5-Methoxy-2-(4-methyl-thiazol-2-yl)-6,7,8,9-tetrahydro-imidazo[1,2-a]quinazoline | 118506-70-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 5-Methoxy-2-(4-methyl-thiazol-2-yl)-6,7,8,9-tetrahydro-imidazo[1,2-a]quinazoline
• 英文别名: 2-(5-Methoxy-6,7,8,9-tetrahydroimidazo[1,2-a]quinazolin-2-yl)-4-methyl-1,3-thiazole
• CAS: 118506-70-0
• 化学式: C₁₅H₁₆N₄OS
• 分子量: 300.384
• InChiKey: NHXNFNNWOHOAJX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  80.6
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  5-methoxy-6,7,8,9-tetrahydroimidazo<1,2-a>quinazoline-2-thiocarboxamide 、 一氯丙酮 以 乙醇 为溶剂， 反应 29.0h， 生成 5-Methoxy-2-(4-methyl-thiazol-2-yl)-6,7,8,9-tetrahydro-imidazo[1,2-a]quinazoline
  参考文献：
  名称：

  2-(Oxadiazolyl)- and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors

  摘要：

  Oxadiazoles, like the benzoyl group in a series of imidazo[1,2-alpha]pyrimidines, have been found to be metabolically stable alternatives to ester groups in benzodiazepine-receptor ligands. This change has lead to a number of compounds which bind to the receptors and which exhibit potent agonist activity in a food-motivated conflict test thought to predict anxiolytic properties. Compounds 4, 5, and 13 were equipotent with chlordiazepoxide but showed little or no myorelaxant effects. Replacing the oxadiazole group by thiazole gave compounds such as 23 which binds to the benzodiazepine receptor but exhibits the intrinsic activity of a partial inverse agonist in vivo.

  DOI：

  10.1021/jm00111a021

文献信息

• TULLY, W. ROGER;GARDNER, COLIN R.;GILLESPIE, ROGER J.;WESTWOOD, ROBERT, J. MED. CHEM., 34,(1991) N, C. 2060-2067
  作者：TULLY, W. ROGER、GARDNER, COLIN R.、GILLESPIE, ROGER J.、WESTWOOD, ROBERT

  DOI：——

  日期：——
• US4925846A
  申请人：——

  公开号：US4925846A

  公开（公告）日：1990-05-15
• 2-(Oxadiazolyl)- and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors
  作者：W. Roger Tully、Colin R. Gardner、Roger J. Gillespie、Robert Westwood

  DOI：10.1021/jm00111a021

  日期：1991.7

  Oxadiazoles, like the benzoyl group in a series of imidazo[1,2-alpha]pyrimidines, have been found to be metabolically stable alternatives to ester groups in benzodiazepine-receptor ligands. This change has lead to a number of compounds which bind to the receptors and which exhibit potent agonist activity in a food-motivated conflict test thought to predict anxiolytic properties. Compounds 4, 5, and 13 were equipotent with chlordiazepoxide but showed little or no myorelaxant effects. Replacing the oxadiazole group by thiazole gave compounds such as 23 which binds to the benzodiazepine receptor but exhibits the intrinsic activity of a partial inverse agonist in vivo.