3-bromo-2-methoxybenzene-1-sulfonyl chloride | 1261794-09-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3-bromo-2-methoxybenzene-1-sulfonyl chloride
• 英文别名: 3-Bromo-2-methoxybenzenesulfonyl chloride；3-bromo-2-methoxybenzenesulfonyl chloride
• CAS: 1261794-09-5
• 化学式: C₇H₆BrClO₃S
• 分子量: 285.546
• InChiKey: JMNPYNBAUDBKPV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  51.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-bromo-2-methoxybenzene-1-sulfonyl chloride 在 氨 作用下， 以 二氯甲烷 为溶剂， 反应 2.17h， 生成 3-Bromo-2-methoxybenzenesulfonamide
  参考文献：
  名称：

  Design and Synthesis of Benzenesulfonamide Derivatives as Potent Anti-Influenza Hemagglutinin Inhibitors

  摘要：

  Structural optimization of salicylamide-based hemagglutinin (HA) inhibitor 1 resulted in the identification of cis-3-(5-hydroxy-1,3,3-timethylcyclohexylmethylamino)benzenesulfonamide 28 and its derivatives as potent anti-influenza agents. The lead compound 28 and its 2-chloro analogue 40 can effectively prevent cytopathic effects (CPE) caused by infection of influenza A/Weiss/43 strain (H1N1) with EC(50) values of 210 and 86 nM, respectively. Mechanism of action studies indicate that 40 and its analogues inhibit the virus fusion with host endosome membrane by binding to HA and stabilizing the prefusion HA structure. With significantly improved metabolic stability, the reported series represents the first generation of orally bioavailable HA inhibitors that have a good selectivity window and potential for further development as novel anti-influenza agents.

  DOI：

  10.1021/ml2000627
• 作为产物：
  描述：

  3-溴-2-甲氧基苯胺 在 盐酸 、 sodium nitrite 、 二氧化硫 、 溶剂黄146 、 copper(l) chloride 作用下， 以 水 为溶剂， 反应 2.0h， 生成 3-bromo-2-methoxybenzene-1-sulfonyl chloride
  参考文献：
  名称：

  Design and Synthesis of Benzenesulfonamide Derivatives as Potent Anti-Influenza Hemagglutinin Inhibitors

  摘要：

  Structural optimization of salicylamide-based hemagglutinin (HA) inhibitor 1 resulted in the identification of cis-3-(5-hydroxy-1,3,3-timethylcyclohexylmethylamino)benzenesulfonamide 28 and its derivatives as potent anti-influenza agents. The lead compound 28 and its 2-chloro analogue 40 can effectively prevent cytopathic effects (CPE) caused by infection of influenza A/Weiss/43 strain (H1N1) with EC(50) values of 210 and 86 nM, respectively. Mechanism of action studies indicate that 40 and its analogues inhibit the virus fusion with host endosome membrane by binding to HA and stabilizing the prefusion HA structure. With significantly improved metabolic stability, the reported series represents the first generation of orally bioavailable HA inhibitors that have a good selectivity window and potential for further development as novel anti-influenza agents.

  DOI：

  10.1021/ml2000627

文献信息

• [EN] MODULATORS OF THE BETA-3 ADRENERGIC RECEPTOR USEFUL FOR THE TREATMENT OR PREVENTION OF DISORDERS RELATED THERETO<br/>[FR] MODULATEURS DU RÉCEPTEUR ADRÉNERGIQUE BÊTA 3 UTILE DANS LE TRAITEMENT OU LA PRÉVENTION DE TROUBLES ASSOCIÉS À CEUX-CI
  申请人：ARENA PHARM INC

  公开号：WO2017214002A1

  公开（公告）日：2017-12-14

  The present invention relates to compounds of Formula (Ia) and pharmaceutical compositions thereof that modulate the activity of the beta-3 adrenergic receptor. Compounds of the present invention and pharmaceutical compositions thereof are directed to methods useful in the treatment of a beta-3 adrenergic receptor-mediated disorder, such as, heart failure; cardiac performance in heart failure; mortality, reinfarction, and/or hospitalization in connection with heart failure; acute heart failure; acute decompensated heart failure; congestive heart failure; severe congestive heart failure; organ damage associated with heart failure (e.g., kidney damage or failure, heart valve problems, heart rhythm problems, and/or liver damage); heart failure due to left ventricular dysfunction; heart failure with normal ejection fraction; cardiovascular mortality following myocardial infarction; cardiovascular mortality in patients with left ventricular failure or left ventricular dysfunction; left ventricular failure; left ventricular dysfunction; class II heart failure using the New York Heart Association (NYHA) classification system; class III heart failure using the New York Heart Association (NYHA) classification system; class IV heart failure using the New York Heart Association (NYHA) classification system; LVEF < 40% by radionuclide ventriculography; LVEF ≤35% by echocardiography or ventricular contrast angiography; and conditions related thereto.

