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N,O-dimethyl-N-hydroxy-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazoleacetamide | 152775-60-5

中文名称
——
中文别名
——
英文名称
N,O-dimethyl-N-hydroxy-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazoleacetamide
英文别名
2-[5-[3-[2,6-dimethyl-4-(2-methyltetrazol-5-yl)phenoxy]propyl]-1,2-oxazol-3-yl]-N-methoxy-N-methylacetamide
N,O-dimethyl-N-hydroxy-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazoleacetamide化学式
CAS
152775-60-5
化学式
C20H26N6O4
mdl
——
分子量
414.464
InChiKey
STLPABOVQUJKKY-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

物化性质

  • 沸点:
    616.8±65.0 °C(predicted)
  • 密度:
    1.28±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.06
  • 重原子数:
    30.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    108.4
  • 氢给体数:
    0.0
  • 氢受体数:
    9.0

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

反应信息

  • 作为反应物:
    描述:
    N,O-dimethyl-N-hydroxy-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazoleacetamide 在 sodium tetrahydroborate 作用下, 以 四氢呋喃乙醚乙醇 为溶剂, 反应 5.0h, 生成 α-methyl-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazolyleethanol
    参考文献:
    名称:
    Antipicornavirus activity of tetrazole analogs related to disoxaril
    摘要:
    A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds. The results of X-ray crystallography studies of several members of the oxazoline series bound to human rhinovirus type IA and 14 have been used to design compounds in the tetrazole series with a broad spectrum of activity. Compound 16b, which has a three-carbon linkage between the isoxazole and phenyl rings and a propyl chain extending from the isoxazole ring, exhibiting an MIC80 for 15 rhinovirus serotypes of 0.20 muM as compared to 0.40 muM for Win 54954. X-ray studies of 16b bound to human rhinovirus-14 show that the propyl side chain extends into a pore in the binding site with the possibility of hydrophobic interactions with a pocket formed by Leu106 and a portion of Ser107.
    DOI:
    10.1021/jm00074a004
  • 作为产物:
    描述:
    5-(4-methoxy-3,5-dimethylphenyl)-2H-tetrazole 在 bis-triphenylphosphine-palladium(II) chloride 、 lithium hydroxide 、 lithium aluminium tetrahydride 、 sodium acetate三溴化硼tribenzylamine hydrochloridepotassium carbonate三乙胺三苯基膦N,N'-羰基二咪唑偶氮二甲酸二乙酯 作用下, 以 四氢呋喃乙醇二氯甲烷氯仿乙腈 为溶剂, 反应 67.67h, 生成 N,O-dimethyl-N-hydroxy-5-<3-<2,6-dimethyl-4-<5-(2-methyl-2H-tetrazolyl)>phenoxy>propyl>-3-isoxazoleacetamide
    参考文献:
    名称:
    Antipicornavirus activity of tetrazole analogs related to disoxaril
    摘要:
    A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds. The results of X-ray crystallography studies of several members of the oxazoline series bound to human rhinovirus type IA and 14 have been used to design compounds in the tetrazole series with a broad spectrum of activity. Compound 16b, which has a three-carbon linkage between the isoxazole and phenyl rings and a propyl chain extending from the isoxazole ring, exhibiting an MIC80 for 15 rhinovirus serotypes of 0.20 muM as compared to 0.40 muM for Win 54954. X-ray studies of 16b bound to human rhinovirus-14 show that the propyl side chain extends into a pore in the binding site with the possibility of hydrophobic interactions with a pocket formed by Leu106 and a portion of Ser107.
    DOI:
    10.1021/jm00074a004
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