1-benzyl-4-(4-methoxyphenyl)-1,2,3,6-tetrahydropyridine hydrochloride

• 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: 1-benzyl-4-(4-methoxyphenyl)-1,2,3,6-tetrahydropyridine hydrochloride
• 英文别名: 1-Benzyl-4-(4-methoxyphenyl)-1,2,3,6-tetrahydropyridine hydrochloride；1-benzyl-4-(4-methoxyphenyl)-3,6-dihydro-2H-pyridine;hydrochloride
• 化学式: C₁₉H₂₁NO*ClH
• 分子量: 315.843
• InChiKey: LEGKVAWVLOPRMT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.41
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  12.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-benzyl-4-(4-methoxyphenyl)-1,2,3,6-tetrahydropyridine hydrochloride 在 palladium on activated charcoal 氢溴酸 、 氢气 作用下， 以 甲醇 、 水 为溶剂， 20.0 ℃ 、101.33 kPa 条件下， 反应 18.0h， 生成 4-(4-羟基苯基)哌啶
  参考文献：
  名称：

  New Strong Fibrates with Piperidine Moiety.

  摘要：

  合成并评估了结构中含有哌啶、4-羟基哌啶、哌啶-3-烯和哌嗪分子的新型纤维化合物。在合成的化合物中，2-[3-[1-（4-氟苯甲酰基）-哌啶-4-基]苯氧基]-2-甲基丙酸（9aA : AHL-157）在降低小鼠和大鼠甘油三酯、胆固醇和血糖方面的活性优于贝扎贝特。

  DOI：

  10.1248/cpb.48.1978
• 作为产物：
  描述：

  1-benzyl-4-(4-methoxy-phenyl)-piperidin-4-ol 在 盐酸 、 甲烷磺酸 作用下， 以 乙醚 、 乙酸乙酯 、 甲苯 为溶剂， 反应 4.0h， 生成 1-benzyl-4-(4-methoxyphenyl)-1,2,3,6-tetrahydropyridine hydrochloride
  参考文献：
  名称：

  Synthesis and SAR study of 4-arylpiperidines and 4-aryl-1,2,3,6-tetrahydropyridines as 5-HT2C agonists

  摘要：

  A series of substituted 4-arylpiperidines and a smaller family of 4-aryl-1,2,3,6-tetrahydropyridines were synthesized and their biological activity at the 5-HT2C receptor studied to determine whether either series showed noteworthy agonist activity. Structure-activity relationships were developed from the performed receptor binding assays and functional studies, and the results of the analysis are presented herein. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.01.122

文献信息

• ALPHA-SYNUCLEIN LIGANDS
  申请人：Washington University

  公开号：US20170189566A1

  公开（公告）日：2017-07-06

  The present invention generally relates to various compounds that are useful as α-synuclein ligands. The invention further relates to methods of using these compounds and their radiolabeled analogs for the detection of synucleinopathies, including Parkinson's disease (PD).

  本发明通常涉及作为α-突触核蛋白配体有用的各种化合物。该发明进一步涉及使用这些化合物及其放射标记类似物用于检测突触核蛋白病，包括帕金森病（PD）的方法。
• Alpha-synuclein ligands
  申请人：Washington University

  公开号：US10300155B2

  公开（公告）日：2019-05-28

  The present invention generally relates to various compounds that are useful as α-synuclein ligands. The invention further relates to methods of using these compounds and their radiolabeled analogs for the detection of synucleinopathies, including Parkinson's disease (PD).

  本发明一般涉及可用作α-突触核蛋白配体的各种化合物。本发明还涉及使用这些化合物及其放射性标记类似物检测突触核蛋白病（包括帕金森病）的方法。
• Synthesis and SAR study of 4-arylpiperidines and 4-aryl-1,2,3,6-tetrahydropyridines as 5-HT2C agonists
  作者：Richard J. Conway、Celine Valant、Arthur Christopoulos、Alan D. Robertson、Ben Capuano、Ian T. Crosby

  DOI：10.1016/j.bmcl.2012.01.122

  日期：2012.4

  A series of substituted 4-arylpiperidines and a smaller family of 4-aryl-1,2,3,6-tetrahydropyridines were synthesized and their biological activity at the 5-HT2C receptor studied to determine whether either series showed noteworthy agonist activity. Structure-activity relationships were developed from the performed receptor binding assays and functional studies, and the results of the analysis are presented herein. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.
• New Strong Fibrates with Piperidine Moiety.
  作者：Teruo KOMOTO、Hiroyuki HIROTA、Mari OTSUKA、Jiro KOTAKE、Susumu HASEGAWA、Hidehiko KOYA、Susumu SATO、Takao SAKAMOTO

  DOI：10.1248/cpb.48.1978

  日期：——

  New fibrates containing piperidine, 4-hydroxypiperidine, piperidin-3-ene, and piperazine moieties in the structures were synthesized and evaluated. Among the synthesized compounds, 2-[3-[1-(4-fluorobenzoyl)-piperidin-4yl]phenoxy]-2-methylpropanoic acid (9aA : AHL-157) showed very superior activities in decreasing triglyceride, cholesterol, and blood sugar compared to bezafibrate in mice and rats.

  合成并评估了结构中含有哌啶、4-羟基哌啶、哌啶-3-烯和哌嗪分子的新型纤维化合物。在合成的化合物中，2-[3-[1-（4-氟苯甲酰基）-哌啶-4-基]苯氧基]-2-甲基丙酸（9aA : AHL-157）在降低小鼠和大鼠甘油三酯、胆固醇和血糖方面的活性优于贝扎贝特。