1-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid hydrazide | 368433-38-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 1-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid hydrazide
• 英文别名: 4-Hydroxy-2-oxo-1-(prop-2-en-1-yl)-1,2-dihydroquinoline-3-carbohydrazide；4-hydroxy-2-oxo-1-prop-2-enylquinoline-3-carbohydrazide
• CAS: 368433-38-9
• 化学式: C₁₃H₁₃N₃O₃
• 分子量: 259.265
• InChiKey: FNLCYVRFFWXKNK-UHFFFAOYSA-N

物化性质

• 密度：
  1.390±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  95.7
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid hydrazide 、 丙酮 反应 1.0h， 以87%的产率得到4-hydroxy-2-oxo-N'-(propan-2-ylidene)-1-(prop-2-en-1-yl)-1,2-dihydroquinoline-3-carbohydrazide
  参考文献：
  名称：

  4-Hydroxy-2-quinolones 171*. Synthesis, isomerism, and antitubercular activity of 1-R-4-hydroxy-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid alkylidenehydrazides

  摘要：

  Alkylidenehydrazides have been synthesized by the reaction of 1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid hydrazides with lower dialkyl ketones in order to reveal a structure-antitubercular activity relationship. It was shown by H-1 NMR spectroscopy that hydrazones obtained from the unsymmetrical ketone-methyl ethyl ketone-exist primarily in the E-isomer form. It was found that the presence of two aliphatic substituents in the alkylidene fragment of the compounds investigated leads to a marked lowering of antimicobacterial properties.

  DOI：

  10.1007/s10593-010-0431-3
• 作为产物：
  描述：

  ethyl 1-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate 在 一水合肼 作用下， 生成 1-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid hydrazide
  参考文献：
  名称：

  4-hydroxy-2-quinolones. 169*. synthesis and bromination of 1-allyl-3-(arylamino-methylene)quinoline-2,4-(1h,3h)-diones

  摘要：

  Bromination of 1-allyl-substituted 3-(arylaminomethylene)quinoline-2,4-(1H,3H)-diones with one equivalent of molecular bromine in glacial acetic acid and subsequent dilution of the reaction mixture with water is accompanied by halocyclization and hydrolysis to form 2-bromomethyl-5-oxo-1,2 dihydro-5H- oxazolo[3,2-a]quinoline-4-carbaldehyde.

  DOI：

  10.1007/s10593-010-0412-6

文献信息

• 4-Hydroxy-2-quinolones. 152*. 3-acetyl-4-hydroxy-2-oxo-1,2-dihydroquinoline and its biologically active derivatives
  作者：I. V. Ukrainets、A. A. Tkach、Liu Yang Yang

  DOI：10.1007/s10593-009-0246-2

  日期：2009.2

  A synthesis and study of the spatial structure of 3-acetyl-4-hydroxy-2-oxo-1,2-dihydroquinoline have been carried. 1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acids [1-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)ethylidene]hydrazides were prepared from this compound by two routes. A comparative analysis of the antitubercular properties of the synthesized compounds and of the closely structurally related N,N'-di(1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carbonyl)hydrazines has been performed.
• 4-Hydroxy-2-quinolones 132. Synthesis, chemical, and biological properties of 1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acids 2-nitrobenzylidenehydrazides
  作者：I. V. Ukrainets、L. V. Sidorenko、O. S. Golovchenko

  DOI：10.1007/s10593-007-0221-8

  日期：2007.11