N-(cyclohexylmethyl)-4-fluorobenzamide | 1178339-86-0

• 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: N-(cyclohexylmethyl)-4-fluorobenzamide
• CAS: 1178339-86-0
• 化学式: C₁₄H₁₈FNO
• 分子量: 235.301
• InChiKey: YRMWGCMKLRATNP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-(cyclohexylmethyl)-4-fluorobenzamide 在 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(hexafluorophosphate) 、 copper(I) bromide 作用下， 以 乙腈 为溶剂， 以65%的产率得到cyclohexanecarboxylic acid 4-fluoro-benzoylamide
  参考文献：
  名称：

  Replacement of BF4− by PF6− makes Selectfluor greener

  摘要：

  A combination of F-TEDA-PF6 and CuBr (0.1 equiv.) provides a potent oxidant that readily oxidizes amides to provide imides at room temperature. Replacement of BF4-, the anion of Selectfluor (F-TEDA-BF4), by PF6-, dramatically reduces CuBr loading in this oxidative reaction. A possible rationale for this dramatic counterion effect is provided. (C) 2012 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jfluchem.2012.05.010
• 作为产物：
  描述：

  对氟苯甲酰氯 、 环己甲胺 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 N-(cyclohexylmethyl)-4-fluorobenzamide
  参考文献：
  名称：

  Copper mediated oxidation of amides to imides by Selectfluor

  摘要：

  The combination of Selectfluor and copper(I) bromide has shown a strong oxidation ability, readily oxidizing amides into the corresponding imides in acetonitrile at room temperature in less than 1 h. This transformation under mild conditions gives good to excellent chemical yields. A possible reaction mechanism is proposed. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.02.059

文献信息

• Nickel-Catalyzed Cross-Dehydrogenative Coupling of α-C(sp³)–H Bonds in <i>N</i>-Methylamides with C(sp³)–H Bonds in Cyclic Alkanes
  作者：Ze-Lin Li、Kang-Kang Sun、Chun Cai

  DOI：10.1021/acs.orglett.8b02736

  日期：2018.10.19

  A nickel-catalyzed cross-dehydrogenative coupling reaction of α-C(sp3)–H bonds in N-methylamides with C(sp3)–H bonds from cyclic alkanes has been developed, which offers a cheap transition-metal-catalyzed C–H activation method for amides without the requirement for any extraneous directing group. This new strategy is highly selective and tolerates a variety of functional groups. Mechanistic investigations

  已开发出镍催化的N-甲酰胺中的α-C（sp 3）-H键与环状烷烃的C（sp 3）-H键的交叉脱氢偶联反应，该反应可提供廉价的过渡金属催化的C -H活化酰胺的方法，不需要任何外来的导向基团。这种新策略具有高度的选择性，并且可以容忍各种功能组。还详细描述了对反应过程的机械研究。
• Inhibitors for GlyT-1
  申请人：Jolidon Synese

  公开号：US20080058331A1

  公开（公告）日：2008-03-06

  The present invention relates to compounds of formula I wherein R 1 , R 2 , R 3 , R 4 , and X are as defined herein or to pharmaceutically acceptable acid addition salts thereof, with the exception of 4-methoxy-N-[2-oxo-2-(phenylamino)ethyl]-N-phenyl-benzamide, 4-chloro-N-[2-[(4-methylphenyl)amino]-2-oxoethyl]-N-phenyl-benzamide, 4-chloro-N-[2-[5-chloro-2-methoxyphenyl)amino]-2-oxoethyl]-N-benzamide, 4-methyl-N-[2-oxo-2-[(2,4,6-trichlorophenyl)amino]ethyl]-N-benzamide, N-[2-[(4-methylphenyl)amino]-2-oxoethyl]-N-phenyl-benzamide, 4-methyl-N-[2-[(4-methylphenyl)amino]-2-oxoethyl]-N-phenyl-benzamide, 4-chloro-N-(2-oxo-2-[(2,4,6-trichlorophenyl)amino]ethyl]-N-benzamide and N-[2-[(2,4-dimethoxyphenyl)amino]-2-oxoethyl]-N-[(2-fluorophenyl)methyl]-benzeneacetamide. The compounds are useful in the treatment of neurological and neuropsychiatric disorders.

  本发明涉及以下式I的化合物其中R1、R2、R3、R4和X如本文所定义或其药学上可接受的酸盐，但不包括4-甲氧基-N-[2-氧代-2-(苯胺)乙基]-N-苯基苯甲酰胺，4-氯-N-[2-[(4-甲基苯基)氨基]-2-氧乙基]-N-苯基苯甲酰胺，4-氯-N-[2-[5-氯-2-甲氧基苯)氨基]-2-氧乙基]-N-苯甲酰胺，4-甲基-N-[2-氧代-2-[(2,4,6-三氯苯基)氨基]乙基]-N-苯甲酰胺，N-[2-[(4-甲基苯基)氨基]-2-氧乙基]-N-苯基苯甲酰胺，4-甲基-N-[2-[(4-甲基苯基)氨基]-2-氧乙基]-N-苯基苯甲酰胺，4-氯-N-(2-氧代-2-[(2,4,6-三氯苯基)氨基]乙基]-N-苯甲酰胺和N-[2-[(2,4-二甲氧基苯基)氨基]-2-氧乙基]-N-[(2-氟苯基)甲基]-苯乙酰胺。这些化合物在治疗神经和神经精神障碍方面是有用的。
• US7589089B2
  申请人：——

  公开号：US7589089B2

  公开（公告）日：2009-09-15
• Copper mediated oxidation of amides to imides by Selectfluor
  作者：Zhuang Jin、Bo Xu、Gerald B. Hammond

  DOI：10.1016/j.tetlet.2011.02.059

  日期：2011.4

  The combination of Selectfluor and copper(I) bromide has shown a strong oxidation ability, readily oxidizing amides into the corresponding imides in acetonitrile at room temperature in less than 1 h. This transformation under mild conditions gives good to excellent chemical yields. A possible reaction mechanism is proposed. (C) 2011 Elsevier Ltd. All rights reserved.
• Replacement of BF4− by PF6− makes Selectfluor greener
  作者：Zhuang Jin、Bo Xu、Stephen G. DiMagno、Gerald B. Hammond

  DOI：10.1016/j.jfluchem.2012.05.010

  日期：2012.11

  A combination of F-TEDA-PF6 and CuBr (0.1 equiv.) provides a potent oxidant that readily oxidizes amides to provide imides at room temperature. Replacement of BF4-, the anion of Selectfluor (F-TEDA-BF4), by PF6-, dramatically reduces CuBr loading in this oxidative reaction. A possible rationale for this dramatic counterion effect is provided. (C) 2012 Elsevier B.V. All rights reserved.