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1-(2-pivaloylpterin-6-yl)-3-<(tert-butyldimethylsilyl)oxy>but-1-yne | 131863-88-2

中文名称
——
中文别名
——
英文名称
1-(2-pivaloylpterin-6-yl)-3-<(tert-butyldimethylsilyl)oxy>but-1-yne
英文别名
1-(2-pivaloylpterin-6-yl)-3-[(tert-butyldimethylsilyl)oxy]but-1-yne;Fyjlrwvyffhknl-uhfffaoysa-;N-[6-[3-[tert-butyl(dimethyl)silyl]oxybut-1-ynyl]-4-oxo-3H-pteridin-2-yl]-2,2-dimethylpropanamide
1-(2-pivaloylpterin-6-yl)-3-<(tert-butyldimethylsilyl)oxy>but-1-yne化学式
CAS
131863-88-2
化学式
C21H31N5O3Si
mdl
——
分子量
429.594
InChiKey
FYJLRWVYFFHKNL-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):
    3.46
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    106
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 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:
    1-(2-pivaloylpterin-6-yl)-3-<(tert-butyldimethylsilyl)oxy>but-1-yne四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 以93%的产率得到1-(2-pivaloylpterin-6-yl)but-1-yn-3-ol
    参考文献:
    名称:
    Model studies directed toward the molybdenum cofactor: 2-alkylidene- and 2-(phenylimino)-1,3-dithioles from acetylenes
    摘要:
    The cycloaddition of activated alkynes, among them 6-alkynylpterins, with the tributylphosphine-carbon disulfide complex followed by a Wittig reaction of the resulting ylid with carbonyl compounds or nitrosobenzene affords novel 2-alkylidene- or 2-(phenylimino)-1,3-dithioles in moderate to very good yields. The pterin-substituted species are potential intermediates in the synthesis of the molybdenum cofactor.
    DOI:
    10.1021/jo00005a029
  • 作为产物:
    描述:
    2-叔丁基二甲基硅氧基丁-3-炔 、 2-pivaloyl-6-chloropterin 在 palladium diacetate 、 copper(l) iodide三乙胺三苯基膦 作用下, 以 乙腈 为溶剂, 反应 1.0h, 以81%的产率得到1-(2-pivaloylpterin-6-yl)-3-<(tert-butyldimethylsilyl)oxy>but-1-yne
    参考文献:
    名称:
    Model studies directed toward the molybdenum cofactor: 2-alkylidene- and 2-(phenylimino)-1,3-dithioles from acetylenes
    摘要:
    The cycloaddition of activated alkynes, among them 6-alkynylpterins, with the tributylphosphine-carbon disulfide complex followed by a Wittig reaction of the resulting ylid with carbonyl compounds or nitrosobenzene affords novel 2-alkylidene- or 2-(phenylimino)-1,3-dithioles in moderate to very good yields. The pterin-substituted species are potential intermediates in the synthesis of the molybdenum cofactor.
    DOI:
    10.1021/jo00005a029
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文献信息

  • TAYLOR, EDWARD C.;DOTZER, REINHARD, J. ORG. CHEM., 56,(1991) N, C. 1816-1822
    作者:TAYLOR, EDWARD C.、DOTZER, REINHARD
    DOI:——
    日期:——
  • Model studies directed toward the molybdenum cofactor: 2-alkylidene- and 2-(phenylimino)-1,3-dithioles from acetylenes
    作者:Edward C. Taylor、Reinhard Doetzer
    DOI:10.1021/jo00005a029
    日期:1991.3
    The cycloaddition of activated alkynes, among them 6-alkynylpterins, with the tributylphosphine-carbon disulfide complex followed by a Wittig reaction of the resulting ylid with carbonyl compounds or nitrosobenzene affords novel 2-alkylidene- or 2-(phenylimino)-1,3-dithioles in moderate to very good yields. The pterin-substituted species are potential intermediates in the synthesis of the molybdenum cofactor.
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