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3,3-dimethyl-N-neopentylpiperidine

中文名称
——
中文别名
——
英文名称
3,3-dimethyl-N-neopentylpiperidine
英文别名
1-(2,2-Dimethylpropyl)-3,3-dimethylpiperidine
3,3-dimethyl-N-neopentylpiperidine化学式
CAS
——
化学式
C12H25N
mdl
——
分子量
183.337
InChiKey
AECXSEFQYOUKII-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):
    3.7
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    3,3-二甲基哌啶吡啶 、 lithium aluminium tetrahydride 作用下, 以 乙醚氯仿 为溶剂, 反应 36.0h, 生成 3,3-dimethyl-N-neopentylpiperidine
    参考文献:
    名称:
    Eclipsed Conformation of the Exocyclic N−CH2 Bond in N-Neopentylpiperidines and the Stereodynamic Consequences As Studied by Dynamic NMR Spectroscopy and Molecular Mechanics Calculations
    摘要:
    The dynamic stereochemistry of a range of N-neopentylpiperidines 1 with an eclipsed N-CH2-t-Bu bond is compared with that of the corresponding range of N-ethylpiperidines 2 with a gauche N-CH2Me bond. By using dynamic NMR spectroscopy, the relative importance of ring inversion, exocyclic bond rotation, and nitrogen inversion are elucidated and barriers are reported and discussed. Minor populations of the neopentyl-axial-eclipsed conformation are detected directly and identified with the help of molecular mechanics calculations. The corresponding N-alkylpyrrolidines are also reported.
    DOI:
    10.1021/jo9720344
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文献信息

  • Benzamide Compounds
    申请人:Gibson Keith Hopkinson
    公开号:US20080293687A1
    公开(公告)日:2008-11-27
    The invention concerns benzamide compounds of Formula (I), wherein R 1a , R 1b , R 1c , R 2 , R 3 , R 4 , m and n have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of histone deacetylase (HDAC).
    这项发明涉及公式(I)的苯甲酰胺化合物,其中R1a、R1b、R1c、R2、R3、R4、m和n具有描述中定义的任意含义;它们的制备过程,含有它们的药物组合物以及它们在制造用作抗增殖剂的药物时的用途,用于预防或治疗对组蛋白去乙酰化酶(HDAC)抑制敏感的肿瘤或其他增殖性疾病。
  • DIAZACARBAZOLES AND METHODS OF USE
    申请人:Chen Huifen
    公开号:US20110118230A1
    公开(公告)日:2011-05-19
    The invention relates to 1,7-diazacarbazole compounds of Formula (I), (I-a) and (I-b) which are useful as kinase inhibitors, more specifically useful as checkpoint kinase 1 (chk1) inhibitors, thus useful as cancer therapeutics. The invention also relates to compositions, more specifically pharmaceutical compositions comprising these compounds and methods of using the same to treat various forms of cancer and hyperproliferative disorders, as well as methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及式(I),(I-a)和(I-b)的1,7-二氮杂咔唑化合物,其作为激酶抑制剂有用,更具体地作为检查点激酶1(chk1)抑制剂有用,因此可用作癌症治疗剂。本发明还涉及包含这些化合物的组合物,更具体地是药物组合物,并使用它们治疗各种形式的癌症和增生性疾病的方法,以及使用这些化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗的方法,或相关的病理条件。
  • Tetracycline Compounds
    申请人:Chen Chi-Li
    公开号:US20120135968A1
    公开(公告)日:2012-05-31
    The present invention is directed to a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof. The variables for Structural Formula I are defined herein. Also described is a pharmaceutical composition comprising the compound of Structural Formula I and its therapeutic use.
    本发明涉及一种由结构式(I)表示的化合物或其药学上可接受的盐。结构式I的变量在此定义。同时还描述了包含结构式I化合物的药物组合物及其治疗用途。
  • METHODS OF USE OF DIAZACARBAZOLES FOR TREATING CANCER
    申请人:Genentech, Inc.
    公开号:US20130261104A1
    公开(公告)日:2013-10-03
    Methods of use of compounds of formula (I) for treating cancer: wherein X, Y, X, R 3 , R 5 and R 6 are as defined herein.
    使用式(I)化合物治疗癌症的方法:其中X、Y、X、R3、R5和R6的定义如本文所述。
  • TETRACYCLINE COMPOUNDS
    申请人:Tetraphase Pharmaceuticals, Inc.
    公开号:US20170044160A1
    公开(公告)日:2017-02-16
    The present invention is directed to a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof. The variables for Structural Formula I are defined herein. Also described is a pharmaceutical composition comprising the compound of Structural Formula I and its therapeutic use.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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