4-(pyrimidin-5-yloxy)benzaldehyde | 1030379-80-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-(pyrimidin-5-yloxy)benzaldehyde
• 英文别名: 4-(Pyrimidin-5-yloxy)benzaldehyde；4-pyrimidin-5-yloxybenzaldehyde
• CAS: 1030379-80-6
• 化学式: C₁₁H₈N₂O₂
• 分子量: 200.197
• InChiKey: UFMGPLUKYBMTMX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  52.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-(pyrimidin-5-yloxy)benzaldehyde 、 甲氧基甲基三苯基氯化膦 在 正丁基锂 作用下， 以 四氢呋喃 为溶剂， 反应 0.67h， 生成 5-(4-(2-methoxyvinyl)phenoxy)pyrimidine
  参考文献：
  名称：

  [EN] TRICYCLIC COMPOUNDS, PREPARATION METHODS, AND THEIR USES
  [FR] COMPOSÉS TRICYCLIQUES, LEURS PROCÉDÉS DE PRÉPARATION ET LEURS UTILISATIONS

  摘要：

  本发明涉及抑制Lp-PLA2活性的新化合物，以及它们的制备方法、含有它们的组合物，以及它们在治疗与Lp-PLA2活性相关的疾病中的应用，例如动脉粥样硬化、阿尔茨海默病和/或糖尿病黄斑水肿。

  公开号：

  WO2012037782A1
• 作为产物：
  描述：

  5-羟基嘧啶 、 对氟苯甲醛 在 sodium methansulfinate 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 以43%的产率得到4-(pyrimidin-5-yloxy)benzaldehyde
  参考文献：
  名称：

  WO2008/65393

  摘要：

  公开号：

文献信息

• 3-PYRIMIDIN-4-YL-OXAZOLIDIN-2-ONES AS INHIBITORS OF MUTANT IDH
  申请人：VESTAS WIND SYSTEMS A/S

  公开号：US20140235620A1

  公开（公告）日：2014-08-21

  The invention is directed to a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein R 1 -R 6 are defined herein. The invention is also directed to compositions containing a compound of formula (I) and to the use of such compounds in the inhibition of mutant IDH proteins having a neomorphic activity. The invention is further directed to the use of a compound of formula (I) in the treatment of diseases or disorders associated with such mutant IDH proteins including, but not limited to, cell-proliferation disorders, such as cancer.

  该发明涉及公式（I）的化合物或其药用盐，其中R1-R6在此处定义。该发明还涉及含有公式（I）化合物的组合物，以及利用这些化合物抑制具有新型活性的突变IDH蛋白。该发明还涉及利用公式（I）的化合物治疗与这些突变IDH蛋白相关的疾病或紊乱，包括但不限于细胞增殖紊乱，如癌症。
• [EN] 3-PYRIMIDIN-4-YL-OXAZOLIDIN-2-ONES AS INHIBITORS OF MUTANT IDH<br/>[FR] 3-PYRIMIDIN-4-YL-OXAZOLIDIN-2-ONES COMME INHIBITEURS D'IDH MUTANTE
  申请人：NOVARTIS AG

  公开号：WO2013046136A1

  公开（公告）日：2013-04-04

  The invention is directed to a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein R1-R6 are defined herein. The invention is also directed to compositions containing a compound of formula (I) and to the use of such compounds in the inhibition of mutant IDH proteins having a neomorphic activity. The invention is further directed to the use of a compound of formual (I) in the treatment of diseases or disorders associated with such mutant IDH proteins including, but not limited to, cell-proliferation disorders, such as cancer.

  该发明涉及公式(I)的化合物或其药学上可接受的盐，其中R1-R6在此处被定义。该发明还涉及含有公式(I)化合物的组合物，以及利用这些化合物抑制具有新型活性的突变IDH蛋白。该发明还涉及利用公式(I)的化合物治疗与这些突变IDH蛋白相关的疾病或紊乱，包括但不限于细胞增殖紊乱，如癌症。
• Novel Compounds
  申请人：Chapman David

  公开号：US20080221139A1

  公开（公告）日：2008-09-11

  The invention provides compounds of formula (I): wherein R 1 and R 2 are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the pharmaceutical compositions; and their use in therapy. The compounds are useful as MMP inhibitors.

  本发明提供了式(I)的化合物：其中R1和R2如规范所定义；它们的制备过程；含有它们的制药组合物；制备制药组合物的过程；以及它们在治疗中的应用。这些化合物可用作MMP抑制剂。
• Hydantoin compounds and pharmaceutical compositions thereof
  申请人：AstraZeneca AB

  公开号：US08183251B2

  公开（公告）日：2012-05-22

  The invention provides compounds of formula (I): wherein R1 and R2 are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the pharmaceutical compositions; and their use in therapy. The compounds are useful as MMP inhibitors.

  本发明提供了式（I）的化合物：其中R1和R2如规范中定义；它们的制备方法；含有它们的制药组合物；制备制药组合物的方法；以及它们在治疗中的使用。这些化合物可用作MMP抑制剂。
• 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH
  申请人：Caferro Thomas Raymond

  公开号：US08957068B2

  公开（公告）日：2015-02-17

  The invention is directed to a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein R1-R6 are defined herein. The invention is also directed to compositions containing a compound of formula (I) and to the use of such compounds in the inhibition of mutant IDH proteins having a neomorphic activity. The invention is further directed to the use of a compound of formula (I) in the treatment of diseases or disorders associated with such mutant IDH proteins including, but not limited to, cell-proliferation disorders, such as cancer.

  本发明涉及式（I）的化合物或其药学上可接受的盐，其中R1-R6在此定义。本发明还涉及含有式（I）的化合物的组合物，并且涉及使用这种化合物来抑制具有新型活性的突变IDH蛋白质。本发明还涉及使用式（I）的化合物来治疗与这种突变IDH蛋白质相关的疾病或紊乱，包括但不限于细胞增殖紊乱，如癌症。