5-phenylpiperazin-2-one | 907973-15-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 5-phenylpiperazin-2-one
• CAS: 907973-15-3
• 化学式: C₁₀H₁₂N₂O
• mdl: MFCD07373505
• 分子量: 176.218
• InChiKey: RMZGIXQVAQTNNP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  41.1
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-phenylpiperazin-2-one 在 tris-(dibenzylideneacetone)dipalladium(0) 、 potassium carbonate 、 4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下， 以 二甲基亚砜 、 乙腈 为溶剂， 反应 10.0h， 生成 4-methyl-1-(7-morpholino-2-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-5-phenylpiperazin-2-one
  参考文献：
  名称：

  [EN] COMPOUNDS AND COMPOSITIONS THAT INHIBIT PIKFYVE
  [FR] COMPOSÉS ET COMPOSITIONS QUI INHIBENT PIKFYVE

  摘要：

  Pyrazolo[1,5-a]pyrimidines are disclosed. These compounds may be useful in the treatment of neurological disorder, including frontotemporal dementia, chronic traumatic encephalopathy, Alzheimer's disease, limbic-predominant age-related TDP-43 encephalopathy, or frontotemporal lobar degeneration. Further, the invention features a method of inhibiting toxicity in a cell related to a protein TDP-43 or C9orf72. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.

  公开号：

  WO2023107557A1
• 作为产物：
  描述：

  ethyl 2-(2-azido-1-phenylethylamino)acetate 在 三苯基膦 作用下， 以 四氢呋喃 为溶剂， 以17 %的产率得到5-phenylpiperazin-2-one
  参考文献：
  名称：

  [EN] COMPOUNDS AND COMPOSITIONS THAT INHIBIT PIKFYVE
  [FR] COMPOSÉS ET COMPOSITIONS QUI INHIBENT PIKFYVE

  摘要：

  Pyrazolo[1,5-a]pyrimidines are disclosed. These compounds may be useful in the treatment of neurological disorder, including frontotemporal dementia, chronic traumatic encephalopathy, Alzheimer's disease, limbic-predominant age-related TDP-43 encephalopathy, or frontotemporal lobar degeneration. Further, the invention features a method of inhibiting toxicity in a cell related to a protein TDP-43 or C9orf72. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.

  公开号：

  WO2023107557A1

文献信息

• CYCLOHEXANE DERIVATIVES AND USES THEREOF
  申请人：BARNES David

  公开号：US20110136735A1

  公开（公告）日：2011-06-09

  The present invention provides a compound of formula I; a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了一种I式化合物；一种制造本发明化合物的方法及其治疗用途。本发明还提供了一种药理活性剂的组合和制药组合物。
• CYCLOHEXANE DERIVATIVES AS INHIBITORS OF ACETYL-COA CARBOXYLASE (ACC)
  申请人：Novartis AG

  公开号：EP2507210B1

  公开（公告）日：2015-04-08
• PHARMACEUTICAL COMPOUNDS AND THEIR USE AS INHIBITORS OF UBIQUITIN SPECIFIC PROTEASE 19 (USP19)
  申请人：Almac Discovery Limited

  公开号：EP3890829A1

  公开（公告）日：2021-10-13
• US8394858B2
  申请人：——

  公开号：US8394858B2

  公开（公告）日：2013-03-12
• [EN] CYCLOHEXANE DERIVATIVES AS INHIBITORS OF ACETYL-COA CARBOXYLASE (ACC)<br/>[FR] DÉRIVÉS DE CYCLOHEXANE COMME INHIBITEURS DE L'ACÉTYL-COA CARBOXYLASE (ACC)
  申请人：NOVARTIS AG

  公开号：WO2011067306A1

  公开（公告）日：2011-06-09

  The present invention provides a compound of formula (I) a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.