2-甲基-5-(4-甲基-1-哌嗪基)苯胺 | 1007211-93-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 中文名称: 2-甲基-5-(4-甲基-1-哌嗪基)苯胺
• 英文名称: 2-methyl-5-(4-methylpiperazin-1-yl)aniline
• 英文别名: 2-methyl-5-(4-methyl-piperazin-1-yl)-phenylamine；2-Methyl-5-(4-methylpiperazin-1-yl)benzenamine
• CAS: 1007211-93-9
• 化学式: C₁₂H₁₉N₃
• 分子量: 205.303
• InChiKey: FCMGLBKFHTXSER-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  15
• 可旋转键数：
  1
• 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：

  2-甲基-5-(4-甲基-1-哌嗪基)苯胺 、 6-(2-chloro-5-fluoropyrimidin-4-yl)spiro[2H-isoindole-3,1'-cyclopropane]-1-one 在 tris-(dibenzylideneacetone)dipalladium(0) 、 caesium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 作用下， 以 1,4-二氧六环 为溶剂， 以122.9 mg的产率得到
  参考文献：
  名称：

  作为PLK1抑制剂的化合物及其制备方法和用途

  摘要：

  本发明提供一类作为PLK1抑制剂的化合物，所述化合物及包含其的组合物能够抑制PLK1，从而可用于预防和/或治疗PLK1相关疾病，例如肿瘤等。

  公开号：

  CN117658987A
• 作为产物：
  描述：

  1-methyl-4-(4-methyl-3-nitrophenyl)piperazine 在 钯 钯 、 二氯甲烷 、 盐酸 、 1,4-二氧六环 、 乙醚 作用下， 以 乙醇 、 环己烯 为溶剂， 反应 6.0h， 生成 2-甲基-5-(4-甲基-1-哌嗪基)苯胺
  参考文献：
  名称：

  SUBSTITUTED DIHYDROPTERIDIN-6-ONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS

  摘要：

  本发明揭示了式（I）中所定义的Dihydropteridin-6-one衍生物及其药学上可接受的盐，以及它们的制备方法和包含它们的制药组合物；本发明的化合物在治疗与蛋白激酶活性失调相关的疾病，如癌症方面可能有用。

  公开号：

  US20110053944A1

文献信息

• PYRIMIDINE DERIVATIVES AS PI3K INHIBITOR AND USE THEREOF
  申请人：Shimma Nobuo

  公开号：US20100069629A1

  公开（公告）日：2010-03-18

  A drug is provided that is useful as a preventive or therapeutic for cancer as a result of having superior PI3K inhibitory effects as well as superior stability in the body and water-solubility. A compound, or pharmaceutically acceptable salt thereof, represented by formula (I): [wherein, X represents a single bond, etc.; Y represents a single bond, etc. (provided that X and Y are not simultaneously single bonds); Z represents a hydrogen atom, etc.; m represents an integer of 1 or 2; and R 1 represents a cyclic substituent].

  提供了一种药物，由于具有优越的PI3K抑制作用以及在体内具有优越的稳定性和水溶性，因此可用作预防或治疗癌症。化合物或其药学上可接受的盐的表示式（I）：[其中，X表示单键等；Y表示单键等（前提是X和Y不同时为单键）；Z表示氢原子等；m表示1或2的整数；R1表示环状取代基]。
• SUBSTITUTED DIHYDROPTERIDIN-6-ONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
  申请人：Caruso Michele

  公开号：US20110053944A1

  公开（公告）日：2011-03-03

  Dihydropteridin-6-one derivatives of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.

  本发明揭示了式（I）中所定义的Dihydropteridin-6-one衍生物及其药学上可接受的盐，以及它们的制备方法和包含它们的制药组合物；本发明的化合物在治疗与蛋白激酶活性失调相关的疾病，如癌症方面可能有用。
• SUBSTITUTED PYRAZOLO-QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
  申请人：Caruso Michele

  公开号：US20100216808A1

  公开（公告）日：2010-08-26

  Pyrazolo-quinazoline derivatives of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.

  本发明揭示了式（I）中所定义的吡唑并喹唑啉衍生物及其药学上可接受的盐，以及它们的制备方法和包含它们的制药组合物；本发明中的化合物在治疗与蛋白激酶活性失调相关的疾病，如癌症中可能有用。
• Pyrimidine derivatives as PI3K inhibitor and use thereof
  申请人：Chugai Seiyaku Kabushiki Kaisha

  公开号：US08022205B2

  公开（公告）日：2011-09-20

  A drug is provided that is useful as a preventive or therapeutic for cancer as a result of having superior PI3K inhibitory effects as well as superior stability in the body and water-solubility. A compound, or pharmaceutically acceptable salt thereof, represented by formula (I): [wherein, X represents a single bond, etc.; Y represents a single bond, etc. (provided that X and Y are not simultaneously single bonds); Z represents a hydrogen atom, etc.; m represents an integer of 1 or 2; and R1 represents a cyclic substituent].

  提供一种药物，由于具有卓越的PI3K抑制作用以及在体内具有卓越的稳定性和水溶性，因此可用作预防或治疗癌症。该化合物或其药学上可接受的盐的化学式为（I）：[其中，X表示单键等；Y表示单键等（前提是X和Y不同时为单键）；Z表示氢原子等；m表示1或2的整数；R1表示环状取代基]。
• Substituted dihydropteridin-6-one derivatives, process for their preparation and their use as kinase inhibitors
  申请人：Caruso Michele

  公开号：US08598172B2

  公开（公告）日：2013-12-03

  Dihydropteridin-6-one derivatives of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.

  本发明公开了式（I）的二氢叶酸6-酮衍生物及其药学上可接受的盐，以及其制备方法和包含它们的药物组合物；本发明的化合物可能在治疗与蛋白激酶活性失调相关的疾病，如癌症方面有用。