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(2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮 | 41854-83-5

中文名称
(2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮
中文别名
——
英文名称
2-methyloctahydroquinolin-4(1H)-one
英文别名
2-methyl-octahydro-quinolin-4-one;2-Methyl-octahydro-chinolin-4-on;γ-2-Methyl-4-oxodecahydrochinolin;2-Methyl-decahydro-4-chinolin;2-methyl-2,3,4a,5,6,7,8,8a-octahydro-1H-quinolin-4-one
(2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮化学式
CAS
41854-83-5
化学式
C10H17NO
mdl
MFCD02932745
分子量
167.251
InChiKey
SEAPKWHFVCCJBB-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

  • 熔点:
    127-128 °C
  • 沸点:
    108 °C(Press: 3 Torr)
  • 密度:
    1.0290 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:7c24493b332bbb72f01081f745d7377b
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反应信息

  • 作为反应物:
    描述:
    (2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮正丁基锂 作用下, 以 乙醚正己烷 为溶剂, 反应 1.5h, 生成
    参考文献:
    名称:
    摘要:
    2e-Methyldecahydroquinolin-4-one was reacted with lithium tert-alkylperoxy acetylides to prepare 4-hydroxy-2e-methyl-4-(2-methyl-2-tert-alkylperoxy-1-butyn-4-yl)decahydroquinolines. The latter readily react with carboxylic acids and methyl iodide, affording the corresponding salts.
    DOI:
    10.1023/a:1012387619776
  • 作为试剂:
    描述:
    2e-methyl-4a-hydroxy-4e-phenylethinyl-trans-decahydroquinoline 在 氢氧化钾(2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮 作用下, 以 1,4-二氧六环 为溶剂, 反应 0.17h, 生成 2e-methyl-4e-hydroxy-4a-phenylethinyl-trans-decahydroquinoline
    参考文献:
    名称:
    Stereochemistry of nitrogenous heterocycles. 71. Isomerization ? Equilibration of stereoisomeric ethinylcarbinols epimeric at the carbinol center
    摘要:
    DOI:
    10.1007/bf00472286
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文献信息

  • Fused, Tricyclic Sulfonamide Inhibitors of Gamma Secretase
    申请人:Konradi W. Andrei
    公开号:US20080021056A1
    公开(公告)日:2008-01-24
    The invention provides compounds of formula I: or pharmaceutically salts thereof where R 1 , R 2 , and the A, B, and C-rings are as defined herein. Compounds of formula I are useful in treating or preventing cognitive disorders, such as Alzheimer's disease. The invention also encompasses pharmaceutical compositions comprising compounds or salts of formula I, methods of preparing the desired compounds, and methods of treating cognitive disorders, such as Alzheimer's disease, using the compounds or salts of formula I.
    该发明提供了公式I的化合物: 或其药用盐,其中R 1 ,R 2 和A、B和C环如本文所定义。公式I的化合物在治疗或预防认知障碍,如阿尔茨海默病方面是有用的。该发明还涵盖了包括公式I的化合物或盐的药物组合物,制备所需化合物的方法,以及使用公式I的化合物或盐治疗认知障碍,如阿尔茨海默病的方法。
  • Fused, tricyclic sulfonamide inhibitors of gamma secretase
    申请人:Elan Pharmaceuticals Inc.
    公开号:EP2450358A1
    公开(公告)日:2012-05-09
    The invention provides compounds of formula I: or pharmaceutically salts thereof, where R1, R2 and the A, B, and C-rings are as defined herein. Compounds of formula I are useful in treating or preventing cognitive disorders, such as Alzheimer's disease. The invention also encompasses pharmaceutical compositions comprising compounds or salts of formula I, methods of preparing the desired compunds, and methods of treating cognitive disorders, such as Alzheimer's disease, using the compounds or salts of formula I.
    本发明提供了式 I 的化合物: 或其药用盐,其中 R1、R2 和 A、B 及 C 环如本文所定义。式 I 的化合物可用于治疗或预防认知障碍,如阿尔茨海默病。本发明还包括包含式 I 化合物或盐的药物组合物、制备所需组合物的方法以及使用式 I 化合物或盐治疗认知障碍(如阿尔茨海默病)的方法。
  • Synthesis of New 1-Adamantanecarboxylic Acid Derivatives
    作者:E. A. Dikusar1'、N. G. Kozlov、V. I. Potkin、A. P. Yuvchenko、N. V. Kovganko
    DOI:10.1023/b:rujo.0000034968.28257.e9
    日期:2004.3
    Reactions of 1-adamantanecarbonyl chloride with functionally substituted alcohols, phenols, amines, thiols, and ketone oximes gave hitherto unknown 1-adamantanecarboxylic acid esters, amides, and thio esters, including those containing a peroxide group.
  • FUSED, TRICYCLIC SULFONAMIDE INHIBITORS OF GAMMA SECRETASE
    申请人:Elan Pharmaceuticals Inc.
    公开号:EP2038280A2
    公开(公告)日:2009-03-25
  • [EN] FUSED, TRICYCLIC SULFONAMIDE INHIBITORS OF GAMMA SECRETASE<br/>[FR] SULFONAMIDES TRICYCLIQUES CONDENSÉS INHIBITEURS DE GAMMA-SECRÉTASE
    申请人:ELAN PHARM INC
    公开号:WO2007143523A2
    公开(公告)日:2007-12-13
    (EN) The invention provides compounds of formula (I): or pharmaceutically salts thereof, where R1, R2 and the A, B, and C-rings are as defined herein. Compounds of formula (I) are useful in treating or preventing cognitive disorders, such as Alzheimer's disease. The invention also encompasses pharmaceutical compositions comprising compounds or salts of formula (I), methods of preparing the desired compunds, and methods of treating cognitive disorders, such as Alzheimer's disease, using the compounds or salts of Formula (I).(FR) La présente invention concerne des composés de formule I : ou des sels pharmaceutiquement acceptables de ceux-ci, où R1, R2 et les cycles A, B et C sont comme présentement défini. Les composés de formule I sont utiles dans le traitement ou la prévention de troubles cognitifs, tels que la maladie d'Alzheimer. L'invention concerne en outre des compositions pharmaceutiques comprenant des composés ou sels de formule I, des procédés de préparation des composés souhaités, et des procédés de traitement de troubles cognitifs, tels que la maladie d'Alzheimer, utilisant les composés ou sels de Formule(I).
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