2-chloro-N-(3-chlorobenzyl)pyrimidin-4-amine | 945895-66-9

• 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: 2-chloro-N-(3-chlorobenzyl)pyrimidin-4-amine
• 英文别名: 2-chloro-N-[(3-chlorophenyl)methyl]pyrimidin-4-amine
• CAS: 945895-66-9
• 化学式: C₁₁H₉Cl₂N₃
• 分子量: 254.119
• InChiKey: VFYLMQDMDWADRX-UHFFFAOYSA-N

物化性质

• 沸点：
  434.8±25.0 °C(Predicted)
• 密度：
  1.412±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  37.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-氨基-1-苄基哌啶 、 2-chloro-N-(3-chlorobenzyl)pyrimidin-4-amine 在 N,N-二异丙基乙胺 作用下， 以 正丁醇 为溶剂， 以51%的产率得到N(2)-(1-benzylpiperidin-4-yl)-N(4)-(3-chlorobenzyl)pyrimidine-2,4-diamine
  参考文献：
  名称：

  Development and evaluation of multifunctional agents for potential treatment of Alzheimer’s disease: Application to a pyrimidine-2,4-diamine template

  摘要：

  We investigated a group of 2-benzylpiperidin-N-benzylpyrimidin-4-amines with various electron-withdrawing or electron-donating groups (EWGs or EDGs, respectively) as multi-targeted Alzheimer's disease (AD) therapeutics. The synthesized derivatives were screened for anti-cholinesterase (AChE and BuChE), anti-A beta-aggregation (AChE- and self-induced) and anti-beta-secretase (BACE-1) activities in an effort to identify lead, multifunctional candidates as part of our multi-targeted approach to treat AD. Biological assessment revealed that the nature of the substituent on the C-4 benzylamine group (e.g., halogen vs methoxy-based) greatly affected the biological profile. In vitro screening identified N-2-(1-benzylpiperidin-4-yl)-N-4-(3,4-dimethoxybenzyl) pyrimidine-2,4-diamine (7h) as the lead candidate with a dual ChE (AChE IC50 = 9.9 mu M; BuChE IC50 = 11.4 mu M), A beta-aggregation (AChE-induced = 59.3%; self-induced = 17.4% at 100 mu M) and BACE-1 (34% inhibition at 10 mu M) inhibitory profile along with good cell viability (% neuroblastoma cell viability at 40 mu M = 81.0%). Molecular modeling studies indicate that a central pyrimidine-2,4-diamine ring serves as a suitable template to develop novel small molecule candidates to target multiple pathological routes in AD. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.05.077
• 作为产物：
  描述：

  3-氯苄胺 在 N,N-二异丙基乙胺 作用下， 生成 2-chloro-N-(3-chlorobenzyl)pyrimidin-4-amine
  参考文献：
  名称：

  Small Molecule Analogs of the Nemo Binding Peptide

  摘要：

  该发明涉及一种抑制活细胞内NF-κB基本调节因子（“NEMO”）与IκB激酶-β（IKK-β）在NEMO结合结构域（NBD）上相互作用的方法，包括将细胞暴露于一种有效量或浓度的该发明化合物，即NEMO结合结构域类似物（NBDA）。该发明进一步涉及一种治疗患者病症的方法，其中在医学上指示抑制NF-κB基本调节因子（“NEMO”）与IκB激酶-β（IKK-β）在NEMO结合结构域（NBD）上的相互作用，包括向患者施用该发明化合物的有效剂量。该发明方法可治疗的病症包括肌肉萎缩症、哮喘、炎性肠病、多发性硬化症、帕金森病、关节炎、糖尿病、移植物抗宿主病、加速衰老、心脏缺血、癌症、紫外线诱导的皮肤损伤或与年龄相关的病理。

  公开号：

  US20180169078A1

文献信息

• Small molecule analogs of the nemo binding peptide
  申请人：THE SCRIPPS RESEARCH INSTITUTE

