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N-(3,5-dimethylbenzyl)quinidinium bromide

中文名称
——
中文别名
——
英文名称
N-(3,5-dimethylbenzyl)quinidinium bromide
英文别名
(S)-[(2R,4S,5R)-1-[(3,5-dimethylphenyl)methyl]-5-ethenyl-1-azoniabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;bromide
N-(3,5-dimethylbenzyl)quinidinium bromide化学式
CAS
——
化学式
Br*C29H35N2O2
mdl
——
分子量
523.513
InChiKey
WFTQVNJMDZBCOI-DZQDBLFASA-M
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):
    2.51
  • 重原子数:
    34
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    42.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    Development and Scale-up of an Organocatalytic Enantioselective Process to Manufacture (S)-Pregabalin
    摘要:
    Herein is reported the development of a new process to manufacture (S)-pregabalin. The method comprises six steps, run under the catalysis of a recyclable polymer bound phase transfer catalyst, and afforded (S)-pregabalin in overall 54% yield, starting from building blocks acetylacetone, isovaleraldehyde, and nitromethane.
    DOI:
    10.1021/acs.oprd.5b00160
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文献信息

  • [EN] PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE ACIDES AMINÉS GAMMA ET INTERMÉDIAIRES UTILISÉS DANS CE PROCÉDÉ
    申请人:ROYAL COLLEGE OF SURGEONS IE
    公开号:WO2013076225A1
    公开(公告)日:2013-05-30
    The invention relates to the preparation of gamma amino acids of formula (I) and pharmaceutically acceptable salts, solvates and prodrugs thereof, and to intermediates used for their preparation. (formula I) wherein R1 is selected from an alkyl group, an alkenyl group, an alkynyl group and a cycloalkyl group, each of which may be optionally substituted and * denotes a chiral centre. In particular, the present invention provides an efficient synthesis of (S)-pregabalin which is suitable for carrying out on an industrial scale.
    该发明涉及制备公式(I)的γ-氨基酸及其药学上可接受的盐、溶剂合物和前药,以及用于其制备的中间体。(公式I)其中R1选自烷基、烯基、炔基和环烷基,每种基团均可选择性地被取代,*表示一个手性中心。特别是,本发明提供了(S)-普瑞巴林的高效合成方法,适用于工业规模生产。
  • PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS
    申请人:Royal College of Surgeons in Ireland
    公开号:US20140336412A1
    公开(公告)日:2014-11-13
    The invention relates to the preparation of gamma amino acids of formula (I) and pharmaceutically acceptable salts, solvates and prodrugs thereof, and to intermediates used for their preparation. (formula I) wherein R 1 is selected from an alkyl group, an alkenyl group, an alkynyl group and a cycloalkyl group, each of which may be optionally substituted and * denotes a chiral centre. In particular, the present invention provides an efficient synthesis of (S)-pregabalin which is suitable for carrying out on an industrial scale.
    本发明涉及制备公式(I)的γ-氨基酸及其药学上可接受的盐、溶剂化物和前药,以及用于它们制备的中间体。(公式I)其中R1选自烷基、烯基、炔基和环烷基,每个基团均可选择性地被取代,*表示手性中心。特别地,本发明提供了一种适用于工业规模的(S)-pregabalin的高效合成方法。
  • EP2782911A1
    申请人:——
    公开号:EP2782911A1
    公开(公告)日:2014-10-01
  • US9593071B2
    申请人:——
    公开号:US9593071B2
    公开(公告)日:2017-03-14
  • Development and Scale-up of an Organocatalytic Enantioselective Process to Manufacture (<i>S</i>)-Pregabalin
    作者:Maria Moccia、Mauro Cortigiani、Claudio Monasterolo、Federica Torri、Claudia Del Fiandra、Geoffrey Fuller、Brian Kelly、Mauro F. A. Adamo
    DOI:10.1021/acs.oprd.5b00160
    日期:2015.9.18
    Herein is reported the development of a new process to manufacture (S)-pregabalin. The method comprises six steps, run under the catalysis of a recyclable polymer bound phase transfer catalyst, and afforded (S)-pregabalin in overall 54% yield, starting from building blocks acetylacetone, isovaleraldehyde, and nitromethane.
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