2-溴-3-(N-叔丁氧羰基-N-甲基)氨基吡啶 | 1393598-48-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: 2-溴-3-(N-叔丁氧羰基-N-甲基)氨基吡啶
• 英文名称: tert-butyl (2-bromopyridin-3-yl)(methyl)carbamate
• 英文别名: 2-Bromo-3-(N-t-butoxycarbonyl-N-methyl)aminopyridine；tert-butyl N-(2-bromopyridin-3-yl)-N-methylcarbamate
• CAS: 1393598-48-5
• 化学式: C₁₁H₁₅BrN₂O₂
• 分子量: 287.156
• InChiKey: PCDDCSUBZHOLGW-UHFFFAOYSA-N

物化性质

• 沸点：
  338.3±27.0 °C(Predicted)
• 密度：
  1.391±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  42.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-溴-3-(N-叔丁氧羰基-N-甲基)氨基吡啶 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 生成 2-溴-N-甲基-3-氨基吡啶
  参考文献：
  名称：

  Practical Way to Imidazo[4,5-b] and [4,5-c]Pyridine-2-ones via Cascade Ureidation/Palladium-Catalyzed Cyclization

  摘要：

  We developed an efficient one-pot tandem carbamoyl chloride amination and palladium-catalyzed intramolecular urea cyclization, which furnished high-throughput access to imidazo[4,5-b]pyridine-2-one and related imidazo[4,5-c]pyridine-2-one ring systems. Moderate to excellent yields were reported.

  DOI：

  10.1021/co300078f
• 作为产物：
  描述：

  (2-溴-3-吡啶基)氨基甲酸叔丁酯 、 碘甲烷 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.5h， 生成 2-溴-3-(N-叔丁氧羰基-N-甲基)氨基吡啶
  参考文献：
  名称：

  Practical Way to Imidazo[4,5-b] and [4,5-c]Pyridine-2-ones via Cascade Ureidation/Palladium-Catalyzed Cyclization

  摘要：

  We developed an efficient one-pot tandem carbamoyl chloride amination and palladium-catalyzed intramolecular urea cyclization, which furnished high-throughput access to imidazo[4,5-b]pyridine-2-one and related imidazo[4,5-c]pyridine-2-one ring systems. Moderate to excellent yields were reported.

  DOI：

  10.1021/co300078f

文献信息

• Fungal cell wall synthesis gene
  申请人：——

  公开号：US20040038239A1

  公开（公告）日：2004-02-26

  A reporter system reflecting the transport process that transports GPI-anchored proteins to the cell wall was constructed and compounds inhibiting this process were discovered. Further, genes conferring resistance to the above compounds were identified and methods of screening for compounds that inhibit the activity of the proteins encoded by these genes were developed. Therefore, through the novel compounds, the present invention showed that antifungal agents having a novel mechanism, i.e. inhibiting the process that transports GPI-anchored proteins to the cell wall, could be achieved.

  构建了一个反映将GPI锚定蛋白转运到细胞壁的运输过程的报告系统，并发现了抑制该过程的化合物。此外，还鉴定了赋予对上述化合物抗性的基因，并开发了筛选抑制这些基因编码的蛋白质活性的化合物的方法。因此，通过新型化合物，本发明展示了可以实现具有新型机制（即抑制将GPI锚定蛋白转运到细胞壁的过程）的抗真菌剂。
• FUNGAL CELL WALL SYNTHESIS GENE
  申请人：Tsukahara Kappei

  公开号：US20090325228A1

  公开（公告）日：2009-12-31

  A reporter system reflecting the transport process that transports GPI-anchored proteins to the cell wall was constructed and compounds inhibiting this process were discovered. Further, genes conferring resistance to the above compounds were identified and methods of screening for compounds that inhibit the activity of the proteins encoded by these genes were developed. Therefore, through the novel compounds, the present invention showed that antifungal agents having a novel mechanism, i.e. inhibiting the process that transports GPI-anchored proteins to the cell wall, could be achieved.

  一个反映将GPI锚定蛋白质运输到细胞壁的传输过程的报告系统被构建，发现了抑制这一过程的化合物。此外，鉴定了赋予对上述化合物抗性的基因，并开发了筛选抑制这些基因编码的蛋白质活性的化合物的方法。因此，通过新型化合物，本发明展示了可以实现一种新颖机制的抗真菌剂，即抑制将GPI锚定蛋白质运输到细胞壁的过程。
• US7375204B2
  申请人：——

  公开号：US7375204B2

  公开（公告）日：2008-05-20
• US7541332B2
  申请人：——

  公开号：US7541332B2

  公开（公告）日：2009-06-02
• US7897387B2
  申请人：——

  公开号：US7897387B2

  公开（公告）日：2011-03-01