9-methyl-9H-carbazol-2-amine | 86439-57-8

• 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: 9-methyl-9H-carbazol-2-amine
• 英文别名: amino-2 methyl-9 carbazole；2-amino-9-methylcarbazole；9-methylcarbazole-2-amine；9-methyl-carbazol-2-ylamine；9-Methyl-carbazol-2-ylamin；9-methylcarbazol-2-amine
• CAS: 86439-57-8
• 化学式: C₁₃H₁₂N₂
• 分子量: 196.252
• InChiKey: ONLJJWBTWXCFHW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  31
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  9-methyl-9H-carbazol-2-amine 在 盐酸 、 sodium azide 、 sodium nitrite 作用下， 生成 2-azido-9-methyl-carbazole
  参考文献：
  名称：

  Preparation and Absorption Spectra of Analogous Dibenzothiophene, Dibenzoselenophene and Carbazole Compounds¹

  摘要：

  DOI：

  10.1021/ja01609a047
• 作为产物：
  描述：

  2-硝基咔唑 在 palladium on activated charcoal 一水合肼 作用下， 以 乙醇 为溶剂， 反应 4.0h， 生成 9-methyl-9H-carbazol-2-amine
  参考文献：
  名称：

  摘要：

  2-, 3- and 4-Pivaloylamino derivatives of dibenzofuran [compounds (5), (4) and (6), respectively] and analogous 3-, 2- and 1-substituted derivatives of 9-methylcarbazole [compounds (8), (7) and (9), respectively] were subjected to lithiation at 0 degreesC and subsequent reaction with dimethylformamide. Aldehyde formation took place at positions alpha to delta to the heteroatom as follows: alpha for (4) and (7); delta for (5); delta and beta (3 : 1) for (8); and alpha' for (6). No formylation occurred with (9).

  DOI：

  10.1071/ch01017

文献信息

• Carbazole and Carboline Compounds for Use in the Diagnosis, Treatment, Alleviation or Prevention of Disorders Associated with Amyloid or Amyloid-Like Proteins
  申请人：AC IMMUNE SA

  公开号：US20170002005A1

  公开（公告）日：2017-01-05

  The present invention relates to novel compounds that can be employed in the diagnosis, treatment, alleviation or prevention of a group of disorders and abnormalities associated with amyloid proteins and amyloid-like proteins, such as Alzheimer's disease. Precursors for the preparation of the compounds according to the present invention are also provided.

  本发明涉及可用于诊断、治疗、缓解或预防与淀粉样蛋白和类淀粉样蛋白相关的一组疾病和异常的新化合物，如阿尔茨海默病。本发明还提供了制备这些化合物的前体。
• [EN] 1-CYANO-PYRROLIDINE DERIVATIVES AS INHIBITORS OF USP30.<br/>[FR] DÉRIVÉS DE 1-CYANO-PYRROLIDINE EN TANT QU'INHIBITEURS DE L'USP 30
  申请人：MISSION THERAPEUTICS LTD

  公开号：WO2017093718A1

  公开（公告）日：2017-06-08

  The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylatingenzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C- terminal hydrolase 30 or Ubiquitin Specific Peptidase 30 (USP30). The invention further relates to the use of DUB inhibitors in the treatment of conditions involving mitochondrial dysfunction and cancer. Compounds of the invention include compounds having the formula (I) (I) or a pharmaceutically acceptable salt thereof, wherein R1, R 2, R 3, m, L and X are as defined herein.

  本发明涉及新颖化合物和制备去泛素酶（DUBs）抑制剂的方法。具体而言，本发明涉及抑制泛素C-末端水解酶30或泛素特异性肽酶30（USP30）。本发明还涉及在治疗涉及线粒体功能障碍和癌症的疾病中使用DUB抑制剂。本发明的化合物包括具有以下结构式（I）的化合物或其药用盐，其中R1、R2、R3、m、L和X如本文所定义。
• Pyrrolo(1',2':1,2)pyrazino(6,5-b)carbazoles.
  作者：JEAN-CHARLES LANCELOT、JEAN-MARIE GAZENGEL、SYLVAIN RAULT、MAX ROBBA

  DOI：10.1248/cpb.31.45

  日期：——

  The synthesis of the new heterocycles pyrrolo [1', 2' : 1, 2] pyrazino [6, 5-b] carbazoles was achieved by the intramolecular cyclisation of 2-(1-pyrrolyl) carbazole derivatives. These latter compounds were obtained by the Clauson-Kaas reaction starting from the corresponding 2-aminocarbazoles, obtained by reduction of 2-nitrocarbazoles. A study of this reduction has shown that the introduction of acetyl grouping in position 9 makes this reaction easier and gives better results than previous methods. 1H-NMR spectra are studied.

  新杂环吡咯 [1', 2' : 1, 2] 吡嗪并 [6, 5-b] 咔唑的合成是通过 2-(1-吡咯基) 咔唑衍生物的分子内环化反应实现的。后一种化合物是通过克劳森-卡斯反应从相应的 2-氨基咔唑（由 2-硝基咔唑还原而成）获得的。对该还原反应的研究表明，在第 9 位引入乙酰基使该反应更容易进行，并比以前的方法得到更好的结果。对 1H-NMR 光谱进行了研究。
• Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
  申请人：Glenn Wayne Robert

  公开号：US20050217038A1

  公开（公告）日：2005-10-06

  Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and one or more tricyclic fused 6-5-6 heteroaromatic keratin dyeing compounds having one heteroatom. A method for oxidative dyeing of keratin fibers, comprising applying such compositions in the presence of an oxidizing agent, for a period sufficient to develop the desired coloration.

  这段话的中文翻译如下： 本发明涉及一种用于氧化染色角蛋白纤维的组合物，包括适合染色的介质和一种或多种三环融合的6-5-6杂环角蛋白染料化合物，其中含有一个杂原子。一种氧化染色角蛋白纤维的方法，包括在氧化剂的存在下应用这种组合物，以便在足够的时间内发展所需的颜色。
• Keratin Dyeing Compounds, Keratin Dyeing Compositions Containing Them, And Use Thereof
  申请人：Glenn Wayne Robert

  公开号：US20080098535A1

  公开（公告）日：2008-05-01

  Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and one or more tricyclic fused 6-5-6 heteroaromatic keratin dyeing compounds having one heteroatom. A method for oxidative dyeing of keratin fibers, comprising applying such compositions in the presence of an oxidizing agent, for a period sufficient to develop the desired coloration.

  含氧化染料的角蛋白纤维氧化染色组合物，包括适于染色的介质和一个或多个三环融合6-5-6杂环角蛋白染料化合物，其中含有一个杂原子。一种氧化染色角蛋白纤维的方法，包括在氧化剂存在下应用这种组合物，以达到所需的着色时间。