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5-[4-(4-methoxyphenyl)piperazine-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one | 485814-86-6

中文名称
——
中文别名
——
英文名称
5-[4-(4-methoxyphenyl)piperazine-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one
英文别名
4-(4-methoxyphenyl)-1-(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-on-5-yl)piperazine;5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one;5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,4,6,7-pentamethyl-benzofuran-3(2H)-one;5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3-one
5-[4-(4-methoxyphenyl)piperazine-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one化学式
CAS
485814-86-6
化学式
C24H30N2O3
mdl
——
分子量
394.514
InChiKey
GNAYTOOUVUIGPH-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):
    4.8
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    42
  • 氢给体数:
    0
  • 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:
    5-[4-(4-methoxyphenyl)piperazine-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one 在 sodium tetrahydroborate 、 sodium hydride 作用下, 以 四氢呋喃甲醇 、 DMF (N,N-dimethyl-formamide) 为溶剂, 反应 3.5h, 生成 1-(3-(benzyloxy)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl)-4-(4-methoxyphenyl)piperazin
    参考文献:
    名称:
    BENZO-FUSED 5-MEMBERED HETROCYCLE COMPOUNDS,PROCESS FOR PREPARATION OF THE SAME, AND USE THEREOF
    摘要:
    公开号:
    EP1411052B1
  • 作为产物:
    描述:
    2,3,5-三甲基苯酚 、 palladium diacetate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦溶剂黄146 、 sodium hydroxide 、 sodium t-butanolate 作用下, 以 甲苯丁酮 为溶剂, 反应 32.0h, 生成 5-[4-(4-methoxyphenyl)piperazine-1-yl]-2,2,4,6,7-pentamethyl-1-benzofuran-3(2H)-one
    参考文献:
    名称:
    Discovery of Benzofuran Derivatives that Collaborate with Insulin-Like Growth Factor 1 (IGF-1) to Promote Neuroprotection
    摘要:
    A series of benzofuran derivatives with neuroprotective activity in collaboration with IGF-1 was discovered using a newly developed cell-based assay involving primary neural cells prepared from rat hippocampal and cerebral cortical tissues. A structure activity relationship study identified compound 8 as exhibiting potent activity and brain penetrability. An in vitro pharmacological study demonstrated that although IGF-1 and 8 individually exhibited the neuroprotective effect, the latter acted in collaboration with IGF-1 to enhance neuroprotective activity.
    DOI:
    10.1021/acs.jmedchem.6b00191
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文献信息

  • Benzofuran derivatives
    申请人:Tsukamoto Tetsuya
    公开号:US20100234357A1
    公开(公告)日:2010-09-16
    The present invention provides a compound represented by the following formula (I): wherein: Ring A represents an optionally substituted piperazine ring, an optionally substituted morpholine ring, or an optionally substituted homopiperazine ring; R 1 and R 2 are the same or different from each other, and represent a hydrogen atom or optionally substituted lower alkyl; R 3 and R 4 are the same or different from each other, and represent a hydrogen atom or halogenated or non-halogenated lower alkyl; R 5 to R 7 are the same or different from each other, and represent a hydrogen atom, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkoxy, optionally substituted cycloalkyl, optionally substituted aryl, an optionally substituted aromatic heterocyclic ring, optionally substituted amino, or acyl; and represents a single bond or double bond, or a salt thereof.
    本发明提供了一种由以下式(I)表示的化合物: 其中: 环A代表可选择地取代的哌嗪环、可选择地取代的吗啉环或可选择地取代的同环丙二胺环; R1和R2彼此相同或不同,代表氢原子或可选择地取代的较低烷基; R3和R4彼此相同或不同,代表氢原子或卤代或非卤代的较低烷基; R5到R7彼此相同或不同,代表氢原子、羟基、可选择地取代的较低烷基、可选择地取代的较低烯基、可选择地取代的较低烷氧基、可选择地取代的环烷基、可选择地取代的芳基、可选择地取代的芳香杂环、可选择地取代的氨基或酰基;和 代表单键或双键,或其盐。
  • Benzo-fused 5-membered hetrocycle compounds, process for preparation of the same, and use thereof
    申请人:——
    公开号:US20040167171A1
    公开(公告)日:2004-08-26
    A compound represented by the formula: 1 (wherein, R 1 and R 2 are the same or different and each represents a hydrogen atom, hydrocarbon group or heterocyclic group, or R 1 and R 2 may form, together with the adjacent carbon atom, a 3-8 membered iso- or heterocyclic group, R 3 represents a cyclic group, a hydroxy group, a mercapto group that may have oxo, or an amino group, R 4 represents a hydrogen atom, a hydrocarbon group, a hydroxy group, a mercapto group which may have oxo, or an amino group, or R 2 and R 4 may link together to form a double bond, X represents a bond or a linear hydrocarbon group, W represents an oxygen atom or a sulfur atom, ring B represents a 5-8 membered nitrogen-containing heterocyclic group, ring C represents a benzene ring, and --- represents a single bond or a double bond), or a salt or a prodrug thereof that has excellent neurodegenerative inhibitory activity and brain penetrability, and is useful as an agent for preventing/treating neurodegenerative diseases.