  本发明涉及式(Ia)化合物及其调节β-3肾上腺素能受体活性的药物组合物。本发明的化合物及其药物组合物针对治疗β-3肾上腺素能受体介导的疾病的方法，例如心力衰竭；心力衰竭中的心脏功能；与心力衰竭相关的死亡率、再梗死和/或住院；急性心力衰竭；急性失代偿性心力衰竭；充血性心力衰竭；重度充血性心力衰竭；与心力衰竭相关的器官损伤（例如肾损伤或衰竭、心脏瓣膜问题、心律问题和/或肝损伤）；因左室功能障碍引起的心力衰竭；射血分数正常的心力衰竭；心肌梗死后心血管死亡率；左室衰竭或左室功能障碍患者的心血管死亡率；左室衰竭；左室功能障碍；纽约心脏协会（NYHA）分类系统的II级心力衰竭；纽约心脏协会（NYHA）分类系统的III级心力衰竭；纽约心脏协会（NYHA）分类系统的IV级心力衰竭；放射性核素心室造影LVEF<40%；超声心动图或心室对比血管造影LVEF≤35%；以及相关病症。
• Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto
  申请人：Arena Pharmaceuticals, Inc.

  公开号：US10479797B2

  公开（公告）日：2019-11-19

  The present invention relates to compounds of Formula (Ia) and pharmaceutical compositions thereof that modulate the activity of the beta-3 adrenergic receptor. Compounds of the present invention and pharmaceutical compositions thereof are directed to methods useful in the treatment of a beta-3 adrenergic receptor-mediated disorder, such as, heart failure; cardiac performance in heart failure; mortality, reinfarction, and/or hospitalization in connection with heart failure; acute heart failure; acute decompensated heart failure; congestive heart failure; severe congestive heart failure; organ damage associated with heart failure (e.g., kidney damage or failure, heart valve problems, heart rhythm problems, and/or liver damage); heart failure due to left ventricular dysfunction; heart failure with normal ejection fraction; cardiovascular mortality following myocardial infarction; cardiovascular mortality in patients with left ventricular failure or left ventricular dysfunction; left ventricular failure; left ventricular dysfunction; class II heart failure using the New York Heart Association (NYHA) classification system; class III heart failure using the New York Heart Association (NYHA) classification system; class IV heart failure using the New York Heart Association (NYHA) classification system; LVEF<40% by radionuclide ventriculography; LVEF≤35% by echocardiography or ventricular contrast angiography; and conditions related thereto.

  本发明涉及调节β-3肾上腺素能受体活性的式(Ia)化合物及其药物组合物。本发明的化合物及其药物组合物用于治疗β-3肾上腺素能受体介导的疾病，如心力衰竭；心力衰竭时的心脏表现；与心力衰竭有关的死亡率、再梗塞和/或住院治疗；急性心力衰竭；急性失代偿性心力衰竭；充血性心力衰竭；严重充血性心力衰竭；与心力衰竭有关的器官损伤（如：肾脏损伤或衰竭、心脏瓣膜问题、心律问题等）、左心室功能不全导致的心力衰竭；射血分数正常的心力衰竭；心肌梗塞后的心血管死亡率；左心室功能不全或左心室功能障碍患者的心血管死亡率；左心室功能不全；左心室功能障碍；根据纽约心脏协会（NYHA）分类系统划分的Ⅱ级心力衰竭；根据纽约心脏协会（NYHA）分类系统划分的Ⅲ级心力衰竭；根据纽约心脏协会（NYHA）分类系统划分的Ⅳ级心力衰竭；根据放射性核素心室造影检查，LVEF<40%；根据超声心动图或心室造影血管造影检查，LVEF≤35%；以及与此相关的情况。
• MODULATORS OF THE BETA-3 ADRENERGIC RECEPTOR USEFUL FOR THE TREATMENT OR PREVENTION OF DISORDERS RELATED THERETO
  申请人：Arena Pharmaceuticals, Inc.

  公开号：EP3464292A1

  公开（公告）日：2019-04-10
• KAT6 TARGETING COMPOUNDS
  申请人：Prelude Therapeutics Incorporated

  公开号：US20230416240A1

  公开（公告）日：2023-12-28

  The present disclosure provides bifunctional compounds comprising a target protein binding moiety and a E3 ubiquitin ligase binding moiety, and associated methods of use.
• Design and Synthesis of Benzenesulfonamide Derivatives as Potent Anti-Influenza Hemagglutinin Inhibitors
  作者：Guozhi Tang、Xianfeng Lin、Zongxing Qiu、Wentao Li、Lei Zhu、Lisha Wang、Shaohua Li、Haodong Li、Wenbin Lin、Mei Yang、Tao Guo、Li Chen、Daniel Lee、Jim Z. Wu、Wengang Yang

  DOI：10.1021/ml2000627

  日期：2011.8.11

  Structural optimization of salicylamide-based hemagglutinin (HA) inhibitor 1 resulted in the identification of cis-3-(5-hydroxy-1,3,3-timethylcyclohexylmethylamino)benzenesulfonamide 28 and its derivatives as potent anti-influenza agents. The lead compound 28 and its 2-chloro analogue 40 can effectively prevent cytopathic effects (CPE) caused by infection of influenza A/Weiss/43 strain (H1N1) with EC(50) values of 210 and 86 nM, respectively. Mechanism of action studies indicate that 40 and its analogues inhibit the virus fusion with host endosome membrane by binding to HA and stabilizing the prefusion HA structure. With significantly improved metabolic stability, the reported series represents the first generation of orally bioavailable HA inhibitors that have a good selectivity window and potential for further development as novel anti-influenza agents.