11-methyl-6,11-dihydrodibenzothiepin | 128044-22-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并硫平类
• 英文名称: 11-methyl-6,11-dihydrodibenzothiepin
• 英文别名: 11-Methyl-6,11-dihydrobenzo[c][1]benzothiepine
• CAS: 128044-22-4
• 化学式: C₁₅H₁₄S
• 分子量: 226.342
• InChiKey: MDNFPMXZOZMYIR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  11-methyl-6,11-dihydrodibenzothiepin 、 N,N-二甲基-3-氯丙胺 在 盐酸 、 正丁基锂 作用下， 生成 N,N-dimethyl-3-(11-methyl-6,11-dihydrodibenzothiepin-6-yl)propylamine hydrochloride
  参考文献：
  名称：

  Polivka, Zdenek; Valenta, Vladimir; Sindelar, Karel, Collection of Czechoslovak Chemical Communications, 1989, vol. 54, # 1, p. 235 - 247

  摘要：

  DOI：
• 作为产物：
  描述：

  11-methyl-6,11-dihydrodibenzothiepin-11-ol 在 磷化氢 、 sodium hypophosphite 、 氢碘酸 、 异丁酸 作用下， 以 溶剂黄146 为溶剂， 反应 3.0h， 以93%的产率得到11-methyl-6,11-dihydrodibenzothiepin
  参考文献：
  名称：

  Polivka, Zdenek; Valenta, Vladimir; Sindelar, Karel, Collection of Czechoslovak Chemical Communications, 1989, vol. 54, # 1, p. 235 - 247

  摘要：

  DOI：

文献信息

• AZA-PYRIDONE COMPOUNDS AND USES THEREOF
  申请人：Alios BioPharma, Inc.

  公开号：US20150072982A1

  公开（公告）日：2015-03-12

  Disclosed herein are aza-pyridone compounds, pharmaceutical compositions that include one or more aza-pyridone compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an orthomyxovirus infection, with an aza-pyridone compounds. Examples of an orthomyxovirus viral infection include an influenza infection.

  本文揭示了氮杂吡啶酮化合物，包括一种或多种氮杂吡啶酮化合物的药物组合物，以及合成这些化合物的方法。本文还揭示了使用氮杂吡啶酮化合物改善和/或治疗疾病和/或病况的方法，包括流感病毒感染在内的正黏液病毒感染。
• PROCESS FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES
  申请人：Shionogi & Co., Ltd.

  公开号：EP2412709A1

  公开（公告）日：2012-02-01

  The present invention provides a pyrone derivative and a pyridone derivative, which are novel intermediates for synthesizing an anti-influenza drug, a method of producing the same, and a method of using the same.

  本发明提供了一种吡酮衍生物和一种吡啶酮衍生物，它们是合成抗流感药物的新型中间体，还提供了一种生产方法和一种使用方法。
• SUBSTITUTED POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE PRODRUG
  申请人：Shionogi & Co., Ltd.

  公开号：EP2620436A1

  公开（公告）日：2013-07-31

  The present invention provides a compound having antiviral effects, particularly having growth inhibitory activity on influenza viruses, a preferred example of the compound being a substituted 3 - hydroxy-4-pyridone derivative prodrug having cap-dependent endonuclease inhibitory activity.

  本发明提供了一种具有抗病毒作用，特别是对流感病毒具有生长抑制活性的化合物，该化合物的一个优选实例是一种具有帽依赖性内切酶抑制活性的取代 3-羟基-4-吡啶酮衍生物原药。
• INFLUENZA VIRUS REPLICATION INHIBITOR AND USE THEREOF
  申请人：Sunshine Lake Pharma Co., Ltd.

  公开号：EP3686201A1

  公开（公告）日：2020-07-29

  Disclosed are a compound as shown in formula (I) as an influenza virus replication inhibitor and a preparation method therefor, a pharmaceutical composition comprising the compound and the use of the compound and pharmaceutical composition thereof in the treatment of influenza.

  公开了作为流感病毒复制抑制剂的式 (I) 所示化合物及其制备方法、包含该化合物的药物组合物以及该化合物及其药物组合物在治疗流感中的用途。
• ARENAVIRUS GROWTH INHIBITOR COMPRISING POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE
  申请人：National University Corporation Hokkaido University

  公开号：EP3815689A1

  公开（公告）日：2021-05-05

  The present invention provides a compound having antiviral activity, especially having arenavirus proliferation inhibitory activity, and/or a medicament comprising the compound. More preferably, the present invention provides a compound having proliferation inhibitory activity on the Old World arenaviruses such as Luna virus, Lassa virus, and lymphocytic choriomeningitis virus and/or the New World arenaviruses such as Junin virus, and/or a medicament comprising the compound. An arenavirus proliferation inhibitor comprising a compound represented by Formula (I) or a prodrug thereof or a pharmaceutically acceptable salt thereof: (wherein R1 is carboxy, or the like; A3 is CR2 or N; R2 is a hydrogen atom, halogen, hydroxy, or the like; R3 is a hydrogen atom, hydroxy, carboxy, cyano, formyl, alkyl optionally substituted with Substituent group F, or the like; either A1 or A2 is CR5R6, and the other is NR7, or A1 is CR8R9, and A2 is CR10R11; and R5, R6, R7, R8, R9, R10, and R11 are each independently a hydrogen atom, carboxy, cyano, alkyl optionally substituted with Substituent group F, or the like).

  本发明提供了一种具有抗病毒活性的化合物，尤其是具有抑制禽流感病毒增殖活性的化合物，和/或包含该化合物的药物。更优选地，本发明提供了一种化合物，该化合物对旧大陆病毒（如卢纳病毒、拉萨病毒和淋巴细胞色素膜炎病毒）和/或新大陆病毒（如朱宁病毒）具有增殖抑制活性，和/或包含该化合物的药物。 一种由式（I）代表的化合物或其原药或其药学上可接受的盐组成的腺病毒增殖抑制剂： (其中 R1 是羧基或类似物；A3 是 CR2 或 N；R2 是氢原子、卤素、羟基或类似物；R3 是氢原子、羟基、羧基、氰基、甲酰基、任选被取代基 F 取代的烷基或类似物；A1 或 A2 是 CR5R6，另一个是 NR7，或 A1 是 CR8R9，A2 是 CR10R11；以及 R5、R6、R7、R8、R9、R10 和 R11 各自独立地是氢原子、羧基、氰基、任选被取代基 F 取代的烷基或类似基团）。