5,5-dimethyl-2-(p-tolyl)-4,5-dihydrofuro[3',2':3,4]naphtho[1,2-d]oxazole | 1410804-53-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 萘并呋喃类
• 英文名称: 5,5-dimethyl-2-(p-tolyl)-4,5-dihydrofuro[3',2':3,4]naphtho[1,2-d]oxazole
• 英文别名: 9,9-Dimethyl-4-(4-methylphenyl)-5,10-dioxa-3-azatetracyclo[10.4.0.02,6.07,11]hexadeca-1(16),2(6),3,7(11),12,14-hexaene；9,9-dimethyl-4-(4-methylphenyl)-5,10-dioxa-3-azatetracyclo[10.4.0.02,6.07,11]hexadeca-1(16),2(6),3,7(11),12,14-hexaene
• CAS: 1410804-53-3
• 化学式: C₂₂H₁₉NO₂
• 分子量: 329.398
• InChiKey: MJFVWXBSSKROCE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  25
• 可旋转键数：
  1
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  35.3
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  黄钟花醌 在 硫酸 、 ammonium acetate 、 双氧水 、 sodium carbonate 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 生成 5,5-dimethyl-2-(p-tolyl)-4,5-dihydrofuro[3',2':3,4]naphtho[1,2-d]oxazole
  参考文献：
  名称：

  1,3-Azoles from ortho-naphthoquinones: Synthesis of aryl substituted imidazoles and oxazoles and their potent activity against Mycobacterium tuberculosis

  摘要：

  Twenty-three naphthoimidazoles and six naphthoxazoles were synthesised and evaluated against susceptible and rifampicin- and isoniazid-resistant strains of Mycobacterium tuberculosis. Among all the compounds evaluated, fourteen presented MIC values in the range of 0.78 to 6.25 mu g/mL against susceptible and resistant strains of M. tuberculosis, Five structures were solved by X-ray crystallographic analysis. These substances are promising antimycobacterial prototypes. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.08.041

文献信息

• 1,3-Azoles from ortho-naphthoquinones: Synthesis of aryl substituted imidazoles and oxazoles and their potent activity against Mycobacterium tuberculosis
  作者：Kelly C.G. Moura、Paula F. Carneiro、Maria do Carmo F.R. Pinto、José A. da Silva、Valéria R.S. Malta、Carlos A. de Simone、Gleiston G. Dias、Guilherme A.M. Jardim、Jéssica Cantos、Tatiane S. Coelho、Pedro E. Almeida da Silva、Eufrânio N. da Silva

  DOI：10.1016/j.bmc.2012.08.041

  日期：2012.11

  Twenty-three naphthoimidazoles and six naphthoxazoles were synthesised and evaluated against susceptible and rifampicin- and isoniazid-resistant strains of Mycobacterium tuberculosis. Among all the compounds evaluated, fourteen presented MIC values in the range of 0.78 to 6.25 mu g/mL against susceptible and resistant strains of M. tuberculosis, Five structures were solved by X-ray crystallographic analysis. These substances are promising antimycobacterial prototypes. (C) 2012 Elsevier Ltd. All rights reserved.