3-(benzyloxy)-2-nitropyridine | 166260-01-1

• 分子结构分类: 有机化合物 - 有机1,3-偶极化合物 - 烯丙基型1,3-偶极有机化合物
• 英文名称: 3-(benzyloxy)-2-nitropyridine
• 英文别名: 2-nitro-3-phenylmethoxypyridine
• CAS: 166260-01-1
• 化学式: C₁₂H₁₀N₂O₃
• mdl: MFCD18909373
• 分子量: 230.223
• InChiKey: DYEWWMLKQRTCII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.083
• 拓扑面积：
  67.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  3-羟基-2-硝基吡啶 、 溴甲苯 在 sodium hydroxide 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 11.0h， 以75%的产率得到3-(benzyloxy)-2-nitropyridine
  参考文献：
  名称：

  通过芳基亚磺酸钠或芳基磺酰氯与水中硝基芳烃的反应合成N-芳基磺酰胺的铁基金属有机骨架

  摘要：

  已经公开了新开发的芳基亚磺酸钠或芳基磺酰氯与硝基芳烃的化学选择反应。化学中分别使用无毒的水和可循环使用的铁基金属-有机骨架作为溶剂和催化剂，为产生N-芳基磺酰胺提供了一种有效的方法，该方法广泛存在于生物活性化合物和药物中，使该方法论对合成化学和药物化学都具有吸引力。

  DOI：

  10.1016/j.tetlet.2018.10.032

文献信息

• ENANTIOMERICALLY PURE AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS
  申请人：CUI Jingrong Jean

  公开号：US20140288086A1

  公开（公告）日：2014-09-25

  Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.

  本发明提供了公式1的对映纯化合物，以及它们的合成和使用方法。首选化合物是c-Met蛋白激酶的强效抑制剂，可用于治疗异常细胞增生性疾病，例如癌症。
• Method for optical measurement of multi-stranded nucleic acid
  申请人：Nakamura Kouki

  公开号：US20050112770A1

  公开（公告）日：2005-05-26

  A method for optical measurement of a multi-stranded nucleic acid which comprises the step of bringing a compound into contact with a multi-stranded nucleic acid wherein said compound is capable of interacting with the multi-stranded nucleic acid, wherein the compound has the following properties: (a) the compound can exist in a substantially colorless and non-fluorescent state under at least one condition in an aqueous solution in the absence of the multi-stranded nucleic acid, and (b) when the multi-stranded nucleic acid is allowed to exist in the condition defined in the above (a), the compound changes to a substantially colored state based on an interaction with the multi-stranded nucleic acid and substantially expresses fluorescent property based on said interaction.

  一种用于多股核酸的光学测量方法，包括以下步骤：将一种化合物与多股核酸接触，所述化合物能够与多股核酸相互作用，且该化合物具有以下性质：(a) 在无多股核酸的情况下，该化合物能够在水溶液中在至少一种条件下处于基本无色和非荧光状态，(b) 当多股核酸存在于上述(a)定义的状态下时，该化合物会因与多股核酸的相互作用而转变为基本上有色的状态，并基于该相互作用而表现出基本上荧光的性质。
• Aminoheteroaryl compounds as protein kinase inhibitors
  申请人：Cui Jean Jingrong

  公开号：US20070072874A1

  公开（公告）日：2007-03-29

  Aminopyridine and aminopyrazine compounds of formula ( 1 ), compositions including these compounds, and methods of their use are provided. Preferred compounds of formula 1 have activity as protein kinase inhibitors, including as inhibitors of c-MET.

  提供了公式（1）的氨基吡啶和氨基吡嗪化合物，包括这些化合物的组合物以及它们的使用方法。公式1的优选化合物具有作为蛋白激酶抑制剂的活性，包括作为c-MET抑制剂。
• METHOD FOR OPTICAL MEASUREMENT OF MULTI-STRANDED NUCLEIC ACID
  申请人：NAKAMURA Kouki

  公开号：US20080124732A1

  公开（公告）日：2008-05-29

  A method for optical measurement of a multi-stranded nucleic acid which comprises the step of bringing a compound into contact with a multi-stranded nucleic acid wherein said compound is capable of interacting with the multi-stranded nucleic acid, wherein the compound has the following properties: (a) the compound can exist in a substantially colorless and non-fluorescent state under at least one condition in an aqueous solution in the absence of the multi-stranded nucleic acid, and (b) when the multi-stranded nucleic acid is allowed to exist in the condition defined in the above (a), the compound changes to a substantially colored state based on an interaction with the multi-stranded nucleic acid and substantially expresses fluorescent property based on said interaction.

  一种用于光学测量多股核酸的方法，包括以下步骤：将一种化合物与多股核酸接触，其中该化合物能够与多股核酸相互作用，该化合物具有以下特性：（a）在无多股核酸存在的情况下，在水溶液中至少有一个条件下，该化合物可以存在于基本无色且不发荧光的状态；（b）当多股核酸被允许在上述（a）所定义的条件下存在时，该化合物会因与多股核酸的相互作用而转变为基本上带色的状态，并基于该相互作用表现出基本上发荧光的特性。
• Method for optical measurement of multi-stranded nucleic acid using cyanine dyes
  申请人：FUJIFILM Corporation

  公开号：EP1362894B1

  公开（公告）日：2007-12-19