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2-(cyclohexylthiocarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine | 121654-78-2

中文名称
——
中文别名
——
英文名称
2-(cyclohexylthiocarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine
英文别名
2-(Cyclohexylthiocarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino[2,1-a][2]benzazepine;2-(cyclohexanecarbothioyl)-1,3,6,7,8,12b-hexahydropyrazino[2,1-a][2]benzazepin-4-one
2-(cyclohexylthiocarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine化学式
CAS
121654-78-2
化学式
C20H26N2OS
mdl
——
分子量
342.505
InChiKey
YYUKRUYAOFPGKZ-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):
    3.6
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    55.6
  • 氢给体数:
    0
  • 氢受体数:
    2

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

反应信息

  • 作为产物:
    描述:
    3-苯基-1-丙胺 在 palladium on activated charcoal sodium tetrahydroborate 、 PPA 、 氢气碳酸氢钠 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 5.0~180.0 ℃ 、101.33 kPa 条件下, 反应 6.75h, 生成 2-(cyclohexylthiocarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine
    参考文献:
    名称:
    Synthesis and anthelmintic activity of a series of of pyrazino[2,1-a][2]benzazepine derivatives
    摘要:
    A series of 1,2,3,4,6,7,8,12b-octahydropyrazino[2,1-alpha][2] benzazepine derivatives was prepared and the cestocidal activity of the compounds evaluated in an in vitro Taenia crassiceps screen. Many of these derivatives proved to be highly active, and 2-(cyclohexylcarbonyl)-4-oxo-1,2,3,4,6,7,8,12b- octahydropyrazino[2,1-alpha][2]benzazepine, epsiprantel (BAN) (22), was selected for further development. The structure-activity relationships are discussed.
    DOI:
    10.1021/jm00129a007
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文献信息

  • Benzazepines, and their use as anthelminthics
    申请人:Beecham Group p.l.c.
    公开号:US04661489A1
    公开(公告)日:1987-04-28
    A compound of formula (I): ##STR1## in which R is optionally substituted phenyl; C.sub.3-8 cycloalkyl; C.sub.5-8 cycloalkenyl; C.sub.1-8 alkyl which may be straight or branched; C.sub.2-8 alkenyl which may be straight or branched; 5- or 6- membered heterocyclyl; or optionally substituted phenyl C.sub.1-4 alkyl, each of Y and Z, which may be the same or different, is oxygen or sulphur; and X is --CH.sub.2 -- or oxygen, a process for the preparation of such compounds and their use in human and veterinary medicine.
    化合物的结构式(I):##STR1## 其中R是可选取代的苯基;C.sub.3-8环烷基;C.sub.5-8环烯基;C.sub.1-8烷基,可以是直链或支链;C.sub.2-8烯基,可以是直链或支链;5-或6-成员杂环基;或可选取代的苯基C.sub.1-4烷基,每个Y和Z都可以相同或不同,是氧或硫;X是--CH.sub.2--或氧,制备这些化合物的方法以及它们在人类和兽医学中的用途。
  • Benzazepines and methods therefor
    申请人:Beecham Group, p.l.c.
    公开号:US04866056A1
    公开(公告)日:1989-09-12
    A compound of formula (I): ##STR1## in which R is optionally substituted phenyl; C.sub.3-8 cycloalkyl; C.sub.5-8 cycloalkenyl; C.sub.1-8 alkyl which may be straight or branched; C.sub.2-8 alkenyl which may be straight or branched; 5- or 6-membered heterocyclyl; or optionally substituted phenyl C.sub.1-4 alkyl, each of Y and Z, which may be the same or different, is oxygen or sulphur; and X is --CH.sub.2 -- or oxygen, a process for the preparation of such compounds and their use in human and veterinary medicine.
    化合物的公式(I):##STR1## 其中R是可选取代的苯基;C.sub.3-8环烷基;C.sub.5-8环烯基;C.sub.1-8烷基,可以是直链或支链;C.sub.2-8烯基,可以是直链或支链;5-或6-成员杂环基;或可选取代的苯基C.sub.1-4烷基,Y和Z中的每一个,可以相同或不同,是氧或硫;X是--CH.sub.2--或氧,一种制备这种化合物的方法以及它们在人类和兽医学中的应用。
  • BREWER, MALCOLM D.;BURGESS, MALCOLM N.;DORGAN, RODERICK J. J.;ELLIOTT, RI+, J. MED. CHEM., 32,(1989) N, C. 2058-2062
    作者:BREWER, MALCOLM D.、BURGESS, MALCOLM N.、DORGAN, RODERICK J. J.、ELLIOTT, RI+
    DOI:——
    日期:——
  • Benzazepine and benzoxazepine derivatives
    申请人:BEECHAM GROUP PLC
    公开号:EP0134984B1
    公开(公告)日:1988-07-13
  • US4661489A
    申请人:——
    公开号:US4661489A
    公开(公告)日:1987-04-28
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