3,5-dichloro-4-fluorobenzenesulfonyl chloride | 1131397-79-9

• 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: 3,5-dichloro-4-fluorobenzenesulfonyl chloride
• 英文别名: 3,5-dichloro-4-fluoro-phenylsulphonyl chloride；3,5-Dichloro-4-fluorobenzene-1-sulfonyl chloride
• CAS: 1131397-79-9
• 化学式: C₆H₂Cl₃FO₂S
• mdl: MFCD12026220
• 分子量: 263.504
• InChiKey: DVAHBTCBQASAHZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  42.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(2,4-二甲氧基苄基)-N-(1,3-噻唑-2-基)胺 、 3,5-dichloro-4-fluorobenzenesulfonyl chloride 在 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 为溶剂， 反应 17.0h， 以76%的产率得到3,5-dichloro-N-(2,4-dimethoxybenzyl)-4-fluoro-N-(thiazol-2-yl)benzenesulfonamide
  参考文献：
  名称：

  BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS

  摘要：

  这项发明涉及苯磺酰胺化合物，作为其立体异构体、对映异构体、互变异构体或它们的混合物；或其药学上可接受的盐、溶剂合物或前药，用于治疗与电压门控钠通道相关的疾病或症状，如癫痫和/或癫痫发作障碍。

  公开号：

  US20180162868A1

文献信息

• BENZOCYCLOHEPTENE ACETIC ACIDS
  申请人：Firooznia Fariborz

  公开号：US20120309796A1

  公开（公告）日：2012-12-06

  Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of inflammatory diseases and disorders such as, for example, asthma and COPD.

  本文提供的是化合物的公式(I)以及其药用盐，其中取代基如规范中所披露的那样。这些化合物及含有它们的药物组合物对于治疗炎症性疾病和紊乱，如哮喘和慢性阻塞性肺病等，具有用处。
• [EN] ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS<br/>[FR] DÉRIVÉS D'ACIDE ARYLSULFONYLAMINOMÉTHYLPHOSPHONIQUE, PRÉPARATION DE CEUX-CI ET UTILISATION DE CEUX-CI COMME COMPOSITIONS PHARMACEUTIQUES
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2009030715A1

  公开（公告）日：2009-03-12

  The invention relates tosubstitutedarylsulphonylaminomethylphosphonic acid derivativesof general formula (I) wherein the groups Ra to Rf, A and Z are defined as mentioned in the specification and claims, which are suitable for preparinga medicament for the treatmentof metabolic disorders, particularlytype 1 or type 2 diabetesmellitus.

  该发明涉及通式（I）的取代芳基磺胺甲基膦酸衍生物，其中基团Ra至Rf、A和Z的定义如规范和权利要求中所述，适用于制备用于治疗代谢紊乱，特别是1型或2型糖尿病的药物。
• ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS
  申请人：Langkopf Elke

  公开号：US20100261677A1

  公开（公告）日：2010-10-14

  The invention relates to substituted arylsulphonylaminomethylphosphonic acid derivatives of general formula (I) wherein the groups R a to R f , A and Z are defined as mentioned in the specification and claims, which are suitable for preparing a medicament for the treatment of metabolic disorders, particularly type 1 or type 2 diabetes mellitus.

  本发明涉及一种通式(I)的取代芳基磺酰氨甲基膦酸衍生物，其中R到Rf，A和Z的基团如说明书和权利要求中所述，适用于制备用于治疗代谢性疾病，特别是1型或2型糖尿病的药物。
• Benzenesulfonamide compouds and their use as therapeutic agents
  申请人：Xenon Pharmaceuticals Inc.

  公开号：US11174268B2

  公开（公告）日：2021-11-16

  This invention is directed to benzenesulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of diseases or conditions associated with voltage-gated sodium channels, such as epilepsy and/or epileptic seizure disorders.

  本发明涉及苯磺酰胺化合物，作为其立体异构体、对映体、同系物或其混合物；或其药学上可接受的盐、溶液剂或原药，用于治疗与电压门控钠通道相关的疾病或病症，如癫痫和/或癫痫发作性疾病。
• α-Aryl pyrrolidine sulfonamides as TRPA1 antagonists
  作者：Vishal A. Verma、Daniel G.M. Shore、Huifen Chen、Jun Chen、Steven Do、David H. Hackos、Aleks Kolesnikov、Joseph P. Lyssikatos、Suzanne Tay、Lan Wang、Anthony A. Estrada

  DOI：10.1016/j.bmcl.2015.11.088

  日期：2016.1

  A series of alpha-aryl pyrrolidine sulfonamide TRPA1 antagonists were advanced from an HTS hit to compounds that were stable in liver microsomes with retention of TRPA1 potency. Metabolite identification studies and physicochemical properties were utilized as a strategy for compound design. These compounds serve as starting points for further compound optimization. (C) 2015 Elsevier Ltd. All rights reserved.