1-methylsulphonyl-2,3,6,7-tetrahydro-1H-azepine | 66207-97-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吖庚因类
• 英文名称: 1-methylsulphonyl-2,3,6,7-tetrahydro-1H-azepine
• 英文别名: 1-Methylsulfonyl-2,3,6,7-tetrahydro-1H-azepin；1-methanesulphonyl-2,3,6,7-tetrahydro-1H-azepine；1-methylsulfonyl-2,3,6,7-tetrahydroazepine
• CAS: 66207-97-4
• 化学式: C₇H₁₃NO₂S
• 分子量: 175.252
• InChiKey: AVERISOFUKEBNQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  45.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-methylsulphonyl-2,3,6,7-tetrahydro-1H-azepine 生成 3-(Methylsulfonyl)-8-oxa-3-azabicyclo[5.1.0]octane
  参考文献：
  名称：

  PAIONI, R.

  摘要：

  DOI：
• 作为产物：
  描述：

  3-hydroxy-4-chloro-1-(β,β,β-trichloroethoxycarbonyl)-pyrrolidine 生成 1-methylsulphonyl-2,3,6,7-tetrahydro-1H-azepine
  参考文献：
  名称：

  PAIONI, R.

  摘要：

  DOI：

文献信息

• Derivatives of perhydro-aza-heterocycles
  申请人：Ciba-Geigy Corporation

  公开号：US04160837A1

  公开（公告）日：1979-07-10

  The present invention provides new derivatives of perhydro-aza-heterocycles of the formula ##STR1## in which X is the oxo radical or hydrogen and the radical OR.sub.1, in which R.sub.1 is hydrogen or a substituted or unsubstituted aliphatic hydrocarbon radical, a substituted or unsubstituted araliphatic hydrocarbon radical or a substituted or unsubstituted aromatic hydrocarbon radical or an acyl radical, R.sub.2 is hydrogen or a substituted or unsubstituted aliphatic hydrocarbon radical, Y is oxygen or sulphur, n.sub.1 and n.sub.2 each are values of 1 to 3, n.sub.1 +n.sub.2 being at most four, and Ar is a substituted or unsubstituted aromatic hydrocarbon radical, and the acid addition salts, in particular the pharmaceutically acceptable acid addition salts thereof. These new substances possess valuable pharmacological properties, in particular antidepressant activity, and can be used for the treatment of mental depressions. Specific embodiments are trans- and cis-3-hydroxy-4-(3,4-dimethyl-phenoxy)-piperidine, trans- and cis-3-hydroxy-4-(2,3-dimethyl-phenoxy)-piperidine, their 1-methyl derivatives and the pharmaceutically acceptable salts of these substances.

  本发明提供了新的perhydro-aza-杂环衍生物，化学式如下：其中X为氧化物基团或氢，基团OR.sub.1中R.sub.1为氢或取代或未取代的脂肪烃基团、取代或未取代的芳基脂肪烃基团或取代或未取代的芳基烃基团或酰基，R.sub.2为氢或取代或未取代的脂肪烃基团，Y为氧或硫，n.sub.1和n.sub.2各自为1至3的值，n.sub.1 +n.sub.2最多为四，Ar为取代或未取代的芳基烃基团，以及其酸盐加合物，特别是其中药学上可接受的酸盐。这些新物质具有有价值的药理特性，特别是抗抑郁活性，并可用于治疗精神抑郁症。具体实施例包括反式和顺式3-羟基-4-(3,4-二甲基苯氧基)-哌啶、反式和顺式3-羟基-4-(2,3-二甲基苯氧基)-哌啶，它们的1-甲基衍生物和这些物质的药学上可接受的盐。
• Direct Synthesis of Previously Inaccessible Bridgehead Azabicyclics by Intramolecular Cyclization of α-Sulfonamido and α-Sulfonimido Radicals
  作者：Leo A. Paquette、Choon Sup Ra、Jeffrey D. Schloss、Silvana M. Leit、Judith C. Gallucci

