(R)-1-((R)-(3,5-bis(trifluoromethyl)phenyl)(2-methyl-2H-tetrazol-5-yl)methyl)-3-ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoxaline | 871834-77-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (R)-1-((R)-(3,5-bis(trifluoromethyl)phenyl)(2-methyl-2H-tetrazol-5-yl)methyl)-3-ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoxaline
• CAS: 871834-77-4
• 化学式: C₂₂H₁₉F₉N₆
• 分子量: 538.419
• InChiKey: LPLOQQSRCZXYAK-CRAIPNDOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.07
• 重原子数：
  37.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  58.87
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  (R)-1-((R)-(3,5-bis(trifluoromethyl)phenyl)(2-methyl-2H-tetrazol-5-yl)methyl)-3-ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoxaline 、 氯甲酸乙酯 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 生成 (R)-ethyl 4-((R)-(3,5-bis(trifluoromethyl)phenyl)(2-methyl-2H-tetrazol-5-yl)methyl)-2-ethyl-6-(trifluoromethyl)-3,4-dihydroquinoxaline-1(2H)-carboxylate
  参考文献：
  名称：

  Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitors

  摘要：

  Cholesteryl ester transfer protein is a plasma glycoprotein that transfers cholesterol ester between lipoprotein particles. Inhibition of this protein, in vitro and in vivo, produces an increase in plasma high density lipoprotein cholesterol (HE)L-Q. This communication will describe the SAR and svnthesis of a series of substituted tetrahydroquinoxaline CETP inhibitors from early P lead to advanced enantiomerically pure anaiogs. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.112
• 作为产物：
  描述：

  在 甲醇 、 sodium azide 、 四丁基碘化铵 、 氯化铵 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 N-甲基吡咯烷酮 、 N,N-二甲基甲酰胺 为溶剂， 生成 (R)-1-((R)-(3,5-bis(trifluoromethyl)phenyl)(2-methyl-2H-tetrazol-5-yl)methyl)-3-ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoxaline
  参考文献：
  名称：

  Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitors

  摘要：

  Cholesteryl ester transfer protein is a plasma glycoprotein that transfers cholesterol ester between lipoprotein particles. Inhibition of this protein, in vitro and in vivo, produces an increase in plasma high density lipoprotein cholesterol (HE)L-Q. This communication will describe the SAR and svnthesis of a series of substituted tetrahydroquinoxaline CETP inhibitors from early P lead to advanced enantiomerically pure anaiogs. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.112