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1-Methyl-4-nitropiperidin | 66909-71-5

中文名称
——
中文别名
——
英文名称
1-Methyl-4-nitropiperidin
英文别名
1-methyl-4-nitro-piperidine;1-Methyl-4-nitropiperidine
1-Methyl-4-nitropiperidin化学式
CAS
66909-71-5
化学式
C6H12N2O2
mdl
——
分子量
144.173
InChiKey
MLYGLYWYVMGNJB-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):
    0.6
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    49.1
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-Methyl-4-nitropiperidin碘甲烷 生成 1,1-dimethyl-4-nitropiperidin-1-ium;iodide
    参考文献:
    名称:
    PIOTROWSKA H.; SAS W.; WINIARSKI J., ROCZ. CHEM. , 1977, 51, NO 12, 2417-2420
    摘要:
    DOI:
  • 作为产物:
    描述:
    4-chloro-1-methyl-4-nitropiperidine;hydrochloride 以53%的产率得到
    参考文献:
    名称:
    PIOTROWSKA H.; SAS W.; WINIARSKI J., ROCZ. CHEM. , 1977, 51, NO 12, 2417-2420
    摘要:
    DOI:
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文献信息

  • N-Aryl Diazaspirocyclic Compounds and Methods of Preparation and Use Thereof
    申请人:Bhatti Balwinder S.
    公开号:US20080214591A1
    公开(公告)日:2008-09-04
    Compounds, pharmaceutical compositions including the compounds, and methods of preparation and use thereof are disclosed. The compounds are N-aryl diazaspirocyclic compounds, bridged analogs of N-heteroaryl diazaspirocyclic compounds, or prodrugs or metabolites of these compounds. The aryl group can be a five- or six-membered heterocyclic ring (heteroaryl). The compounds and compositions can be used to treat and/or prevent a wide variety of conditions or disorders, particularly those disorders characterized by dysfunction of nicotinic cholinergic neurotransmission, including disorders involving neuromodulation of neurotransmitter release, such as dopamine release. CNS disorders, which are characterized by an alteration in normal neurotransmitter release, are another example of disorders that can be treated and/or prevented. The compounds and compositions can also be used to alleviate pain. The compounds can: (i) alter the number of nicotinic cholinergic receptors of the brain of the patient, (ii) exhibit neuroprotective effects and (iii) when employed in effective amounts, not result in appreciable adverse side effects (e.g., side effects such as significant increases in blood pressure and heart rate, significant negative effects upon the gastro-intestinal tract, and significant effects upon skeletal muscle).
    本文揭示了化合物、包含这些化合物的药物组合物以及其制备和使用方法。这些化合物是N-芳基二氮杂螺环化合物、N-杂芳基二氮杂螺环化合物的桥接类似物,或这些化合物的前药或代谢物。芳基基团可以是五元或六元杂环环(杂芳基)。这些化合物和组合物可用于治疗和/或预防各种疾病或障碍,特别是那些以尼古丁胆碱能神经递质功能障碍为特征的障碍,包括涉及神经递质释放的神经调节障碍,如多巴胺释放。中枢神经系统障碍是另一个可以治疗和/或预防的障碍的例子,其特征是正常神经递质释放的改变。这些化合物和组合物还可用于缓解疼痛。这些化合物可以:(i)改变患者大脑中尼古丁胆碱能受体的数量,(ii)表现出神经保护作用,(iii)在有效剂量下,不会产生明显的不良副作用(例如,明显增加血压和心率、对胃肠道产生明显的负面影响以及对骨骼肌产生明显的影响)。
  • N-ARYL DIAZASPIROCYCLIC COMPOUNDS AND METHODS OF PREPARATION AND USE THEREOF
    申请人:Bhatti Balwinder S.
    公开号:US20110105548A1
    公开(公告)日:2011-05-05
    Compounds, pharmaceutical compositions including the compounds, and methods of preparation and use thereof are disclosed. The compounds are N-aryl diazaspirocyclic compounds, bridged analogs of N-heteroaryl diazaspirocyclic compounds, or prodrugs or metabolites of these compounds. The aryl group can be a five- or six-membered heterocyclic ring (heteroaryl). The compounds and compositions can be used to treat and/or prevent a wide variety of conditions or disorders, particularly those disorders characterized by dysfunction of nicotinic cholinergic neurotransmission, including disorders involving neuromodulation of neurotransmitter release, such as dopamine release. CNS disorders, which are characterized by an alteration in normal neurotransmitter release, are another example of disorders that can be treated and/or prevented. The compounds and compositions can also be used to alleviate pain. The compounds can: (i) alter the number of nicotinic cholinergic receptors of the brain of the patient, (ii) exhibit neuroprotective effects and (iii) when employed in effective amounts, not result in appreciable adverse side effects (e.g., side effects such as significant increases in blood pressure and heart rate, significant negative effects upon the gastro-intestinal tract, and significant effects upon skeletal muscle).
    本文介绍了N-芳基二氮杂螺环化合物、N-杂芳基二氮杂螺环化合物的桥接类似物以及这些化合物的前药或代谢物。芳基可以是五元或六元杂环环(杂芳基)。这些化合物和组合物可以用于治疗和/或预防各种条件或疾病,特别是那些以尼古丁乙酰胆碱神经递质功能障碍为特征的疾病,包括涉及神经递质释放的神经调节疾病,如多巴胺释放。中枢神经系统疾病是另一种可以治疗和/或预防的疾病,其特征是正常神经递质释放的改变。这些化合物和组合物也可以用于缓解疼痛。这些化合物可以:(i)改变患者大脑中尼古丁乙酰胆碱受体的数量,(ii)表现出神经保护效果,以及(iii)在有效剂量下,不会产生明显的不良副作用(例如,明显增加血压和心率、对胃肠道产生明显负面影响和对骨骼肌产生明显影响等副作用)。
  • US7291731B2
    申请人:——
    公开号:US7291731B2
    公开(公告)日:2007-11-06
  • US7375110B2
    申请人:——
    公开号:US7375110B2
    公开(公告)日:2008-05-20
  • US7923559B2
    申请人:——
    公开号:US7923559B2
    公开(公告)日:2011-04-12
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