4-methyl-6-naphthalen-2-yl-2H-pyridazin-3-one | 28734-27-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 4-methyl-6-naphthalen-2-yl-2H-pyridazin-3-one
• 英文别名: 5-methyl-3-naphthalen-2-yl-1H-pyridazin-6-one
• CAS: 28734-27-2
• 化学式: C₁₅H₁₂N₂O
• 分子量: 236.273
• InChiKey: TXKPQKVAXDCHNI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  41.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-methyl-6-naphthalen-2-yl-2H-pyridazin-3-one 在 三氯氧磷 作用下， 生成 3-chloro-4-methyl-6-naphthalen-2-yl-pyridazine
  参考文献：
  名称：

  3-Aminopyridazine derivatives with atypical antidepressant, serotonergic and dopaminergic activities

  摘要：

  Minaprine [3-[(beta-morpholinoethyl)amino]-4-methyl-6-phenylpyridazine dihydrochloride] is active in most animal models of depression and exhibits in vivo a dual dopaminomimetic and serotoninomimetic activity profile. In an attempt to dissociate these two effects and to characterize the responsible structural requirements, a series of 47 diversely substituted analogues of minaprine were synthesized and tested for their potential antidepressant, serotonergic, and dopaminergic activities. The structure-activity relationships show that dopaminergic and serotonergic activities can be dissociated. Serotonergic activity appears to be correlated mainly with the substituent in the 4-position of the pyridazine ring whereas the dopaminergic activity appears to be dependent on the presence, or in the formation, of a para-hydroxylated aryl ring in the 6-position of the pyridazine ring.

  DOI：

  10.1021/jm00123a004
• 作为产物：
  描述：

  衣康酸酐 在 三氯化铝 、 sodium acetate 、 potassium carbonate 、 一水合肼 作用下， 以 甲醇 、 硝基苯 、 丙酮 为溶剂， 生成 4-methyl-6-naphthalen-2-yl-2H-pyridazin-3-one
  参考文献：
  名称：

  Siddiqui, Anees A.; Wani, Sachin M., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 7, p. 1574 - 1579

  摘要：

  DOI：

文献信息

• Siddiqui, Anees A.; Wani, Sachin M., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 7, p. 1574 - 1579
  作者：Siddiqui, Anees A.、Wani, Sachin M.

  DOI：——

  日期：——
• 3-Aminopyridazine derivatives with atypical antidepressant, serotonergic and dopaminergic activities
  作者：Camille Georges Wermuth、Gilbert Schlewer、Jean Jacques Bourguignon、Georges Maghioros、Marie Jeanne Bouchet、Claudine Moire、Jean Paul Kan、Paul Worms、Kathleen Biziere

  DOI：10.1021/jm00123a004

  日期：1989.3

  Minaprine [3-[(beta-morpholinoethyl)amino]-4-methyl-6-phenylpyridazine dihydrochloride] is active in most animal models of depression and exhibits in vivo a dual dopaminomimetic and serotoninomimetic activity profile. In an attempt to dissociate these two effects and to characterize the responsible structural requirements, a series of 47 diversely substituted analogues of minaprine were synthesized and tested for their potential antidepressant, serotonergic, and dopaminergic activities. The structure-activity relationships show that dopaminergic and serotonergic activities can be dissociated. Serotonergic activity appears to be correlated mainly with the substituent in the 4-position of the pyridazine ring whereas the dopaminergic activity appears to be dependent on the presence, or in the formation, of a para-hydroxylated aryl ring in the 6-position of the pyridazine ring.