  公开号：US10758522B2

  公开（公告）日：2020-09-01

  The invention is directed to a method of inhibiting, within a living cell, the interaction between NF-κB essential modulator (“NEMO”) with IκB kinase-β (IKK-β) at the NEMO binding domain (NBD), comprising exposing the cell to an effective amount or concentration of a compound of the invention, a NEMO-binding domain analog (NBDA). The invention is further directed to a method of treating a condition in a patient, wherein inhibiting the interaction between NF-κB essential modulator (“NEMO”) with IκB kinase-β (IKK-β) at the NEMO binding domain (NBD) is medically indicated, comprising administering to the patient an effective dose of a compound of the invention. Conditions that can be treated by a method of the invention includes muscular dystrophy, asthma, inflammatory bowel disease, multiple sclerosis, Parkinson's Disease, arthritis, diabetes, graft versus host disease, accelerated aging, heart ischemia, cancer, UV-induced skin damage, or an age-related pathology.

  本发明涉及一种在活细胞内抑制NF-κB基本调节剂（"NEMO"）与IκB激酶-β（IKK-β）在NEMO结合结构域（NBD）处相互作用的方法，包括将细胞暴露于有效量或有效浓度的本发明化合物--NEMO结合结构域类似物（NBDA）。本发明进一步涉及一种治疗患者病症的方法，其中抑制 NF-κB 基本调节剂（"NEMO"）与 IκB 激酶-β（IKK-β）在 NEMO 结合结构域（NBD）处的相互作用具有医学指征，包括向患者施用有效剂量的本发明化合物。本发明方法可治疗的疾病包括肌肉萎缩症、哮喘、炎症性肠病、多发性硬化症、帕金森病、关节炎、糖尿病、移植物抗宿主疾病、加速衰老、心脏缺血、癌症、紫外线引起的皮肤损伤或与年龄相关的病理。
• NOVEL PYRIMIDINE DERIVATIVES 698
  申请人：AstraZeneca AB

  公开号：EP2132184A1

  公开（公告）日：2009-12-16
• SMALL MOLECULE ANALOGS OF THE NEMO BINDING PEPTIDE
  申请人：The Scripps Research Institute

  公开号：EP3302468A1

  公开（公告）日：2018-04-11
• [EN] NOVEL PYRIMIDINE DERIVATIVES 698<br/>[FR] NOUVEAUX DÉRIVÉS 698 DE PYRIMIDINE
  申请人：ASTRAZENECA AB

  公开号：WO2008104754A1

  公开（公告）日：2008-09-04

  [EN] The invention concerns compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R¹, n, R², R³, and R⁴ are as defined in the description. The present invention also relates to processes for the preparation of such compounds, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of EphB4 kinases.
  [FR] La présente invention concerne des composés représentés par la formule (I) ou l'un de ses sels pharmaceutiquement admis, dans laquelle R1, n, R2, R3 et R4 sont tels que définis dans la description. L'invention concerne également des procédés d'élaboration de tels composés, des compositions pharmaceutiques les contenant, et leur utilisation dans la fabrication d'un médicament à utiliser comme anti-proliférant en prévention ou traitement de tumeurs ou d'autres états proliférants réagissant à l'inhibition des kinases EphB4.
• [EN] SMALL MOLECULE ANALOGS OF THE NEMO BINDING PEPTIDE<br/>[FR] ANALOGUES À PETITES MOLÉCULES DU PEPTIDE DE LIAISON NEMO
  申请人：SCRIPPS RESEARCH INST

  公开号：WO2016196117A1

  公开（公告）日：2016-12-08

  The invention is directed to a method of inhibiting, within a living cell, the interaction between NF-κB essential modulator ("NEMO") with IκB kinase-β (IKK-β) at the NEMO binding domain (NBD), comprising exposing the cell to an effective amount or concentration of a compound of the invention, a NEMO-binding domain analog (NBDA). The invention is further directed to a method of treating a condition in a patient, wherein inhibiting the interaction between NF-κB essential modulator ("NEMO") with IκB kinase-β (IKK-β) at the NEMO binding domain (NBD) is medically indicated, comprising administering to the patient an effective dose of a compound of the invention. Conditions that can be treated by a method of the invention includes muscular dystrophy, asthma, inflammatory bowel disease, multiple sclerosis, Parkinson's Disease, arthritis, diabetes, graft versus host disease, accelerated aging, heart ischemia, cancer, UV-induced skin damage, or an age-related pathology.