  DOI：10.1021/jo010216z

  日期：2001.5.1

  Syntheses of the first bridgehead sultams and the only known bridgehead disulfonimide are described. Both approaches capitalize on the electrophilicity of alpha-sulfonyl radicals and their propensity to undergo intramolecular ring closure. Where double bonds are concerned, 5-exo and 6-exo pathways operate preferentially as long as structural strain is not excessive. When the reaction center is a carbon-carbon

  描述了第一个桥头磺胺和唯一已知的桥头二磺酰亚胺的合成。两种方法都利用了α-磺酰基的亲电性和它们进行分子内闭环的倾向。在涉及双键的情况下，只要结构应变不过度，5-exo和6-exo途径就优先起作用。当反应中心是碳-碳三键时，第一个环化反应会产生乙烯基，该乙烯基具有足够的反应活性以捕获溶剂苯。在45的情况下，该顺序反应重要地导致引入足够活化的苯乙烯官能团以允许第二个闭环在动力学上可行。通过X射线晶体学方法已经阐明了12和17的固态结构特征。尽管与氮孤对相对于相邻磺酰基的排列方式的规范存在重大差异，但这些化合物仍具有良好的水解稳定性。对于13，可能产生α-磺酰胺碳负离子，并且已经实现了用乙酸铬酰的区域特异性氧化。
• Antidepressant piperidinones
  申请人：Ciba-Geigy Corporation

  公开号：US04246269A1

  公开（公告）日：1981-01-20

  The present invention provides new derivatives of perhydro-aza-heterocycles of the formula ##STR1## in which X is the oxo radical or hydrogen and the radical OR.sub.1, in which R.sub.1 is hydrogen or a substituted or unsubstituted aliphatic hydrocarbon radical, a substituted or unsubstituted araliphatic hydrocarbon radical or a substituted or unsubstituted aromatic hydrocarbon radical or an acyl radical, R.sub.2 is hydrogen or a substituted or unsubstituted aliphatic hydrocarbon radical, Y is oxygen or sulphur, n.sub.1 and n.sub.2 each are values of 1 to 3, n.sub.1 +n.sub.2 being at most four, and Ar is a substituted or unsubstituted aromatic hydrocarbon radical, and the acid addition salts, in particular the pharmaceutically acceptable acid addition salts thereof. These new substances possess valuable pharmacological properties, in particular antidepressant activity, and can be used for the treatment of mental depressions. Specific embodiments are trans- and cis-3-hydroxy-4-(3,4-dimethyl-phenoxy)-piperidine, trans- and cis-3-hydroxy-4-(2,3-dimethyl-phenoxy)-piperidine, their 1-methyl derivatives and the pharmaceutically acceptable salts of these substances.

  本发明提供了新的过氢化-氮杂杂环衍生物的衍生物，其化学式为##STR1## 其中X是氧代基或氢，基OR.sub.1是氢或取代或未取代的脂肪烃基、取代或未取代的芳杂烃基或取代或未取代的芳香烃基或酰基，R.sub.2是氢或取代或未取代的脂肪烃基，Y是氧或硫，n.sub.1和n.sub.2分别是1到3的值，n.sub.1 + n.sub.2最多为4，Ar是取代或未取代的芳香烃基，以及其酸加成盐，特别是其药用可接受的酸加成盐。这些新物质具有有价值的药理学特性，特别是抗抑郁活性，可用于治疗精神抑郁症。具体实施例包括顺式和反式3-羟基-4-(3,4-二甲基-苯氧基)-哌啶、顺式和反式3-羟基-4-(2,3-二甲基-苯氧基)-哌啶、它们的1-甲基衍生物和这些物质的药用可接受的盐。
• The First Examples of Bridgehead Bicyclic Sultams
  作者：Leo A. Paquette、Silvana M. Leit

  DOI：10.1021/ja992161c

  日期：1999.9.1
• PAIONI, R.
  作者：PAIONI, R.

  DOI：——

  日期：——