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4-(5,6-dihydro-11H-imidazo[2,1-b][3]-benzazepin-11-ylidene)-1-piperidineacetonitrile | 147083-09-8

中文名称
——
中文别名
——
英文名称
4-(5,6-dihydro-11H-imidazo[2,1-b][3]-benzazepin-11-ylidene)-1-piperidineacetonitrile
英文别名
2-[4-(5,6-Dihydroimidazo[2,1-b][3]benzazepin-11-ylidene)piperidin-1-yl]acetonitrile
4-(5,6-dihydro-11H-imidazo[2,1-b][3]-benzazepin-11-ylidene)-1-piperidineacetonitrile化学式
CAS
147083-09-8
化学式
C19H20N4
mdl
——
分子量
304.395
InChiKey
DLLNYCOSBLTSDB-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):
    1.7
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • [EN] IMIDAZO(2,1-B)(3)BENZAZEPINE DERIVATIVES, COMPOSITIONS AND METHOD OF USE
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:WO1992022551A1
    公开(公告)日:1992-12-23
    (EN) The present invention is concerned with novel imidazo[2,1-b][3]benzazepines of formula (I), the pharmaceutically acceptable addition salts and stereochemically isomeric forms thereof, wherein each of the dotted lines independently represents an optional bond; R1 represents hydrogen, halo, C1-4alkyl or C1-4alkyloxy; R2 represents hydrogen, halo, C1-4alkyl or C1-4alkyloxy; R3 represents hydrogen, C1-4alkyl, ethenyl substituted with hydroxycarbonyl or C1-4alkyloxycarbonyl, C1-4alkyl substituted with hydroxycarbonyl or C1-4alkyloxycarbonyl, hydroxyC1-4alkyl, formyl or hydroxycarbonyl; R4 represents hydrogen, C1-4alkyl, hydroxyC1-4alkyl, phenyl or halo; R5 represents hydrogen, C1-4alkyl or halo; L represents hydrogen; C1-6alkyl; C1-6alkyl substituted with one substituent selected from the group consisting of hydroxy, halo, C1-4alkyloxy, hydroxycarbonyl, C1-4alkyloxycarbonyl, C1-4alkyloxycarbonyl-C1-4alkyloxy, hydroxycarbonylC1-4alkyloxy, C1-4alkyloxycarbonylamino, C1-4alkylaminocarbonyl, C1-4alkylaminocarbonylamino, C1-4alkylaminothiocarbonylamino, aryl, aryloxy and arylcarbonyl; C1-6alkyl substituted with both hydroxy and aryloxy; C3-6alkenyl; C3-6alkenyl substituted with aryl; or, L represents a radical of formula -Alk-Y-Het1 (a-1), -Alk-NH-CO-Het2 (a-2) or -Alk-Het3 (a-3); provided that 6,11-dihydro-11-(4-piperidinylidene)-5$i(H)-imidazo[2,1-b][3]benzazepine is excluded, which are useful antiallergic compounds. Compositions comprising said compounds, methods of using and processes for preparing the same.(FR) La présente invention concerne de nouvelles imidazo[2,1-b][3]benzazépines de la formule (I), les sels d'addition pharmaceutiquement acceptables et les formes stéréochimiquement isomerés de celles-ci, dans laquelle chacune des lignes pointillées représente indépendamment une liaison optionnelle; R1 représente hydrogène, halo, C1-4alkyle ou C1-4alkyloxy; R3 représente hydrogène, C1-4alkyle, éthényle substitué avec hydroxycarbonyle ou C1-4alkyloxycarbonyle, C1-4alkyle substitué avec hydroxycarbonyle ou C1-4 alkyloxycarbonyle, hydroxy-C1-4alkyle, formyle ou hydroxycarbonyle; R4 représente hydrogène, C1-4alkyle, hydroxyC1-4alkyle, phényle ou halo; R5 représente hydrogène, C1-4alkyle ou halo; L représente hydrogène; C1-6alkyle; C1-6alkyle substitué avec un substituant choisi dans le groupe comportant hydroxy, halo, C1-4alkyloxy, hydroxycarbonyle, C1-4alkyloxycarbonyle, C1-4alkyloxycarbonyle-C1-4alkyloxy, hydroxycarbonyleC1-4alkyloxycarbonylamino, C1-4alkylaminocarbonyle, C1-4alkylaminocarbonylamino, C1-4alkylaminothiocarbonylamino, aryle, aryloxy et arylcarbonyle; C1-6alkyle substitué avec hydroxy et aryloxy; C3-6alcényle; C3-6alcényle substitué avec aryle; ou bien, L représente un radical de la formule -Alk-Y-Het1 (a-1), -Alk-NH-CO-Het2 (a-2) ou -Alk-Het3 (a-3); à condition que 6,11-dihydro-11-(4-pipéridinylidène)-5-$i(H)-imidazo[2,1-b][3]benzazépine soit exclu; ils sont utilisés comme composés antiallergiques. Compositions contenant lesdits composés, méthodes d'utilisation et procédés pour leur préparation.
