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(E)-3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-acrylamide | 689299-71-6

中文名称
——
中文别名
——
英文名称
(E)-3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-acrylamide
英文别名
(E)-3-(4'-chlorobiphenyl-4-yl)-N-(4-piperidin-1-ylmethylphenyl)acrylamide;(E)-3-[4-(4-chlorophenyl)phenyl]-N-[4-(piperidin-1-ylmethyl)phenyl]prop-2-enamide
(E)-3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-acrylamide化学式
CAS
689299-71-6
化学式
C27H27ClN2O
mdl
——
分子量
430.977
InChiKey
HSFWTAVXXXJJRW-CAOOACKPSA-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):
    6.1
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (E)-3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-acrylamide 乙醚 作用下, 以 乙酸乙酯 为溶剂, 生成 3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-propionamide
    参考文献:
    名称:
    Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds
    摘要:
    本发明涉及一般式I的酰胺化合物,其中A、B、b、W、X、Y、Z、R1、R2和R3基团和残基具有权利要求1中所给出的意义。此外,本发明涉及包含至少一种根据本发明的酰胺的制药组合物。鉴于MCH受体拮抗活性,本发明的制药组合物适用于治疗代谢紊乱和/或进食障碍,特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
    公开号:
    US07351719B2
  • 作为产物:
    描述:
    4-(1-哌啶基甲基)苯胺3-(4'-chloro-biphenyl-4-yl)-acrylic acid1-羟基苯并三唑 、 O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate 、 三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以63%的产率得到(E)-3-(4'-chloro-biphenyl-4-yl)-N-(4-piperidin-1-ylmethyl-phenyl)-acrylamide
    参考文献:
    名称:
    Design, synthesis and evaluation of MCH receptor 1 antagonists—Part II: Optimization of pyridazines toward reduced phospholipidosis and hERG inhibition
    摘要:
    Despite recent success there remains a high therapeutic need for the development of drugs targeting diseases associated with the metabolic syndrome. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, a series of 3,6-disubstituted pyridazines was evaluated. During optimization several issues of the initial lead structures had to be resolved, such as selectivity over related GPCRs, inhibition of the hERG channel as well as the potential to induce phospholipidosis. Utilizing property-based design, we could demonstrate that all parameters can significantly be improved by consequently increasing the polarity of the compounds. By this strategy, we succeeded in identifying potent and orally available MCH-R1 antagonists with good selectivity over M1 and 5-HT2A and an improved safety profile with respect to hERG inhibition and phospholipidosis. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2015.05.074
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文献信息

  • [DE] 3-(4-PIPERIDIN-1YLMETHYL-PHENYL) -PROPIONSÄURE-PHRNYLAMID-DERIVATE UND VERWANDTE VERBINDUNGEN ALS MCH (MELANINE CONCENTRATING HORMONE) ANTAGONISTEN ZUR BEHANDLUNG VON ESSSTÖRUNGEN<br/>[EN] 3-(4-PIPERIDINE-1YLMETHYL-PHENYL)-PROPION ACID-PHENYLAMIDE-DERIVATIVES AND RELATED COMPOUNDS USED IN THE FORM OF MCH ANTAGONISTS (MELANINE CONCENTRATING HORMONE) FOR TREATING EATING DISORDERS<br/>[FR] DERIVES D'ACIDE 3-(4-PIPERIDINE-1YLMETHYL-PHENYL) PROPIONIQUE-PHENYLAMIDE ET COMPOSES APPARENTES, UTILISES COMME ANTAGONISTES MCH (HORMONE DE CONCENTRATION EN MELANINE) POUR LE TRAITEMENT DE TROUBLES DUS A L'ALIMENTATION
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2005063239A1
    公开(公告)日:2005-07-14
    Die vorliegende Erfindung betrifft Amid-Verbindungen der allgemeinen Formel (I), in der die Gruppen und Reste A, B, b, W, X, Y, Z, R1, R2 und R3 die in Anspruch 1 angegebenen Bedeutungen aufweisen. Ferner betrifft die Erfindung Arzneimittel enthaltend mindestens ein erfindungsgemäßes Amid. Auf Grund der MCH-Rezeptor antagonistischen Aktivität eignen sich die erfindungsgemäßen Arzneimittel zur Behandlung von metabolischen Störungen und/oder Essstörungen, insbesondere von Adipositas, Bulimie, Anorexie, Hyperphagia und Diabetes.