    一种化合物的化学式为1(其中,R1和R2相同或不同,分别代表氢原子、烃基或杂环基,或R1和R2可以与相邻的碳原子形成一个3-8个成员的同分异构环基,R3代表一个环状基团,一个羟基,一个硫醇基,可以具有氧化物,或者一个氨基,R4代表一个氢原子,一个烃基,一个羟基,一个硫醇基,可以具有氧化物,或者一个氨基,或者R2和R4可以连接形成一个双键,X代表一个键或一个线性烃基,W代表一个氧原子或一个硫原子,环B代表一个5-8个成员的含氮杂环基,环C代表一个苯环,而---代表一个单键或一个双键),或其盐或前药,具有出色的神经退行性抑制活性和脑穿透性,可用作预防/治疗神经退行性疾病的药物。
  • Benzo-fused 5-membered heterocyclic compounds, their production and use
    申请人:Ohkawa Shigenori
    公开号:US20070149558A1
    公开(公告)日:2007-06-28
    A compound represented by the formula: (wherein, R 1 and R 2 are the same or different and each represents a hydrogen atom, hydrocarbon group or heterocyclic group, or R 1 and R 2 may form, together with the adjacent carbon atom, a 3-8 membered iso- or heterocyclic group, R 3 represents a cyclic group, a hydroxy group, a mercapto group that may have oxo, or an amino group, R 4 represents a hydrogen atom, a hydrocarbon group, a hydroxy group, a mercapto group which may have oxo, or an amino group, or R 2 and R 4 may link together to form a double bond, X represents a bond or a linear hydrocarbon group, W represents an oxygen atom or a sulfur atom, ring B represents a 5-8 membered nitrogen-containing heterocyclic group, ring C represents a benzene ring, and represents a single bond or a double bond), or a salt or a prodrug thereof that has excellent neurodegenerative inhibitory activity and brain penetrability, and is useful as an agent for preventing/treating neurodegenerative diseases.
    该化合物的化学式为:(其中,R1和R2相同或不同,每个代表氢原子,烃基或杂环基,或者R1和R2可以与相邻的碳原子一起形成3-8个成员的异构或杂环基,R3代表环状基团,羟基,硫醇基,可能具有氧化作用的氨基基团,或R4代表氢原子,烃基,羟基,可能具有氧化作用的硫醇基或氨基基团,或R2和R4可以连接形成双键,X代表键或线性烃基,W代表氧原子或硫原子,环B代表一个5-8成员的含氮杂环基,环C代表苯环,并且代表单键或双键),或其盐或前药,具有优异的神经退行性抑制活性和脑穿透性,可用作预防/治疗神经退行性疾病的药物。
  • BENZOFURAN DERIVATIVES
    申请人:Tsukamoto Tetsuya
    公开号:US20120046277A1
    公开(公告)日:2012-02-23
    The present invention provides a compound represented by the following formula (I): wherein: Ring A represents an optionally substituted piperazine ring, an optionally substituted morpholine ring, or an optionally substituted bromopiperazine ring; R 1 and R 2 are the same or different from each other, and represent a hydrogen atom or optionally substituted lower alkyl; R 3 and R 4 are the same or different from each other, and represent a hydrogen atom or halogenated or non-halogenated lower alkyl; R 3 to R 7 are the same or different from each other, and represent a hydrogen atom, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkoxy, optionally substituted cycloakyl, optionally substituted aryl, an optionally substituted aromatic heterocyclic ring, optionally substituted amino, or acyl; and represents a single bond or double bond, wherein R 2 and R 3 do not exist when carbon atoms respectively adjacent to R 2 : and R 3 form a double bond, and there is no case where all of R 1 to R 7 are hydrogen atoms, and R 1 and R 2 ; may form a ring together with an adjacent carbon atom; or a salt thereof.
    本发明提供了以下式(I)所表示的化合物:其中:环A表示可选取代的哌嗪环、可选取代的吗啡环或可选取代的溴代哌嗪环;R1和R2相同或不同,表示氢原子或可选取代的较低烷基;R3和R4相同或不同,表示氢原子或卤代或非卤代的较低烷基;R3到R7相同或不同,表示氢原子、羟基、可选取代的较低烷基、可选取代的较低烯基、可选取代的较低烷氧基、可选取代的环烷基、可选取代的芳基、可选取代的芳香族杂环环、可选取代的氨基或酰基;表示单键或双键,其中当R2和R3分别相邻的碳原子形成双键时,R2和R3不存在,且不存在R1到R7全为氢原子的情况,R1和R2可以与相邻碳原子共同形成环;或其盐。
  • US7208495B2
    申请人:——
    公开号:US7208495B2
    公开(公告)日:2007-04-24
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