3-Butyl-8-<3-(2p-fluorophenyl-2-dioxolanyl)propyl>-4-oxo-1-phenyl-1,3,8-triazaspiro<4.5>decan | 54080-22-7

• 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: 3-Butyl-8-<3-(2p-fluorophenyl-2-dioxolanyl)propyl>-4-oxo-1-phenyl-1,3,8-triazaspiro<4.5>decan
• 英文别名: 8-{3-[2-(4-fluoro-phenyl)-[1,3]dioxolan-2-yl]-propyl}-3-isobutyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one；8-[3-[2-(4-Fluorophenyl)-1,3-dioxolan-2-yl]propyl]-3-(2-methylpropyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one
• CAS: 54080-22-7
• 化学式: C₂₉H₃₈FN₃O₃
• 分子量: 495.637
• InChiKey: UGPDZVNNGGGPCY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  36
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  45.2
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-Butyl-8-<3-(2p-fluorophenyl-2-dioxolanyl)propyl>-4-oxo-1-phenyl-1,3,8-triazaspiro<4.5>decan 在 盐酸 作用下， 以 乙醇 为溶剂， 反应 0.25h， 生成 8-[4-(4-Fluoro-phenyl)-4-oxo-butyl]-3-isobutyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one
  参考文献：
  名称：

  Effect of N-alkylation on the affinities of analogs of spiperone for dopamine D2 and serotonin 5-HT2 receptors

  摘要：

  Two series of N-substituted spiperone analogues were prepared and evaluated in vitro to measure their affinities for dopamine D2 and serotonin 5-HT2 receptors. Substitution of the amide nitrogen with an alkyl group of five carbon units or less resulted in analogues displaying a low selectivity for D2 compared to 5-HT2 receptors. However, a moderate improvement in selectivity for D2 receptors was observed with N-benzylspiperone. Substitution at either the ortho or para position of the benzyl group resulted in a further reduction in affinity for 5-HT2 receptors and improvement in the selectivity ratio. Examination of N-substituted analogues of spiperone may provide insights into the topography of the antagonist binding region of the 5-HT2 receptor. The results also suggest that an F-18-labeled analogue of N-(4-nitrobenzyl)spiperone (4p) may be a suitable tracer for studying D2 receptors with positron emission tomography since this compound displays a high selectivity for D2 receptors relative to that of spiperone and N-methylspiperone.

  DOI：

  10.1021/jm00081a002
• 作为产物：
  描述：

  乙烯二氧基螺哌隆 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydride 作用下， 生成 3-Butyl-8-<3-(2p-fluorophenyl-2-dioxolanyl)propyl>-4-oxo-1-phenyl-1,3,8-triazaspiro<4.5>decan
  参考文献：
  名称：

  Effect of N-alkylation on the affinities of analogs of spiperone for dopamine D2 and serotonin 5-HT2 receptors

  摘要：

  Two series of N-substituted spiperone analogues were prepared and evaluated in vitro to measure their affinities for dopamine D2 and serotonin 5-HT2 receptors. Substitution of the amide nitrogen with an alkyl group of five carbon units or less resulted in analogues displaying a low selectivity for D2 compared to 5-HT2 receptors. However, a moderate improvement in selectivity for D2 receptors was observed with N-benzylspiperone. Substitution at either the ortho or para position of the benzyl group resulted in a further reduction in affinity for 5-HT2 receptors and improvement in the selectivity ratio. Examination of N-substituted analogues of spiperone may provide insights into the topography of the antagonist binding region of the 5-HT2 receptor. The results also suggest that an F-18-labeled analogue of N-(4-nitrobenzyl)spiperone (4p) may be a suitable tracer for studying D2 receptors with positron emission tomography since this compound displays a high selectivity for D2 receptors relative to that of spiperone and N-methylspiperone.

  DOI：

  10.1021/jm00081a002

文献信息

• Effect of N-alkylation on the affinities of analogs of spiperone for dopamine D2 and serotonin 5-HT2 receptors
  作者：Robert H. Mach、Joseph R. Jackson、Robert R. Luedtke、Kathryn J. Ivins、Perry B. Molinoff、Richard L. Ehrenkaufer

  DOI：10.1021/jm00081a002

  日期：1992.2

  Two series of N-substituted spiperone analogues were prepared and evaluated in vitro to measure their affinities for dopamine D2 and serotonin 5-HT2 receptors. Substitution of the amide nitrogen with an alkyl group of five carbon units or less resulted in analogues displaying a low selectivity for D2 compared to 5-HT2 receptors. However, a moderate improvement in selectivity for D2 receptors was observed with N-benzylspiperone. Substitution at either the ortho or para position of the benzyl group resulted in a further reduction in affinity for 5-HT2 receptors and improvement in the selectivity ratio. Examination of N-substituted analogues of spiperone may provide insights into the topography of the antagonist binding region of the 5-HT2 receptor. The results also suggest that an F-18-labeled analogue of N-(4-nitrobenzyl)spiperone (4p) may be a suitable tracer for studying D2 receptors with positron emission tomography since this compound displays a high selectivity for D2 receptors relative to that of spiperone and N-methylspiperone.