N-(4-chlorobenzyl)-1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido [1,2,3-de]quinoxaline-6-carboxamide | 552883-98-4

• 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-(4-chlorobenzyl)-1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido [1,2,3-de]quinoxaline-6-carboxamide
• 英文别名: N-(4-chlorobenzyl)-1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamide；N-(4-chlorobenzyl)-1-methyl-9-(morpholinomethyl)-2,7-dioxo-1,2,3,7-tetrahydropyrido[1,2,3-de]quinoxaline-6-carboxamide；N-[(4-chlorophenyl)methyl]-4-methyl-7-(morpholin-4-ylmethyl)-3,10-dioxo-1,4-diazatricyclo[7.3.1.05,13]trideca-5,7,9(13),11-tetraene-11-carboxamide
• CAS: 552883-98-4
• 化学式: C₂₅H₂₅ClN₄O₄
• 分子量: 480.951
• InChiKey: GOUFCWPWLUOOBL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  34
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  82.2
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  N-(4-chlorobenzyl)-1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido [1,2,3-de]quinoxaline-6-carboxamide 在 氯甲酸乙酯 作用下， 以 氯仿 为溶剂， 以92%的产率得到N-(4-chlorobenzyl)-9-(chloromethyl)-1-methyl-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamide
  参考文献：
  名称：

  The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase

  摘要：

  Discovery efforts were focused on identifying a non-nucleoside antiviral for treating infections caused by human cytomegalovirus (HCMV) with equal or better potency and diminished toxicity compared to current therapeutics. This Letter describes the HCMV DNA polymerase inhibition and in vitro antiviral activity of various 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.01.094
• 作为产物：
  描述：

  ethyl 1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxylate 以 甲醇 、 乙醇 、 二氯甲烷 、 乙二醇 、 对氯苄胺 为溶剂， 生成 N-(4-chlorobenzyl)-1-methyl-9-(morpholin-4-ylmethyl)-2,7-dioxo-2,3-dihydro-1H,7H-pyrido [1,2,3-de]quinoxaline-6-carboxamide
  参考文献：
  名称：

  PYRIDOQUINOXALINE ANTIVIRALS

  摘要：

  本发明提供了一种具有化学式I1的化合物或其药用可接受的盐，其中R1和R2如规范中定义。这些化合物对于治疗病毒感染是有用的。

  公开号：

  US20030130255A1

文献信息

• Pyridoquinoxaline antivirals
  申请人：——

  公开号：US20030207877A1

  公开（公告）日：2003-11-06

  The present invention provides a compound of formula I 1 or a pharmaceutically acceptable salt thereof wherein R 1 , R 2 and R 3 are as defined in the specification. The compounds are useful for the treatment of viral infections.

  本发明提供了一种具有以下结构的化合物I或其药学上可接受的盐，其中R1、R2和R3如规范中定义。这些化合物对于治疗病毒感染是有用的。
• US6686356B2
  申请人：——

  公开号：US6686356B2

  公开（公告）日：2004-02-03
• [EN] PYRIDOQUINOXALINE ANTIVIRALS<br/>[FR] ANTIVIRAUX A BASE DE PYRIDOQUINOXALINE
  申请人：UPJOHN CO

  公开号：WO2003053971A1

  公开（公告）日：2003-07-03

  The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein R?1, R2 and R3¿ are as defined in the specification. The compounds are useful for the treatment of viral infections.
• [EN] PYRIDOQUINOXALINE ANTIVIRALS<br/>[FR] ANTIVIRAUX DE PYRIDOQUINOXALINE
  申请人：UPJOHN CO

  公开号：WO2003053972A1

  公开（公告）日：2003-07-03

  The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein R?1 and R2¿ are as defined in the specification. The compounds are useful for the treatment of viral infections.
• The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase
  作者：Steven P. Tanis、Joseph W. Strohbach、Timothy T. Parker、Malcom W. Moon、Suvit Thaisrivongs、William R. Perrault、Todd A. Hopkins、Mary L. Knechtel、Nancee L. Oien、Janet L. Wieber、Kevin J. Stephanski、Michael W. Wathen

  DOI：10.1016/j.bmcl.2010.01.094

  日期：2010.3

  Discovery efforts were focused on identifying a non-nucleoside antiviral for treating infections caused by human cytomegalovirus (HCMV) with equal or better potency and diminished toxicity compared to current therapeutics. This Letter describes the HCMV DNA polymerase inhibition and in vitro antiviral activity of various 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides. (C) 2010 Elsevier Ltd. All rights reserved.