6-bromo-N-(2-phenylethyl)-2,3,4,9-tetrahydro-1H-carbazol-1-amine | 132214-09-6

• 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: 6-bromo-N-(2-phenylethyl)-2,3,4,9-tetrahydro-1H-carbazol-1-amine
• CAS: 132214-09-6
• 化学式: C₂₀H₂₁BrN₂
• 分子量: 369.304
• InChiKey: TZMBEIZTFFHEHF-UHFFFAOYSA-N

物化性质

• 沸点：
  535.0±50.0 °C(Predicted)
• 密度：
  1.40±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  27.8
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  6-溴-2,3,4,9-四氢咔唑-1-酮 在 sodium tetrahydroborate 作用下， 以 乙醇 、 xylene 为溶剂， 反应 9.0h， 生成 6-bromo-N-(2-phenylethyl)-2,3,4,9-tetrahydro-1H-carbazol-1-amine
  参考文献：
  名称：

  Antitubercular, antifungal, and antibacterial activity in vitro of 1-phenethylamino-1,2,3,4-tetrahydrocarbazoles

  摘要：

  DOI：

  10.1007/bf00768385

文献信息

• [EN] COMPOSITIONS AND METHODS FOR VIRAL INHIBITION<br/>[FR] COMPOSITIONS ET PROCEDES D'INHIBITION VIRALE
  申请人：CHIRON CORP

  公开号：WO2005037791A1

  公开（公告）日：2005-04-28

  The present invention discloses methods and compositions for viral inhibition, particularly inhibition of HCV and SARS. The invention also provides compositions including carbazole derivatives useful for viral inhibition.

  本发明公开了用于病毒抑制的方法和组合物，特别是用于HCV和SARS的抑制。该发明还提供了包括对病毒抑制有用的咔唑衍生物的组合物。
• [EN] NOVEL MEANS AND METHODS FOR TREATING DISEASES OF THE CENTRAL NERVOUS SYSTEM, METABOLIC AND CARDIAC DISEASES AND AGING<br/>[FR] NOUVEAUX MOYENS ET MÉTHODES POUR LE TRAITEMENT DE MALADIES DU SYSTÈME NERVEUX CENTRAL, DE MALADIES CARDIAQUES ET MÉTABOLIQUES ET DU VIEILLISSEMENT
  申请人：UNIV MUENCHEN L MAXIMILIANS

  公开号：WO2013139929A1

  公开（公告）日：2013-09-26

  This invention relates to a compound of formula (la) or (Ila) wherein either (A) R1 is I and R2 is selected from substituted or unsubstituted piperidinyl, preferably N-substituted or unsubstituted piperidin-4-yl; substituted or unsubstituted cyclohexyl, cyclopentyl, or cyclohexyl alkyl; substituted or unsubstituted aryl-alkyl; alkyl; aryl; - CHO; and hydrogen; or (B) R1 is selected from halogen; substituted or unsubstituted alkoxy; substituted or unsubstituted alkyl; cyano; and hydrogen; and R2 is substituted or unsubstituted piperidinyl, preferably N-substituted or unsubstituted piperidin-4-yl; and R3, R4 and R5 independently are either H or defined as R1; R6 is H; alkyl or aryl-alkyl, or R2 and R6 together with the N attached thereto form a 5- or 6-membered ring, preferably pyrrol; each of the m occurrences of R7 is independently selected from C1 to C4 alkyl, C1 to C4 alkoxy and halogen, preferably F; and m being 0, 1, 2, 3 or 4; X is selected from NH; N-alkyl, preferably NCH3; N- aryl-alkyl; S; and O; wherein in formula (la) R2 and X together may alternatively form or comprise a 6-membered ring, said 6-membered ring preferably being piperazine; n is 0, 1 or 2; the substituents being independently selected from alkyl, aryl-alkyl; alkoxy, aryl, hydroxy; halogen; oxo; and thio; alkyl being branched, unbranched and/or cyclic C1 to C10 alkyl, preferably branched or unbranched C1 to C4 alkyl, more preferably methyl, ethyl, n-propyl, i- propyl, i-butyl or t-butyl; alkoxy being C1 to C4 alkoxy, preferably methoxy; aryl being phenyl, naphthyl or tetrahydronaphthyl, preferably phenyl; or a compound of any one of Tables 3 to 46; or a salt or hydrate thereof.

  本发明涉及一种化合物，其化学式为（Ia）或（IIa），其中（A）R1为I，R2选自取代或未取代的哌啶基，优选N-取代或未取代的哌啶-4-基；取代或未取代的环己基、环戊基或环己基烷基；取代或未取代的芳基-烷基；烷基；芳基；-CHO；和氢；或者（B）R1选自卤素；取代或未取代的烷氧基；取代或未取代的烷基；氰基；和氢；R2为取代或未取代的哌啶基，优选N-取代或未取代的哌啶-4-基；R3、R4和R5独立地为H或被定义为R1；R6为H；烷基或芳基-烷基，或者R2和R6与其连接的N共同形成5-或6-成员环，优选吡咯；每个R7的m次出现独立地选自C1到C4烷基、C1到C4烷氧基和卤素，优选F；m为0、1、2、3或4；X选自NH；N-烷基，优选NCH3；N-芳基-烷基；S；和O；其中在化学式（Ia）中，R2和X共同可以形成或包含一个6-成员环，该6-成员环优选为哌嗪；n为0、1或2；取代基独立地选自烷基、芳基-烷基；烷氧基、芳基、羟基；卤素；氧化物；和硫代基；烷基为支链、直链和/或环状C1到C10烷基，优选支链或直链C1到C4烷基，更优选甲基、乙基、正丙基、异丙基、异丁基或叔丁基；烷氧基为C1到C4烷氧基，优选甲氧基；芳基为苯基、萘基或四氢萘基，优选苯基；或者为表3至表46中的任一化合物；或其盐或水合物。
• Compositions and Methods for Viral Inhibition
  申请人：Ni Zhi-Jie

  公开号：US20070276009A1

  公开（公告）日：2007-11-29

  The present invention discloses methods and compositions for viral inhibition, particularly inhibition of HCV and SARS. The invention also provides compositions including carbazole derivatives useful for viral inhibition.

  本发明揭示了病毒抑制的方法和组合物，特别是对HCV和SARS的抑制。本发明还提供了包括咔唑衍生物的组合物，用于病毒抑制。
• NOVEL CYCLOALKYL[B] CONDENSED INDOLES
  申请人：SMITHKLINE BEECHAM CORPORATION

  公开号：EP1658068B1

  公开（公告）日：2009-02-18
• COMPOSITIONS AND METHODS FOR VIRAL INHIBITION
  申请人：CHIRON CORPORATION

  公开号：EP1678137A1

  公开（公告）日：2006-07-12