6'-bromo-4,4-difluorospiro[cyclohexane-1,3'-pyrrolo[3,2-b]pyridin]-2'(1'H)-one | 1190862-25-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: 6'-bromo-4,4-difluorospiro[cyclohexane-1,3'-pyrrolo[3,2-b]pyridin]-2'(1'H)-one
• 英文别名: 6'-Bromo-4,4-difluoro-1',2'-dihydrospiro[cyclohexane-1,3'-pyrrolo[3,2-b]pyridine]-2'-one；6-bromo-4',4'-difluorospiro[1H-pyrrolo[3,2-b]pyridine-3,1'-cyclohexane]-2-one
• CAS: 1190862-25-9
• 化学式: C₁₂H₁₁BrF₂N₂O
• 分子量: 317.133
• InChiKey: LVEBWQIKGWUCGZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  18
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  42
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolanyl)benzamide 、 6'-bromo-4,4-difluorospiro[cyclohexane-1,3'-pyrrolo[3,2-b]pyridin]-2'(1'H)-one 在 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 caesium carbonate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 生成 N-cyclopropyl-3-(4',4'-difluoro-2-oxospiro[1H-pyrrolo[3,2-b]pyridine-3,1'-cyclohexane]-6-yl)-4-methylbenzamide
  参考文献：
  名称：

  Indolin-2-one p38α inhibitors II: Lead optimisation

  摘要：

  Optimisation of a series of indolin-2-one p38 alpha inhibitors was achieved via both blocking of a potential metabolic 'hot spot' and by increasing overall polarity of the lead series leading to non-cytotoxic compounds which showed improved oral bioavailabilities in the rat. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.07.033
• 作为产物：
  描述：

  6-溴4-氮杂-吲哚-2-酮 在 DAST 、 potassium tert-butylate 作用下， 以 二氯甲烷 、 二甲基亚砜 为溶剂， 生成 6'-bromo-4,4-difluorospiro[cyclohexane-1,3'-pyrrolo[3,2-b]pyridin]-2'(1'H)-one
  参考文献：
  名称：

  Indolin-2-one p38α inhibitors II: Lead optimisation

  摘要：

  Optimisation of a series of indolin-2-one p38 alpha inhibitors was achieved via both blocking of a potential metabolic 'hot spot' and by increasing overall polarity of the lead series leading to non-cytotoxic compounds which showed improved oral bioavailabilities in the rat. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.07.033

文献信息

• New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
  申请人：Laboratorios Almirall, S.A.

  公开号：EP2108641A1

  公开（公告）日：2009-10-14

  This invention is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I) to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.

  这项发明涉及具有一般式(I)的新p38丝裂原活化蛋白激酶抑制剂；其制备方法；包含它们的药物组合物；以及它们在治疗中的应用。
• SUBSTITUTED SPIRO[CYCLOALKYL-1,3'-INDOL]-2'(1'H)-ONE DERIVATIVES AND THEIR USE AS P38 MITOGEN-ACTIVATED KINASE INHIBITORS
  申请人：Eastwood Paul Robert

  公开号：US20110053936A1

  公开（公告）日：2011-03-03

  The present disclosure is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I), processes for preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

  本公开涉及新的p38丝裂原活化蛋白激酶抑制剂，其具有一般式(I)，其制备方法，其药物组合物以及其使用方法。
• NEW SUBSTITUTED SPIRO[CYCLOALKYL-1,3'-INDO]-2'(1'H)-ONE DERIVATIVES AND THEIR USE AS P38 MITOGEN-ACTIVATED KINASE INHIBITORS
  申请人：Almirall, S.A.

  公开号：EP2280943B1

  公开（公告）日：2013-11-06
• US8772288B2
  申请人：——

  公开号：US8772288B2

  公开（公告）日：2014-07-08
• [EN] NEW SUBSTITUTED SPIRO[CYCLOALKYL-1,3'-INDOL]-2'(1'H)-ONE DERIVATIVES AND THEIR USE AS P38 MITOGEN-ACTIVATED KINASE INHIBITORS.<br/>[FR] NOUVEAUX DÉRIVÉS SUBSTITUÉS DE SPIRO[CYCLOALKYL-1,3'-INDOL]-2'(1'H)-ONE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE LA KINASE ACTIVÉE PAR LE MITOGÈNE P38
  申请人：ALMIRALL SA

  公开号：WO2009124692A1

  公开（公告）日：2009-10-15

  This invention is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I) to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.