1-(benzenesulfonyl)-4-(2-nitrovinyl)-1H-indole | 1059131-14-4

• 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-(benzenesulfonyl)-4-(2-nitrovinyl)-1H-indole
• 英文别名: 1-(Benzenesulphonyl)-4-(2-nitrovinyl)-1H-indole；4-[(E)-2-nitrovinyl]-1-(phenylsulfonyl)-1H-indole；1-(benzenesulfonyl)-4-[(E)-2-nitroethenyl]indole
• CAS: 1059131-14-4
• 化学式: C₁₆H₁₂N₂O₄S
• 分子量: 328.348
• InChiKey: RDIKXFQGJIOBQY-FMIVXFBMSA-N

物化性质

• 沸点：
  565.7±42.0 °C(Predicted)
• 密度：
  1.36±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  93.3
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(benzenesulfonyl)-4-(2-nitrovinyl)-1H-indole 在 nickel boride sodium tetrahydroborate 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 3.58h， 生成 2-[1-(benzenesulphonyl)-1H-indol-4-yl]ethylamine
  参考文献：
  名称：

  WO2008/110598

  摘要：

  公开号：
• 作为产物：
  描述：

  4-吲哚甲醛 在 ammonium acetate 、 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.05h， 生成 1-(benzenesulfonyl)-4-(2-nitrovinyl)-1H-indole
  参考文献：
  名称：

  WO2008/110598

  摘要：

  公开号：

文献信息

• Indole and indoline derivatives as 5-HT6 selective ligands
  申请人：Merck Sharp & Dohme Ltd.

  公开号：US06187805B1

  公开（公告）日：2001-02-13

  Three classes of indole and indoline derivatives are disclosed as ligands selective for the 5-HT6 receptors, and hence of value in the treatment or prevention of CNS disorders, including Alzheimer's disease, Parkinson's disease, schizophrenia, depression and anxiety. A particular class, 1-substituted-4-(&ohgr;-N,N-dialkyl-aminoalkyl)indoles, are claimed as novel compounds.

  揭示了三类吲哚和吲哚啉衍生物作为选择性结合到5-HT6受体的配体，因此在治疗或预防中枢神经系统疾病方面具有价值，包括阿尔茨海默病、帕金森病、精神分裂症、抑郁症和焦虑症。其中一类称为1-取代-4-(&ohgr;-N,N-二烷基氨基烷基)吲哚，被称为新型化合物。
• New compounds
  申请人：Angbrant Johan

  公开号：US20080293694A1

  公开（公告）日：2008-11-27

  The present invention relates to novel compounds of formula (I): wherein R 1 , R 2 , R 3 , R 4 , and R 5 are as described herein, to pharmaceutical compositions comprising the compounds, to processes for their preparation, as well as to the use of the compounds for the preparation of a medicament against 5-HT 6 receptor-related disorders.

  本发明涉及一种新型化合物，其化学式为(I)：其中R1、R2、R3、R4和R5如本文所述，以及包含该化合物的制药组合物，其制备过程以及利用该化合物制备用于治疗5-HT6受体相关疾病的药物的使用。
• Sulfonyl-indole derivatives
  申请人：Proximagen Limited

  公开号：US08138333B2

  公开（公告）日：2012-03-20

  The present invention relates to novel compounds of formula (I): wherein R1, R2, R3, R4, and R5 are as described herein, to pharmaceutical compositions comprising the compounds, to processes for their preparation, as well as to the use of the compounds for the preparation of a medicament against 5-HT6 receptor-related disorders.

  本发明涉及公式（I）的新化合物：其中R1、R2、R3、R4和R5如本文所述，以及包含这些化合物的制药组合物，其制备过程，以及使用这些化合物制备针对5-HT6受体相关疾病的药物的用途。
• <i>N</i>-Arylsulfonylindole Derivatives as Serotonin 5-HT₆ Receptor Ligands
  作者：Michael G. N. Russell、Robert J. Baker、Laura Barden、Margaret S. Beer、Linda Bristow、Howard B. Broughton、Michael Knowles、George McAllister、Smita Patel、José L. Castro

  DOI：10.1021/jm010943m

  日期：2001.11.1

  A series of N-1-arylsulfonyltryptamines were found to be potent ligands of the human serotonin 5-HT6 receptor with the 5-methoxy-1-benzenesulfonyl analogue (19) having the highest affinity. Additionally, it was discovered that a group such as 3-(3-methoxybenzyl)-1,2,4-oxadiazol-5-yI in the 2-position of the indole ring (43) can replace the arylsulfonyl substituent in the 1-position with no loss of affinity. This suggested that the binding conformation of the aminoethyl side chain at this receptor was toward the 4-position of the indole ring and was supported by the fact that the 4-(aminoethyl)indoles (45) also displayed high affinity, as did the conformationally rigid 1,3,4,5-tetrahydrobenz[c,d]indole (49). Molecular modeling showed that 19, 43, and 45 all had low-energy conformers that overlaid well onto 49. Both 19 and 49 had good selectivity over other serotonin receptors tested, with 49 also showing excellent selectivity over all dopamine receptors. In a functional adenylate cyclase stimulation assay, 19 and 49 had no agonist activity, whereas 45 behaved as a partial agonist. Finally, it was shown that 19 had good activity in the 5-HT2A centrally mediated mescaline-induced head twitch assay, which implies that it is brain-penetrant.
• US6187805B1
  申请人：——

  公开号：US6187805B1

  公开（公告）日：2001-02-13