N-(1-naphthyl)-5H-chromeno [2,3-d]pyrimidin-4-amine | 1219126-51-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: N-(1-naphthyl)-5H-chromeno [2,3-d]pyrimidin-4-amine
• 英文别名: N-(1-Naphthyl)-10H-9-oxa-1,3-diazaanthracen-4-amine；N-naphthalen-1-yl-5H-chromeno[2,3-d]pyrimidin-4-amine
• CAS: 1219126-51-8
• 化学式: C₂₁H₁₅N₃O
• 分子量: 325.37
• InChiKey: XFVBCYXQHOQFQM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  25
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  47
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  N'-(3-cyano-3,4-dihydro-2H-chromen-2-yl)-N,N-dimethylimidoformamide 、 1-萘胺 在 溶剂黄146 作用下， 反应 0.08h， 以71%的产率得到N-(1-naphthyl)-5H-chromeno [2,3-d]pyrimidin-4-amine
  参考文献：
  名称：

  Novel chromeno [2,3-b]-pyrimidine derivatives as potential anti-microbial agents

  摘要：

  An efficient, microwave irradiated synthesis of novel chromeno[2,3-b]-pyrimidine derivatives was carried out. 2-Amino-3,4-dihydro-2H-chromene-3-carbonitrile was converted into imine using N,N-Dimethylacetaldehyde dimethylacetal to give the core intermediate, which was used for the preparation of chromenopyrimidine library, using acetic acid and different amine in microwave irradiation for 5 min. Structures of newly synthesized compounds were confirmed by spectral studies. Compound 6g was characterized by single crystal X-ray analysis. All the compounds were also screened for their antimicrobial activity. Few of the compounds are found to be potential antimicrobials.

  DOI：

  10.1016/j.ejmech.2010.02.040

文献信息

• Novel chromeno [2,3-b]-pyrimidine derivatives as potential anti-microbial agents
  作者：U. Sankappa Rai、Arun M. Isloor、Prakash shetty、A.M. Vijesh、Nithin Prabhu、Shrikrishna Isloor、M. Thiageeswaran、Hoong-Kun Fun

  DOI：10.1016/j.ejmech.2010.02.040

  日期：2010.6

  An efficient, microwave irradiated synthesis of novel chromeno[2,3-b]-pyrimidine derivatives was carried out. 2-Amino-3,4-dihydro-2H-chromene-3-carbonitrile was converted into imine using N,N-Dimethylacetaldehyde dimethylacetal to give the core intermediate, which was used for the preparation of chromenopyrimidine library, using acetic acid and different amine in microwave irradiation for 5 min. Structures of newly synthesized compounds were confirmed by spectral studies. Compound 6g was characterized by single crystal X-ray analysis. All the compounds were also screened for their antimicrobial activity. Few of the compounds are found to be potential antimicrobials.