3-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline
• 英文别名: [3-(4-Fluorophenyl)-4,4-dimethylimidazo[1,5-a]quinoxalin-5-yl]-pyrrolidin-1-ylmethanone
• 化学式: C₂₃H₂₃FN₄O
• 分子量: 390.46
• InChiKey: BISSZWKXAHVKPH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  29
• 可旋转键数：
  1
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  41.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  N-(4-fluorobenzyl)formamide 在 potassium tert-butylate 、 sodium carbonate 、 三乙胺 、 三氯氧磷 作用下， 以 四氢呋喃 为溶剂， 反应 5.0h， 生成 3-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-5-[(pyrrolidino)carbonyl]imidazo[1,5-a]quinoxaline
  参考文献：
  名称：

  3-Phenyl-Substituted Imidazo[1,5-a]quinoxalin-4-ones and Imidazo[1,5-a]quinoxaline Ureas That Have High Affinity at the GABA_A/Benzodiazepine Receptor Complex

  摘要：

  A series of imidazo[1,5-alpha]quinoxalin-4-ones and imidazo[1,5-alpha]quinoxaline ureas containing substituted phenyl groups at the 3-position was developed. Compounds within the imidazo-[1,5-alpha]quinoxaline urea series had high affinity for the GABA(A)/benzodiazepine receptor complex with varying in vitro efficacy, although most analogs were partial agonists as indicated by [S-35]TBPS and Cl- current ratios. Interestingly, a subseries of piperazine ureas was identified which had biphasic efficacy, becoming more antagonistic with increasing concentration. Analogs within the imidazo [1,5-alpha] quinoxalin-4-one series had substantially decreased binding affinity as compared to the quinoxaline urea series. These compounds ranged from antagonists to full agonists by in. vitro analysis, with several derivatives having roughly 4-fold greater intrinsic activity than diazepam as indicated by Cl- current measurement. Numerous compounds from both series were effective in antagonizing metrazole-induced seizures, consistent with anti-convulsant properties and possible anxiolytic activity. Most of the quinoxaline ureas and quinoxalin-4-ones were active in an acute electroshock physical dependence side effect assay in mice precluding further development.

  DOI：

  10.1021/jm960070+

文献信息

• IMIDAZO 1,5-a]QUINOXALINES
  申请人：THE UPJOHN COMPANY

  公开号：EP0590022A1

  公开（公告）日：1994-04-06
• US5541324A
  申请人：——

  公开号：US5541324A

  公开（公告）日：1996-07-30
• [EN] IMIDAZO[1,5-a]QUINOXALINES
  申请人：THE UPJOHN COMPANY

  公开号：WO1992022552A1

  公开（公告）日：1992-12-23

  (EN) Imidazo[1,5-a]quinoxalines (I) which do not contain an endocyclic carbonyl group are useful as anxiolytic and sedative/hypnotic agents.(FR) Des imidazo[1,5-a]quinoxalines de formule (I) qui ne contiennent pas un groupe carbonyle endocyclique sont utilisées comme agents anxyolytiques et sédatifs/hypnotiques.