4'-methoxy-4-nitro-[1,1'-biphenyl]-3-amine

• 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: 4'-methoxy-4-nitro-[1,1'-biphenyl]-3-amine
• 英文别名: 5-(4'-methoxyphenyl)-2-nitroaniline；5-(4-methoxyphenyl)-2-nitroaniline
• 化学式: C₁₃H₁₂N₂O₃
• 分子量: 244.25
• InChiKey: XSGILIZRYWPJCB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  81.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4'-methoxy-4-nitro-[1,1'-biphenyl]-3-amine 在 palladium on activated charcoal 、 甲酸铵 、 溶剂黄146 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 生成
  参考文献：
  名称：

  Identification of novel HDAC inhibitors through cell based screening and their evaluation as potential anticancer agents

  摘要：

  A series of benzimidazole based HDAC inhibitors have been rationally designed, synthesized and screened. The SAR of this new chemotype is described. The lead compound, 11e, showed strong activity in several cellular assays and demonstrated in vivo efficacy in mouse xenograft pancreatic cancer models. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.07.001
• 作为产物：
  描述：

  5-溴-2-硝基苯胺 、 4-甲氧基苯硼酸 在 四(三苯基膦)钯 、 potassium carbonate 作用下， 生成 4'-methoxy-4-nitro-[1,1'-biphenyl]-3-amine
  参考文献：
  名称：

  Identification of novel HDAC inhibitors through cell based screening and their evaluation as potential anticancer agents

  摘要：

  A series of benzimidazole based HDAC inhibitors have been rationally designed, synthesized and screened. The SAR of this new chemotype is described. The lead compound, 11e, showed strong activity in several cellular assays and demonstrated in vivo efficacy in mouse xenograft pancreatic cancer models. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.07.001

文献信息

• Cu-Catalyzed π-Core Evolution of Benzoxadiazoles with Diaryliodonium Salts for Regioselective Synthesis of Phenazine Scaffolds
  作者：Jinyu Sheng、Ru He、Jie Xue、Chao Wu、Juan Qiao、Chao Chen

  DOI：10.1021/acs.orglett.8b01748

  日期：2018.8.3

  The Cu-catalyzed regioselective synthesis of phenazine N-oxides was realized from benzoxadiazoles and diaryliodonium salts. The process was initiated by the electrophilic arylation of benzoxadiazoles with diaryliodonium salts and followed by benzocyclization reactions. The further reduction of N-oxides in situ to phenazine scaffolds and deviation to organic fluorescent materials were readily accomplished

  由苯并恶二唑和二芳基碘鎓盐实现了铜催化的吩嗪N-氧化物的区域选择性合成。该过程通过苯并恶二唑与二芳基碘鎓盐的亲电芳基化反应开始，然后进行苯并环化反应。容易将原位N-氧化物进一步还原为吩嗪支架并偏离有机荧光材料。
• 吡唑类脾酪氨酸激酶抑制剂及其制备方法与用途
  申请人：中国药科大学

  公开号：CN112047932B

  公开（公告）日：2022-11-08

  本发明公开了一种吡唑类脾酪氨酸激酶抑制剂，并公开了其制备方法，本发明还公开了包含上述化合物的药物组合物，以及它们在制备治疗由Syk介导的疾病药物中的用途，所述疾病包括癌症和炎性疾病等。
• Propane-1,3-dione derivatives
  申请人：——

  公开号：US20030191164A1

  公开（公告）日：2003-10-09

  Provided is a pharmaceutical composition containing a propane-1,3-dione derivative as the active ingredient, particularly a GnRH receptor antagonist. Also, provided is a propane-1,3-dione derivative having a GnRH antagonistic effect.

  提供的是一种含有丙酮-1,3-二酮衍生物作为活性成分的制药组合物，特别是一种GnRH受体拮抗剂。同时，也提供了一种具有GnRH拮抗作用的丙酮-1,3-二酮衍生物。
• Propane-1, 3-dione derivative
  申请人：Hirano Masaaki

  公开号：US20050267110A1

  公开（公告）日：2005-12-01

  Provided is a pharmaceutical composition containing a propane-1,3-dione derivative as the active ingredient, particularly a GnRH receptor antagonist. Also, provided is a propane-1,3-dione derivative having a GnRH antagonistic effect.

  提供的是一种药物组合物，其活性成分为丙酮酸丙烷-1,3-二酮衍生物，特别是GnRH受体拮抗剂。同时，提供了一种具有GnRH拮抗作用的丙酮酸丙烷-1,3-二酮衍生物。
• Propane-1,3-dione derivative
  申请人：Hirano Masaaki

  公开号：US06960591B2

  公开（公告）日：2005-11-01

  Provided is a pharmaceutical composition containing a propane-1,3-dione derivative as the active ingredient, particularly a GnRH receptor antagonist. Also, provided is a propane-1,3-dione derivative having a GnRH antagonistic effect.

  提供了一种含有丙酮-1,3-二酮衍生物作为活性成分的药物组合物，特别是GnRH受体拮抗剂。同时，还提供了一种具有GnRH拮抗作用的丙酮-1,3-二酮衍生物。