4-(Pyridin-4-yloxy)-benzenethiol | 193022-95-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-(Pyridin-4-yloxy)-benzenethiol
• 英文别名: 4-(4-pyridyloxy)thiophenol；4-pyridin-4-yloxybenzenethiol
• CAS: 193022-95-6
• 化学式: C₁₁H₉NOS
• 分子量: 203.265
• InChiKey: QDAJYXULPGKGRC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  23.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(Pyridin-4-yloxy)-benzenethiol 在 air 作用下， 以 四氢呋喃 为溶剂， 反应 19.0h， 以0.061 g的产率得到4-(4-pyridoxy)phenyl disulfide
  参考文献：
  名称：

  Synthesis of dihydroindolizines for potential photoinduced work function alteration

  摘要：

  Seeking to immobilize photochromophores on metallic surfaces, we have synthesized four molecules which contain both a photoresponsive dihydroindolizine (DHI) core and a sulfur containing moiety, which allow for their assembly onto gold substrates. Sonogashira, Suzuki, or Ullmann couplings are employed to generate pyridines with pendant thioacetates (or disulfides). The pyridines are condensed with spiro[2-cyclopropene-1,9'[9H]fluorene]-2,3-dimethyl ester affording the targeted DHIs. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.10.097
• 作为产物：
  描述：

  4-碘吡啶 在 copper(l) iodide 、 四丁基氟化铵 、 caesium carbonate 、 聚甘氨酸 作用下， 以 四氢呋喃 、 二甲基亚砜 为溶剂， 反应 27.5h， 生成 4-(Pyridin-4-yloxy)-benzenethiol
  参考文献：
  名称：

  Synthesis of dihydroindolizines for potential photoinduced work function alteration

  摘要：

  Seeking to immobilize photochromophores on metallic surfaces, we have synthesized four molecules which contain both a photoresponsive dihydroindolizine (DHI) core and a sulfur containing moiety, which allow for their assembly onto gold substrates. Sonogashira, Suzuki, or Ullmann couplings are employed to generate pyridines with pendant thioacetates (or disulfides). The pyridines are condensed with spiro[2-cyclopropene-1,9'[9H]fluorene]-2,3-dimethyl ester affording the targeted DHIs. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.10.097

文献信息

• Aromatic sulfone hydroxamic acid metalloprotease inhibitor
  申请人：——

  公开号：US20040235818A1

  公开（公告）日：2004-11-25

  A treatment process is disclosed that comprises administering an effective amount of an aromatic sulfone hydroxamic acid that exhibits excellent inhibitory activity of one or more matrix metalloprotease (MMP) enzymes, such as MMP-2, MMP-9 and MMP-13, while exhibiting substantially less inhibition at least of MMP-1 to a host having a condition associated with pathological matrix metalloprotease activity. Also disclosed are metalloprotease inhibitor compounds having those selective activities, processes for manufacture of such compounds and pharmaceutical compositions using an inhibitor. A contemplated compound corresponds in structure to formula B, below, 1

  本发明揭示了一种治疗过程，其中包括向患有与病理基质金属蛋白酶活性相关的病情的宿主施用一种有效量的芳香磺酰羟肟酸，该肟酸表现出对一种或多种基质金属蛋白酶（MMP）酶的出色抑制活性，例如MMP-2、MMP-9和MMP-13，同时对至少MMP-1的抑制作用明显较少。还揭示了具有这些选择性活性的金属蛋白酶抑制剂化合物，制造这种化合物的过程以及使用抑制剂的制药组合物。考虑的化合物与下面的B式结构相对应，1。
• Hydroxamic and carboxylic acid derivatives having MMP and TNF inhibitory activity
  申请人：——

  公开号：US20030207889A1

  公开（公告）日：2003-11-06

  Hydroxamic and carboxylic acid derivatives having MMP and TNF inhibitory activity.

  具有MMP和TNF抑制活性的羟肟酸和羧酸衍生物。
• Matrix metalloprotease inhibitors
  申请人：F. HOFFMANN-LA ROCHE AG

  公开号：EP0780386B1

  公开（公告）日：2002-10-02
• AROMATIC SULFONE HYDROXAMIC ACID METALLOPROTEASE INHIBITOR
  申请人：G.D. SEARLE & CO.

  公开号：EP1183239A1

  公开（公告）日：2002-03-06
• US5932595A
  申请人：——

  公开号：US5932595A

  公开（公告）日：1999-08-03