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2-氧代-2-(1-Boc-4-氧代-3-哌啶)乙酸乙酯 | 518990-24-4

中文名称
2-氧代-2-(1-Boc-4-氧代-3-哌啶)乙酸乙酯
中文别名
3-乙氧草酰基-4-氧代哌啶-1-羧酸叔丁酯
英文名称
tert-butyl 3-(2-ethoxy-2-oxoacetyl)-4-oxopiperidine-1-carboxylate
英文别名
——
2-氧代-2-(1-Boc-4-氧代-3-哌啶)乙酸乙酯化学式
CAS
518990-24-4
化学式
C14H21NO6
mdl
——
分子量
299.324
InChiKey
RSNKXJXWNHBZEU-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

物化性质

  • 沸点:
    420.1±45.0 °C(Predicted)
  • 密度:
    1.202

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    90
  • 氢给体数:
    0
  • 氢受体数:
    6

安全信息

  • 海关编码:
    2933399090

SDS

SDS:282e0f289ee0f0ac019b83b2e8e88951
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反应信息

  • 作为反应物:
    描述:
    2-氧代-2-(1-Boc-4-氧代-3-哌啶)乙酸乙酯甲醇sodium一水合肼溶剂黄146 作用下, 反应 17.5h, 生成 tert-butyl 3-[hydroxy(methyl)carbamoyl]-1,4,6,7-tetrahydropyrazolo[4,3-c]pyridine-5-carboxylate
    参考文献:
    名称:
    [EN] DIAZEPINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF HEPATITIS B INFECTIONS
    [FR] DÉRIVÉS DE DIAZÉPINONE ET LEUR UTILISATION DANS LE TRAITEMENT DES INFECTIONS PAR L'HÉPATITE B
    摘要:
    本文提供了一种用于治疗HBV感染的化合物(I)和(V),以及其药物组合物和抑制、抑制或预防受试者HBV感染的方法。
    公开号:
    WO2018005883A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and evaluation of tetrahydropyrazolopyridine inhibitors of anion exchange protein SLC26A4 (pendrin)
    摘要:
    Pendrin is a transmembrane chloride/anion antiporter that is strongly upregulated in the airways in rhinoviral infection, asthma, cystic fibrosis and chronic rhinosinusitis. Based on its role in the regulation of airway surface liquid depth, pendrin inhibitors have potential indications for treatment of inflammatory airways diseases. Here, a completely regioselective route to tetrahydro-pyrazolopyridine pendrin inhibitors based on 1,3-diketone and substituted hydrazine condensation was been developed. Structure-activity relationships at the tetrahydropyridyl nitrogen were investigated using a focused library, establishing the privileged nature of N-phenyl ureas and improving inhibitor potency by greater than 2-fold.
    DOI:
    10.1016/j.bmcl.2019.07.003
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文献信息

  • [EN] OXADIAZEPINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF HEPATITIS B INFECTIONS<br/>[FR] DÉRIVÉS D'OXADIAZÉPINONE ET LEUR UTILISATION DANS LE TRAITEMENT D'INFECTIONS PAR L'HÉPATITE B
    申请人:NOVIRA THERAPEUTICS INC
    公开号:WO2018005881A1
    公开(公告)日:2018-01-04
    Provided herein are compounds of formula (IA) and (III) useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.
    本文提供了公式(IA)和(III)的化合物,用于治疗需要治疗HBV感染的受试者,以及其药物组合物和抑制、抑制或预防受试者HBV感染的方法。
  • [EN] ALKYNYL ALCOHOLS AND METHODS OF USE<br/>[FR] ALCOOLS D'ALCYNYLE ET PROCÉDÉS D'UTILISATION CORRESPONDANTS
    申请人:HOFFMANN LA ROCHE
    公开号:WO2015025025A1
    公开(公告)日:2015-02-26
    The invention relates to compounds of Formula (0): wherein Q, A1-A8, R4 and R5 and each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over- activation of NF-kB signaling is observed.
    这项发明涉及以下式的化合物(0):其中Q,A1-A8,R4和R5分别具有如本文所述的含义。式(0)的化合物及其药物组成物在治疗观察到NF-kB信号通路的不良或过度活化的疾病和紊乱中是有用的。
  • [EN] NOVEL INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV)<br/>[FR] NOUVEAUX INDOLE-2-CARBOXAMIDES ACTIFS CONTRE LE VIRUS DE L'HÉPATITE B (VHB)
    申请人:AICURIS GMBH & CO KG
    公开号:WO2020221826A1
    公开(公告)日:2020-11-05
    The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV replication cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes and intermediates for making the compounds.
    本发明一般涉及新型抗病毒药剂。具体地,本发明涉及能够抑制乙型肝炎病毒(HBV)编码的蛋白质或干扰HBV复制周期功能的化合物,包括这种化合物的组合物,抑制HBV病毒复制的方法,治疗或预防HBV感染的方法,以及制备这些化合物的工艺和中间体。
  • [EN] NOVEL INDOLIZINE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV)<br/>[FR] NOUVEAUX INDOLIZINE-2-CARBOXAMIDES ACTIFS CONTRE LE VIRUS DE L'HÉPATITE B (VHB)
    申请人:AICURIS GMBH & CO KG
    公开号:WO2020221824A1
    公开(公告)日:2020-11-05
    The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV replication cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes and intermediates for making the compounds.
    本发明一般涉及新型抗病毒剂。具体地,本发明涉及能够抑制乙型肝炎病毒(HBV)编码的蛋白质或干扰HBV复制周期功能的化合物,包括这种化合物的组合物,抑制HBV病毒复制的方法,治疗或预防HBV感染的方法,以及制备这些化合物的工艺和中间体。
  • [EN] NOVEL PHENYL AND PYRIDYL UREAS ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV)<br/>[FR] NOUVELLES URÉES DE PHÉNYLE ET DE PYRIDYLE ACTIVES CONTRE LE VIRUS DE L'HÉPATITE B (VHB)
    申请人:AICURIS GMBH & CO KG
    公开号:WO2020221816A1
    公开(公告)日:2020-11-05
    The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV replication cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes and intermediates for making the compounds.
    本发明一般涉及新型抗病毒剂。具体地,本发明涉及能够抑制乙型肝炎病毒(HBV)编码的蛋白质或干扰HBV复制周期功能的化合物,包含这种化合物的组合物,抑制HBV病毒复制的方法,治疗或预防HBV感染的方法,以及制备这些化合物的工艺和中间体。
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