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2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid | 220658-28-6

中文名称
——
中文别名
——
英文名称
2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid
英文别名
——
2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzo<b>furan-5-carboxylic acid化学式
CAS
220658-28-6
化学式
C23H24O6
mdl
——
分子量
396.44
InChiKey
NWSLXVAGYGTJIE-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):
    5.3
  • 重原子数:
    29.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    85.97
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid盐酸4-二甲氨基吡啶2,4,6-三异丙基苯磺酰氯三乙胺 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 反应 5.0h, 生成 4-<2-<5-(N-diphenylmethylcarbamoyl)benzofuran-2-yl>phenyloxy>butyric acid
    参考文献:
    名称:
    A Convenient Synthesis of 2-Phenylbenzofuran Derivatives with Potent Testosterone 5a-Reductase Inhibitory Activities
    摘要:
    A convenient method for the synthesis of 4-[2-(benzo[b]furan-2-yl)phenyloxy]butyric acid derivatives with a carbamoyl group at the 5 or 6 position of the benzofuran ring showing potent 5 alpha-reductase inhibitory activities was developed. Oxazolin-2-ylbenzofuran derivatives were treated with tert-BuLi followed by tri(n-butyl)tin chloride, to give 2-tri(1-butyl)stannylbenzofuran derivatives. A palladium-catalyzed cross-coupling reaction of these benzofuran derivatives with tert-butyl 4-(2-iodophenyloxy)butyrate afforded the 2-phenyl benzofuran compounds in good yields.
    DOI:
    10.3987/com-98-8342
  • 作为产物:
    参考文献:
    名称:
    A Convenient Synthesis of 2-Phenylbenzofuran Derivatives with Potent Testosterone 5a-Reductase Inhibitory Activities
    摘要:
    A convenient method for the synthesis of 4-[2-(benzo[b]furan-2-yl)phenyloxy]butyric acid derivatives with a carbamoyl group at the 5 or 6 position of the benzofuran ring showing potent 5 alpha-reductase inhibitory activities was developed. Oxazolin-2-ylbenzofuran derivatives were treated with tert-BuLi followed by tri(n-butyl)tin chloride, to give 2-tri(1-butyl)stannylbenzofuran derivatives. A palladium-catalyzed cross-coupling reaction of these benzofuran derivatives with tert-butyl 4-(2-iodophenyloxy)butyrate afforded the 2-phenyl benzofuran compounds in good yields.
    DOI:
    10.3987/com-98-8342
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