    该发明涉及通式(I)的酰胺化合物,其中基团和残基A、B、b、W、X、Y、Z、R1、R2和R3具有权利要求1中所述的含义。此外,该发明涉及含有至少一种根据本发明的酰胺的药物。由于MCH受体拮抗活性,根据本发明的药物适用于治疗代谢紊乱和/或进食障碍,特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
  • [DE] NEUE AMID-VERBINDUNGEN MIT MCH-ANTAGONISTISCHER WIRKUNG UND DIESE VERBINDUNGEN ENTHALTENDE ARZNEIMITTEL<br/>[EN] NOVEL AMIDE COMPOUNDS WITH MCH ANTAGONISTIC EFFECT AND MEDICAMENTS COMPRISING SAID COMPOUNDS<br/>[FR] NOUVEAUX COMPOSES DE TYPE AMIDE EXERÇANT UNE ACTION ANTAGONISTE SUR L'HORMONE MCH, ET MEDICAMENTS CONTENANT CES COMPOSES
    申请人:BOEHRINGER INGELHEIM PHARMA
    公开号:WO2004039764A1
    公开(公告)日:2004-05-13
    Die vorliegende Erfindung betrifft Amid-Verbindungen der allgemeinen Formel (I), in der die Gruppen und Reste A, B, b, W, X, Y, Z, R1, R2 und R3 die in Anspruch 1 angegebenen Bedeutungen aufweisen. Ferner betrifft die Erfindung Arzneimittel enthaltend mindestens ein erfindungsgemässes Amid. Auf Grund der MCH-Rezeptor antagonistischen Aktivität eignen sich die erfindungsgemässen Arzneimittel zur Behandlung von metabolischen Störungen und/oder Essstörungen, insbesondere von Obesitas, Bulimie, Anorexie, Hyperphagia und Diabetes.
    该发明涉及通式(I)的酰胺化合物,其中基团和残基A、B、b、W、X、Y、Z、R1、R2和R3具有权利要求1中所述的含义。此外,该发明涉及含有至少一种根据本发明的酰胺的药物。由于MCH受体拮抗活性,根据本发明的药物适用于治疗代谢紊乱和/或进食障碍,特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
  • Amide compounds with MCH antagonistic activity and medicaments comprising these compounds
    申请人:Lehmann-Lintz Thorsten
    公开号:US20050267093A1
    公开(公告)日:2005-12-01
    Compounds of formula (I) wherein A, B, b, W, X, Y, Z, R 1 , R 2 , and R 3 have the meanings given in claim 1, pharmaceutical compositions these compounds, and methods of preventing or treating metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia, and diabetes using these compounds.
    化合物的公式(I),其中A,B,b,W,X,Y,Z,R1,R2和R3具有权利要求1所给出的含义,制备这些化合物的药物组合物,以及使用这些化合物预防或治疗代谢紊乱和/或进食障碍,特别是肥胖症,暴食症,厌食症,暴饮暴食和糖尿病的方法。
  • Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds
    申请人:Boehringer Ingelheim Pharma GmbH & Co. KG
    公开号:US20040152742A1
    公开(公告)日:2004-08-05
    The present invention relates to amide compounds of general formula I 1 wherein the groups and residues A, B, b, W, X, Y, Z, R 1 , R 2 and R 3 have the meanings given in claim 1. Moreover the invention relates to pharmaceutical compositions containing at least one amide according to the invention. In view of the MCH receptor-antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.
    本发明涉及一般式I1的酰胺化合物,其中基团和残基A、B、b、W、X、Y、Z、R1、R2和R3具有权利要求1中给出的含义。此外,本发明涉及至少含有本发明中一种酰胺的药物组合物。鉴于MCH受体拮抗活性,本发明中的药物组合物适用于治疗代谢性疾病和/或进食障碍,特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
  • NEUE AMID-VERBINDUNGEN MIT MCH-ANTAGONISTISCHER WIRKUNG UND DIESE VERBINDUNGEN ENTHALTENDE ARZNEIMITTEL
    申请人:BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG
    公开号:EP1558567A1
    公开(公告)日:2005-08-03
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