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(2S,5R,6R)-5-methyl-6-(3-morpholinophenyl)piperidine-2-carboxylic acid | 916914-58-4

中文名称
——
中文别名
——
英文名称
(2S,5R,6R)-5-methyl-6-(3-morpholinophenyl)piperidine-2-carboxylic acid
英文别名
(2S,5R,6R)-5-methyl-6-(3-morpholin-4-ylphenyl)piperidine-2-carboxylic acid
(2S,5R,6R)-5-methyl-6-(3-morpholinophenyl)piperidine-2-carboxylic acid化学式
CAS
916914-58-4
化学式
C17H24N2O3
mdl
——
分子量
304.389
InChiKey
DHTWOSUFEXXKBS-UHOFOFEASA-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):
    -0.3
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    61.8
  • 氢给体数:
    2
  • 氢受体数:
    5

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2S,5R,6R)-6-(3-bromophenyl)-5-methylpiperidine-2-carboxylic acid(2S,5R,6R)-5-methyl-6-(3-morpholinophenyl)piperidine-2-carboxylic acid2,3,5-三甲基吡啶 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 19.0h, 以28%的产率得到(3R,4R,7R,8R,9aS,10aS)-4-(3-Bromo-phenyl)-3,7-dimethyl-8-(3-morpholin-4-yl-phenyl)-octahydro-4a,8a-diaza-anthraquinone
    参考文献:
    名称:
    Convergent Synthesis of Complex Diketopiperazines Derived from Pipecolic Acid Scaffolds and Parallel Screening against GPCR Targets
    摘要:
    A convergent approach to highly functionalized diketopiperazines (DKPs) using enantioenriched pipecolic acids is described. Scandium triflate-catalyzed [4 + 2] aza-annulation was employed to produce stereochemically well-defined building blocks. A resin "catch and release" strategy was devised to convert annulation products to pipecolic acid monomers. Complex diketopiperazines were efficiently assembled utilizing one-pot cyclodimerization of pipecolic acids. Massively parallel screening of the complex DKPs against a panel of molecular targets identified novel ligands for a number of G-protein-coupled receptors (GPCRs).
    DOI:
    10.1021/jo061758p
  • 作为产物:
    描述:
    (E)-(2R,3R)-2-Amino-3-(dimethyl-phenyl-silanyl)-hex-4-enoic acid methyl esterplatinum(IV) oxide 、 tris(dibenzylideneacetone)dipalladium (0) sodium tetrahydroborate 、 potassium phosphate 、 Amberlyst A26 hydroxide resin 、 氢气 、 magnesium sulfate 、 三氟乙酸三氟乙酸酐2-(二环己基膦基)联苯scandium tris(trifluoromethanesulfonate) 作用下, 以 四氢呋喃甲醇乙二醇二甲醚二氯甲烷乙酸乙酯 为溶剂, 反应 15.0h, 生成 (2S,5R,6R)-5-methyl-6-(3-morpholinophenyl)piperidine-2-carboxylic acid
    参考文献:
    名称:
    Convergent Synthesis of Complex Diketopiperazines Derived from Pipecolic Acid Scaffolds and Parallel Screening against GPCR Targets
    摘要:
    A convergent approach to highly functionalized diketopiperazines (DKPs) using enantioenriched pipecolic acids is described. Scandium triflate-catalyzed [4 + 2] aza-annulation was employed to produce stereochemically well-defined building blocks. A resin "catch and release" strategy was devised to convert annulation products to pipecolic acid monomers. Complex diketopiperazines were efficiently assembled utilizing one-pot cyclodimerization of pipecolic acids. Massively parallel screening of the complex DKPs against a panel of molecular targets identified novel ligands for a number of G-protein-coupled receptors (GPCRs).
    DOI:
    10.1021/jo061758p
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