2,5-dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine | 1236130-57-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2,5-dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine
• 英文别名: 2,5-dichloro-N-[(3-methoxyphenyl)methyl]pyrimidin-4-amine
• CAS: 1236130-57-6
• 化学式: C₁₂H₁₁Cl₂N₃O
• mdl: MFCD23328991
• 分子量: 284.145
• InChiKey: DBVLODROPIAOQC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.166
• 拓扑面积：
  47
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2,5-dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine 、 间氨基苯甲醚 在 对甲苯磺酸 作用下， 以 1,4-二氧六环 为溶剂， 反应 48.0h， 以30%的产率得到5-chloro-N(4)-(3-methoxybenzyl)-N(2)-(3-methoxyphenyl)pyrimidine-2,4-diamine
  参考文献：
  名称：

  MACROCYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS

  摘要：

  本发明涉及以下式I的大环化合物：或其药用可接受的盐或季铵盐，其中所述成员组分在此提供，并且它们的组合物和使用方法，这些JAK/ALK抑制剂在治疗JAK/ALK相关疾病中有用，包括例如炎症和自身免疫性疾病，以及癌症。

  公开号：

  US20100190804A1
• 作为产物：
  描述：

  3-甲氧基苄胺 、 2,4,5-三氯嘧啶 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以92%的产率得到2,5-dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine
  参考文献：
  名称：

  MACROCYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS

  摘要：

  本发明涉及以下式I的大环化合物：或其药用可接受的盐或季铵盐，其中所述成员组分在此提供，并且它们的组合物和使用方法，这些JAK/ALK抑制剂在治疗JAK/ALK相关疾病中有用，包括例如炎症和自身免疫性疾病，以及癌症。

  公开号：

  US20100190804A1

文献信息

• Macrocyclic compounds and their use as kinase inhibitors
  申请人：Combs Andrew Paul

  公开号：US08765727B2

  公开（公告）日：2014-07-01

  The present invention relates to macrocyclic compounds of Formula I: or pharmaceutically acceptable salts thereof or quaternary ammonium salts thereof wherein constituent members are provided hereinwith, as well as their compositions and methods of use, which are JAK/ALK inhibitors useful in the treatment of JAK/ALK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer.

  本发明涉及以下式子的大环化合物：或其药学上可接受的盐或季铵盐，其中其组成成员在此提供，以及它们的组合物和使用方法，这些JAK/ALK抑制剂可用于治疗JAK/ALK相关疾病，包括例如炎症和自身免疫性疾病以及癌症。
• US8765727B2
  申请人：——

  公开号：US8765727B2

  公开（公告）日：2014-07-01
• [EN] MACROCYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS<br/>[FR] COMPOSÉS MACROCYCLIQUES ET LEUR UTILISATION EN TANT QU'INHIBITEURS DES KINASES
  申请人：INCYTE CORP

  公开号：WO2010085597A1

  公开（公告）日：2010-07-29

  The present invention relates to macrocyclic compounds of Formula I: or pharmaceutically acceptable salts thereof or quaternary ammonium salts thereof wherein constituent members are provided hereinwith, as well as their compositions and methods of use, which are JAK/ ALK inhibitors useful in the treatment of JAK/ALK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer.
• Discovery and SARs of 5-Chloro-<i>N</i>⁴-phenyl-<i>N</i>²-(pyridin-2-yl)pyrimidine-2,4-diamine Derivatives as Oral Available and Dual CDK 6 and 9 Inhibitors with Potent Antitumor Activity
  作者：Yang Wang、Xing Chen、Yaoyao Yan、Xiaochen Zhu、Mingming Liu、Xinhua Liu

  DOI：10.1021/acs.jmedchem.9b02121

  日期：2020.3.26

  Cyclin-dependent kinases (CDKs) are promising therapeutic targets for cancer therapy. Herein, we describe our efforts toward the discovery of a series of 5-chloro-N-4-phenyl-N-2(pyridin-2-yl)pyrimidine-2,4-diamine derivatives as dual CDK6 and 9 inhibitors. Intensive structural modifications lead to the identification of compound 66 as the most active dual CDK6/9 inhibitor with balancing potency against these two targets and good selectivity over CDK2. Further biological studies revealed that compound 66 was directly bound to CDK6/9, resulting in suppression of their downstream signaling pathway and inhibition of cell proliferation by blocking cell cycle progression and inducing cellular apoptosis. More importantly, compound 66 significantly inhibited tumor growth in a xenograft mouse model with no obvious toxicity, indicating the promising therapeutic potential of CDK6/9 dual inhibitors for cancer treatment. Therefore, the above results are of great importance in the development of dual CDK6/9 inhibitors for cancer therapy.
• MACROCYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS
  申请人：Combs Andrew Paul

  公开号：US20100190804A1

  公开（公告）日：2010-07-29

  The present invention relates to macrocyclic compounds of Formula I: or pharmaceutically acceptable salts thereof or quaternary ammonium salts thereof wherein constituent members are provided hereinwith, as well as their compositions and methods of use, which are JAK/ALK inhibitors useful in the treatment of JAK/ALK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer.

  本发明涉及以下式I的大环化合物：或其药用可接受的盐或季铵盐，其中所述成员组分在此提供，并且它们的组合物和使用方法，这些JAK/ALK抑制剂在治疗JAK/ALK相关疾病中有用，包括例如炎症和自身免疫性疾病，以及癌症。