2-bromo-1-(imidazo[1,2-a]pyrazin-3-yl)ethanone monohydrobromide | 358780-17-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并吡嗪类
• 英文名称: 2-bromo-1-(imidazo[1,2-a]pyrazin-3-yl)ethanone monohydrobromide
• 英文别名: 2-Bromo-1-imidazo[1,2-a]pyrazin-3-ylethanone;hydrobromide
• CAS: 358780-17-3
• 化学式: BrH*C₈H₆BrN₃O
• 分子量: 320.971
• InChiKey: GCZWCGMIOBILNG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.88
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  47.3
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• 2,4-Disubstituted thiazolyl derivatives
  申请人：——

  公开号：US20030203897A1

  公开（公告）日：2003-10-30

  This invention concerns the use of a compound of formula (I′) 1 a N-oxide, pharmaceutically acceptable addition salt, quaternary amine and stereochemically isomeric form thereof, wherein Q is optionally substituted C 3-6 cycloalkyl, phenyl, naphthyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, benzthiazolyl, benzoxazolyl, benzimidazolyl, indazolyl, or imidazopyridyl; or Q is a radical of formula 2 wherein X and Y each independently are O, NR 3 , CH 2 or S, with R 3 being hydrogen or C 1-4 alkyl; q is 1 to 4; Z is O or NR 4 with R 4 being hydrogen or C 1-4 alkyl; r is 1 to 3; L is optionally substituted phenyl or L is Het with Het being an optionally substituted five- or six-membered heterocyclic ring or an optionally substituted bicyclic heterocyclic ring; for the manufacture of a medicament for the prevention or the treatment of diseases mediated through cytokines.

  这项发明涉及使用化合物的公式(I′)1a N-氧化物，药学上可接受的加成盐，季铵盐和其立体化学异构体，其中Q是可选择取代的C3-6环烷基，苯基，萘基，吡啶基，嘧啶基，吡嗪基，吡啶并嘧啶基，苯噻唑基，苯氧唑基，苯并咪唑基，吲哚基，或咪唑吡啶基；或Q是公式2的基团，其中X和Y分别独立地是O，NR3，CH2或S，R3为氢或C1-4烷基；q为1到4；Z为O或NR4，其中R4为氢或C1-4烷基；r为1到3；L是可选择取代的苯基或L是Het，其中Het是可选择取代的五元或六元杂环环或可选择取代的双环杂环环；用于制造用于预防或治疗通过细胞因子介导的疾病的药物。
• 2,4-DISUBSTITUTED THIAZOLYL DERIVATIVES
  申请人：Janssen Pharmaceutica N.V.

  公开号：EP1261607A1

  公开（公告）日：2002-12-04
• US7105550B2
  申请人：——

  公开号：US7105550B2

  公开（公告）日：2006-09-12
• US7893280B2
  申请人：——

  公开号：US7893280B2

  公开（公告）日：2011-02-22
• [EN] 2,4-DISUBSTITUTED THIAZOLYL DERIVATIVES<br/>[FR] DERIVES DE THIAZOLYLE 2,4-DISUBSTITUE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2001064674A1

  公开（公告）日：2001-09-07

  This invention concerns the use of a compound of formula (I'), an (N)-oxide, pharmaceutically acceptable addition salt, quaternary amine and stereochemically isomeric form thereof, wherein Q is optionally substituted C3-6cycloalkyl, phenyl, naphthyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, benzthiazolyl, benzoxazolyl, benzimidazolyl, indazolyl, or imidazopyridyl; or Q is a radical of formula (b-1, b-2, b-3), wherein X and Y each independently are O, NR3, CH2 or S, with R3 being hydrogen or C¿1-4?alkyl; q is 1 to 4; Z is O or NR?4 with R4¿ being hydrogen or C¿1-4?alkyl; r is 1 to 3; L is optionally substituted phenyl or L is Het with Het being an optionally substituted five- or six-membered heterocyclic ring or an optionally substituted bicyclic heterocyclic ring; for the manufacture of a medicament for the prevention or the treatment of diseases mediated through cytokines.