4-cyanopyridine-2-sulfonamide | 1251259-15-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 4-cyanopyridine-2-sulfonamide
• CAS: 1251259-15-0
• 化学式: C₆H₅N₃O₂S
• 分子量: 183.191
• InChiKey: RLKJGADWGKBXSV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  12
• 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：
  105
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-cyanopyridine-2-sulfonamide 在 氨 、 氢气 作用下， 以 甲醇 、 N,N-二甲基乙酰胺 为溶剂， 20.0~130.0 ℃ 、3.0 MPa 条件下， 反应 26.0h， 生成 4,4-dimethyl-6-oxo-N-phenyl-2-[(2-sulfamoylpyridin-4-yl)methylamino]cyclohexene-1-carbothioamide
  参考文献：
  名称：

  [EN] 3-AMINO-1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONES
  [FR] 3-AMINO -1,5,6,7-TÉTRAHYDRO-4 H-INDOL-4-ONES

  摘要：

  式(I)的化合物是Bub1激酶的抑制剂，其制备方法及其作为药物的用途。

  公开号：

  WO2015193339A1

文献信息

• [EN] ACYL SULFONAMIDES FOR TREATING CANCER<br/>[FR] ACYLSULFONAMIDES POUR LE TRAITEMENT DU CANCER
  申请人：BAYER AG

  公开号：WO2020216701A1

  公开（公告）日：2020-10-29

  The present invention provides acyl sulfonamide compounds of general formula (I): in which X, R1, R2, R3, R4, R5, R6, Ra and Rb are as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, as a sole agent or in combination with other active ingredients as well as methods of treating and/or prophylaxing diseases, particularly cancer, more particularly cancer in which KAT6A and/or KAT6B is focally amplified, said method comprising administering an effective amount of at least one compound of formula (I) to a subject in need thereof.

  本发明提供了一般式(I)的酰基磺酰胺化合物：其中X、R1、R2、R3、R4、R5、R6、Ra和Rb如本文所述和定义的那样，制备所述化合物的方法，用于制备所述化合物的有用中间体化合物，包含所述化合物的药物组合物和组合物，以及利用所述化合物制造用于治疗或预防疾病的药物组合物，特别是治疗或预防过度增殖性疾病的药物组合物，作为唯一药剂或与其他活性成分结合使用，以及治疗和/或预防疾病的方法，特别是癌症，更特别是KAT6A和/或KAT6B在局部扩增的癌症，所述方法包括向需要的受试者施用至少一种式(I)化合物的有效量。
• TARGETED DRUG DELIVERY USING SULFONAMIDE DERIVATIVES
  申请人：——

  公开号：US20030109555A1

  公开（公告）日：2003-06-12

  The present invention relates to Glutathione S-transferase (GST)/Reduced Glutathione (GSH) as a means for the in-vivo release of a drug that has been conjugated to specific electrophilic moieties via a sulfonamide bond. The drug may be an anticancer agent (or one with other therapeutic properties) carrying a free —NH— which has been derivatized by the attachment of an electrophile containing a moiety, such as p-CN— or p-NO 2-pyridinylsulfonyl groups, or p-NO 2- or 2,4 dinitrophenylsulfonyl groups, or suitable derivatives thereof, to make a prodrug. Optionally, the sulfonamide moiety may have attached to it a targeting molecule. The present invention also provides Glutathione S-transferase (GST)/Reduced Gluthathione (GSH) as a means for the release of a protected amino derivative that has been conjugated to specific electrophilic moieties via a sulfonamide bond. The precursor is a synthetic intermediate carrying a free —NH— which has been derivatized by the attachment of an electrophile via a sulfonamide bond.

  本发明涉及谷胱甘肽S-转移酶（GST）/还原谷胱甘肽（GSH）作为体内释放已通过磺酰胺键与特定亲电性基团结合的药物的手段。该药物可能是一种抗癌剂（或具有其他治疗性能）携带有一个自由的-NH-，通过连接含有一个基团的亲电子试剂，如p-CN-或p-NO2-吡啶基磺酰基团，或p- -或2,4-二硝基苯基磺酰基团，或其适当的衍生物，制备成前药。可选地，磺酰胺基团上可能连接有一个靶向分子。本发明还提供谷胱甘肽S-转移酶（GST）/还原谷胱甘肽（GSH）作为释放已通过磺酰胺键与特定亲电性基团结合的保护氨基衍生物的手段。前体是一种合成中间体，携带有一个自由的-NH-，通过连接一个亲电子试剂通过磺酰胺键进行衍生化。
• 3-amino-1,5,6,7-tetrahydro-4H-indol-4-ones
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：US10428044B2

  公开（公告）日：2019-10-01

  Compounds of formula (I) which are inhibitors of Bub1 kinase, processes for their production and their use as pharmaceuticals.

  作为 Bub1 激酶抑制剂的式 (I) 化合物、其生产工艺及其制药用途。
• 3-AMINO-1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONES
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：EP3157914A1

  公开（公告）日：2017-04-26
• ACYL SULFONAMIDES FOR TREATING CANCER
  申请人：Bayer Aktiengesellschaft

  公开号：US20220226279A1

  公开（公告）日：2022-07-21

  The present invention provides acyl sulfonamide compounds of general formula (I): in which X, R 1 , R 2 , R 3 , R 4 , R 5 , R 6′ R a and R b are as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, as a sole agent or in combination with other active ingredients as well as methods of treating and/or prophylaxing diseases, particularly cancer, more particularly cancer in which KAT6A and/or KAT6B is focally amplified, said method comprising administering an effective amount of at least one compound of formula (I) to a subject in need thereof.