(2-Hydroxy-3-nitrophenyl)-(4-methyl-1,4-diazepan-1-yl)methanone | 934275-52-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: (2-Hydroxy-3-nitrophenyl)-(4-methyl-1,4-diazepan-1-yl)methanone
• 英文别名: (2-hydroxy-3-nitrophenyl)-(4-methyl-1,4-diazepan-1-yl)methanone
• CAS: 934275-52-2
• 化学式: C₁₃H₁₇N₃O₄
• 分子量: 279.296
• InChiKey: OFGYHUNYNOTGAI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  89.6
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2-Hydroxy-3-nitrophenyl)-(4-methyl-1,4-diazepan-1-yl)methanone 在 platinum on activated charcoal 氢气 作用下， 生成 (3-Amino-2-hydroxyphenyl)-(4-methyl-1,4-diazepan-1-yl)methanone
  参考文献：
  名称：

  Comparison of N,N′-diarylsquaramides and N,N′-diarylureas as antagonists of the CXCR2 chemokine receptor

  摘要：

  N,N'-diarylsquaramides were prepared and evaluated as antagonists of CXCR2. The compounds were found to be potent and selective antagonists of CXCR2. Significant differences in SAR was observed relative to the previously described N,N'-diarylurea series. As was the case in the N,N'-diarylurea series, placing sulfonamide substituent adjacent to the acidic phenol significantly reduced the clearance in rat pharmacokinetic studies. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.12.067
• 作为产物：
  描述：

  2-氯-3-硝基苯甲酸 在 水 、 sodium hydride 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 (2-Hydroxy-3-nitrophenyl)-(4-methyl-1,4-diazepan-1-yl)methanone
  参考文献：
  名称：

  Comparison of N,N′-diarylsquaramides and N,N′-diarylureas as antagonists of the CXCR2 chemokine receptor

  摘要：

  N,N'-diarylsquaramides were prepared and evaluated as antagonists of CXCR2. The compounds were found to be potent and selective antagonists of CXCR2. Significant differences in SAR was observed relative to the previously described N,N'-diarylurea series. As was the case in the N,N'-diarylurea series, placing sulfonamide substituent adjacent to the acidic phenol significantly reduced the clearance in rat pharmacokinetic studies. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.12.067

文献信息

• Comparison of N,N′-diarylsquaramides and N,N′-diarylureas as antagonists of the CXCR2 chemokine receptor
  作者：Brent W. McCleland、Roderick S. Davis、Michael R. Palovich、Katherine L. Widdowson、Michelle L. Werner、Miriam Burman、James J. Foley、Dulcie B. Schmidt、Henry M. Sarau、Martin Rogers、Kevin L. Salyers、Peter D. Gorycki、Theresa J. Roethke、Gary J. Stelman、Leonard M. Azzarano、Keith W. Ward、Jakob Busch-Petersen

  DOI：10.1016/j.bmcl.2006.12.067

  日期：2007.3

  N,N'-diarylsquaramides were prepared and evaluated as antagonists of CXCR2. The compounds were found to be potent and selective antagonists of CXCR2. Significant differences in SAR was observed relative to the previously described N,N'-diarylurea series. As was the case in the N,N'-diarylurea series, placing sulfonamide substituent adjacent to the acidic phenol significantly reduced the clearance in rat pharmacokinetic studies. (c) 2007 Elsevier Ltd. All rights reserved.