7-chloro-4-methyl-10-(4-methyl-piperazin-1-yl)-4H-benzo[b]thieno[3,4-e][1,4]diazepine | 59681-64-0

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 7-chloro-4-methyl-10-(4-methyl-piperazin-1-yl)-4H-benzo[b]thieno[3,4-e][1,4]diazepine
• 英文别名: 7-Chloro-4-methyl-10-(4-methyl-1-piperazinyl)-4H-thieno[ 3,4-b] [1,5] benzodiazepine；7-Chloro-10-methyl-4-(4-methylpiperazin-1-yl)thieno[3,4-b][1,5]benzodiazepine
• CAS: 59681-64-0
• 化学式: C₁₇H₁₉ClN₄S
• 分子量: 346.884
• InChiKey: SQMAXHXDGPAQLM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  23
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  50.3
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  7-Chloro-4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one 在 氢氧化钾 、 tetraphosphorus decasulfide 作用下， 以 1,4-二氧六环 、 吡啶 、 甲醇 为溶剂， 生成 7-chloro-4-methyl-10-(4-methyl-piperazin-1-yl)-4H-benzo[b]thieno[3,4-e][1,4]diazepine
  参考文献：
  名称：

  10-(Alkylamino)-4H-thieno[3,4-b][1,5]benzodiazepines. A novel class of potential neuroleptic agents

  摘要：

  An investigation of the structural requirements for CNS activity of the title compounds was undertaken. A synthesis of the precursor dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-ones was achieved and three routes for their conversion to the title compounds were developed. The compounds were tested for neuroleptic activity by means of the blockade or d-amphetamine lethality in aggregated mice and/or effects on locomotor activity in rats. Antidepressant activity was examined using inhibition of tetrabenazine-induced depression in mice. Most of the compounds were found to be potent neuroleptic agents with several exhibiting additional antidepressant activity.

  DOI：

  10.1021/jm00192a020

文献信息

• US3951981A
  申请人：——

  公开号：US3951981A

  公开（公告）日：1976-04-20
• US4087421A
  申请人：——

  公开号：US4087421A

  公开（公告）日：1978-05-02