[(R)-7-bromo-4,4-difluoro-1-((R)-2-methyl-propane-2-sulfinylamino)-1,2,3,4-tetrahydro-naphthalen-1-yl]-difluoro-acetic acid ethyl ester | 1415108-31-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: [(R)-7-bromo-4,4-difluoro-1-((R)-2-methyl-propane-2-sulfinylamino)-1,2,3,4-tetrahydro-naphthalen-1-yl]-difluoro-acetic acid ethyl ester
• 英文别名: ethyl 2-[(1R)-7-bromo-1-[[(R)-tert-butylsulfinyl]amino]-4,4-difluoro-2,3-dihydronaphthalen-1-yl]-2,2-difluoroacetate
• CAS: 1415108-31-4
• 化学式: C₁₈H₂₂BrF₄NO₃S
• 分子量: 488.341
• InChiKey: RUKAJUNVWBXLSY-WVDZOPJMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  74.6
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  (R)-2-methyl-propane-2-sulfinic acid [7-bromo-4,4-difluoro-3,4-dihydro-2H-naphthalen-(1E)-ylidene]-amide 、 二氟溴乙酸乙酯 以the product [(R)-7-bromo-4,4-difluoro-1-((R)-2-methyl-propane-2-sulfinylamino)-1,2,3,4-tetrahydro-naphthalen-1-yl]-difluoro-acetic acid ethyl ester (58% yield) was obtained as a brown solid的产率得到[(R)-7-bromo-4,4-difluoro-1-((R)-2-methyl-propane-2-sulfinylamino)-1,2,3,4-tetrahydro-naphthalen-1-yl]-difluoro-acetic acid ethyl ester
  参考文献：
  名称：

  SPIRO-[1,3]-OXAZINES AND SPIRO-[1,4]-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS

  摘要：

  本发明提供了具有BACE1和/或BACE2抑制活性的公式I的螺环-[1,3]-噁唑和螺环-[1,4]-噁唑烷，它们的制造方法，含有它们的制药组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防阿尔茨海默病和2型糖尿病等疾病方面是有用的。

  公开号：

  US20120302549A1

文献信息

• [EN] SPIRO-[1,3]-OXAZINES AND SPIRO-[1,4]-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS<br/>[FR] SPIRO-[1,3]-OXAZINES ET SPIRO-[1,4]-OXAZÉPINES EN TANT QU'INHIBITEURS DE BAEC1 ET/OU BACE2
  申请人：HOFFMANN LA ROCHE

  公开号：WO2012163790A1

  公开（公告）日：2012-12-06

  The present invention provides spiro-[l,3]-oxazines and spiro-[l,4]-oxazepines of formula (I) having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.

  本发明提供了具有BACE1和/或BACE2抑制活性的式(I)的螺-[1,3]-噁唑和螺-[1,4]-噁唑啉，其制备方法，含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗例如阿尔茨海默病和2型糖尿病等疾病方面是有用的。
• SPIRO-[1,3]-OXAZINES AND SPIRO-[1,4]-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS
  申请人：Narquizian Robert

  公开号：US20120302549A1

  公开（公告）日：2012-11-29

  The present invention provides spiro-[1,3]-oxazines and spiro-[1,4]-oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.

  本发明提供了具有BACE1和/或BACE2抑制活性的式I的螺[1,3]-噁唑和螺[1,4]-噁唑环烯化合物，其制备方法，包含它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗例如阿尔茨海默病和2型糖尿病等疾病方面非常有用。
• US9079919B2
  申请人：——

  公开号：US9079919B2

  公开（公告）日：2015-07-14
• Spiro-[1,3]-oxazines and spiro-[1,4]-oxazepines as BACE1 and/or BACE2 inhibitors
  申请人：Narquizian Robert

  公开号：US09079919B2

  公开（公告）日：2015-07-14

  The present invention provides spiro-[1,3]-oxazines and spiro-[1,4]-oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.

  本发明提供了具有BACE1和/或BACE2抑制活性的公式I的螺环[1,3]-噁唑和螺环[1,4]-噁唑烷，其制造、含有它们的制药组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防例如阿尔茨海默病和2型糖尿病等方面具有用途。