N-(3-Trifluormethylphenyl)-pyridin-3-amidin | 23564-97-8

• 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-Trifluormethylphenyl)-pyridin-3-amidin
• 英文别名: N-(3-trifluoromethyl-phenyl)-nicotinamidine；N-(alpha,alpha,alpha-Trifluoro-m-tolyl)nicotinamidine；N'-[3-(trifluoromethyl)phenyl]pyridine-3-carboximidamide
• CAS: 23564-97-8
• 化学式: C₁₃H₁₀F₃N₃
• 分子量: 265.238
• InChiKey: OWXPTUNZVBFFRK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  51.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-氰基吡啶 、 间氨基三氟甲苯 在 三氯化铝 作用下， 以 various solvent(s) 为溶剂， 反应 0.5h， 以3%的产率得到N-(3-Trifluormethylphenyl)-pyridin-3-amidin
  参考文献：
  名称：

  Synthesis and antiinflammatory activity of N1-(substituted phenyl)pyridinecarboxamidines.

  摘要：

  通过在氯化铝或钠胺的存在下，将取代的芳香胺与氰基吡啶缩合，合成了一系列N1-(取代苯基)吡啶羧氨基。在合成N1-烷氧基苯基吡啶羧氨基的过程中，发现邻烷氧基芳香胺与氯化铝反应生成邻氨基酚，而间位和对位的烷氧基芳香胺几乎没有去烷基化。成功地使用钠胺将邻烷氧基芳香胺与氰基吡啶进行缩合。在几种活性衍生物中，N1-(2,4-二氯苯基)吡啶羧氨基和N1-(4-氯苯基)吡啶羧氨基表现出显著的抗炎活性。

  DOI：

  10.1248/cpb.31.2484

文献信息

• AMIDINOHETEROCYCLES AS MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE
  申请人：Combs Andrew P.

  公开号：US20080119491A1

  公开（公告）日：2008-05-22

  The present invention is directed to amidino heterocyclic compounds which are modulators of indoleamine 2,3-dioxygenase (IDO), as well as to pharmaceutical compositions comprising such compounds and to pharmaceutical methods of treatment comprising administration of such compounds and pharmaceutical compositions.

  本发明涉及对吲哌酮胺 2,3-双氧酶 (IDO) 的调节剂的酰胺杂环化合物，以及包含这种化合物的药物组合物和包括给予这种化合物和药物组合物的治疗药物方法。
• HISANO, TAKUZO;TASAKI, MASANOBU;TSUMOTO, KONOSUKE;MATSUOKA, TOSHIKAZU;ICH+, CHEM. AND PHARM. BULL., 1983, 31, N 7, 2484-2490
  作者：HISANO, TAKUZO、TASAKI, MASANOBU、TSUMOTO, KONOSUKE、MATSUOKA, TOSHIKAZU、ICH+

  DOI：——

  日期：——
• [EN] AMIDINOHETEROCYCLES AS MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE<br/>[FR] AMIDINOHÉTÉROCYCLES MODULATEURS DE L'INDOLÉAMINE 2,3-DIOXYGÉNASE
  申请人：INCYTE CORP

  公开号：WO2008036643A2

  公开（公告）日：2008-03-27

  [EN] The present invention is directed to amidino heterocyclic compounds which are modulators of indoleamine 2,3-dioxygenase (IDO), as well as to pharmaceutical compositions comprising such compounds and to pharmaceutical methods of treatment comprising administration of such compounds and pharmaceutical compositions.
  [FR] La présente invention concerne des composés amidino hétérocycliques modulateurs de l'indoléamine 2,3-dioxygénase (IDO), des compositions pharmaceutiques comprenant de tels composés, et des traitements pharmaceutiques comprenant l'administration de tels composés et compositions pharmaceutiques.
• Synthesis and antiinflammatory activity of N1-(substituted phenyl)pyridinecarboxamidines.
  作者：TAKUZO HISANO、MASANOBU TASAKI、KONOSUKE TSUMOTO、TOSHIKAZU MATSUOKA、MASATAKA ICHIKAWA

  DOI：10.1248/cpb.31.2484

  日期：——

  A series of N1-(substituted phenyl) pyridinecarboxamidines was synthesized by the condensation of substituted anilines with cyanopyridines in the presence of aluminum chloride or sodium amide and these compounds were evaluated for antiinflammatory activity by the carrageenin-induced rat paw edema assay. In the synthesis of N1-alkoxyphenyl pyridinecarboxamidines, it was found that o-alkoxyanilines reacted with aluminum chloride to afford o-aminophenol, while m- and p-alkoxyanilines were scarcely dealkylated. Sodium amide was successfully used for the condensation of o-alkoxyanilines with cyanopyridines. Among several active derivatives, N1-(2, 4-dichlorophenyl) pyridinecarboxamidine and N1-(4-chlorophenyl)-pyridinecarboxamidine exhibited significant antiinflammatory activities.

  通过在氯化铝或钠胺的存在下，将取代的芳香胺与氰基吡啶缩合，合成了一系列N1-(取代苯基)吡啶羧氨基。在合成N1-烷氧基苯基吡啶羧氨基的过程中，发现邻烷氧基芳香胺与氯化铝反应生成邻氨基酚，而间位和对位的烷氧基芳香胺几乎没有去烷基化。成功地使用钠胺将邻烷氧基芳香胺与氰基吡啶进行缩合。在几种活性衍生物中，N1-(2,4-二氯苯基)吡啶羧氨基和N1-(4-氯苯基)吡啶羧氨基表现出显著的抗炎活性。