N-[[2-(dimethylcarbamoyl)-4-fluoro-phenyl]methyl]-5-(1,1-dioxothiazinan-2-yl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: N-[[2-(dimethylcarbamoyl)-4-fluoro-phenyl]methyl]-5-(1,1-dioxothiazinan-2-yl)-8-hydroxy-1,6-naphthyridine-7-carboxamide
• 英文别名: N-[[2-(dimethylcarbamoyl)-4-fluorophenyl]methyl]-5-(1,1-dioxothiazinan-2-yl)-8-hydroxy-1,6-naphthyridine-7-carboxamide
• 化学式: C₂₃H₂₄FN₅O₅S
• 分子量: 501.538
• InChiKey: ZXPCMQIDAHRMPC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  35
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  141
• 氢给体数：
  2
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  5-氟-2-甲基苯甲酸甲酯 在 盐酸 、 N-溴代丁二酰亚胺(NBS) 、 N-羟基-7-氮杂苯并三氮唑 、 sodium hydride 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 、 过氧化苯甲酰 作用下， 以 甲醇 、 四氯化碳 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 生成 N-[[2-(dimethylcarbamoyl)-4-fluoro-phenyl]methyl]-5-(1,1-dioxothiazinan-2-yl)-8-hydroxy-1,6-naphthyridine-7-carboxamide
  参考文献：
  名称：

  A potent and orally active HIV-1 integrase inhibitor

  摘要：

  A 1,6-naphthyridine inhibitor of HIV-1 integrase has been discovered with excellent inhibitory activity in cells, good pharmacokinetics, and an excellent ability to inhibit virus with mutant enzyme. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.11.080

文献信息

• N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as hiv integrase inhibitors
  申请人：Egbertson Melissa

  公开号：US20050176955A1

  公开（公告）日：2005-08-11

  N-(Substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides are inhibitors of HIV integrase and inhibitors of HIV replication. The naphthyridine carboxamides are of Formula (I): wherein R 1 ′, R 2 ′ and R 3 ′ are defined herein. The compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are described.

  N-(取代苯基)-8-羟基-1,6-萘啶-7-羧酰胺是HIV整合酶的抑制剂和HIV复制的抑制剂。萘啶羧酰胺的化学式为(I):其中R1'，R2'和R3'在此被定义。这些化合物在预防和治疗HIV感染以及预防、延迟发病和治疗艾滋病方面非常有用。这些化合物可以作为化合物本身或作为药物可接受的盐形式用于对抗HIV感染和艾滋病。这些化合物及其盐可以作为药物组合物中的成分，可选择与其他抗病毒药物、免疫调节剂、抗生素或疫苗组合使用。描述了预防、治疗或延迟艾滋病发病的方法以及预防或治疗HIV感染的方法。
• N-(SUBSTITUTED BENZYL)-8-HYDROXY-1,6-NAPHTHYRIDINE-7- CARBOXAMIDES USEFUL AS HIV INTEGRASE INHIBITORS
  申请人：Merck & Co., Inc.

  公开号：EP1496836A2

  公开（公告）日：2005-01-19
• EP1496836A4
  申请人：——

  公开号：EP1496836A4

  公开（公告）日：2006-03-22
• US7323460B2
  申请人：——

  公开号：US7323460B2

  公开（公告）日：2008-01-29
• [EN] N-(SUBSTITUTED BENZYL)-8-HYDROXY-1,6-NAPHTHYRIDINE-7- CARBOXAMIDES USEFUL AS HIV INTEGRASE INHIBITORS<br/>[FR] N-(BENZYL SUBSTITUE)-8-HYDROXY-1,6-NAPHTHYRIDINE-7- CARBOXAMIDES UTILES EN TANT QU'INHIBITEURS D'INTEGRASE DE HIV
  申请人：MERCK & CO INC

  公开号：WO2003077850A2

  公开（公告）日：2003-09-25

  N-(Substituted benzyl)-8-hydroxy- 1,6-naphthyridine-7-carboxamides are inhibitors of HIV integrase and inhibitors of HIV replication. The naphthyridine carboxamides are of Formula (I): wherein R1', R2' and R3' are defined herein. The compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are described.