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1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol | 474539-18-9

中文名称
——
中文别名
——
英文名称
1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol
英文别名
(4-ethoxy-3-methoxyphenyl)-(4-hydroxy-2-methyl-3,4-dihydro-2H-quinolin-1-yl)methanone
1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol化学式
CAS
474539-18-9
化学式
C20H23NO4
mdl
——
分子量
341.407
InChiKey
QAANAVWGTNEUKT-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):
    3
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol1,2,3,4-四氢喹啉 以to give the titled compound (288 mg, yield: 36%) as a white crystal的产率得到cis-1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-4-(1,2,3,4-tetrahydroquinolin-1-yl)1,2,3,4-tetrahydroquinoline
    参考文献:
    名称:
    Novel heterocyclic derivatives
    摘要:
    本发明的目的是提供可溶性β-淀粉样前体蛋白分泌刺激剂,其对治疗神经退行性疾病以及脑血管疾病引起的神经病变具有有效性。更具体地说,本发明提供了以下式(I)的新化合物或其盐或前药:1 [其中,R1和R2分别代表氢原子或较低的烷基等,Ar1和环B分别代表可选取代的芳香族基团,环A代表可选取代的苯环,环C代表可选取代的4-至8-成员环,可以进一步与可选取代的环融合,X代表CH或N,Y代表CH或N]。
    公开号:
    US20040157850A1
  • 作为产物:
    描述:
    4-乙氧基-3-甲氧基苯甲酰氯2-methyl-1,2,3,4-tetrahydroquinoline-4-ol吡啶 作用下, 反应 16.0h, 以30%的产率得到1-(4-ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol
    参考文献:
    名称:
    EP1382598
    摘要:
    公开号:
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文献信息

  • Novel heterocyclic derivatives
    申请人:——
    公开号:US20040157850A1
    公开(公告)日:2004-08-12
    The object of the present invention is to provide soluble &bgr;-amyloid precursor protein secretory stimulators, which are effective in treating neurodegenerative diseases as well as cerebrovascular disorder-induced neuronopathy. More specifically, the present invention provides a novel compound of the following Formula (I) or a salt or prodrug thereof: 1 [wherein R 1 and R 2 each represent a hydrogen atom or a lower alkyl group, etc., Ar 1 and the ring B each represent an optionally substituted aromatic group, the ring A represents an optionally substituted benzene ring, the ring C represents an optionally substituted 4- to 8-membered ring which may further be condensed with an optionally substituted ring, X represents CH or N, and Y represents CH or N].
    本发明的目的是提供可溶性β-淀粉样前体蛋白分泌刺激剂,其对治疗神经退行性疾病以及脑血管疾病引起的神经病变具有有效性。更具体地说,本发明提供了以下式(I)的新化合物或其盐或前药:1 [其中,R1和R2分别代表氢原子或较低的烷基等,Ar1和环B分别代表可选取代的芳香族基团,环A代表可选取代的苯环,环C代表可选取代的4-至8-成员环,可以进一步与可选取代的环融合,X代表CH或N,Y代表CH或N]。
  • NOVEL HETEROCYCLIC DERIVATIVES
    申请人:Takeda Chemical Industries, Ltd.
    公开号:EP1382598A1
    公开(公告)日:2004-01-21
    The object of the present invention is to provide soluble β-amyloid precursor protein secretory stimulators, which are effective in treating neurodegenerative diseases as well as cerebrovascular disorder-induced neuronopathy. More specifically, the present invention provides a novel compound of the following Formula (I) or a salt or prodrug thereof: [wherein R1 and R2 each represent a hydrogen atom or a lower alkyl group, etc., Ar1 and the ring B each represent an optionally substituted aromatic group, the ring A represents an optionally substituted benzene ring, the ring C represents an optionally substituted 4- to 8-membered ring which may further be condensed with an optionally substituted ring, X represents CH or N, and Y represents CH or N].
    本发明的目的是提供可溶性β-淀粉样前体蛋白分泌刺激剂,它能有效治疗神经退行性疾病以及脑血管疾病引起的神经元病变。更具体地说,本发明提供了下式(I)的新型化合物或其盐或原药: [其中 R1 和 R2 分别代表氢原子或低级烷基等,Ar1 和环 B 分别代表任选取代的芳香基团,环 A 代表任选取代的苯环,环 C 代表任选取代的 4 至 8 元环,可进一步缩合任选取代的环,X 代表 CH 或 N,Y 代表 CH 或 N]。
  • US6930104B2
    申请人:——
    公开号:US6930104B2
    公开(公告)日:2005-08-16
  • EP1382598
    申请人:——
    公开号:——
    公开(公告)日:——
  • Heterocyclic derivatives
    申请人:Kakihana Mitsuru
    公开号:US06930104B2
    公开(公告)日:2005-08-16
    The object of the present invention is to provide soluble β-amyloid precursor protein secretory stimulators, which are effective in treating neurodegenerative diseases as well as cerebrovascular disorder-induced neuronopathy. More specifically, the present invention provides a novel compound of the following Formula (I) or a salt or prodrug thereof: [wherein R 1 and R 2 each represent a hydrogen atom or a lower alkyl group, etc., Ar 1 and the ring B each represent an optionally substituted aromatic group, the ring A represents an optionally substituted benzene ring, the ring C represents an optionally substituted 4- to 8-membered ring which may further be condensed with an optionally substituted ring, X represents CH or N, and Y represents CH or N].
    本发明的目的是提供可溶性β-淀粉样前体蛋白分泌刺激剂,其对治疗神经退行性疾病以及脑血管疾病引起的神经病变具有有效性。更具体地,本发明提供以下式(I)的新化合物或其盐或前药:[其中R1和R2各代表氢原子或较低的烷基等,Ar1和环B各代表可选择取代的芳香基,环A代表可选择取代的苯环,环C代表可选择取代的4-至8-环,该环可能进一步与可选择取代的环融合,X代表CH或N,Y代表CH或N]。
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