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4,5,6,7-四氢吡唑并[1,5-a]吡啶-3-甲醛 | 307308-03-8

中文名称
4,5,6,7-四氢吡唑并[1,5-a]吡啶-3-甲醛
中文别名
4,5,6,7-四氢吡唑并[1,5-A]吡啶-3-甲醛
英文名称
4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-3-carbaldehyde
英文别名
——
4,5,6,7-四氢吡唑并[1,5-a]吡啶-3-甲醛化学式
CAS
307308-03-8
化学式
C8H10N2O
mdl
MFCD09834817
分子量
150.18
InChiKey
CSPINDKIWMCRNX-UHFFFAOYSA-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):
    0.4
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    34.9
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P280,P304+P340,P305+P351+P338,P405,P501
  • 危险性描述:
    H302

SDS

SDS:854ce372c0cf86d3f6ea2cc5ca151a91
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反应信息

  • 作为反应物:
    描述:
    4,5,6,7-四氢吡唑并[1,5-a]吡啶-3-甲醛titanium(IV) isopropylateN,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 甲醇乙腈 为溶剂, 反应 17.5h, 生成 (1R,2S,5S)-N-[cyano(4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl)methyl]-3-[(2S)-3,3-dimethyl-2-[(2,2,2-trifluoroacetyl)amino]butanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide
    参考文献:
    名称:
    [EN] INHIBITORS OF CYSTEINE PROTEASES AND METHODS OF USE THEREOF
    [FR] INHIBITEURS DE CYSTÉINE PROTÉASES ET LEURS MÉTHODES D'UTILISATION
    摘要:
    The disclosure provides compounds with nitrile warheads and their use in treating medical diseases or disorders, such as viral infections. Pharmaceutical compositions and methods of making various compounds with nitrile warheads are provided. The compounds are contemplated to inhibit proteases, such as the 3C, CL- or 3CL-like protease.
    公开号:
    WO2023044171A1
  • 作为产物:
    描述:
    吡唑并[1,5-a]吡啶-3-基甲醇 在 palladium on activated charcoal 、 氢气戴斯-马丁氧化剂 作用下, 以 乙醇二氯甲烷 为溶剂, 生成 4,5,6,7-四氢吡唑并[1,5-a]吡啶-3-甲醛
    参考文献:
    名称:
    [EN] IMIDAZOTRIAZINONE COMPOUNDS
    [FR] COMPOSÉS D'IMIDAZOTRIAZINONE
    摘要:
    本发明提供了咪唑三唑酮化合物,它们是磷酸二酯酶9的抑制剂及其药用盐。本发明还提供了用于治疗哺乳动物,包括人类,PDE9相关疾病或疾病的过程、药物组成、药物制剂和化合物的药用。
    公开号:
    WO2013142269A1
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文献信息

  • AMINO-HETEROCYCLIC COMPOUNDS
    申请人:Verhoest Patrick R.
    公开号:US20090030003A1
    公开(公告)日:2009-01-29
    The invention provides PDE9-inhibiting compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein R, R 1 , R 2 and R 3 are as defined herein. Pharmaceutical compositions containing the compounds of Formula I, and uses thereof in treating neurodegenerative and cognitive disorders, such as Alzheimer's disease and schizophrenia, are also provided.
    该发明提供了式(I)的PDE9抑制化合物及其药用盐,其中R、R1、R2和R3如本文所定义。还提供了含有式I化合物的药物组合物,并将其用于治疗神经退行性和认知障碍,如阿尔茨海默病和精神分裂症。
  • Pyrazolo[3,4-d]pyrimidine compounds
    申请人:Pfizer Inc.
    公开号:US07964607B2
    公开(公告)日:2011-06-21
    The invention provides PDE9-inhibiting compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein R, R1, R2 and R3 are as defined herein. Pharmaceutical compositions containing the compounds of Formula I, and uses thereof in treating neurodegenerative and cognitive disorders, such as Alzheimer's disease and schizophrenia, are also provided.
    本发明提供了PDE9抑制化合物的公式(I),以及其药学上可接受的盐,其中R,R1,R2和R3的定义如本文所述。还提供了含有公式I化合物的药物组合物,并用于治疗神经退行性和认知障碍,例如阿尔茨海默病和精神分裂症的用途。
  • Imidazotriazinone Compounds
    申请人:FORUM Pharmaceuticals, Inc.
    公开号:US20150191476A1
    公开(公告)日:2015-07-09
    The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.
    本发明提供了咪唑三嗪酮类化合物及其医药上可接受的盐,这些化合物是磷酸二酯酶9的抑制剂。本发明还提供了制备该化合物的方法、药物组合物、药物制剂以及在哺乳动物,包括人类中治疗PDE9相关疾病或疾病的药物用途。
  • MONOACYLGLYCEROL LIPASE MODULATORS
    申请人:Janssen Pharmaceutica NV
    公开号:EP3856178A1
    公开(公告)日:2021-08-04
  • IMIDAZOTRIAZINONE COMPOUNDS
    申请人:Ironwood Pharmaceuticals, Inc.
    公开号:US20170327502A1
    公开(公告)日:2017-11-16
    The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.
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