(1R,2S)-1-({3,6-diethyl-5-[(5-methylpyridin-2-yl) oxy] pyrazin-2-yl}amino) indan-2-ol

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1R,2S)-1-({3,6-diethyl-5-[(5-methylpyridin-2-yl) oxy] pyrazin-2-yl}amino) indan-2-ol
• 英文别名: (1R,2S)-1-[[3,6-diethyl-5-(5-methylpyridin-2-yl)oxypyrazin-2-yl]amino]-2,3-dihydro-1H-inden-2-ol
• 化学式: C₂₃H₂₆N₄O₂
• 分子量: 390.485
• InChiKey: NLAVRZIFFTXNTC-PZJWPPBQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  29
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  80.2
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (1R,2S)-1-({3,6-diethyl-5-[(5-methylpyridin-2-yl) oxy] pyrazin-2-yl}amino) indan-2-ol 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 N-[(1R,2S)-2-ethoxy-2,3-dihydro-1H-inden-1-yl]-3,6-DIETHYL-5-[(5-methylpyridin-2-yl)oxy]pyrazin-2-amine
  参考文献：
  名称：

  Heteroatom-linked indanylpyrazines are corticotropin releasing factor type-1 receptor antagonists

  摘要：

  Low nanomolar corticotropin releasing factor type-1 (CRF1) receptor antagonists containing unique indanylamines were identified from the heteroatom-linked pyrazine chemotype. The most potent indanylpyrazine had a K-i = 11 +/- 1 nM. The oxygen-linked pyrazinyl derivatives were prepared through a copper-catalyzed coupling of a pyridinone to a bromo- or iodopyrazine. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.09.008
• 作为产物：
  描述：

  2-羟基-5-甲基嘧啶 、 alkaline earth salt of/the/ methylsulfuric acid 在 copper(l) iodide 、 caesium carbonate 、 N,N'-二甲基乙二胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 (1R,2S)-1-({3,6-diethyl-5-[(5-methylpyridin-2-yl) oxy] pyrazin-2-yl}amino) indan-2-ol
  参考文献：
  名称：

  Heteroatom-linked indanylpyrazines are corticotropin releasing factor type-1 receptor antagonists

  摘要：

  Low nanomolar corticotropin releasing factor type-1 (CRF1) receptor antagonists containing unique indanylamines were identified from the heteroatom-linked pyrazine chemotype. The most potent indanylpyrazine had a K-i = 11 +/- 1 nM. The oxygen-linked pyrazinyl derivatives were prepared through a copper-catalyzed coupling of a pyridinone to a bromo- or iodopyrazine. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.09.008

文献信息

• [EN] SUBSTITUTED 1,4-PYRAZINE DERIVATIVES<br/>[FR] DERIVES 1,4-PYRAZINE SUBSTITUES
  申请人：UPJOHN CO

  公开号：WO2004024719A1

  公开（公告）日：2004-03-25

  Substituted aryl 1,4-pyrazine derivatives and their use in treating anxiety disorders, depression and stress related disorders are disclosed.

  揭示了替代芳基1,4-吡嗪衍生物及其在治疗焦虑症、抑郁症和与压力有关的疾病中的应用。
• Substituted 1,4-pyrazine derivatives
  申请人：——

  公开号：US20040116444A1

  公开（公告）日：2004-06-17

  Substituted aryl 1,4-pyrazine derivatives and their use in treating anxiety disorders, depression and stress related disorders are disclosed.

  本发明揭示了取代芳基1,4-吡嗪衍生物及其在治疗焦虑症、抑郁症和与压力相关的疾病中的应用。
• SUBSTITUTED 1,4-PYRAZINE DERIVATIVES
  申请人：Pharmacia & Upjohn Company LLC

  公开号：EP1539736A1

  公开（公告）日：2005-06-15