3-(3,4-二氯苯基)苯磺酰氯 | 731779-90-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-(3,4-二氯苯基)苯磺酰氯
• 英文名称: 3-(3,4-dichlorophenyl)-phenylsulfonyl chloride
• 英文别名: 3-(3,4-dichlorophenyl)benzenesulfonyl Chloride
• CAS: 731779-90-1
• 化学式: C₁₂H₇Cl₃O₂S
• mdl: MFCD01631884
• 分子量: 321.611
• InChiKey: IGFBHZODFKDWRW-UHFFFAOYSA-N

物化性质

• 沸点：
  451.2±35.0 °C(Predicted)
• 密度：
  1.493±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• 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：
  2

反应信息

• 作为反应物：
  描述：

  3-(3,4-二氯苯基)苯磺酰氯 、 3-chloro-5-amino-7-isobutylamino-1(2)H-indazole 在 吡啶 作用下， 生成 N-[3-chloro-7-(isobutylamino)-1H-indazol-5-yl]-3-(3,4-dichlorophenyl)benzenesulfonamide
  参考文献：
  名称：

  Structure-Based Design, Synthesis, and Antimicrobial Activity of Indazole-Derived SAH/MTA Nucleosidase Inhibitors

  摘要：

  The structure-based design, synthesis, and biological activity of a novel indazole-containing inhibitor series for S-adenosyl homocysteine/methylthioadenosine (SAH/MTA) nucleosidase are described. Use of 5-aminoindazole as the core scaffold provided a structure-guided series of low nanomolar inhibitors with broad-spectrum antimicrobial activity. The implementation of structure-based methodologies provided a 6000-fold increase in potency over a short timeline (several months) and an economy of synthesized compounds.

  DOI：

  10.1021/jm0302039

文献信息

• Bis-(Sulfonylamino) Derivatives in Therapy 205
  申请人：Bylund Johan

  公开号：US20090163586A1

  公开（公告）日：2009-06-25

  The invention provides compounds of formula (I) wherein R 1 , R 3 , L 1 , L 2 , G 1 , G 2 , A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1.

  该发明提供了式（I）的化合物 其中R 1 ，R 3 ，L 1 ，L 2 ，G 1 ，G 2 ，A和m如规范中定义的那样，以及其光学异构体，消旋体和互变异构体，以及其药学上可接受的盐；以及它们的制备方法，含有它们的药物组合物以及它们在治疗中的应用。这些化合物是微粒体前列腺素E合成酶-1的抑制剂。
• 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] BISARYLSULFONAMIDES USEFUL AS KINASE INHIBITORS IN THE TREATMENT OF INFLAMMATION AND CANCER<br/>[FR] BISARYLSULFONAMIDES UTILISÉS COMME INHIBITEURS DE LA KINASE DANS LE TRAITEMENT DE L'INFLAMMATION ET DU CANCER
  申请人：KANCERA AB

  公开号：WO2011161201A1

  公开（公告）日：2011-12-29

  A compound of formula (I). The compound is useful for treating cancer and inflammatory diseases. A pharmaceutical composition containing the compound.

  一种化合物的化学式（I）。该化合物可用于治疗癌症和炎症性疾病。含有该化合物的药物组合物。
• SULFONAMIDE COMPOUNDS
  申请人：Bystrom Styrbjorn

  公开号：US20130172339A1

  公开（公告）日：2013-07-04

  A compound of formula (I), wherein A is S, O or a double bond, and L is a substituted thiazolyl, phenyl or pyridyl. The compound is useful for the treatment of inflammation and cancer.

  式(I)的化合物，其中A为S、O或双键，L为取代的噻唑基、苯基或吡啶基。该化合物可用于治疗炎症和癌症。
• Bis-(sulfonylamino) derivatives for use in therapy
  申请人：Bylund Johan

  公开号：US09145380B2

  公开（公告）日：2015-09-29

  The invention provides compounds of formula (I) wherein R1, R3, L1, L2, G1, G2, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1.

  本发明提供了式（I）的化合物，其中R1、R3、L1、L2、G1、G2、A和m如规范中所定义，并提供其光学异构体、外消旋体和互变异构体，以及其药学上可接受的盐；以及制备它们的方法、包含它们的制药组合物和它们在治疗中的用途。这些化合物是微粒体前列腺素E合成酶-1的抑制剂。