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(αR,3R)-3-bromo-N-(2-hydroxy-1-phenylethyl)piperidin-2-one

中文名称
——
中文别名
——
英文名称
(αR,3R)-3-bromo-N-(2-hydroxy-1-phenylethyl)piperidin-2-one
英文别名
——
(αR,3R)-3-bromo-N-(2-hydroxy-1-phenylethyl)piperidin-2-one化学式
CAS
——
化学式
C13H16BrNO2
mdl
——
分子量
298.18
InChiKey
FYQBQYVRMOBJSV-NEPJUHHUSA-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):
    2.11
  • 重原子数:
    17.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    40.54
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

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:
    参考文献:
    名称:
    Asymmetric synthesis. XXXIX.1 Synthesis of 3-substituted piperidin-2-ones from chiral non-racemic lactams
    摘要:
    A series of 3-substituted piperidines in enantiomerically pure form has been synthesized from lactam 1 via the bromo derivative 2i. t-Butyl acetate and 5-methylpyridine derivatives 2g and 2h were obtained optically pure by direct alkylation of 1 with corresponding halides. Azido, amino or benzyloxy products were obtained by diastereoselective substitution of 2i. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/s0040-4020(96)00339-0
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文献信息

  • Conformationally restricted analogues of methionine: Synthesis of chiral 3-Amino-5-methylthio-2-piperidones
    作者:Ricardo Rodríguez、M. Angels Estiarte、Anna Diez、Mario Rubiralta、Anna Colell、Carmen García-Ruiz、JoséC. Fernández-Checa
    DOI:10.1016/s0040-4020(96)00340-7
    日期:1996.5
    (alpha R, 3RS, 5S)-3-amino-N-(2-hydroxy-1-phenylethyl)-5-methylthio-2-piperidones 1 have been synthesized from enamide 2 by subsequent free radical addition of methanothiol on position 5 and amination of 3-position. Copyright (C) 1996 Elsevier Science Ltd
  • Asymmetric synthesis. XXXIX.1 Synthesis of 3-substituted piperidin-2-ones from chiral non-racemic lactams
    作者:Laurent Micouin、Martine Bonin、Marie-Pierre Cherrier、Alain Mazurier、Alain Tomas、Jean-Charles Quirion、Henri-Philippe Husson
    DOI:10.1016/s0040-4020(96)00339-0
    日期:1996.5
    A series of 3-substituted piperidines in enantiomerically pure form has been synthesized from lactam 1 via the bromo derivative 2i. t-Butyl acetate and 5-methylpyridine derivatives 2g and 2h were obtained optically pure by direct alkylation of 1 with corresponding halides. Azido, amino or benzyloxy products were obtained by diastereoselective substitution of 2i. Copyright (C) 1996 Elsevier Science Ltd
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