4-chloro-6-(2-thienyl)pyrimidin-2-amine | 569657-91-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-chloro-6-(2-thienyl)pyrimidin-2-amine
• 英文别名: 2-amino-4-chloro-6-(thien-2-yl)pyrimidine；2-Amino-4-chloro-6-(2-thienyl)pyrimidine；4-chloro-6-thiophen-2-ylpyrimidin-2-amine
• CAS: 569657-91-6
• 化学式: C₈H₆ClN₃S
• 分子量: 211.675
• InChiKey: KMFPVBIHZXWKIP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  80
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-chloro-6-(2-thienyl)pyrimidin-2-amine 在 N,O-双三甲硅基乙酰胺 作用下， 以 正丁醇 为溶剂， 生成 5-Amino-2-(furan-2-yl)-7-(thien-2-yl)[1,2,4]triazolo[1,5-c]pyrimidine
  参考文献：
  名称：

  2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: Highly potent, orally active, adenosine A2A antagonists. Part 1

  摘要：

  The structure-activity relationship of this novel class of compounds based on 2-(2-furanyl)-7-phenyl[1,2,4]-triazolo[1,5-c]pyrimidin-5-amine, 1, and its analogs was evaluated for their in vitro and in vivo adenosine A(2A) receptor antagonism. Several compounds displayed oral activity at 3 mg/kg in a rat catalepsy model. Specifically, compound 8g displayed an excellent in vitro profile, as well as a highly promising in vivo profile. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.05.086
• 作为产物：
  描述：

  2-噻吩硼酸 、 2-氨基-4,6-二氯嘧啶 在 四(三苯基膦)钯 、 potassium carbonate 作用下， 以 乙腈 为溶剂， 生成 4-chloro-6-(2-thienyl)pyrimidin-2-amine
  参考文献：
  名称：

  2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: Highly potent, orally active, adenosine A2A antagonists. Part 1

  摘要：

  The structure-activity relationship of this novel class of compounds based on 2-(2-furanyl)-7-phenyl[1,2,4]-triazolo[1,5-c]pyrimidin-5-amine, 1, and its analogs was evaluated for their in vitro and in vivo adenosine A(2A) receptor antagonism. Several compounds displayed oral activity at 3 mg/kg in a rat catalepsy model. Specifically, compound 8g displayed an excellent in vitro profile, as well as a highly promising in vivo profile. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.05.086

文献信息

• Rho-kinase inhibitors
  申请人：BAYER CORPORATION

  公开号：US20040002508A1

  公开（公告）日：2004-01-01

  Disclosed are compounds and derivatives thereof, their synthesis, and their use as Rho-kinase inhibitors. These compounds are useful for inhibiting tumor growth, treating erectile dysfunction, and treating other indications mediated by Rho-kinase, e.g., coronary heart disease.

  本文披露了化合物及其衍生物、它们的合成以及它们作为Rho激酶抑制剂的用途。这些化合物可用于抑制肿瘤生长、治疗勃起功能障碍，以及治疗其他由Rho激酶介导的疾病，例如冠心病。
• Pyrimidine derivatives for treatment of hyperproliferative disorders
  申请人：Dixon A. Julie

  公开号：US20050277640A1

  公开（公告）日：2005-12-15

  Pyrimidine derivatives of formula (I) in which J and Y represent aromatic or heteroaromatic rings; R 2 , G, G′, and G″ represent substituent groups and R 2a represents H or halogen; L represents a linking group; and M represents CH or N. Pharmaceutical compositions containing these compounds, and methods of using these compounds in treatment of hyperproliferative diseases such as cancer are also disclosed and claimed.

  式(I)中的嘧啶衍生物，其中J和Y代表芳香环或杂芳环；R2、G、G′和G″代表取代基，而R2a代表氢或卤素；L代表连接基团；M代表CH或N。还公开和声明了含有这些化合物的药物组合物，并使用这些化合物治疗增殖过度性疾病，如癌症的方法。
• PYRIMIDINE DERIVATIVES FOR TREATMENT OF HYPERPROLIFERATIVE DISORDERS
  申请人：Dixon Julie A.

  公开号：US20100075967A1

  公开（公告）日：2010-03-25

  Pyrimidine derivatives of formula (I) in which J and Y represent aromatic or heteroaromatic rings; R 2 , G, G′, and G″ represent substituent groups and R 2a represents H or halogen; L represents a linking group; and M represents CH or N. Pharmaceutical compositions containing these compounds, and methods of using these compounds in treatment of hyperproliferative diseases such as cancer are also disclosed and claimed.

  公式（I）的嘧啶衍生物，其中J和Y代表芳香或杂芳环；R2，G，G'和G''代表取代基，R2a代表H或卤素；L代表连接基团；M代表CH或N。本发明还公开和声明了包含这些化合物的制药组合物，并使用这些化合物治疗高增殖性疾病，如癌症的方法。
• Rho-Kinase Inhibitors
  申请人：Nagarathnam Dhanapalan

  公开号：US20120053179A1

  公开（公告）日：2012-03-01

  Disclosed are compounds and derivatives thereof, their synthesis, and their use as Rho-kinase inhibitors. These compounds are useful for inhibiting tumor growth, treating erectile dysfunction, and treating other indications mediated by Rho-kinase, e.g., coronary heart disease.

  本发明揭示了化合物及其衍生物，它们的合成以及它们作为Rho-kinase抑制剂的用途。这些化合物对于抑制肿瘤生长、治疗勃起功能障碍以及治疗其他由Rho-kinase介导的适应症，例如冠心病，是有用的。
• Pyrimidine Derivatives for Treatment of Hyperproliferative Disorders
  申请人：Dixon Julie A.

  公开号：US20110098301A1

  公开（公告）日：2011-04-28

  Pyrimidine derivatives of formula pharmaceutical compositions containing these compounds, and methods of using these compounds in treatment of hyperproliferative diseases such as cancer are disclosed and claimed.

  本发明揭示并声明了式的嘧啶衍生物、含有这些化合物的制药组合物以及使用这些化合物治疗癌症等增殖性疾病的方法。