trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[7-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide | 1192312-63-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[7-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide
• CAS: 1192312-63-2
• 化学式: C₂₃H₂₀N₄O₃
• 分子量: 400.437
• InChiKey: FJAKPAPUGHHPRR-QXONSOMPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.73
• 重原子数：
  30.0
• 可旋转键数：
  3.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  94.07
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  5-苯基-2-嘧啶胺 、 trans-3-oxo-3H-spiro[7-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxylic acid 在 吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以45%的产率得到trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[7-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide
  参考文献：
  名称：

  Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1′-cyclohexane]-4′-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist

  摘要：

  A series of trans-3-oxospiro[(aza)isobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide derivatives were synthesized to identify potent NPY Y5 receptor antagonists. Of the compounds, 21j showed high Y5 binding affinity, metabolic stability and brain and cerebrospinal fluid (CSF) penetration, and low susceptibility to P-glycoprotein transporters. Oral administration of 21j significantly inhibited the Y5 agonist-induced food intake in rats with a minimum effective dose of 1 mg/kg. This compound was selected for proof-of-concept studies in human clinical trials. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.08.019

文献信息

• Identification of positron emission tomography ligands for NPY Y5 receptors in the brain
  作者：Hirobumi Takahashi、Yuji Haga、Takunobu Shibata、Katsumasa Nonoshita、Toshihiro Sakamoto、Minoru Moriya、Tomoyuki Ohe、Masato Chiba、Yuko Mitobe、Hidefumi Kitazawa、Hisashi Iwaasa、Akane Ishihara、Yasuyuki Ishii、Akio Kanatani、Takehiro Fukami

  DOI：10.1016/j.bmcl.2009.07.103

  日期：2009.9

  A series of trans-3-oxospiro[(aza)isobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide derivatives were synthesized and profiled for NPY Y5 binding affinity, brain and CSF penetrability in rats, and susceptibility to human and mouse P-glycoprotein transporters in order to develop a PET ligand. Compound 12b exhibited an acceptable profile for a PET ligand, and [C-11]12b was successfully utilized in clinical settings as a Y5 PET ligand. (C) 2009 Elsevier Ltd. All rights reserved.
• Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1′-cyclohexane]-4′-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist
  作者：Yuji Haga、Toshihiro Sakamoto、Takunobu Shibata、Katsumasa Nonoshita、Makoto Ishikawa、Takuya Suga、Hirobumi Takahashi、Toshiyuki Takahashi、Hidekazu Takahashi、Makoto Ando、Takashi Murai、Akira Gomori、Zenjun Oda、Hidefumi Kitazawa、Yuko Mitobe、Maki Kanesaka、Tomoyuki Ohe、Hisashi Iwaasa、Yasuyuki Ishii、Akane Ishihara、Akio Kanatani、Takehiro Fukami

  DOI：10.1016/j.bmc.2009.08.019

  日期：2009.10

  A series of trans-3-oxospiro[(aza)isobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide derivatives were synthesized to identify potent NPY Y5 receptor antagonists. Of the compounds, 21j showed high Y5 binding affinity, metabolic stability and brain and cerebrospinal fluid (CSF) penetration, and low susceptibility to P-glycoprotein transporters. Oral administration of 21j significantly inhibited the Y5 agonist-induced food intake in rats with a minimum effective dose of 1 mg/kg. This compound was selected for proof-of-concept studies in human clinical trials. (C) 2009 Elsevier Ltd. All rights reserved.