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(+/-)-trans-1-(4-chlorophenyl)-2-(4,6-dichloro[1,3,5]triazin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester

中文名称
——
中文别名
——
英文名称
(+/-)-trans-1-(4-chlorophenyl)-2-(4,6-dichloro[1,3,5]triazin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
英文别名
methyl (1R,3S)-1-(4-chlorophenyl)-2-(4,6-dichloro-1,3,5-triazin-2-yl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-3-carboxylate
(+/-)-trans-1-(4-chlorophenyl)-2-(4,6-dichloro[1,3,5]triazin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester化学式
CAS
——
化学式
C22H16Cl3N5O2
mdl
——
分子量
488.76
InChiKey
IEWPZEMQOJQBQO-FUHWJXTLSA-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):
    6.3
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    84
  • 氢给体数:
    1
  • 氢受体数:
    6

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-甲基哌嗪(+/-)-trans-1-(4-chlorophenyl)-2-(4,6-dichloro[1,3,5]triazin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl esterpotassium carbonate 作用下, 以 四氢呋喃 为溶剂, 反应 6.0h, 以65%的产率得到(+/-)-trans-2-[4,6-bis(4-methylpiperazin-1-yl)[1,3,5]triazin-2-yl]-1-(4-chlorophenyl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
    参考文献:
    名称:
    Syntheses of new substituted triazino tetrahydroisoquinolines and β-carbolines as novel antileishmanial agents1
    摘要:
    A series of triazino tetrahydroisoquinolines (3-5) and beta-carboline derivatives (15-27) have been synthesized as novel antileishmanial agents. Among them, compounds 15, 16 and 25 have shown 78.0%, 78.6% and 68.0% in vivo inhibition against Leishmania donovani at a dose of 50 mg kg(-1) x 5 days, respectively, while compounds 3 and 18 exhibited 55.6% and 53.3% in vivo inhibitions, respectively, against L. donovani at a dose of 50 mg kg(-1) x 5 days. (c) 2005 Elsevier SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2005.09.007
  • 作为产物:
    参考文献:
    名称:
    Syntheses of new substituted triazino tetrahydroisoquinolines and β-carbolines as novel antileishmanial agents1
    摘要:
    A series of triazino tetrahydroisoquinolines (3-5) and beta-carboline derivatives (15-27) have been synthesized as novel antileishmanial agents. Among them, compounds 15, 16 and 25 have shown 78.0%, 78.6% and 68.0% in vivo inhibition against Leishmania donovani at a dose of 50 mg kg(-1) x 5 days, respectively, while compounds 3 and 18 exhibited 55.6% and 53.3% in vivo inhibitions, respectively, against L. donovani at a dose of 50 mg kg(-1) x 5 days. (c) 2005 Elsevier SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2005.09.007
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文献信息

  • Syntheses of new substituted triazino tetrahydroisoquinolines and β-carbolines as novel antileishmanial agents1
    作者:A KUMAR、S KATIYAR、S GUPTA、P CHAUHAN
    DOI:10.1016/j.ejmech.2005.09.007
    日期:2006.1
    A series of triazino tetrahydroisoquinolines (3-5) and beta-carboline derivatives (15-27) have been synthesized as novel antileishmanial agents. Among them, compounds 15, 16 and 25 have shown 78.0%, 78.6% and 68.0% in vivo inhibition against Leishmania donovani at a dose of 50 mg kg(-1) x 5 days, respectively, while compounds 3 and 18 exhibited 55.6% and 53.3% in vivo inhibitions, respectively, against L. donovani at a dose of 50 mg kg(-1) x 5 days. (c) 2005 Elsevier SAS. All rights reserved.
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