ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-pyrazolo[4,3-b]pyridin-3-yl)cyclohex-3-enecarboxylate

• 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: ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-pyrazolo[4,3-b]pyridin-3-yl)cyclohex-3-enecarboxylate
• 化学式: C₂₃H₁₉ClF₃N₃O₃
• 分子量: 477.87
• InChiKey: JNYSGHZKTAFAGN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.54
• 重原子数：
  33.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  74.08
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-pyrazolo[4,3-b]pyridin-3-yl)cyclohex-3-enecarboxylate 在 钯 氢气 作用下， 以 乙酸乙酯 为溶剂， 40.0 ℃ 、13.51 MPa 条件下， 反应 24.0h， 以to give the title compound (500 mg, yield: 99%) as a yellow oil的产率得到ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-pyrazolo[4,3-b]pyridin-3-yl)cyclohexanecarboxylate
  参考文献：
  名称：

  3-CYCLOHEXENYL AND CYCLOHEXYL SUBSTITUTED INDOLE AND INDAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF

  摘要：

  本发明涉及公式I所示的化合物及其药学上可接受的盐或溶剂。这样的化合物可用于治疗RORgammaT介导的疾病或病状。

  公开号：

  US20150191434A1
• 作为产物：
  描述：

  4-(三氟甲基磺酰氧基)-3-环己烯羧酸乙酯 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 potassium acetate 、 sodium carbonate 作用下， 以 1,4-二氧六环 、 乙醇 、 甲苯 为溶剂， 反应 8.0h， 生成 ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-pyrazolo[4,3-b]pyridin-3-yl)cyclohex-3-enecarboxylate
  参考文献：
  名称：

  3-CYCLOHEXENYL AND CYCLOHEXYL SUBSTITUTED INDOLE AND INDAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF

  摘要：

  本发明涉及式I化合物以及药用可接受的盐或溶剂化物。这类化合物可用于治疗RORgammaT介导的疾病或状况。

  公开号：

  US20150191434A1

文献信息

• Discovery of <i>N</i>-(Indazol-3-yl)piperidine-4-carboxylic Acids as RORγt Allosteric Inhibitors for Autoimmune Diseases
  作者：Hongjun Zhang、Blair T. Lapointe、Neville Anthony、Rita Azevedo、Jos Cals、Craig C. Correll、Matthew Daniels、Sujal Deshmukh、Hans van Eenenaam、Heidi Ferguson、Laxminarayan G. Hegde、Willem Jan Karstens、John Maclean、J. Richard Miller、Lily Y. Moy、Vladimir Simov、Sunil Nagpal、Arthur Oubrie、Rachel L. Palte、Gopal Parthasarathy、Nunzio Sciammetta、Mario van der Stelt、Janice D. Woodhouse、B. Wesley Trotter、Kenneth Barr

  DOI：10.1021/acsmedchemlett.9b00431

  日期：2020.2.13

  The clinical success of anti-IL-17 monoclonal antibodies (i.e., Cosentyx and Taltz) has validated Th17 pathway modulation for the treatment of autoimmune diseases. The nuclear hormone receptor ROR gamma t is a master regulator of Th17 cells and affects the production of a host of cytokines, including IL-17A, IL-17F, IL -22, IL-26, and GMCSF. Substantial interest has been spurred across both academia and industry to seek small molecules suitable for ROR gamma t inhibition. A variety of ROR gamma t inhibitors have been reported in the past few years, the majority of which are orthosteric binders. Here we disclose the discovery and optimization of a class of inhibitors, which bind differently to an allosteric binding pocket. Starting from a weakly active hit 1, a tool compound 14 was quickly identified that demonstrated superior potency, selectivity, and off-target profile. Further optimization focused on improving metabolic stability. Replacing the benzoic acid moiety with piperidinyl carboxylate, modifying the 4-aza-indazole core in 14 to 4-F-indazole, and incorporating a key hydroxyl group led to the discovery of 25, which possesses exquisite potency and selectivity, as well as an improved pharmacokinetic profile suitable for oral dosing.
• [EN] 3-CYCLOHEXENYL AND CYCLOHEXYL SUBSTITUTED INDOLE AND INDAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF<br/>[FR] COMPOSÉS INDAZOLE ET INDOLE À SUBSTITUTION CYCLOHEXYL ET 3-CYCLOHEXENYL
  申请人：MERCK SHARP & DOHME

  公开号：WO2014028597A3

  公开（公告）日：2014-05-01
• US9487490B2
  申请人：——

  公开号：US9487490B2

  公开（公告）日：2016-11-08
• 3-CYCLOHEXENYL AND CYCLOHEXYL SUBSTITUTED INDOLE AND INDAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
  申请人：Merck Sharp & Dohme Corp.

  公开号：US20150191434A1

  公开（公告）日：2015-07-09

  The present invention relates to compounds according to Formula I and pharmaceutically acceptable salts or solvates thereof. Such compounds can be used in the treatment of RORgammaT-mediated diseases or conditions.

  本发明涉及式I化合物以及药用可接受的盐或溶剂化物。这类化合物可用于治疗RORgammaT介导的疾病或状况。