N-[(3-methoxyphenyl)acetyl]piperidine | 92912-56-6

• 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-[(3-methoxyphenyl)acetyl]piperidine
• 英文别名: 2-(3-Methoxyphenyl)-1-piperidin-1-ylethanone
• CAS: 92912-56-6
• 化学式: C₁₄H₁₉NO₂
• mdl: MFCD20538554
• 分子量: 233.31
• InChiKey: NQCZVUZTEALFRK-UHFFFAOYSA-N

物化性质

• 沸点：
  402.3±28.0 °C(Predicted)
• 密度：
  1.092±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 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：
  29.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-[(3-methoxyphenyl)acetyl]piperidine 在 lithium aluminium tetrahydride 、 氢溴酸 作用下， 以 乙醚 、 水 为溶剂， 反应 3.0h， 生成 1-[2-(3-羟基苯基)乙基]哌啶
  参考文献：
  名称：

  Synthesis and cholinesterase activity of phenylcarbamates related to Rivastigmine, a therapeutic agent for Alzheimer's disease

  摘要：

  In order to develop new cholinesterase agents effective against Alzheimer's disease (AD) we synthesized some phenylcarbamates structurally related to Rivastigmine and evaluated their in vitro and in vivo biological activity. Among the compounds which displayed the most significant in vitro activity, 1-[1-(3-dimethylcarbamoyloxyphenyl)ethyl]piperidine (31b), in addition to a simple and cheaper synthesis, showed lower toxicity and very similar therapeutic index in comparison with Rivastigmine. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.

  DOI：

  10.1016/s0223-5234(01)01324-1
• 作为产物：
  描述：

  哌啶 、 3-甲氧基苯基乙酰氯 在 formylated piperidine 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 以36%的产率得到N-[(3-methoxyphenyl)acetyl]piperidine
  参考文献：
  名称：

  Palasz, Peter D.; Utley, James H. P.; Hardstone, J. David, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1984, vol. 38, # 4, p. 281 - 292

  摘要：

  DOI：

文献信息

• A Facile One-Carbon Homologation of Aryl Aldehydes to Amides
  作者：Wang Shen、Aaron Kunzer

  DOI：10.1021/ol025608m

  日期：2002.4.1

  in good to excellent yields. Both electron-donating and electron-withdrawing substitutions on the aromatic rings are tolerated, and the reaction works well with hindered alkylamines. This simple homologation could find broad applications. [reaction: see text]

  容易获得的2-芳基-1,1-二溴-1-烯烃可以在异常温和的条件下以良好或极好的收率转化为酰胺。芳环上的给电子取代和吸电子取代都是可容忍的，并且该反应与受阻烷基胺反应良好。这种简单的认证可以找到广泛的应用。[反应：看文字]
• Lee, Ving J.; Curran, William V.; Fields, Thomas F., Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1873 - 1891
  作者：Lee, Ving J.、Curran, William V.、Fields, Thomas F.、Learn, Keith

  DOI：——

  日期：——
• Palasz, Peter D.; Utley, James H. P.; Hardstone, J. David, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1984, vol. 38, # 4, p. 281 - 292
  作者：Palasz, Peter D.、Utley, James H. P.、Hardstone, J. David

  DOI：——

  日期：——
• LEE, VING J.;CURRAN, WILLIAM V.;FIELDS, THOMAS F.;LEARN, KEITH, J. HETEROCYCL. CHEM., 25,(1988) N, C. 1873-1891
  作者：LEE, VING J.、CURRAN, WILLIAM V.、FIELDS, THOMAS F.、LEARN, KEITH

  DOI：——

  日期：——
• Synthesis and cholinesterase activity of phenylcarbamates related to Rivastigmine, a therapeutic agent for Alzheimer's disease
  作者：C MUSTAZZA、A BORIONI、M GIUDICE、F GATTA、R FERRETTI、A MENEGUZ、M VOLPE、P LORENZINI

  DOI：10.1016/s0223-5234(01)01324-1

  日期：2002.2

  In order to develop new cholinesterase agents effective against Alzheimer's disease (AD) we synthesized some phenylcarbamates structurally related to Rivastigmine and evaluated their in vitro and in vivo biological activity. Among the compounds which displayed the most significant in vitro activity, 1-[1-(3-dimethylcarbamoyloxyphenyl)ethyl]piperidine (31b), in addition to a simple and cheaper synthesis, showed lower toxicity and very similar therapeutic index in comparison with Rivastigmine. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.