1-o-tolyl-piperidine-4-carboxylic acid | 607354-74-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 1-o-tolyl-piperidine-4-carboxylic acid
• 英文别名: 1-(2-Methylphenyl)piperidine-4-carboxylic acid
• CAS: 607354-74-5
• 化学式: C₁₃H₁₇NO₂
• 分子量: 219.283
• InChiKey: QYDPRJUEQSCLHS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  40.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-氨基-2H-1,4-苯并吗啉-3(4H)-酮 、 1-o-tolyl-piperidine-4-carboxylic acid 生成 1-o-Tolyl-piperidine-4-carboxylic acid (3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-amide
  参考文献：
  名称：

  Discovery of piperidine carboxamide TRPV1 antagonists

  摘要：

  A series of piperidine carboxamides were developed as potent antagonists of the transient receptor potential vanilloid-1 (TRPV1), an emerging target for the treatment of pain. A focused library of polar head groups led to the identification of a benzoxazinone amide that afforded good potency in cell-based assays. Synthesis and a QSAR model will be presented. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.07.035
• 作为产物：
  描述：

  哌啶-4-甲酸乙酯 在 氢氧化钾 、 tris(dibenzylideneacetone)dipalladium (0) 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 、 sodium t-butanolate 作用下， 以 四氢呋喃 、 甲醇 、 甲苯 为溶剂， 反应 2.0h， 生成 1-o-tolyl-piperidine-4-carboxylic acid
  参考文献：
  名称：

  Preparation of a Series of Aryl Isonipecotic Acids Using Microwave Irradiation

  摘要：

  Rapid parallel synthesis of arylisonipecotic acids was achieved using microwave irradiation of a palladium catalyzed amination reaction.

  DOI：

  10.1081/scc-120021042

文献信息

• 4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
  申请人：Calvo R. Raul

  公开号：US20060116368A1

  公开（公告）日：2006-06-01

  This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.

  这项发明涉及辣椒素受体VR1配体。更具体地说，这项发明涉及对VR1具有潜在调节作用的杂环异尼泊酸酰胺，这些化合物对于治疗和预防哺乳动物的疾病状况是有用的。
• Hetero isonipecotic modulators of vanilloid VR1 receptor
  申请人：Gaul D. Michael

  公开号：US20050288281A1

  公开（公告）日：2005-12-29

  This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.

  这项发明涉及辣椒素受体VR1配体，更具体地说，涉及异构异壳胺酰胺，它们是VR1的有效调节剂，可用于哺乳动物的疾病的治疗和预防。
• AZOLECARBOXAMIDE DERIVATIVE
  申请人：Sugasawa Keizo

  公开号：US20090286766A1

  公开（公告）日：2009-11-19

  Provided is an agent for treating or preventing urinary frequency, urinary urgency and urinary, incontinence which are associated with overactive bladder, a lower urinary tract disease such as interstitial cystitis and chronic prostatitis accompanied by lower urinary tract pain, and various diseases accompanied by pain. A novel azolecarboxamide derivative in which an azole ring such as thioazole or oxazole is bonded to a benzene ring, pyridine ring or pyrimidine ring through carboxamide was confirmed to have a potent trkA receptor-inhibitory activity and found to be an agent for treating or preventing lower urinary tract disease and various diseases accompanied by pain, which is excellent in efficacy and safety, and thus the present invention was accomplished.

  提供了一种用于治疗或预防与过度活跃膀胱、下泌尿道疾病（如间质性膀胱炎和慢性前列腺炎伴随下泌尿道疼痛）以及伴随疼痛的各种疾病相关的尿频、尿急和尿失禁的药剂。一种新型的唑烷羧酰胺衍生物，其中唑环（如硫唑环或噁唑环）通过羧酰胺键连接到苯环、吡啶环或嘧啶环上，被证实具有强效的trkA受体抑制活性，并被发现是一种用于治疗或预防下泌尿道疾病和伴随疼痛的各种疾病的药剂，其疗效和安全性优异，因此本发明得以完成。
• US8163746B2
  申请人：——

  公开号：US8163746B2

  公开（公告）日：2012-04-24
• [EN] 4-PIPERIDINECARBOXAMIDE MODULATORS OF VANILLOID VR1 RECEPTOR<br/>[FR] MODULATEURS DE 4-PIPERIDINECARBOXAMIDE DU RECEPTEUR VANILLOIDE VR1
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2006058338A2

  公开（公告）日：2006-06-01

  [EN] This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
  [FR] Cette invention concerne des ligands du récepteur vanilloïde VR1. Plus particulièrement, l'invention concerne des amides isonipecotiques qui sont des modulateurs puissants convenant pour le traitement et la prévention de divers états pathologiques chez les mammifères.