N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide | 1038402-16-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻二嗪
• 英文名称: N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide
• 英文别名: N-[3-[2-(3,3-dimethylpentyl)-5-hydroxy-3-oxo-6-(2-thienyl)pyridazin-4-yl]-1,1-dioxo-4H-1$l^{6},2,4-benzothiadiazin-7-yl]methanesulfonamide；N-[3-[2-(3,3-dimethylpentyl)-5-hydroxy-3-oxo-6-thiophen-2-ylpyridazin-4-yl]-1,1-dioxo-4H-1λ6,2,4-benzothiadiazin-7-yl]methanesulfonamide
• CAS: 1038402-16-2
• 化学式: C₂₃H₂₇N₅O₆S₃
• 分子量: 565.695
• InChiKey: BJJRKIKPFDBGGQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  37
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  203
• 氢给体数：
  3
• 氢受体数：
  10

反应信息

• 作为产物：
  描述：

  2-(3.3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2.3-dihydro-pyridazine-4-carboxylic acid ethyl ester 、 2-amino-5-(methanesulfonylamino)benzenesulfonamide 在 氩 、 甲醇 、 N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide 作用下， 以 吡啶 为溶剂， 反应 16.0h， 以to afford the desired product, N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,2-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-methanesulfonamide (5n) (0.0274 g, 16% yield)的产率得到N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide
  参考文献：
  名称：

  Pyridazinone compounds

  摘要：

  这项发明涉及吡啶并咪唑酮化合物以及包含这些化合物的药物组合物，这些化合物在治疗丙型肝炎病毒感染方面具有用处。

  公开号：

  US20080275032A1
• 作为试剂：
  描述：

  2-(3.3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2.3-dihydro-pyridazine-4-carboxylic acid ethyl ester 、 2-amino-5-(methanesulfonylamino)benzenesulfonamide 在 氩 、 甲醇 、 N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide 作用下， 以 吡啶 为溶剂， 反应 16.0h， 以to afford the desired product, N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,2-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-methanesulfonamide (5n) (0.0274 g, 16% yield)的产率得到N-{3-[2-(3,3-dimethyl-pentyl)-5-hydroxy-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}-methanesulfonamide
  参考文献：
  名称：

  Pyridazinone compounds

  摘要：

  这项发明涉及吡啶并咪唑酮化合物以及包含这些化合物的药物组合物，这些化合物在治疗丙型肝炎病毒感染方面具有用处。

  公开号：

  US20080275032A1

文献信息

• WO2008/82725
  申请人：——

  公开号：——

  公开（公告）日：——
• [EN] PYRIDAZINONE COMPOUNDS<br/>[FR] COMPOSÉS DE TYPE PYRIDAZINONE
  申请人：ANADYS PHARMACEUTICALS INC

  公开号：WO2008082725A1

  公开（公告）日：2008-07-10

  [EN] The invention is directed to pyridazinone compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.
  [FR] L'invention porte sur des composés de type pyridazinone et sur des compositions pharmaceutiques contenant de tels composés qui sont utiles dans le traitement d'infections par le virus de l'hépatite C.
• Novel HCV NS5B polymerase inhibitors derived from 4-(1′,1′-dioxo-1′,4′-dihydro-1′λ6-benzo[1′,2′,4′]thiadiazin-3′-yl)-5-hydroxy-2H-pyridazin-3-ones. Part 3: Further optimization of the 2-, 6-, and 7′-substituents and initial pharmacokinetic assessments
  作者：Lian-Sheng Li、Yuefen Zhou、Douglas E. Murphy、Nebojsa Stankovic、Jingjing Zhao、Peter S. Dragovich、Thomas Bertolini、Zhongxiang Sun、Benjamin Ayida、Chinh V. Tran、Frank Ruebsam、Stephen E. Webber、Amit M. Shah、Mei Tsan、Richard E. Showalter、Rupal Patel、Laurie A. LeBrun、Darian M. Bartkowski、Thomas G. Nolan、Daniel A. Norris、Ruhi Kamran、Jennifer Brooks、Maria V. Sergeeva、Leo Kirkovsky、Qiang Zhao、Charles R. Kissinger

  DOI：10.1016/j.bmcl.2008.02.072

  日期：2008.6

  5-Hydroxy-3(2H)-pyridazinone derivatives were investigated as inhibitors of genotype 1 HCV NS5B polymerase. Lead optimization led to the discovery of compound 3a, which displayed potent inhibitory activities in biochemical and replicon assays [IC50 (1b) < 10 nM; IC50 (1a) = 22 nM; EC50 (1b) = 5 nM], good stability toward human liver microsomes (HLM t(1/2) > 60 min), and high ratios of liver to plasma concentrations 12 h after a single oral administration to rats. (c) 2008 Published by Elsevier Ltd.
• Pyridazinone compounds
  申请人：Zhou Yuefen

  公开号：US20080275032A1

  公开（公告）日：2008-11-06

  The invention is directed to pyridazinone compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.

  这项发明涉及吡啶并咪唑酮化合物以及包含这些化合物的药物组合物，这些化合物在治疗丙型肝炎病毒感染方面具有用处。