7-Bromo-2-(4-fluorophenyl)-3-methylimidazo[4,5-c]pyridine | 1239720-39-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 7-Bromo-2-(4-fluorophenyl)-3-methylimidazo[4,5-c]pyridine
• CAS: 1239720-39-8
• 化学式: C₁₃H₉BrFN₃
• 分子量: 306.137
• InChiKey: NKSLIOARMFWZEK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  30.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  5-bromo-N-methyl-4-nitro-1-oxidopyridin-1-ium-3-amine 、 对氟苯甲醛 在 sodium dithionite 作用下， 以 乙醇 为溶剂， 反应 0.75h， 以68%的产率得到7-Bromo-2-(4-fluorophenyl)-3-methylimidazo[4,5-c]pyridine
  参考文献：
  名称：

  [EN] NOVEL SUBSTITUTED BENZOXAZOLE, BENZIMIDAZOLE, OXAZOLOPYRIDINE AND IMIDAZOPYRIDINE DERIVATIVES AS GAMMA SECRETASE MODULATORS
  [FR] NOUVEAUX DÉRIVÉS SUBSTITUÉS DU BENZOXAZOLE, DU BENZIMIDAZOLE, DE L'OXAZOLOPYRIDINE ET DE L'IMIDAZOPYRIDINE COMME MODULATEURS DE LA GAMMA-SECRÉTASE

  摘要：

  本发明涉及具有以下式（I）的新颖取代苯并噁唑、苯并咪唑、噁唑吡啶和咪唑吡啶衍生物，其中R1、R2、R3、R4、X、A1、A2、A3、A4、Y1、Y2、Y3和Z的含义如索赔中所定义。根据本发明的化合物可用作γ-分泌酶调节剂。本发明还涉及制备这种新化合物的方法、包含所述化合物作为活性成分的药物组合物以及将所述化合物用作药物的用途。

  公开号：

  WO2010094647A1

文献信息

• [EN] NOVEL SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS AS GAMMA SECRETASE MODULATORS<br/>[FR] NOUVEAUX COMPOSÉS HÉTÉROCYCLIQUES BICYCLIQUES SUBSTITUÉS EN TANT QUE MODULATEURS DE LA GAMMA-SÉCRÉTASE
  申请人：ORTHO MCNEIL JANSSEN PHARM

  公开号：WO2010089292A1

  公开（公告）日：2010-08-12

  The present invention is concerned with substituted bicyclic heterocyclic compounds of Formula (I) wherein Het1, Het2, A1, A2, A3 and A4 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.

  本发明涉及式（I）的取代双环杂环化合物，其中Het1、Het2、A1、A2、A3和A4的含义如权利要求中所定义。根据本发明的化合物可用作γ-分泌酶调节剂。本发明还涉及制备这种新化合物的方法，包含所述化合物作为活性成分的药物组合物，以及将所述化合物用作药物的用途。
• NOVEL SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS AS GAMMA SECRETASE MODULATORS
  申请人：Gijsen Henricus, Jacobus, Maria

  公开号：US20110281881A1

  公开（公告）日：2011-11-17

  The present invention is concerned with substituted bicyclic heterocyclic compounds of Formula (I) wherein Het 1 , Het 2 , A 1 , A 2 , A 3 and A 4 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
• NOVEL SUBSTITUTED BENZOXAZOLE, BENZIMIDAZOLE, OXAZOLOPYRIDINE AND IMIDAZOPYRIDINE DERIVATIVES AS GAMMA SECRETASE MODULATORS
  申请人：Gijsen Henricu Jacobus Maria

  公开号：US20120022090A1

  公开（公告）日：2012-01-26

  The present invention is concerned with novel substituted benzoxazole, benzimidazole, oxazolopyridine and imidazopyridine derivatives of Formula (I) wherein R 1 , R 2 , R 3 , R 4 , X, A 1 , A 2 , A 3 , A 4 , Y 1 , Y 2 , Y 3 and Z have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
• US8772504B2
  申请人：——

  公开号：US8772504B2

  公开（公告）日：2014-07-08
• US8946426B2
  申请人：——

  公开号：US8946426B2

  公开（公告）日：2015-02-03