摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

9-Methoxycarbonylmethyl-2-methyl-2H-[1,2,3]triazolo[4,5-f]quinoline-8-carboxylic acid methyl ester | 173317-19-6

中文名称
——
中文别名
——
英文名称
9-Methoxycarbonylmethyl-2-methyl-2H-[1,2,3]triazolo[4,5-f]quinoline-8-carboxylic acid methyl ester
英文别名
methyl 9-(2-methoxy-2-oxoethyl)-2-methyltriazolo[4,5-f]quinoline-8-carboxylate
9-Methoxycarbonylmethyl-2-methyl-2H-[1,2,3]triazolo[4,5-f]quinoline-8-carboxylic acid methyl ester化学式
CAS
173317-19-6
化学式
C15H14N4O4
mdl
——
分子量
314.301
InChiKey
KRKLQTAMUOTRGE-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):
    1.02
  • 重原子数:
    23.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    96.2
  • 氢给体数:
    0.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    9-Methoxycarbonylmethyl-2-methyl-2H-[1,2,3]triazolo[4,5-f]quinoline-8-carboxylic acid methyl ester 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 反应 12.0h, 以25%的产率得到8-hydroxymethyl-9-(2-hydroxyethyl)-2-methyl-2H-triazolo<4,5-f>quinoline
    参考文献:
    名称:
    Reaction of 5-Aminobenzotriazoles with Methyl Propiolate. Formation of Triazolo[4,5-f]quinolines and Related Compounds. Unusual Products in the Michael Addition Reaction of 2-Methyl-2H-5-aminobenzotriazole
    摘要:
    Reaction of 5-aminobenzotriazoles (1b-d) with methyl propiolate gives (Z/E)-3-[1(2)(3)-methyl(benzotriazol-5-yl)]aminomonopropenoates (5b-d) and (E)-3-[1(2)(3)-methyl(benzotriazol-5-yl)]aminobispropenoates (6b-d), while in the case of la addition took place on the nitrogen of the triazole ring to give mixtures of (E)-3-(5-aminobenzotriazol-1(2)(3)-yl)propenoates (2,3,4). Mono- (5b-d) and bis-adducts (6b-d) underwent further reaction which also led to the isolation of triazolo[4,5-f]quinolines, of a triazolo[4,5-f]carbostyril and 1-[benzotriazol-5-yl]-2-pyridones. Formation of these compounds depends on the reaction conditions: the solvent employed and the temperature. Thermal cyclization of Michael adduct (Z/E)-(5c) gave triazoloquinolinone (9c) and the rearranged product (13) in various ratio depending on the concentration of Dowtherm used.
    DOI:
    10.3987/com-95-7145
  • 作为产物:
    参考文献:
    名称:
    Reaction of 5-Aminobenzotriazoles with Methyl Propiolate. Formation of Triazolo[4,5-f]quinolines and Related Compounds. Unusual Products in the Michael Addition Reaction of 2-Methyl-2H-5-aminobenzotriazole
    摘要:
    Reaction of 5-aminobenzotriazoles (1b-d) with methyl propiolate gives (Z/E)-3-[1(2)(3)-methyl(benzotriazol-5-yl)]aminomonopropenoates (5b-d) and (E)-3-[1(2)(3)-methyl(benzotriazol-5-yl)]aminobispropenoates (6b-d), while in the case of la addition took place on the nitrogen of the triazole ring to give mixtures of (E)-3-(5-aminobenzotriazol-1(2)(3)-yl)propenoates (2,3,4). Mono- (5b-d) and bis-adducts (6b-d) underwent further reaction which also led to the isolation of triazolo[4,5-f]quinolines, of a triazolo[4,5-f]carbostyril and 1-[benzotriazol-5-yl]-2-pyridones. Formation of these compounds depends on the reaction conditions: the solvent employed and the temperature. Thermal cyclization of Michael adduct (Z/E)-(5c) gave triazoloquinolinone (9c) and the rearranged product (13) in various ratio depending on the concentration of Dowtherm used.
    DOI:
    10.3987/com-95-7145
点击查看最新优质反应信息