(R,S)-6-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine | 824430-68-4

• 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: (R,S)-6-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
• 英文别名: 9-chloro-5-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
• CAS: 824430-68-4
• 化学式: C₁₁H₁₄ClN
• 分子量: 195.692
• InChiKey: HMGASYPJYKHVCW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-氯苯乙胺 在 吡啶 、 三氯化铝 、 硼烷 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 生成 (R,S)-6-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
  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

• Discovery and Structure−Activity Relationship of (1<i>R</i>)-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1<i>H</i>-3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT_2C Receptor Agonist 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、Peter I. Dosa、Jon A. Covel、Albert Ren、Robert R. Webb、Nigel R. A. Beeley、Michael Martin、Michael Morgan、Stephen Espitia、Hazel R. Saldana、Christina Bjenning、Kevin T. Whelan、Andrew J. Grottick、Frederique Menzaghi、William J. Thomsen

  DOI：10.1021/jm0709034

  日期：2008.1.1

  The synthesis and SAR of a novel 3-benzazepine series of 5-HT2C agonists is described. Compound 7d (lorcaserin, APD356) was identified as one of the more potent and selective compounds in vitro (pEC50 values in functional assays measuring [(3)H]phosphoinositol turnover: 5-HT2C = 8.1; 5-HT2A = 6.8; 5-HT2B = 6.1) and was potent in an acute in vivo rat food intake model upon oral administration (ED50

  描述了新型3-苯并ze庚因系列的5-HT 2C激动剂的合成和SAR。在体外，化合物7d（lorcaserin，APD356）被鉴定为更有效和选择性的化合物之一（在功能测定中，通过[[3] H]磷酸肌醇周转率测定的pEC50值：5-HT2C = 8.1; 5-HT2A = 6.8; 5- HT2B = 6.1），并且在口服后在急性体内大鼠食物摄入模型中有效（在6 h时的ED50 = 18 mg / kg）。Lorcaserin在大鼠单剂量药代动力学研究中进一步表征（t1 / 2 = 3.7小时； F = 86％），以及在生长的Sprague-Dawley大鼠中28天的体重增加模型（在60℃时观察到体重增加减少8.5％） 36 mg / kg出价）。选择洛卡西林在肥胖症的临床试验中进行进一步评估。
• BENZAZEPINE DERIVATIVES USEFUL FOR TREATMENT OF 5HT2C RECEPTOR ASSOCIATED DISEASES
  申请人：Brian Smith

  公开号：US20130172322A1

  公开（公告）日：2013-07-04

  The present invention relates to certain 1-substituted-2,3,4,5-tetrahydro-3-benzazepine derivatives of Formula (I), that are modulators of the 5HT2C receptor. Accordingly, compounds of the present invention are useful for the prophylaxis or treatment of 5HT2C receptor associated diseases, conditions or disorders, such as, obesity and related disorders.

  本发明涉及某些1-取代-2,3,4,5-四氢-3-苯并哌啶衍生物，其为5HT2C受体调节剂。因此，本发明化合物对于预防或治疗与5HT2C受体相关的疾病、病况或障碍，如肥胖症及相关疾病，是有用的。
• Benzazepine derivatives and methods of prophylaxis or treatment of 5ht2c receptor associated diseases
  申请人：Smith Brian

  公开号：US20070142357A1

  公开（公告）日：2007-06-21

  The present invention relates to certain 1-substituted-2,3,4,5-tetrahydro-3-benzazepine derivatives of Formula (I), that are modulators of the 5HT2C receptor. Accordingly, compounds of the present invention are useful for the prophylaxis or treatment of 5HT2C receptor associated diseases, conditions or disorders, such as, obesity and related disorders.

  本发明涉及某些1-取代-2,3,4,5-四氢-3-苯并咪唑衍生物，其为5HT2C受体调节剂。因此，本发明化合物可用于预防或治疗与5HT2C受体相关的疾病、病况或障碍，如肥胖症及相关疾病。
• BENZAZEPINE DERIVATIVES AND METHODS OF PROPHYLAXIS OR TREATMENT OF 5HT2C RECEPTOR ASSOCIATED DISEASES
  申请人：Brian Smith

  公开号：US20100173894A1

  公开（公告）日：2010-07-08

  The present invention relates to certain 1-substituted-2,3,4,5-tetrahydro-3-benzazepine derivatives of Formula (I), that are modulators of the 5HT2C receptor. Accordingly, compounds of the present invention are useful for the prophylaxis or treatment of 5HT2C receptor associated diseases, conditions or disorders, such as, obesity and related disorders.

  本发明涉及某些1-取代的2,3,4,5-四氢-3-苯并噻吩衍生物(I式)，它们是5HT2C受体调节剂。因此，本发明化合物对于预防或治疗5HT2C受体相关的疾病、状况或障碍，如肥胖症及相关疾病，是有用的。
• THERAPEUTIC AGENT FOR STRESS URINARY INCONTINENCE AND FECAL INCONTINENCE
  申请人：Takeda Pharmaceutical Company Limited

  公开号：EP3733204A1

  公开（公告）日：2020-11-04

  The present invention provides a medicament for use in treating stress urinary incontinence with fewer adverse effects including a body weight lowering effect. The present invention also provides a medicament for use in treating a disease such as incontinence of feces and further provide a medicament for use in treating a disease such as incontinence of feces with fewer adverse effects including a body weight lowering effect. A medicament for use in treating stress urinary incontinence, comprising a 5-HT2C receptor agonist, wherein the medicament is administered at a dosage lower than the minimum dosage of the agonist as an anti-obesity drug. A medicament for use in treating incontinence of feces, etc., comprising a 5-HT2C receptor agonist. A medicament for use in treating incontinence of feces, comprising a 5-HT2C receptor agonist, wherein the medicament is administered at a dosage lower than the minimum dosage of the agonist as an anti-obesity drug.

  本发明提供了一种用于治疗压力性尿失禁的药物，其不良反应较少，包括降低体重的效果。本发明还提供了一种用于治疗大便失禁等疾病的药物，并进一步提供了一种用于治疗大便失禁等疾病的药物，其不良反应较少，包括有降低体重的作用。 一种用于治疗压力性尿失禁的药物，包含一种5-HT2C受体激动剂，其中该药物的给药剂量低于作为抗肥胖药物的激动剂的最小剂量。一种用于治疗大便失禁等的药物，包含一种 5-HT2C 受体激动剂。一种用于治疗大便失禁等的药物，包含一种5-HT2C受体激动剂，其中该药物作为抗肥胖药物以低于该激动剂最小剂量的剂量给药。