(+/-)-cis-1-tert-butyl 3-methyl-4-(2-(isopropoxycarbonyl)-3-(trifluoromethyl)phenyl)pyrrolidine-1,3-dicarboxylate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (+/-)-cis-1-tert-butyl 3-methyl-4-(2-(isopropoxycarbonyl)-3-(trifluoromethyl)phenyl)pyrrolidine-1,3-dicarboxylate
• 英文别名: 1-O-tert-butyl 3-O-methyl (3R,4R)-4-[2-propan-2-yloxycarbonyl-3-(trifluoromethyl)phenyl]pyrrolidine-1,3-dicarboxylate
• 化学式: C₂₂H₂₈F₃NO₆
• 分子量: 459.463
• InChiKey: IYRQSUWALZQPQI-GJZGRUSLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  32
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  82.1
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  (+/-)-cis-1-tert-butyl 3-methyl-4-(2-(isopropoxycarbonyl)-3-(trifluoromethyl)phenyl)pyrrolidine-1,3-dicarboxylate 在 三乙胺 、 lithium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and SAR of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones as 5-HT2C receptor agonists

  摘要：

  A series of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones is described, several examples of which exhibit potent 5-HT2C agonism with excellent selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compounds such as 38 and 44 were shown to be effective in reducing food intake in an acute rat feeding model. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.091
• 作为产物：
  描述：

  2-三氟甲基苯甲酰氯 在 盐酸 、 18-冠醚-6 、 四甲基乙二胺 、 palladium 10% on activated carbon 、 氢气 、 仲丁基锂 、 双(三甲基硅烷基)氨基钾 、 potassium carbonate 、 三氟乙酸 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 水 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， -78.0~65.0 ℃ 、101.33 kPa 条件下， 生成 (+/-)-cis-1-tert-butyl 3-methyl-4-(2-(isopropoxycarbonyl)-3-(trifluoromethyl)phenyl)pyrrolidine-1,3-dicarboxylate
  参考文献：
  名称：

  Synthesis and SAR of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones as 5-HT2C receptor agonists

  摘要：

  A series of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones is described, several examples of which exhibit potent 5-HT2C agonism with excellent selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compounds such as 38 and 44 were shown to be effective in reducing food intake in an acute rat feeding model. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.091

文献信息

• Pyrrolo(oxo)isoquinolines as 5HT ligands
  申请人：Fevig M. John

  公开号：US20060014777A1

  公开（公告）日：2006-01-19

  The present application describes compounds according to Formula I, pharmaceutical compositions, comprising at least one compound according to Formula I and optionally at least one additional therapeutic agent and methods of treating various diseases, conditions and disorders associated with modulation of serotonin receptors such as, for example: metabolic diseases, which includes but is not limited to obesity, diabetes, diabetic complications, atherosclerosis, impared glucose tolerance and dyslipidemia; central nervous system diseases which includes but is not limited to, anxiety, depression, obsessive compulsive disorder, panic disorder, psychosis, schizophrenia, sleep disorder, sexual disorder and social phobias; cephalic pain; migraine; and gastrointestinal disorders using compounds according to Formula I or pharmaceutically acceptable salt forms thereof, wherein A, B, D, E, m, n, R 3 , R 7 , R 8 , R 9 , R 10 , R 11 and X are described herein.

  本申请描述了根据式I的化合物，包括至少一种根据式I的化合物和可选地至少一种额外的治疗剂的药物组合物，以及治疗与调节5-羟色胺受体相关的各种疾病、症状和紊乱的方法，例如：代谢性疾病，包括但不限于肥胖症、糖尿病、糖尿病并发症、动脉粥样硬化、糖耐量受损和血脂异常；中枢神经系统疾病，包括但不限于焦虑、抑郁症、强迫症、恐慌症、精神病、精神分裂症、睡眠障碍、性功能障碍和社交恐惧症；头痛；偏头痛；以及使用根据式I的化合物或其药用盐形式治疗胃肠道紊乱，其中A、B、D、E、m、n、R3、R7、R8、R9、R10、R11和X在此处描述。
• PYRROLO(OXO)ISOQUINOLINES AS 5HT LIGANDS
  申请人：Bristol-Myers Squibb Company

  公开号：EP1778225A2

  公开（公告）日：2007-05-02
• US7572805B2
  申请人：——

  公开号：US7572805B2

  公开（公告）日：2009-08-11
• [EN] PYRROLO(OXO)ISOQUINOLINES AS 5HT LIGANDS<br/>[FR] PYRROLO(OXO)ISOQUINOLEINES UTILISEES COMME LIGANDS 5HT
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2006019886A2

  公开（公告）日：2006-02-23

  The present application describes compounds according to Formula I, pharmaceutical compositions, comprising at least one compound according to Formula I and optionally at least one additional therapeutic agent and methods of treating various diseases, conditions and disorders associated with modulation of serotonin receptors such as, for example: metabolic diseases, which includes but is not limited to obesity, diabetes, diabetic complications, atherosclerosis, impared glucose tolerance and dyslipidemia; central nervous system diseases which includes but is not limited to, anxiety, depression, obsessive compulsive disorder, panic disorder, psychosis, schizophrenia, sleep disorder, sexual disorder and social phobias; cephalic pain; migraine; and gastrointestinal disorders using compounds according to Formula I or pharmaceutically acceptable salt forms thereof, wherein A, B, D, E, m, n, R3, R7, R8, R9, R10, R11 and X are described herein.
• Synthesis and SAR of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones as 5-HT2C receptor agonists
  作者：John M. Fevig、Jianxin Feng、Karen A. Rossi、Keith J. Miller、Ginger Wu、Chen-Pin Hung、Thao Ung、Sarah E. Malmstrom、Ge Zhang、William J. Keim、Mary Jane Cullen、Kenneth W. Rohrbach、Qinling Qu、Jinping Gan、Mary Ann Pelleymounter、Jeffrey A. Robl

  DOI：10.1016/j.bmcl.2012.10.091

  日期：2013.1

  A series of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones is described, several examples of which exhibit potent 5-HT2C agonism with excellent selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compounds such as 38 and 44 were shown to be effective in reducing food intake in an acute rat feeding model. (C) 2012 Elsevier Ltd. All rights reserved.