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dichloro-[3-acetoxymethyl-7-bromo-1,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one-N,N]palladium(II) | 502963-04-4

中文名称
——
中文别名
——
英文名称
dichloro-[3-acetoxymethyl-7-bromo-1,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one-N,N]palladium(II)
英文别名
——
dichloro-[3-acetoxymethyl-7-bromo-1,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one-N,N]palladium(II)化学式
CAS
502963-04-4
化学式
C18H16BrCl2N3O3Pd
mdl
——
分子量
579.573
InChiKey
PXPHCZUQOOYXEF-HKPSJHCMSA-L
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

反应信息

  • 作为产物:
    描述:
    sodium tetrachloropalladate(II) trihydrate 、 rac-3-acetoxymethyl-7-bromo-2,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one 以 甲醇二氯甲烷 为溶剂, 以80%的产率得到dichloro-[3-acetoxymethyl-7-bromo-1,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one-N,N]palladium(II)
    参考文献:
    名称:
    Synthesis, structural characterisation and biological activity of Zn(II) and Pd(II) complexes of 3-substituted 5-(2′-pyridyl)-1,4-benzodiazepin-2-one derivatives
    摘要:
    Zn-II and Pd-II complexes of 7-bromo-1,3-dihydro-3-hydroxymethyl-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one ((+)-L1), and 3-acetoxymethyl-7-bromo-1,3-dihydro-1-methyl-5-(2'-pyridyl)-2H-1,4-benzodiazepin-2-one ((+/-)-L2) were prepared and determined by spectroscopic studies (IR and H-1 NMR) and X-ray structure analysis. The influence of the metal coordination on the absolute configuration at the stereogenic centre of the chiral ligands was studied. In ZnL1Cl(2) (1) a distorted trigonal bipyramid was formed in which L1 acts as a tridentate N,N,O-Iigand, while in the case of ZnL2Cl(2) (3), Zn-II is in a distorted tetrahedral environment coordinated by two azomethine nitrogen and two chlorine atoms. Zn-II complexes 1 and 3 are the first zinc complexes of benzodiazepines reported so far. In Pd-II complexes 2 and 4, the expected square-planar coordination was observed. The free ligands and their complexes were evaluated for their in vitro cytostatic activity against the murine L1210/0 and human T-lymphoblast Molt/ C8 and CEM/0 cell lines, as well as for their in vitro-antiviral activity in different assay systems. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(02)01251-2
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