    本发明涉及一种新型的Imidazo[2,1-b][3]benzazepines化合物,其化学式为(I),包括其药学上可接受的加合物盐和立体化学异构体,其中每个虚线独立地表示一个可选键;R1代表、卤素、C1-4烷基或C1-4烷基;R2代表、卤素、C1-4烷基或C1-4烷基;R3代表、C1-4烷基、丙基取代的羟基羧酰基或C1-4烷羰基、C1-4烷基取代的羟基羧酰基或C1-4烷羰基、羟基C1-4烷基、甲酰基或羟基羧酰基;R4代表、C1-4烷基、羟基C1-4烷基、基或卤素;R5代表、C1-4烷基或卤素;L代表;C1-6烷基;C1-6烷基取代一个选自羟基、卤素、C1-4烷基、羟基羧酰基、C1-4烷羰基、C1-4烷羰基-C1-4烷基、羟基羧酰基C1-4烷基、C1-4烷羰基基、C1-4烷基基羰基、C1-4烷基基羰基基、C1-4烷基代羰基基、芳基、芳基和芳基羧酰基的取代基;C1-6烷基取代羟基和芳基;C3-6基;C3-6基取代芳基;或L代表公式-Alk-Y-Het1(a-1)、-Alk-NH-CO-Het2(a-2)或-Alk-Het3(a-3)的基团;但不包括6,11-二-11-(4-哌啶基亚胺)-5$i(H)-imidazo[2,1-b][3]benzazepine,其作为抗过敏化合物。本发明还涉及包括该化合物的组合物、使用方法以及制备该化合物的方法。
  • Imidazo[2,1-b][3]benzazepine derivatives, compositions and method of use
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP0518435A1
    公开(公告)日:1992-12-16
    The present invention is concerned with novel imidazo[2,1-b][3]benzazepines of formula the pharmaceutically acceptable addition salts and stereochemically isomeric forms thereof, wherein each of the dotted lines independently represents an optional bond; R¹ represents hydrogen, halo, C₁₋₄alkyl or C₁₋₄alkyloxy; R² represents hydrogen, halo, C₁₋₄alkyl or C₁₋₄alkyloxy; R³ represents hydrogen, C₁₋₄alkyl, ethenyl substituted with hydroxycarbonyl or C₁₋₄alkyloxycarbonyl, C₁₋₄alkyl substituted with hydroxycarbonyl or C₁₋₄alkyloxycarbonyl, hydroxyC₁₋₄alkyl, formyl or hydroxycarbonyl; R⁴ represents hydrogen, C₁₋₄alkyl, hydroxyC₁₋₄alkyl, phenyl or halo; R⁵ represents hydrogen, C₁₋₄alkyl or halo; L represents hydrogen; C₁₋₆alkyl; C₁₋₆alkyl substituted with one substituent selected from the group consisting of hydroxy, halo, C₁₋₄alkyloxy, hydroxycarbonyl, C₁₋₄alkyloxycarbonyl, C₁₋₄alkyloxycarbonyl-C₁₋₄alkyloxy, hydroxycarbonylC₁₋₄alkyloxy, C₁₋₄alkyloxycarbonylamino, C₁₋₄alkylaminocarbonyl, C₁₋₄alkylaminocarbonylamino, C₁₋₄alkylaminothiocarbonylamino, aryl, aryloxy and arylcarbonyl; C₁₋₆alkyl substituted with both hydroxy and aryloxy; C₃₋₆alkenyl; C₃₋₆alkenyl substituted with aryl; or, L represents a radical of formula -Alk-Y-Het¹ (a-1), -Alk-NH-CO-Het² (a-2) or -Alk-Het³ (a-3); provided that 6,11-dihydro-11-(4-piperidinylidene)-5H-imidazo[2,1-b][3]benzazepine is ecxluded, which are useful antiallergic compounds. Compositions comprising said compounds, methods of using and processes for preparing the same.
    本发明涉及一种新型的imidazo[2,1-b][3]benzazepines化合物,其分子式为药学上可接受的加盐和立体异构体形式,其中每个虚线独立表示可选键;R¹表示、卤素、C₁₋₄烷基或C₁₋₄烷基;R²表示、卤素、C₁₋₄烷基或C₁₋₄烷基;R³表示、C₁₋₄烷基、丙基取代羟基羧酰基或C₁₋₄烷羰基、C₁₋₄烷基取代羟基羧酰基或C₁₋₄烷羰基、羟基C₁₋₄烷基、甲酰基或羟基羧酰基;R⁴表示、C₁₋₄烷基、羟基C₁₋₄烷基、基或卤素;R⁵表示、C₁₋₄烷基或卤素;L表示、C₁₋₆烷基、取代一个取代基的C₁₋₆烷基,所述取代基选自羟基、卤素、C₁₋₄烷基、羟基羧酰基、C₁₋₄烷羰基、C₁₋₄烷羰基-C₁₋₄烷基、羟基羧酰基C₁₋₄烷基、C₁₋₄烷羰基基、C₁₋₄烷基羰基、C₁₋₄烷基羰基基、C₁₋₄烷代羰基基、芳基、芳基和芳基羧酰基;取代羟基和芳基的C₁₋₆烷基;C₃₋₆基;取代芳基的C₃₋₆基;或L表示式-Alk-Y-Het¹(a-1)、-Alk-NH-CO-Het²(a-2)或-Alk-Het³(a-3)的基团;但不包括6,11-二-11-(4-哌啶甲基)-5H-imidazo[2,1-b][3]benzazepine,它们是有用的抗过敏化合物。本发明还涉及包含上述化合物的组合物、使用方法和制备方法。
  • IMIDAZO 2,1-b] 3]BENZAZEPINE DERIVATIVES, COMPOSITIONS AND METHOD OF USE
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP0588858B1
    公开(公告)日:2003-09-17
  • US5468743A
    申请人:——
    公开号:US5468743A
    公开(公告)日:1995-11-21
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