N-benzyl-2-chloro-3-nitroquinolin-4-amine | 879000-70-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: N-benzyl-2-chloro-3-nitroquinolin-4-amine
• CAS: 879000-70-1
• 化学式: C₁₆H₁₂ClN₃O₂
• 分子量: 313.743
• InChiKey: TXGWZRMBTBLSQM-UHFFFAOYSA-N

物化性质

• 沸点：
  490.3±45.0 °C(Predicted)
• 密度：
  1.421±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  70.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-benzyl-2-chloro-3-nitroquinolin-4-amine 在 盐酸 、 tin 作用下， 以 甲醇 、 水 为溶剂， 反应 1.0h， 以30%的产率得到N4-benzyl-2-chloroquinoline-3,4-diamine
  参考文献：
  名称：

  Dual inhibitors of epidermal growth factor receptor and topoisomerase IIα derived from a quinoline scaffold

  摘要：

  基于含有喹唑啉基团的EGFR抑制剂，合成并评估了一系列含有喹啉骨架的三十四种化合物的EGFR激酶抑制和抗癌活性。

  DOI：

  10.1039/c6ra15118c
• 作为产物：
  描述：

  4-羟基-3-硝基-2(1H)-喹啉酮 在 苯膦酰二氯 、 三乙胺 作用下， 以 水 为溶剂， 反应 4.0h， 生成 N-benzyl-2-chloro-3-nitroquinolin-4-amine
  参考文献：
  名称：

  Dual inhibitors of epidermal growth factor receptor and topoisomerase IIα derived from a quinoline scaffold

  摘要：

  基于含有喹唑啉基团的EGFR抑制剂，合成并评估了一系列含有喹啉骨架的三十四种化合物的EGFR激酶抑制和抗癌活性。

  DOI：

  10.1039/c6ra15118c

文献信息

• HYDROXY AND ALKOXY SUBSTITUTED 1H-IMIDAZOQUINOLINES AND METHODS
  申请人：Kshirsagar Tushar A.

  公开号：US20090221556A1

  公开（公告）日：2009-09-03

  1H-Imidazo[4,5-c]quinolin-4-amines with a hydroxy, alkoxy, hydroxyalkoxy, or alkoxyalkoxy substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

  本文介绍了在2位置具有羟基，烷氧基，羟基烷氧基或烷氧基烷氧基取代基的1H-咪唑并[4,5-c]喹啉-4-胺类化合物、含有这些化合物的制药组合物、制备这些化合物的方法、中间体以及这些化合物作为免疫调节剂的用途，用于诱导动物细胞因子生物合成和治疗包括病毒和肿瘤疾病在内的疾病。
• 2-Amino 1H-Imidazo Ring Systems and Methods
  申请人：Kshirsagar Tushar A.

  公开号：US20090023720A1

  公开（公告）日：2009-01-22

  1H-Imidazo ring systems (e.g., imidazopyridines, imidazoquinolines, imidazonaphthyridines, 6,7,8,9-tetrahydro imidazoquinolines and imidazonaphthyridines) with an amino substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

  本发明揭示了在2-位置具有氨基取代基的咪唑环系统（例如咪唑吡啶，咪唑喹啉，咪唑萘啉，6,7,8,9-四氢咪唑喹啉和咪唑萘啉），含有这些化合物的制药组合物，制备这些化合物的方法，中间体以及这些化合物作为免疫调节剂的用途，用于调节动物细胞因子生物合成以及治疗包括病毒和肿瘤性疾病在内的疾病的方法。
• Hydroxy and alkoxy substituted 1H-imidazoquinolines and methods
  申请人：3M Innovative Properties Company

  公开号：US08088790B2

  公开（公告）日：2012-01-03

  1H-Imidazo[4,5-c]quinolin-4-amines with a hydroxy, alkoxy, hydroxyalkoxy, or alkoxyalkoxy substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

  本发明公开了在2位具有羟基、烷氧基、羟基烷氧基或烷氧基烷氧基取代基的1H-咪唑并[4,5-c]喹啉-4-胺类化合物、含有这些化合物的制药组合物、制备这些化合物的方法、中间体以及这些化合物作为免疫调节剂的使用方法，用于诱导动物细胞因子生物合成和治疗包括病毒和肿瘤性疾病在内的疾病。
• 2-amino 1H-in-imidazo ring systems and methods
  申请人：3M Innovative Properties Company

  公开号：US08143270B2

  公开（公告）日：2012-03-27

  1H-Imidazo ring systems (e.g., imidazopyridines, imidazoquinolines, imidazonaphthyridines, 6,7,8,9-tetrahydro imidazoquinolines and imidazonaphthyridines) with an amino substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

  本发明公开了在2位具有氨基取代基的1H-咪唑环系（例如咪唑吡啶、咪唑喹啉、咪唑萘啉、6,7,8,9-四氢咪唑喹啉和咪唑萘啉）及其制药组合物、制备上述化合物的方法、中间体以及这些化合物的用途，包括作为免疫调节剂，调节动物的细胞因子生物合成，用于治疗包括病毒和肿瘤疾病在内的疾病。
• Design, microwave-mediated synthesis and biological evaluation of novel 4-aryl(alkyl)amino-3-nitroquinoline and 2,4-diaryl(dialkyl)amino-3-nitroquinolines as anticancer agents
  作者：Monika Chauhan、Anil Rana、Jimi Marin Alex、Arvind Negi、Sandeep Singh、Raj Kumar

  DOI：10.1016/j.bioorg.2014.11.004

  日期：2015.2

  Design, microwave-assisted synthesis of novel 4-aryl (alkyl) amino-3-nitroquinoline (1a-1l) and 2,4-diaryl (dialkyl) amino-3-nitroquinolines (2a-2k and 3a) via regioselective and complete nucleophilic substitution of 2,4-dichloro-3-nitroquinoline, respectively in water are presented. The newly synthesized compounds were evaluated for the first time for antiproliferative activity against EGFR overexpressing human lung (A-549 and H-460) and colon (HCT-116-wild type and HCT-116-p53 null) cancer cell lines. Some notions about structure-activity relationships (SAR) are presented. Compounds 2e, 2f, 2j and 3a overall exhibited excellent anticancer activity comparable to erlotinib which was used as a positive control. Molecular modeling studies disclosed the recognition pattern of the compounds and also supported the observed SAR. (C) 2014 Elsevier Inc. All rights reserved.