(7R)-19-methoxy-5-methyl-2,5-diazatetracyclo[13.4.0.02,7.08,13]nonadeca-1(15),8,10,12,16,18-hexaene | 448296-34-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯氮卓类
• 英文名称: (7R)-19-methoxy-5-methyl-2,5-diazatetracyclo[13.4.0.02,7.08,13]nonadeca-1(15),8,10,12,16,18-hexaene
• CAS: 448296-34-2
• 化学式: C₁₉H₂₂N₂O
• 分子量: 294.396
• InChiKey: GZXNMNCAWGIAAW-KRWDZBQOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.37
• 拓扑面积：
  15.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (7R)-19-methoxy-5-methyl-2,5-diazatetracyclo[13.4.0.02,7.08,13]nonadeca-1(15),8,10,12,16,18-hexaene 在 palladium diacetate 、 三氯化铝 、 三乙胺 、 三苯基膦 作用下， 以 甲醇 、 二氯甲烷 、 苯 为溶剂， 反应 82.0h， 生成 (14bR)-1,2,3,4,10,14b-六氢-2-甲基-二苯并(c,f)吡嗪并(1,2-a)氮杂卓
  参考文献：
  名称：

  Synthesis and Pharmacological Testing of 1,2,3,4,10,14b-Hexahydro-6-methoxy-2-methyldibenzo[c,f]pyrazino[1,2-a]azepin and Its Enantiomers in Comparison with the Two Antidepressants Mianserin and Mirtazapine

  摘要：

  The synthesis and resolution of 1,2,3,4,10,14b-hexahydro-6-methoxy-2-methyldibenzo[cf]-pyrazino[1,2-alpha]azepin (6-methoxymianserin, 6) are described. Furthermore, the in vitro and in vivo effects of 6 and its enantiomers are presented. 6 displayed high affinity for the 5-HT2A/2C receptors, only moderate affinity for the adrenoceptors, and no affinity for the NA reuptake site. Surprisingly, 6 also showed moderate to high affinity for the dopamine D2 receptor, an effect that resides in the (R)-(-)-enantiomer.

  DOI：

  10.1021/jm010566d
• 作为产物：
  描述：

  (2-氯乙基)-(2-氯-2-苯乙基)-甲胺 在 PPA 、 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 反应 25.0h， 生成 (7R)-19-methoxy-5-methyl-2,5-diazatetracyclo[13.4.0.02,7.08,13]nonadeca-1(15),8,10,12,16,18-hexaene
  参考文献：
  名称：

  Synthesis and Pharmacological Testing of 1,2,3,4,10,14b-Hexahydro-6-methoxy-2-methyldibenzo[c,f]pyrazino[1,2-a]azepin and Its Enantiomers in Comparison with the Two Antidepressants Mianserin and Mirtazapine

  摘要：

  The synthesis and resolution of 1,2,3,4,10,14b-hexahydro-6-methoxy-2-methyldibenzo[cf]-pyrazino[1,2-alpha]azepin (6-methoxymianserin, 6) are described. Furthermore, the in vitro and in vivo effects of 6 and its enantiomers are presented. 6 displayed high affinity for the 5-HT2A/2C receptors, only moderate affinity for the adrenoceptors, and no affinity for the NA reuptake site. Surprisingly, 6 also showed moderate to high affinity for the dopamine D2 receptor, an effect that resides in the (R)-(-)-enantiomer.

  DOI：

  10.1021/jm010566d

文献信息

• Synthesis and Pharmacological Testing of 1,2,3,4,10,14b-Hexahydro-6-methoxy-2-methyldibenzo[<i>c</i>,<i>f</i>]pyrazino[1,2-<i>a</i>]azepin and Its Enantiomers in Comparison with the Two Antidepressants Mianserin and Mirtazapine
  作者：Håkan V. Wikström、Marguérite M. Mensonides-Harsema、Thomas I. F. H. Cremers、Ejner K. Moltzen、Jørn Arnt

  DOI：10.1021/jm010566d

  日期：2002.7.1

  The synthesis and resolution of 1,2,3,4,10,14b-hexahydro-6-methoxy-2-methyldibenzo[cf]-pyrazino[1,2-alpha]azepin (6-methoxymianserin, 6) are described. Furthermore, the in vitro and in vivo effects of 6 and its enantiomers are presented. 6 displayed high affinity for the 5-HT2A/2C receptors, only moderate affinity for the adrenoceptors, and no affinity for the NA reuptake site. Surprisingly, 6 also showed moderate to high affinity for the dopamine D2 receptor, an effect that resides in the (R)-(-)-enantiomer.