DOI：

  10.1016/s0223-5234(99)80047-6

文献信息

• Synthesis of N-heterocyclic carbene-Pd(II)-5-phenyloxazole complexes and initial studies of their catalytic activity toward the Buchwald-Hartwig amination of aryl chlorides
  作者：Zhi-Mao Zhang、Yu-Ting Xu、Li-Xiong Shao

  DOI：10.1016/j.jorganchem.2021.121683

  日期：2021.5

  N-heterocyclic carbene (NHC)-Pd(II) complexes using 5-phenyloxazole as the ancillary ligand have been obtained in moderate to good yields by a one-pot reaction of the corresponding imidazolium salts, palladium chloride and 5-phenyloxazole under mild conditions. Initial studies showed that one of the complexes is an efficient catalyst for the Buchwald-Hartwig amination of aryl chlorides with various secondary

  通过在相应的咪唑鎓盐，氯化钯和5-苯基恶唑的单锅反应下，以中等至良好的产率获得了三种以5-苯基恶唑为辅助配体的新的N-杂环卡宾（NHC）-Pd（II）配合物。温和的条件。初步研究表明，该配合物是在0.01-0.05 mol％的不同催化剂负载量下，用各种仲胺和伯胺对芳基氯化物进行Buchwald-Hartwig胺化反应的有效催化剂，因此它将丰富NHC的化学性质并得到用于偶合具有挑战性且成本较低的芳基氯化物的替代催化剂。
• N-Heterocyclic carbene-palladacyclic complexes: synthesis, characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides
  作者：Feng Liu、Yuan-Yuan Hu、Di Li、Quan Zhou、Jian-Mei Lu

  DOI：10.1016/j.tet.2018.07.052

  日期：2018.9

  a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01 mol%).

  在温和条件下，通过一锅法成功地获得了N-杂环卡宾-四环复合物3。通过X射线单晶衍射明确证实了3a的结构，即使在极低的催化剂负载量（0.01摩尔％）下，它仍是Buchwald-Hartwig胺化和酮的α-芳基化反应中的活性催化剂。
• Debenzylative Sulfonylation of Tertiary Benzylamines Promoted by Visible Light
  作者：Ying Fu、Qing‐Kui Wu、Zhengyin Du

  DOI：10.1002/ejoc.202100144

  日期：2021.3.26

  A visible light photocatalytic debenzylative sulfonylation of tertiary benzylamines is described, affording a series of sulfonamides in high yields. This operationally simple transformation showed high functional group compatibility and wide substrate scope.

  描述了叔苄胺的可见光光催化脱苄基磺酰化，以高收率提供了一系列磺酰胺。该操作简单的转化显示出高官能团相容性和广泛的底物范围。
• Synthesis of N-heterocyclic carbene-Pd(II) complexes and their catalytic activity in the Buchwald-Hartwig amination of aryl chlorides
  作者：Zhi-Mao Zhang、Yu-Jue Gao、Jian-Mei Lu

  DOI：10.1016/j.tet.2017.11.026

  日期：2017.12

  Novel N-heterocyclic carbene-palladium(II) complexes using 2-picolinic acid as the ancillary ligand have been successfully developed under mild conditions. Their catalytic activity in organic synthesis has been initially tested in the Buchwald-Hartwig amination of secondary and primary amines with aryl chlorides. Various substituents on both substrates can be tolerated, giving the desired coupling

  使用2-吡啶甲酸作为辅助配体的新型N-杂环卡宾-钯（II）配合物已在温和条件下成功开发。最初已经在仲胺和伯胺与芳基氯化物的布赫瓦尔德-哈特维格胺胺化中测试了它们在有机合成中的催化活性。可以容忍两种底物上的各种取代基，从而以良好或几乎定量的产率提供所需的偶联产物。最小催化剂负载量可以为0.01 mol％，这意味着它们在工业过程中的潜在应用。
• Photoconductive devices containing novel squaraine compounds
  申请人：XEROX CORPORATION

  公开号：EP0145400A2

  公开（公告）日：1985-06-19

  This invention is generally directed to fluorinated squaraine compositions of the formula: wherein R,. R2, R3, and R4, are independently selected from alkyl groups, containing from about 1 to about 20 carbon atoms, and layered photoresponsive devices containing such compositions.

  本发明一般涉及式中的氟化方碱组合物： 其中RR2、R3 和 R4 分别独立地选自含有约 1 至约 20 个碳原子的烷基，以及含有此类组合物的层状光致发光器件。