5-chloro-6-(1H-indol-7-yl)-2,2,3,3,8-pentamethyl-2,3-dihydroquinolin-4(1H)-one | 1268469-81-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 5-chloro-6-(1H-indol-7-yl)-2,2,3,3,8-pentamethyl-2,3-dihydroquinolin-4(1H)-one
• 英文别名: 5-chloro-6-(1H-indol-7-yl)-2,2,3,3,8-pentamethyl-1H-quinolin-4-one
• CAS: 1268469-81-3
• 化学式: C₂₂H₂₃ClN₂O
• 分子量: 366.89
• InChiKey: JQKOMAQFUWNONV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  26
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  44.9
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  、 吲哚-7-硼酸 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 sodium carbonate 作用下， 以 1,4-二氧六环 为溶剂， 生成 5-chloro-6-(1H-indol-7-yl)-2,2,3,3,8-pentamethyl-2,3-dihydroquinolin-4(1H)-one
  参考文献：
  名称：

  Tetrahydroquinoline glucocorticoid receptor agonists: Discovery of a 3-hydroxyl for improving receptor selectivity

  摘要：

  We have previously disclosed a series of glucocorticoid receptor (GR) ligands derived from 6-indole-1,2,3,4-tetrahydroquinolines through structure-activity relationship (SAR) of the pendent C6-indole ring. In parallel with this effort, we now report SAR of the tetrahydroquinoline A-ring that identified the importance of a C3 hydroxyl in improving GR selectivity within a series of non-steroidal GR agonists. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.11.047

文献信息

• Tetrahydroquinoline glucocorticoid receptor agonists: Discovery of a 3-hydroxyl for improving receptor selectivity
  作者：Steven L. Roach、Robert I. Higuchi、Andrew R. Hudson、Mark E. Adams、Peter M. Syka、Dale E. Mais、Jeffrey N. Miner、Keith B. Marschke、Lin Zhi

  DOI：10.1016/j.bmcl.2010.11.047

  日期：2011.1

  We have previously disclosed a series of glucocorticoid receptor (GR) ligands derived from 6-indole-1,2,3,4-tetrahydroquinolines through structure-activity relationship (SAR) of the pendent C6-indole ring. In parallel with this effort, we now report SAR of the tetrahydroquinoline A-ring that identified the importance of a C3 hydroxyl in improving GR selectivity within a series of non-steroidal GR agonists. (C) 2010 Elsevier Ltd. All rights reserved.