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7-[(S)-3,4-dihydroxybutyl]-7H-7a,9-diazacyclopenta[b]phenanthrene-8,10-dione | 948307-65-1

中文名称
——
中文别名
——
英文名称
7-[(S)-3,4-dihydroxybutyl]-7H-7a,9-diazacyclopenta[b]phenanthrene-8,10-dione
英文别名
——
7-[(S)-3,4-dihydroxybutyl]-7H-7a,9-diazacyclopenta[b]phenanthrene-8,10-dione化学式
CAS
948307-65-1
化学式
C19H18N2O4
mdl
——
分子量
338.363
InChiKey
FYDWTZCRNIFJLO-HKALDPMFSA-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):
    1.92
  • 重原子数:
    25.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    89.87
  • 氢给体数:
    3.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    7-[(S)-3,4-dihydroxybutyl]-7H-7a,9-diazacyclopenta[b]phenanthrene-8,10-dione二异丙基铵盐四氮唑三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 78.0h, 生成 7-[(S)-3-O-(2-cyanoethoxy(diisopropylamino)phosphino)-4-(4,4'-dimethoxytrityloxy)butyl]-7H-7a,9-diazacyclopenta[b]phenanthrene-8,10-dione
    参考文献:
    名称:
    Synthesis and DNA Binding Properties of a New Benzo[f]Imidazo[1,5b]-Isoquinoline-Butan-1,2-Diol Derivative
    摘要:
    A benzo[f]imidazo[1,5b]-isoquinoline derivative 4 with a 1,2-butandiol linker was prepared by reaction of a trimethylsilylated 5-naphthylidenehydantoin 3 with a 2,3-dideoxy-D-glyceropentafuranoside 2 in 22% yield. After deprotection, the resulting compound 5 was converted to a DMT protected phosphoramidite building block 7 for standard DNA synthesis. DNA/DNA, DNA/RNA duplexes with 5 inserted as bulges were destabilized, except when the new amidite was used for the synthesis of a zipping duplex.
    DOI:
    10.1080/15257770600918524
  • 作为产物:
    参考文献:
    名称:
    Synthesis and DNA Binding Properties of a New Benzo[f]Imidazo[1,5b]-Isoquinoline-Butan-1,2-Diol Derivative
    摘要:
    A benzo[f]imidazo[1,5b]-isoquinoline derivative 4 with a 1,2-butandiol linker was prepared by reaction of a trimethylsilylated 5-naphthylidenehydantoin 3 with a 2,3-dideoxy-D-glyceropentafuranoside 2 in 22% yield. After deprotection, the resulting compound 5 was converted to a DMT protected phosphoramidite building block 7 for standard DNA synthesis. DNA/DNA, DNA/RNA duplexes with 5 inserted as bulges were destabilized, except when the new amidite was used for the synthesis of a zipping duplex.
    DOI:
    10.1080/15257770600918524
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