3-[N-(2-hydroxycarbonylmethyl)carboxamide]-4-methyl-9H-carbazole | 1262229-39-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 3-[N-(2-hydroxycarbonylmethyl)carboxamide]-4-methyl-9H-carbazole
• 英文别名: 2-[(4-methyl-9H-carbazole-3-carbonyl)amino]acetic acid
• CAS: 1262229-39-9
• 化学式: C₁₆H₁₄N₂O₃
• 分子量: 282.299
• InChiKey: RDFHWEYMONXLKO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  82.2
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-[N-(2-hydroxycarbonylmethyl)carboxamide]-4-methyl-9H-carbazole 、 对甲基苯甲醛 在 sodium acetate 、 乙酸酐 作用下， 反应 2.0h， 生成 4-(4-methylbenzylidene)-2-(4-methyl-9H-carbazol-3-yl)oxazol-5(4H)-one
  参考文献：
  名称：

  Gündogdu, Cevher; Göçmentürk, Mustafa; Ergün, Yavuz, Asian Journal of Chemistry, 2011, vol. 23, # 8, p. 3543 - 3545

  摘要：

  DOI：
• 作为产物：
  描述：

  methyl (4-methyl-9H-carbazole-3-carbonyl)glycinate 在 lithium hydroxide monohydrate 、 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 2.0h， 以91%的产率得到3-[N-(2-hydroxycarbonylmethyl)carboxamide]-4-methyl-9H-carbazole
  参考文献：
  名称：

  Synthesis of novel carbazolyl-oxazolone derivatives and their spectroscopic properties

  摘要：

  Abstract magnified image Novel carbazolyl‐oxazolones, 3a, 3b, 3c, 3d, were synthesized with 3‐[N‐(2‐hydroxycarbonylmethyl)‐carboxamide]‐4‐methyl‐9H‐carbazole and several aryl aldehydes for the first time. Photo physical characterization of synthesized 2‐carbazolyl‐4‐arylidene‐5‐oxazolones (3a, 3b, 3c, 3d) in dichloromethane, chloroform, and toluene was performed. J. Heterocyclic Chem., (2010).

  DOI：

  10.1002/jhet.499

文献信息

• Synthesis of novel carbazolyl-oxazolone derivatives and their spectroscopic properties
  作者：Cevher Gündoğdu、Derya Topkaya、Gülsiye Öztürk、Serap Alp、Yavuz Ergün

  DOI：10.1002/jhet.499

  日期：2010.11

  Abstract magnified image Novel carbazolyl‐oxazolones, 3a, 3b, 3c, 3d, were synthesized with 3‐[N‐(2‐hydroxycarbonylmethyl)‐carboxamide]‐4‐methyl‐9H‐carbazole and several aryl aldehydes for the first time. Photo physical characterization of synthesized 2‐carbazolyl‐4‐arylidene‐5‐oxazolones (3a, 3b, 3c, 3d) in dichloromethane, chloroform, and toluene was performed. J. Heterocyclic Chem., (2010).
• Gündogdu, Cevher; Göçmentürk, Mustafa; Ergün, Yavuz, Asian Journal of Chemistry, 2011, vol. 23, # 8, p. 3543 - 3545
  作者：Gündogdu, Cevher、Göçmentürk, Mustafa、Ergün, Yavuz

  DOI：——

  日期：——