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(1r,4r)-6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-imine hydrochloride | 1383985-61-2

中文名称
——
中文别名
——
英文名称
(1r,4r)-6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-imine hydrochloride
英文别名
(1r,4r)-6'-bromo-4-methoxyspiro[cyclohexane-1,2'-indene]-1'(3'H)imine hydrochloride
(1r,4r)-6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-imine hydrochloride化学式
CAS
1383985-61-2
化学式
C15H18BrNO*ClH
mdl
——
分子量
344.679
InChiKey
FDVIYQRSGKCUIF-HUZMHWHNSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.37
  • 重原子数:
    19.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    33.08
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

点击查看最新优质反应信息

文献信息

  • Compounds and their use as BACE Inhibitors
    申请人:Csjernyik Gabor
    公开号:US20120165347A1
    公开(公告)日:2012-06-28
    The present invention relates to compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and/or prevention of Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI (“mild cognitive impairment”), Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.
    本发明涉及式(I)的化合物及其药物组合物。此外,本发明涉及治疗方法,用于治疗和/或预防与Aβ相关的病理,如唐氏综合症,β-淀粉样蛋白血管病,如但不限于脑淀粉样蛋白血管病或遗传性脑出血,与认知损害相关的疾病,如但不限于MCI(“轻度认知损害”),阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,与疾病如阿尔茨海默病或痴呆症相关的神经退行性疾病,包括混合性血管性和退行性起源的痴呆,早老性痴呆,老年性痴呆和与帕森病、进行性上核性麻痹或皮层基底节变性相关的痴呆。
  • [EN] CYCLOALKYL ETHER COMPOUNDS AND THEIR USE AS BACE INHIBITORS<br/>[FR] COMPOSÉS CYCLOALKYLE-ÉTHER ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE BACE
    申请人:ASTRAZENECA AB
    公开号:WO2013190301A1
    公开(公告)日:2013-12-27
    Cycloalkyl ether compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Αβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration and pharmaceutical compositions containing such compounds. Formula (I) wherein A is -O-, or -CH2-, n is 0 or 1.
    环烷醚化合物及其治疗上可接受的盐,其制备方法,这些化合物的治疗用途,用于治疗与Αβ相关的病理,如唐氏综合症,β-淀粉样蛋白血管病,阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,与阿尔茨海默病或痴呆症等疾病相关的神经退行性变化,包括以血管性和退行性为主的混合性痴呆,早老性痴呆,老年痴呆和与帕森病、进行性核上性麻痹或皮层基底变性相关的痴呆,以及含有这些化合物的药物组合物。式(I)中,A为-O-,或-CH2-,n为0或1。
  • Process Intensification and Integration Studies for the Generation of a Key Aminoimidazole Intermediate in the Synthesis of Lanabecestat
    作者:Desiree Znidar、David Cantillo、Phillip Inglesby、Alistair Boyd、C. Oliver Kappe
    DOI:10.1021/acs.oprd.8b00089
    日期:2018.5.18
    multistep synthesis of aminoimidazole 6, a key intermediate in the preparation of lanabecestat (AZD3293/LY3314814), is described. Under intensified conditions (high temperature and elevated pressure), the overall processing time and required amounts of reagents could be significantly reduced, thus potentially minimizing manufacturing costs and improving the sustainability footprint. Process integration
    描述了一种改进的合成程序,用于多步合成咪唑6,这是制备lanabecestat的关键中间体(AZD3293 / LY3314814)。在高温条件下(高温和高压),可以大大减少总的处理时间和所需的试剂量,从而有可能最大程度地降低制造成本并改善可持续性足迹。已经尝试了从酮中间体2开始的三个连续步骤的过程集成,从而为潜在的多步连续制造路线奠定了基础。该过程包括通过用和Ti(i PrO)处理酮2初步形成亚胺3如图4所示,将3与酰胺4进行环缩合以形成醇5,并使用和Zn(OAc)2进行解,从而可以以47%的总产率获得目标结构单元6。
  • [EN] 2H-IMIDAZOL-4-AMINE COMPOUNDS AND THEIR USE AS BACE INHIBITORS<br/>[FR] COMPOSÉS 2H-IMIDAZOL-4-AMINE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE BACE
    申请人:ASTRAZENECA AB
    公开号:WO2013190298A1
    公开(公告)日:2013-12-27
    2H-imidazol-4-amine compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Αβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration methods of therapy, and pharmaceutical compositions containing such compounds. Formula (I) wherein A is -O- or -CH2-, n is 1 or 1.
    2H-咪唑-4-胺化合物,其治疗上可接受的盐,其制备过程,这些化合物的治疗用途,用于治疗与Αβ相关的病理,如唐氏综合症,β-淀粉样蛋白血管病,阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,与疾病如阿尔茨海默病或痴呆症相关的神经退行性疾病,包括混合性血管性和退行性起源的痴呆,早老性痴呆,老年痴呆和与帕森病、进行性上核性麻痹或皮层基底变性相关的痴呆的治疗方法,以及含有这些化合物的药物组合物。 公式(I)其中A为-O-或-CH2-,n为1或1。
  • [EN] PROCESSES FOR THE STEREOSELECTIVE PREPARATION OF BACE INHIBITORS<br/>[FR] PROCÉDÉS POUR LA PRÉPARATION STÉRÉOSÉLECTIVE D'INHIBITEURS DE BACE
    申请人:ASTRAZENECA AB
    公开号:WO2019122268A1
    公开(公告)日:2019-06-27
    The present application relates to processes for the stereoselective preparation of dihydroimidazole ring systems. Compounds prepared according to the disclosed processes are useful in treating at least one condition associated with inhibitition of the deposition of amyloid ß peptide (Aß) and portions thereof by inhibiting or the beta site APP Cleaving Enzyme (BACE).
    本申请涉及用于立体选择性制备二氢咪唑环系统的过程。根据所公开的过程制备的化合物可用于治疗至少一种与抑制淀粉样蛋白ß肽(Aß)及其部分沉积有关的疾病,通过抑制β位点APP裂解酶(BACE)。
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