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(2-ethyl-1-azabicyclo[2.2.2]octan-3-yl) 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate

中文名称
——
中文别名
——
英文名称
(2-ethyl-1-azabicyclo[2.2.2]octan-3-yl) 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate
英文别名
——
(2-ethyl-1-azabicyclo[2.2.2]octan-3-yl) 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate化学式
CAS
——
化学式
C25H30N2O2
mdl
——
分子量
390.5
InChiKey
WGRUWZBYEFGUQI-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    32.8
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Method for producing solifenacin or salts thereof
    申请人:Inakoshi Masatoshi
    公开号:US20070185329A1
    公开(公告)日:2007-08-09
    There is provided a novel method for producing solifenacin or a salt thereof which is useful as a medicine, particularly a therapeutic agent and/or a preventive agent for a urinary organ system disease such as pollakiuria or urinary incontinence. Illustratively, there are provided (1) a method for producing solifenacin in which 2-(1H-imidazolylcarbonyl)-1-phenyltetrahydroisoquinoline is used as the starting material, (2) a method for producing solifenacin succinate in which (1RS)-phenyltetrahydroisoquinoline-carboxylic acid quinuclidinyl ester is used as the starting material, (3) a method for producing solifenacin in which a lower alkyl quinuclidinyl carbonate is used as the starting material and (4) a method for producing solifenacin in which phenyltetrahydroisoquinoline-carboxylic acid secondary lower alkyl or tertiary lower alkyl ester is used as the starting material and allowed to react with an alkali metal lower alkoxide.
    提供了一种新的制备索利费南或其盐的方法,该方法可用作药物,特别是用于治疗和/或预防尿生殖器官疾病,如尿频或尿失禁的治疗剂和/或预防剂。例如,提供了以下四种方法:(1)使用2-(1H-咪唑基)-1-苯基四氢异喹啉作为起始材料制备索利费南的方法;(2)使用(1RS)-苯基四氢异喹啉-羧酸奎尼克啶酯作为起始材料制备索利费南琥珀酸盐的方法;(3)使用较低烷基奎尼库啶碳酸酯作为起始材料制备索利费南的方法;(4)使用苯基四氢异喹啉-羧酸次级较低烷基或三级较低烷基酯作为起始材料,并与碱金属较低烷氧化物反应制备索利费南的方法。
  • Solifenacin-containing composition
    申请人:Inakoshi Masatoshi
    公开号:US20070191425A1
    公开(公告)日:2007-08-16
    To provide a novel method for producing a composition comprising solifenacin or a salt thereof, and a composition comprising solifenacin or a salt thereof as produced by the method, wherein an optionally substituted lower alkyl is added to the 2-position of the quinuclidine of solifenacin. The composition of the present invention contains a highly pure solifenacin, while the unexpected compounds specific to the method in an extremely low content, so that it has very preferable properties as a bulk for pharmaceutical products.
    提供一种生产含有索利那汀或其盐的组合物的新方法,以及由该方法生产的含有索利那汀或其盐的组合物,其中在索利那汀的喹啉环的2位加入一个可选的取代较低的烷基。本发明的组合物含有高度纯净的索利那汀,同时非常低的意外化合物含量,因此作为药品产品原料非常有优越性能。
  • SOLIFENACIN-CONTAINING COMPOSITION
    申请人:Astellas Pharma Inc.
    公开号:EP1726304A1
    公开(公告)日:2006-11-29
    To provide a novel method for producing a composition comprising solifenacin or a salt thereof, and a composition comprising solifenacin or a salt thereof as produced by the method, wherein an optionally substituted lower alkyl is added to the 2-position of the quinuclidine of solifenacin. The composition of the present invention contains a highly pure solifenacin, while the unexpected compounds specific to the method in an extremely low content, so that it has very preferable properties as a bulk for pharmaceutical products.
    提供一种生产包含索非那新或其盐的组合物的新方法,以及一种包含由该方法生产的索非那新或其盐的组合物,其中在索非那新的奎宁环的 2 位上添加了一个任选取代的低级烷基。本发明的组合物含有高纯度的索非那新,而该方法所特有的意外化合物的含量极低,因此它作为医药产品的散装物具有非常优越的性能。
  • PROCESS FOR PRODUCING SOLIFENACIN OR ITS SALT
    申请人:Astellas Pharma Inc.
    公开号:EP1757604A1
    公开(公告)日:2007-02-28
    There is provided a novel method for producing solifenacin or a salt thereof which is useful as a medicine, particularly a therapeutic agent and/or a preventive agent for a urinary organ system disease such as pollakiuria or urinary incontinence. Illustratively, there are provided (1) a method for producing solifenacin in which 2-(1H-imidazolylcarbonyl)-1-phenyltetrahydroisoquinoline is used as the starting material, (2) a method for producing solifenacin succinate in which (1RS)-phenyltetrahydroisoquinoline-carboxylic acid quinuclidinyl ester is used as the starting material, (3) a method for producing solifenacin in which a lower alkyl quinuclidinyl carbonate is used as the starting material and (4) a method for producing solifenacin in which phenyltetrahydroisoquinoline-carboxylic acid secondary lower alkyl or tertiary lower alkyl ester is used as the starting material and allowed to react with an alkali metal lower alkoxide.
    本发明提供了一种生产索利芬那新或其盐的新方法,该方法可用作药物,特别是泌尿器官系统疾病(如花粉尿症或尿失禁)的治疗剂和/或预防剂。示例性地,提供了(1)一种生产索利那新的方法,其中使用 2-(1H-咪唑羰基)-1-苯基四氢异喹啉作为起始原料;(2)一种生产索利那新琥珀酸酯的方法,其中使用(1RS)-苯基四氢异喹啉-羧酸奎宁酯作为起始原料、(4) 以苯基四氢异喹啉-羧酸仲低级烷基酯或叔低级烷基酯为起始原料,使其与碱金属低级烷氧基化合物反应,生产索利那新的方法。
  • Synthesis of solifenacin monosuccinate
    申请人:Astellas Pharma Inc.
    公开号:EP2305676A1
    公开(公告)日:2011-04-06
    There is provided a method for producing solifenacin succinate, which comprises allowing succinic acid to react with a compound represented by formula (II): [in the formula, stereochemistry of the 1-position of phenyl-substituted tetrahydroisoquinoline is a mixture of (R)-form and (S)-form].
    提供了一种生产琥珀酸索利那新的方法,该方法包括让琥珀酸与式 (II) 所代表的化合物反应: [式中,苯基取代的四氢异喹啉 1 位的立体化学结构为(R)-形式和(S)-形式的混合物]。
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