4-amino-2-phenyl-chromeno[3,4-c]pyridin-5-ylideneamine | 30144-15-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 4-amino-2-phenyl-chromeno[3,4-c]pyridin-5-ylideneamine
• 英文别名: 5-Imino-2-phenylchromeno[3,4-c]pyridine-4-ylamine；5-imino-2-phenylchromeno[3,4-c]pyridin-4-amine
• CAS: 30144-15-1
• 化学式: C₁₈H₁₃N₃O
• 分子量: 287.321
• InChiKey: FECRHUHFSQLLIK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  72
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-amino-2-phenyl-chromeno[3,4-c]pyridin-5-ylideneamine 在 盐酸 作用下， 以 溶剂黄146 为溶剂， 生成 (4-amino-2-phenyl-chromeno[3,4-c]pyridin-5-ylidene)-phenyl-amine
  参考文献：
  名称：

  Reynolds,G.A. et al., Journal of Heterocyclic Chemistry, 1970, vol. 7, p. 1061 - 1069

  摘要：

  DOI：
• 作为产物：
  描述：

  2-(2-phenyl-4H-chromen-4-ylidene)malononitrile 在 ammonium hydroxide 作用下， 以 吡啶 为溶剂， 生成 4-amino-2-phenyl-chromeno[3,4-c]pyridin-5-ylideneamine
  参考文献：
  名称：

  Reynolds,G.A. et al., Journal of Heterocyclic Chemistry, 1970, vol. 7, p. 1061 - 1069

  摘要：

  DOI：

文献信息

• Rangnekar, D.W.,; Dhamnaskar, S.V.,, Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1767 - 1768
  作者：Rangnekar, D.W.,、Dhamnaskar, S.V.,

  DOI：——

  日期：——
• Substituted benzopyranopyridopyrimidine ring syntheses by the ternary condensation of malononitrile, salicylaldehyde, and aromatic ketones in the presence of ammonium acetate
  作者：Akio Sakurai、Yoshito Motomura、Hiroshi Midorikawa

  DOI：10.1021/jo00975a013

  日期：1972.5
• A convenient one-pot synthesis of new chromeno[3,4-c]chromene and chromeno[3,4-c]pyridine derivatives in the presence of high surface area of magnesium oxide
  作者：Iman Mohammadzadeh、Hassan Sheibani

  DOI：10.1016/j.cclet.2012.10.007

  日期：2012.12

  In this investigation a new strategy involves the one-pot, three-component reaction of malononitrile, salycilaldehyde and phenol derivatives in the presence of high surface area of MgO is extended to the formation of chromeno[3,4-c]chromene derivatives in good to excellent yields in a short reaction time. Also, the three component reactions of an aldehyde such as salycilaldehyde and ketones with malononitril for the formation of chromeno[3,4-c]pyridines are investigated. (C) 2012 Iman Mohammadzadeh. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
• Reynolds,G.A. et al., Journal of Heterocyclic Chemistry, 1970, vol. 7, p. 1061 - 1069
  作者：Reynolds,G.A. et al.

  DOI：——

  日期：——