1-((2-dimethylamino)ethyl)-2,3-dihydro-1H-indol-6-yl-amine | 174567-28-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 1-((2-dimethylamino)ethyl)-2,3-dihydro-1H-indol-6-yl-amine
• 英文别名: 1-(2-dimethylaminoethyl)-2,3-dihydro-1H-indol-6-ylamine；1-[2-(dimethylamino)ethyl]-2,3-dihydroindol-6-amine
• CAS: 174567-28-3
• 化学式: C₁₂H₁₉N₃
• 分子量: 205.303
• InChiKey: PPRQIXZNPDSXMR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  32.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-((2-dimethylamino)ethyl)-2,3-dihydro-1H-indol-6-yl-amine 、 5-氯-3-甲基苯并(B)噻吩-2-磺酰氯 生成 5-Chloro-3-methylbenzo[b]thiophene-2-sulfonic acid [1-(2-dimethylaminoethyl)-2,3-dihydro-1H-indol-6-yl]amide
  参考文献：
  名称：

  Sulphonamide derivatives, process for their preparation, and their use as medicaments

  摘要：

  本发明揭示了具有中枢神经系统活性的新型磺酰胺衍生物，其制备过程以及它们作为药物的用途。本化合物的结构式如下（I）或其盐：其中：P为苯并噻吩、苯并噻二唑、喹啉、苯并呋喃或吲哚；A为单键、C1-6烷基或C2-6烯基基团；R1为卤素、C1-6烷基（可选择地被一个或多个卤素原子取代）、C3-6环烷基、COC1-6烷基、C1-6烷氧基、OCF3、羟基、羟基C1-6烷基、羟基C1-6烷氧基、C1-6烷氧基C1-6烷氧基、硝基、氨基、C1-6烷基氨基或C1-6二烷基氨基、氰基，或R1为苯基、萘基；n为0、1、2、3、4、5或6；R2为氢、C1-6烷基或C1-6烷基芳基或R2与R3连接形成(CH2)2或(CH2)3基团；R3为R5基团或与R5共同形成(CH2)2O或(CH2)3O基团，或R3与R2连接形成(CH2)2或(CH2)3基团；R4为N-哌嗪环，可选择地被C1-6烷基取代；R5为氢、卤素、C1-6烷基、C3-6环烷基、COC1-6烷基、C1-6烷氧基、羟基、羟基C1-6烷基、羟基C1-6烷氧基、C1-6烷氧基C1-6烷氧基、硝基、三氟甲基、氰基或芳基。

  公开号：

  US06599904B2

文献信息

• Substitited indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds, their prepartion and use in medicaments
  申请人：Esteve Laboratorios Dr. Esteve S.A.

  公开号：EP1676841A1

  公开（公告）日：2006-07-05

  The present invention relates to substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds of general formula I, a process for their preparation, medicaments comprising said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds as well as the use of said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds for the preparation of medicaments, which are particularly suitable for the prophylaxis and/or treatment of disorders or diseases that are at least partially mediated via 5-HT6 receptors.

  本发明涉及通式I的取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物，其制备方法，包含所述取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物的药物，以及利用所述取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物制备药物，该药物特别适用于预防和/或治疗至少部分通过5-HT6受体介导的疾病或疾病。
• [EN] SULPHONAMIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS MEDICAMENTS<br/>[FR] DERIVES DE SULFAMIDE, PROCEDE DE PREPARATION DE CES DERIVES ET UTILISATION DE CES DERNIERS EN TANT QUE MEDICAMENTS
  申请人：SMITHKLINE BEECHAM PLC

  公开号：WO1998027081A1

  公开（公告）日：1998-06-25

  (EN) Novel sulphonamide derivatives having CNS activity, processes for their preparation and their use as medicaments.(FR) On décrit de nouveaux dérivés de sulfamique ayant une activité sur le système nerveux central (SNC), des procédés de préparation de ces nouveaux composés ainsi que leur utilisation en tant que médicaments.

  （中）描述了具有中枢神经系统活性的新型磺酰胺衍生物，其制备过程以及它们作为药物的用途。
• Substituted Indazolyl Sulfonamide and 2,3-Dihydro-Indolyl Sulfonamide Compounds, their Preparation and Use in Medicaments
  申请人：Merce Vidal Ramon

  公开号：US20090005417A1

  公开（公告）日：2009-01-01

  The present invention relates to substituted indazolyl sulfonamide and 2,3-dihydroindolyl sulfonamide compounds of general formula I, a process for their preparation, medicaments comprising said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds as well as the use of said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds for the preparation of medicaments, which are particularly suitable for the prophylaxis and/or treatment of disorders or diseases that are at least partially mediated via 5-HT 6 receptors.

  本发明涉及一般式I的取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物，以及它们的制备方法、包含所述取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物的药物，以及利用所述取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物制备药物，特别适用于预防和/或治疗通过5-HT6受体介导的至少部分疾病或疾病的用途。
• Melanin concentrating hormone antagonist
  申请人：Kato Kaneyoshi

  公开号：US20070173498A1

  公开（公告）日：2007-07-26

  A melanin-concentrating hormone antagonist which comprises a compound of the formula: wherein Ar 1 is a cyclic group which may have substituents; X is a spacer having a main chain of 1 to 6 atoms; Y is a bond or a spacer having a main chain of 1 to 6 atoms; Ar is a monocyclic aromatic ring which may be condensed with a 4 to 8 membered non-aromatic ring, and may have further substituents; R 1 and R 2 are independently hydrogen atom or a hydrocarbon group which may have substituents; R 1 and R 2 , together with the adjacent nitrogen atom, may form a nitrogen-containing hetero ring which may have substituents; R 2 may form a spiro ring together with Ar; or R 2 , together with the adjacent nitrogen atom and Y, may form a nitrogen-containing hetero ring which may have substituents; or a salt thereof; which is useful as an agent for preventing or treating obesity, etc.

  一种黑色素浓集激素拮抗剂，包括一个化合物，其化学式为：其中Ar1是一个环状基团，可能具有取代基；X是一个具有1到6个原子主链的间隔物；Y是一条键或具有1到6个原子主链的间隔物；Ar是一个单环芳香环，可以与一个4到8个成员的非芳香环融合，并且可能有进一步的取代基；R1和R2分别是氢原子或一个可能具有取代基的碳氢基团；R1和R2连同相邻的氮原子可以形成一个含氮杂环，该杂环可能具有取代基；R2可以与Ar一起形成一个螺环；或者R2连同相邻的氮原子和Y可以形成一个含氮杂环，该杂环可能具有取代基；或其盐；用作预防或治疗肥胖等的药剂。
• AMIDE DERIVATIVES HAVING 5HT1D-ANTAGONIST ACTIVITY
  申请人：SMITHKLINE BEECHAM PLC

  公开号：EP0763034A1

  公开（公告）日：1997-03-19