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(2R,3S,5S)-5-hydroxymethyl-3-isopropyl-2-[4-methoxy-3-(3-methoxy-propoxy)-phenyl]pyrrolidine-1-carboxylic acid tert-butyl ester | 916793-67-4

中文名称
——
中文别名
——
英文名称
(2R,3S,5S)-5-hydroxymethyl-3-isopropyl-2-[4-methoxy-3-(3-methoxy-propoxy)-phenyl]pyrrolidine-1-carboxylic acid tert-butyl ester
英文别名
(2R,3S,5S)-5-hydroxymethyl-3-isopropyI-2-[4-methoxy-3-(3-methoxy-propoxy)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester;(2R,3S,5S)-5-Hydroxymethyl-3-isopropyl-2-[4-methoxy-3-(3-methoxy-propoxy)phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester;tert-butyl (2R,3S,5S)-5-(hydroxymethyl)-2-[4-methoxy-3-(3-methoxypropoxy)phenyl]-3-propan-2-ylpyrrolidine-1-carboxylate
(2R,3S,5S)-5-hydroxymethyl-3-isopropyl-2-[4-methoxy-3-(3-methoxy-propoxy)-phenyl]pyrrolidine-1-carboxylic acid tert-butyl ester化学式
CAS
916793-67-4
化学式
C24H39NO6
mdl
——
分子量
437.577
InChiKey
UJUQVWCQRYEENF-IPJJNNNSSA-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):
    3.9
  • 重原子数:
    31
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    77.5
  • 氢给体数:
    1
  • 氢受体数:
    6

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

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文献信息

  • ORGANIC COMPOUNDS
    申请人:Mickel Stuart John
    公开号:US20100274027A1
    公开(公告)日:2010-10-28
    The invention provides a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially renin inhibitors, such as Allskiren. Inter alia, the invention provides a process for the manufacture of a compound of the formula III, wherein R, R 1 , R 2 , R 3 and PG are as defined in the specification, or a salt thereof. The manufacture comprises (preferably consists of) reacting a compound of the formula I, with a reagent able to transform hydroxy into X where X is for example a leaving group.
    本发明提供了一种新的过程、新的过程步骤和新的中间体,用于合成药物活性化合物,特别是肾素抑制剂,例如Allskiren。此外,本发明还提供了一种制备式III化合物或其盐的方法,其中R、R1、R2、R3和PG如规范中所定义。该制备方法包括(最好是由)将式I化合物与能够将羟基转化为X的试剂反应,其中X例如是一个离去基团。
  • Organic Compounds
    申请人:Mickel Stuart John
    公开号:US20080207921A1
    公开(公告)日:2008-08-28
    The invention related to a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially renin inhibitors, such as Aliskiren. Inter alia, the invention relates to a process for the manufacture of a compound of the formula III, wherein R, R 1 , R 2 , R 3 and PG are as defined in the specification, or a salt thereof, said manufacture comprising (preferably consisting in) reacting a compound of the formula I,
    本发明涉及一种新颖的过程、新颖的过程步骤和新颖的中间体,用于合成药物活性化合物,特别是肾素抑制剂,如阿利司他。此外,本发明涉及一种制备式III化合物的过程,其中R、R1、R2、R3和PG如规范中所定义,或其盐,所述制备包括(最好是由)反应式I化合物。
  • Synthesis of Renin Inhibitors Involving a Cycloaddition Reaction
    申请人:Mickel Stuart John
    公开号:US20080255369A1
    公开(公告)日:2008-10-16
    The invention related to a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially renin inhibitors, such as Aliskiren. Inter alia, the invention relates to a process for the manufacture of a compound of the formula III, wherein R, R 1 , and R′ are as defined in the specification, or a salt thereof, and a compound of formula IV wherein R, R 1 , R 2 and R′ are as defined in the specification, and processes of manufacturing these.
    该发明涉及一种新颖的工艺、新颖的工艺步骤和新颖的中间体,可用于合成药物活性化合物,特别是肾素抑制剂,例如阿利司他。此外,该发明涉及一种制备式III化合物的工艺,其中R、R1和R′如规范中定义,或其盐,以及式IV化合物的工艺,其中R、R1、R2和R′如规范中定义,并制备这些化合物的工艺。
  • Synthesis of renin inhibitors involving a cycloaddition reaction
    申请人:Novartis AG
    公开号:US07973175B2
    公开(公告)日:2011-07-05
    The invention related to a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially renin inhibitors, such as Aliskiren. Inter alia, the invention relates to a process for the manufacture of a compound of the formula III, wherein R, R1, and R′ are as defined in the specification, or a salt thereof, and a compound of formula IV wherein R, R1, R2 and R′ are as defined in the specification, and processes of manufacturing these.
    本发明涉及一种新型工艺、新型工艺步骤和新型中间体,用于合成药物活性化合物,特别是肾素抑制剂,如阿利司他。本发明还涉及一种制造式III化合物或其盐的工艺,其中R、R1和R′如规范中所定义,以及制造式IV化合物的工艺,其中R、R1、R2和R′如规范中所定义。
  • Process for preparing renin inhibitors
    申请人:Novartis AG
    公开号:US07767831B2
    公开(公告)日:2010-08-03
    The present invention provides a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially renin inhibitors, such as Aliskiren. Inter alia, the invention provides a process for the manufacture of a compound of the formula III, wherein R, R1, R2, R3 and PG are as defined in the specification, or a salt thereof. The manufacture comprises (preferably consists of) reacting a compound of the formula I, with a reagent able to transform hydroxy into X where X is for example a leaving group.
    本发明提供了一种新颖的过程、新颖的过程步骤和新颖的中间体,可用于合成药物活性化合物,特别是肾素抑制剂,如阿利司他。此外,本发明提供了一种用于制造公式III化合物或其盐的方法,其中R、R1、R2、R3和PG如规范中所定义。制造包括(最好仅包括)将公式I化合物与能将羟基转化为X的试剂反应,其中X例如是一个离去基团。
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