N-[(2-acetamido-4-fluorophenyl)methyl]acetamide | 936363-99-4

• 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: N-[(2-acetamido-4-fluorophenyl)methyl]acetamide
• CAS: 936363-99-4
• 化学式: C₁₁H₁₃FN₂O₂
• 分子量: 224.235
• InChiKey: IIXAZBWMQKWAMT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  58.2
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  N-(2-cyano-5-fluorophenyl)acetamide 在 palladium 10% on activated carbon 氢气 作用下， 以 乙醇 、 水 为溶剂， 反应 72.0h， 生成 N-[(2-acetamido-4-fluorophenyl)methyl]acetamide
  参考文献：
  名称：

  HIV INTEGRASE INHIBITORS

  摘要：

  这项发明涵盖了一系列公式I的双环嘧啶酮化合物，这些化合物抑制HIV整合酶并防止病毒整合到人类DNA中。这种作用使得这些化合物对治疗HIV感染和艾滋病有用。该发明还涵盖了用于治疗HIV感染者的药物组合物和方法。

  公开号：

  US20070129379A1

文献信息

• HIV integrase inhibitors
  申请人：Naidu Narasimhulu B.

  公开号：US20070111984A1

  公开（公告）日：2007-05-17

  The invention encompasses a series bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

  这项发明涵盖了一系列公式I的双环嘧啶酮化合物，它们能抑制HIV整合酶，防止病毒整合到人类DNA中。这一作用使得这些化合物对治疗HIV感染和艾滋病具有用处。该发明还涵盖了用于治疗HIV感染者的药物组合物和方法。
• WO2007/64316
  申请人：——

  公开号：——

  公开（公告）日：——
• [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-NAPHTYRIDINE-7-CARBOXAMIDES UTILES COMME INHIBITEURS DE L'INTEGRASE DU VIH
  申请人：MERCK & CO INC

  公开号：WO2003077857A2

  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. In one embodiment, the naphthyridine carboxamides are of Formula (II): (II),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.
• HIV INTEGRASE INHIBITORS
  申请人：Naidu B. Narasimhulu

  公开号：US20070129379A1

  公开（公告）日：2007-06-07

  The invention encompasses a series bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

  这项发明涵盖了一系列公式I的双环嘧啶酮化合物，这些化合物抑制HIV整合酶并防止病毒整合到人类DNA中。这种作用使得这些化合物对治疗HIV感染和艾滋病有用。该发明还涵盖了用于治疗HIV感染者的药物组合物和方法。