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<(4-Methoxy-2-quinolyl)methyl>formamide | 132833-02-4

中文名称
——
中文别名
——
英文名称
<(4-Methoxy-2-quinolyl)methyl>formamide
英文别名
2-formamidomethyl-4-methoxyquinoline;N-[(4-methoxyquinolin-2-yl)methyl]formamide
<(4-Methoxy-2-quinolyl)methyl>formamide化学式
CAS
132833-02-4
化学式
C12H12N2O2
mdl
——
分子量
216.239
InChiKey
DEXKSGHKFQNJFZ-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):
    1.6
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    51.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    <(4-Methoxy-2-quinolyl)methyl>formamide 在 TEA 、 三氯氧磷 作用下, 以 二氯甲烷 为溶剂, 反应 0.07h, 以73%的产率得到5-Methoxyimidazo<1,5-a>quinoline
    参考文献:
    名称:
    Langry, Kevin C., Organic Preparations and Procedures International, 1994, vol. 26, # 4, p. 429 - 438
    摘要:
    DOI:
  • 作为产物:
    描述:
    甲酸丙酯 、 2-(Aminomethyl)-4-methoxyquinoline dihydrochloride 在 TEA 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以74%的产率得到<(4-Methoxy-2-quinolyl)methyl>formamide
    参考文献:
    名称:
    Langry, Kevin C., Organic Preparations and Procedures International, 1994, vol. 26, # 4, p. 429 - 438
    摘要:
    DOI:
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文献信息

  • Formation of imidazopyridines by the phase transfer catalyzed reaction of .alpha.-(aminomethyl)pyridines and CHCl3 with alkaline hydroxide
    作者:Kevin C. Langry
    DOI:10.1021/jo00007a028
    日期:1991.3
    The reaction of chloroform with 2-(aminomethyl)pyridine (1) under basic phase-transfer catalysis affords the highly fluorescent imidazo[1,5-alpha]pyridine (2) in 25% isolated yield. Despite the formation of considerable tarry residue, GC-MS indicates that the volatile fraction of the reaction is simple and consists of 2 and two minor residue, GC-MS indicates that the volatile fraction of the reaction is simple and consists of 2 and two minor components identified as N-(2-pyridylmethyl)formamide (6) and (2-pyridylmethyl)isonitrile (7). The basic phase transfer catalyzed reaction of chloroform with a series of alpha-(aminomethyl)azanaphthalenes was found to be general and yield the corresponding annulated imidazo derivaties in comparable yields. Despite product yields in the 25% range, GC of the reaction mixtures indicates that the volatile fractions generally consist of residual starting aminomethyl compound, the imidazo product, and a minor amount of the (alpha-azanaphthylmethyl)formamide. However, 3-(aminomethyl)isoquinoline (18) failed to provide any of the expected imidazo[1,5-b]isoquinoline (19). The failure to detect 19 was investigated.
  • LANGRY, KEVIN C., J. ORG. CHEM. , 56,(1991) N, C. 2400-2404
    作者:LANGRY, KEVIN C.
    DOI:——
    日期:——
  • Langry Kevin C., Org. Prep. and Proced. Int, 26 (1994) N 4, S 429-438
    作者:Langry Kevin C.
    DOI:——
    日期:——
  • Langry, Kevin C., Organic Preparations and Procedures International, 1994, vol. 26, # 4, p. 429 - 438
    作者:Langry, Kevin C.
    DOI:——
    日期:——
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