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6-(dipropylamino)-6,7-dihydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one | 132874-91-0

中文名称
——
中文别名
——
英文名称
6-(dipropylamino)-6,7-dihydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one
英文别名
6,7-Dihydro-6-(dipropylamino)-3H,5H-pyrido(1,2,3-de)quinoxalin-3-one;6-Dipropylamino-6,7-dihydro-5H-pyrido[1,2,3-de]quinoxalin-3-one;11-(dipropylamino)-1,4-diazatricyclo[7.3.1.05,13]trideca-3,5,7,9(13)-tetraen-2-one
6-(dipropylamino)-6,7-dihydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one化学式
CAS
132874-91-0
化学式
C17H23N3O
mdl
——
分子量
285.389
InChiKey
ZUNQTXSGJHYWAG-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):
    2.8
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    35.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    N-(1-formyl-1,2,3,4-tetrahydro-3-quinolyl)formamide 在 palladium on activated charcoal 盐酸sodium nitrate氢气sodium acetate 、 sodium carbonate 、 溶剂黄146 作用下, 以 1,4-二氧六环乙醇N,N-二甲基甲酰胺三氟乙酸 为溶剂, 反应 44.5h, 生成 6-(dipropylamino)-6,7-dihydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one
    参考文献:
    名称:
    Dopaminergic and serotonergic activities of imidazoquinolinones and related compounds
    摘要:
    The synthesis of 5-(dipropylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (5), a potent dopamine D2 agonist showing high dopamine/serotonin (5HT1A) selectivity, is described. Dopaminergic activity is associated with the (R)-enantiomer of 5; the (S)-enantiomer shows no dopaminergic activity. A series of analogues where the imidazolone ring was modified to various 5- or 6-membered heterocyclic rings were prepared. Some of these compounds showed a combination of dopaminergic and serotonergic activity, while one compound, 6-(dipropylamino)-1,2,6,7-tetrahydro-3H,5H-pyrido[3,2,1-ij]quinazolin-3-one (24), was a selective serotonergic agonist. Various analogues of 5 where the dipropylamine substituent was modified were prepared. Most of these showed reduced dopaminergic activity, while several were as potent as 5 at the serotonin 5HT1A receptor. Orientations for the new compounds at dopamine and serotonin receptors are proposed and compared with those of other tricyclic ligands known to have high affinity at these receptors.
    DOI:
    10.1021/jm00084a013
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文献信息

  • HETEROCYCLIC AMINES HAVING CENTRAL NERVOUS SYSTEM ACTIVITY
    申请人:THE UPJOHN COMPANY
    公开号:EP0480939B1
    公开(公告)日:1995-01-25
  • CHIRAL CATALYSTS, CATALYTIC OXIDATION AND DISPROPORTIONATION REACTIONS, AND METHODS OF PRODUCING EPOXYCHROMANS AND TAXOL
    申请人:RESEARCH CORPORATION TECHNOLOGIES, INC.
    公开号:EP0643626A1
    公开(公告)日:1995-03-22
  • EP0643626A4
    申请人:——
    公开号:EP0643626A4
    公开(公告)日:1995-12-06
  • US5273975A
    申请人:——
    公开号:US5273975A
    公开(公告)日:1993-12-28
  • US5436240A
    申请人:——
    公开号:US5436240A
    公开(公告)日:1995-07-25
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