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(2'R)-cis-5-[2',5'-dihydro-4'-((tert-butyldiphenyl)silyl)oxy-2'-furanyl]-2-aminoquinazoline | 503321-53-7

中文名称
——
中文别名
——
英文名称
(2'R)-cis-5-[2',5'-dihydro-4'-((tert-butyldiphenyl)silyl)oxy-2'-furanyl]-2-aminoquinazoline
英文别名
[(2R,5R)-5-(2-aminoquinazolin-5-yl)-3-[tert-butyl(diphenyl)silyl]oxy-2,5-dihydrofuran-2-yl]methanol
(2'R)-cis-5-[2',5'-dihydro-4'-((tert-butyldiphenyl)silyl)oxy-2'-furanyl]-2-aminoquinazoline化学式
CAS
503321-53-7
化学式
C29H31N3O3Si
mdl
——
分子量
497.669
InChiKey
HCNALUGOSSHWRF-XNMGPUDCSA-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):
    4.1
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    90.5
  • 氢给体数:
    2
  • 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:
    (2'R)-cis-5-[2',5'-dihydro-4'-((tert-butyldiphenyl)silyl)oxy-2'-furanyl]-2-aminoquinazoline吡啶4-二甲氨基吡啶三甲基氯硅烷四丁基氟化铵三乙酰氧基硼氢化钠溶剂黄146三乙胺N,N-二异丙基乙胺 作用下, 以 四氢呋喃二氯甲烷乙腈 为溶剂, 反应 29.67h, 生成 N2-isobutyryl-5-[2'-deoxy-β-D-threo-pentofuranosyl-3'-O-(2-cyanoethoxy)(diisopropylamino)phosphino-5'-O-(4,4'-dimethoxytrityl)]-2-aminoquinazoline
    参考文献:
    名称:
    Design of Triple Helix Forming C-Glycoside Molecules
    摘要:
    The modeling, synthesis, and characterization of oligomers containing 2-aminoquinazolin-5-yl 2'-deoxynucleotide residues are reported. The 2-arninoquinazoline residues sequence specifically bind via Hoogsteen base pairing as a third strand in the center of the major groove at TA base pair Watson-Crick duplex sequences. Evidence for the formation of a sequence specific three-stranded structure is based on thermal denaturation UV-vis and fluorescence studies. The novel 2-aminoquinazoline C-nucleoticle is a component of a system designed to overcome the homopurine requirement for triple helix structures.
    DOI:
    10.1021/ja028033x
  • 作为产物:
    描述:
    2-溴-6-硝基苄溴盐酸 、 palladium bis(dibenzylideneacetone)palladium(0)三叔丁基膦硫酸铁粉三乙胺 作用下, 以 四氢呋喃乙二醇乙醚乙醇 为溶剂, 反应 2.51h, 生成 (2'R)-cis-5-[2',5'-dihydro-4'-((tert-butyldiphenyl)silyl)oxy-2'-furanyl]-2-aminoquinazoline
    参考文献:
    名称:
    Design of Triple Helix Forming C-Glycoside Molecules
    摘要:
    The modeling, synthesis, and characterization of oligomers containing 2-aminoquinazolin-5-yl 2'-deoxynucleotide residues are reported. The 2-arninoquinazoline residues sequence specifically bind via Hoogsteen base pairing as a third strand in the center of the major groove at TA base pair Watson-Crick duplex sequences. Evidence for the formation of a sequence specific three-stranded structure is based on thermal denaturation UV-vis and fluorescence studies. The novel 2-aminoquinazoline C-nucleoticle is a component of a system designed to overcome the homopurine requirement for triple helix structures.
    DOI:
    10.1021/ja028033x
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文献信息

  • Design of Triple Helix Forming C-Glycoside Molecules
    作者:Jian-Sen Li、Yun-Hua Fan、Yi Zhang、Luis A. Marky、Barry Gold
    DOI:10.1021/ja028033x
    日期:2003.2.1
    The modeling, synthesis, and characterization of oligomers containing 2-aminoquinazolin-5-yl 2'-deoxynucleotide residues are reported. The 2-arninoquinazoline residues sequence specifically bind via Hoogsteen base pairing as a third strand in the center of the major groove at TA base pair Watson-Crick duplex sequences. Evidence for the formation of a sequence specific three-stranded structure is based on thermal denaturation UV-vis and fluorescence studies. The novel 2-aminoquinazoline C-nucleoticle is a component of a system designed to overcome the homopurine requirement for triple helix structures.
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