2-(2-dimethylamino-ethyl)-5,6-bis-(4-methoxy-phenyl)-2H-pyridazin-3-one | 70777-02-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-(2-dimethylamino-ethyl)-5,6-bis-(4-methoxy-phenyl)-2H-pyridazin-3-one
• 英文别名: 2-[2-(Dimethylamino)ethyl]-5,6-bis(4-methoxyphenyl)pyridazin-3-one
• CAS: 70777-02-5
• 化学式: C₂₂H₂₅N₃O₃
• 分子量: 379.459
• InChiKey: VUJOOQRBGPUAMY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  54.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  5,6-bis(4-methoxyphenyl)-2H-pyridazin-3-one 、 2-氯-N,N-二甲基乙胺 以82%的产率得到
  参考文献：
  名称：

  NANNINI G.; BIASOII G.; PERRONE E.; FORGIONE A.; BUTTINONI A.; FERRARI M., EUR. J. MED. CHEM. CHIM. THER., 1979, 14, NO 1, 53-60

  摘要：

  DOI：

文献信息

• NOVEL PYRIDAZINE DERIVATIVES AND MEDICINES CONTAINING THE SAME AS EFFECTIVE INGREDIENTS
  申请人：OHKUCHI Masao

  公开号：US20090270399A1

  公开（公告）日：2009-10-29

  This invention relates to pyridazine derivatives represented by the formula (1): wherein R 1 represents a (substituted) aryl group, R 2 represents a phenyl group substituted at 4-position by a lower alkoxyl, group or a lower alkylthio group, R 3 represents a lower alkoxyl group, a halogenated lower alkyl group, a lower cycloalkyl group, a (substituted) aryl group, a (substituted) aryloxy group, a (substituted) nitrogen-containing heterocyclic ring residue, a (substituted) aminocarbonyl group or a lower alkylcarbonyl group, A represents a single bond, a lower alkylene group or a lower alkenylene group, X represents O or S, and the dashed line indicates that the carbon-carbon bond between the 4-position and the 5-position is a single bond or a double bond, or salts thereof; and also to medicines containing them as effective ingredients. These compounds have excellent inhibitory activity against interleukin-1β production, and are useful as preventives and therapeutics for immune system diseases, inflammatory diseases, ischemic diseases and the like.

  本发明涉及由式（1）表示的吡嗪衍生物： 其中R1表示（取代的）芳基基团，R2表示在4位被低烷氧基团或低烷硫基团取代的苯基基团，R3表示低烷氧基团、卤代的低烷基团、低环烷基团、（取代的）芳基基团、（取代的）芳氧基基团、（取代的）含氮杂环环残基、（取代的）氨基甲酰基团或低烷基甲酰基团，A表示单键、低烷基烷基或低烯基烷基，X表示O或S，虚线表示4位和5位之间的碳-碳键为单键或双键，或其盐；以及含有它们作为有效成分的药物。这些化合物具有优异的抑制白细胞介素-1β产生的活性，可用作预防和治疗免疫系统疾病、炎症性疾病、缺血性疾病等。
• NANNINI G.; BIASOII G.; PERRONE E.; FORGIONE A.; BUTTINONI A.; FERRARI M., EUR. J. MED. CHEM. CHIM. THER., 1979, 14, NO 1, 53-60
  作者：NANNINI G.、 BIASOII G.、 PERRONE E.、 FORGIONE A.、 BUTTINONI A.、 FERRARI M.

  DOI：——

  日期：——