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4-(tert-butoxycarbonyl)-3,5-diphenyl-2-[hydroxy-(3,4,5-trimethoxyphenyl)-methyl]-4H-[1,4]oxazine | 943818-48-2

中文名称
——
中文别名
——
英文名称
4-(tert-butoxycarbonyl)-3,5-diphenyl-2-[hydroxy-(3,4,5-trimethoxyphenyl)-methyl]-4H-[1,4]oxazine
英文别名
Tert-butyl 2-[hydroxy-(3,4,5-trimethoxyphenyl)methyl]-3,5-diphenyl-1,4-oxazine-4-carboxylate;tert-butyl 2-[hydroxy-(3,4,5-trimethoxyphenyl)methyl]-3,5-diphenyl-1,4-oxazine-4-carboxylate
4-(tert-butoxycarbonyl)-3,5-diphenyl-2-[hydroxy-(3,4,5-trimethoxyphenyl)-methyl]-4H-[1,4]oxazine化学式
CAS
943818-48-2
化学式
C31H33NO7
mdl
——
分子量
531.606
InChiKey
LHTHUZDAHZFRDS-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):
    5
  • 重原子数:
    39
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    86.7
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    4-(tert-butoxycarbonyl)-3,5-diphenyl-2-[hydroxy-(3,4,5-trimethoxyphenyl)-methyl]-4H-[1,4]oxazine咪唑正丁基锂 作用下, 以 四氢呋喃正己烷N,N-二甲基甲酰胺 为溶剂, 反应 22.75h, 生成 4-(tert-butoxycarbonyl)-2-[(tert-butyl-dimethyl-silanyloxy)-(3,4,5-trimethoxy-phenyl)-methyl]-3,5-diphenyl-6-formyl-4H-[1,4]oxazine
    参考文献:
    名称:
    Easy Access to New Heterocyclic Systems:  1,4-Oxazine and Substituted 1,4-Oxazines
    摘要:
    In the course of our investigations on the synthesis of new nitrogen heterocyclic derivatives, we were interested in the synthesis and study of new 1,4-oxazine rings. To this aim, the desired bisvinylphosphate was prepared from N-Boc morpholine-3,5-dione and was then engaged in palladium-catalyzed reactions (reduction, Suzuki, and Stille cross-coupling reactions). The 1,4-oxazine and its corresponding 3,5-disubstituted derivatives were obtained in fair to good yields and were then functionalized under anionic conditions.
    DOI:
    10.1021/jo070528n
  • 作为产物:
    描述:
    3,5-bis{[bis(phenyloxy)phosphoryl]oxy}-4-(tert-butoxycarbonyl)-[1,4]oxazine 在 bis-triphenylphosphine-palladium(II) chloride barium dihydroxide正丁基锂 作用下, 以 四氢呋喃乙醇正己烷 为溶剂, 反应 10.75h, 生成 4-(tert-butoxycarbonyl)-3,5-diphenyl-2-[hydroxy-(3,4,5-trimethoxyphenyl)-methyl]-4H-[1,4]oxazine
    参考文献:
    名称:
    Easy Access to New Heterocyclic Systems:  1,4-Oxazine and Substituted 1,4-Oxazines
    摘要:
    In the course of our investigations on the synthesis of new nitrogen heterocyclic derivatives, we were interested in the synthesis and study of new 1,4-oxazine rings. To this aim, the desired bisvinylphosphate was prepared from N-Boc morpholine-3,5-dione and was then engaged in palladium-catalyzed reactions (reduction, Suzuki, and Stille cross-coupling reactions). The 1,4-oxazine and its corresponding 3,5-disubstituted derivatives were obtained in fair to good yields and were then functionalized under anionic conditions.
    DOI:
    10.1021/jo070528n
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文献信息

  • Easy Access to New Heterocyclic Systems:  1,4-Oxazine and Substituted 1,4-Oxazines
    作者:Elise Claveau、Isabelle Gillaizeau、Jérome Blu、Amélie Bruel、Gérard Coudert
    DOI:10.1021/jo070528n
    日期:2007.6.1
    In the course of our investigations on the synthesis of new nitrogen heterocyclic derivatives, we were interested in the synthesis and study of new 1,4-oxazine rings. To this aim, the desired bisvinylphosphate was prepared from N-Boc morpholine-3,5-dione and was then engaged in palladium-catalyzed reactions (reduction, Suzuki, and Stille cross-coupling reactions). The 1,4-oxazine and its corresponding 3,5-disubstituted derivatives were obtained in fair to good yields and were then functionalized under anionic conditions.
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