8-methoxy-1-methyl-1,3,4,5-tetrahydro-benzo[d]azepin-2-one | 849663-11-2

• 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: 8-methoxy-1-methyl-1,3,4,5-tetrahydro-benzo[d]azepin-2-one
• 英文别名: 7-methoxy-5-methyl-1,2,3,5-tetrahydro-3-benzazepin-4-one
• CAS: 849663-11-2
• 化学式: C₁₂H₁₅NO₂
• 分子量: 205.257
• InChiKey: HLCVUAUNVLGJEG-UHFFFAOYSA-N

物化性质

• 沸点：
  401.5±45.0 °C(Predicted)
• 密度：
  1.077±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  8-methoxy-1-methyl-1,3,4,5-tetrahydro-benzo[d]azepin-2-one 在 硼烷四氢呋喃络合物 、 盐酸 、 sodium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 5.0h， 以72%的产率得到8-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine
  参考文献：
  名称：

  BENZOAZEPIN-OXY-ACETIC ACID DERIVATIVES AS PPAR-DELTA AGONISTS USED FOR THE INCREASE OF HDL-C, LOWER LDL-C AND LOWER CHOLESTEROL

  摘要：

  该发明涉及一种化合物，其化学式为（I），可用作PPAR激动剂。还描述了使用该发明的化合物治疗糖尿病、肾病、神经病、视网膜病变、多囊卵巢综合征、高血压、缺血、中风、肠易激综合征、炎症、白内障、心血管疾病、代谢X综合征、高LDL胆固醇血症、血脂异常（包括高甘油三酯血症、高胆固醇血症、混合性高脂血症和低HDL胆固醇血症）、动脉粥样硬化、肥胖以及其他与脂质代谢和能量稳态并发症相关的疾病的药物组合物和治疗方法。

  公开号：

  US20070244094A1
• 作为产物：
  描述：

  2-chloro-N-[2-(4-methoxyphenyl)ethyl]propionamide 在 三氯化铝 作用下， 生成 8-methoxy-1-methyl-1,3,4,5-tetrahydro-benzo[d]azepin-2-one
  参考文献：
  名称：

  Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

  摘要：

  We report on the synthesis, biological evaluation and structure-activity relationships for a series of 3-benzazepine derivatives as 5-HT2C receptor agonists. The compounds were evaluated in functional assays measuring [H-3] phosphoinositol turnover in HEK-293 cells transiently transfected with h5-HT2C, h5-HT2A or h5-HT2B receptors. Several compounds are shown to be potent and selective 5-HT2C receptor agonists, which decrease food intake in a rat feeding model. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.12.080

文献信息

• BENZOAZEPIN-OXY-ACETIC ACID DERIVATIVES AS PPAR-DELTA AGONISTS USED FOR THE INCREASE OF HDL-C, LOWER LDL-C AND LOWER CHOLESTEROL
  申请人：Kuo Gee-Hong

  公开号：US20070244094A1

  公开（公告）日：2007-10-18

  The invention is directed to compounds of Formula (I) useful as PPAR agonists. Pharmaceutical compositions and methods of treating one or more conditions including, but not limited to, diabetes, nephropathy, neuropathy, retinopathy, polycystic ovary syndrome, hypertension, ischemia, stroke, irritable bowel disorder, inflammation, cataract, cardiovascular diseases, Metabolic X Syndrome, hyper-LDL-cholesterolemia, dyslipidemia (including hypertriglyceridemia, hypercholesterolemia, mixed hyperlipidemia, and hypo-HDL-cholesterolemia), atherosclerosis, obesity, and other disorders related to lipid metabolism and energy homeostasis complications thereof, using compounds of the invention are also described.

  该发明涉及一种化合物，其化学式为（I），可用作PPAR激动剂。还描述了使用该发明的化合物治疗糖尿病、肾病、神经病、视网膜病变、多囊卵巢综合征、高血压、缺血、中风、肠易激综合征、炎症、白内障、心血管疾病、代谢X综合征、高LDL胆固醇血症、血脂异常（包括高甘油三酯血症、高胆固醇血症、混合性高脂血症和低HDL胆固醇血症）、动脉粥样硬化、肥胖以及其他与脂质代谢和能量稳态并发症相关的疾病的药物组合物和治疗方法。
• US7678786B2
  申请人：——

  公开号：US7678786B2

  公开（公告）日：2010-03-16
• US8633184B2
  申请人：——

  公开号：US8633184B2

  公开（公告）日：2014-01-21
• Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity
  作者：Brian M. Smith、Jeffrey M. Smith、James H. Tsai、Jeffrey A. Schultz、Charles A. Gilson、Scott A. Estrada、Rita R. Chen、Douglas M. Park、Emily B. Prieto、Charlemagne S. Gallardo、Dipanjan Sengupta、William J. Thomsen、Hazel R. Saldana、Kevin T. Whelan、Frederique Menzaghi、Robert R. Webb、Nigel R.A. Beeley

  DOI：10.1016/j.bmcl.2004.12.080

  日期：2005.3

  We report on the synthesis, biological evaluation and structure-activity relationships for a series of 3-benzazepine derivatives as 5-HT2C receptor agonists. The compounds were evaluated in functional assays measuring [H-3] phosphoinositol turnover in HEK-293 cells transiently transfected with h5-HT2C, h5-HT2A or h5-HT2B receptors. Several compounds are shown to be potent and selective 5-HT2C receptor agonists, which decrease food intake in a rat feeding model. (c) 2005 Elsevier Ltd. All rights reserved.