N-(5-acetyl-2-hydroxyphenyl)-2,2-dichloroacetamide | 871946-59-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: N-(5-acetyl-2-hydroxyphenyl)-2,2-dichloroacetamide
• CAS: 871946-59-7
• 化学式: C₁₀H₉Cl₂NO₃
• 分子量: 262.092
• InChiKey: SVBPESXUZGXVQY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(5-acetyl-2-hydroxyphenyl)-2,2-dichloroacetamide 在 咪唑 、 盐酸 、 碳酸氢钠 、 potassium carbonate 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 82.42h， 生成 6-acetyl-2-butoxy-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-one
  参考文献：
  名称：

  Design, Synthesis, and Microbiological Evaluation of New Candida albicans CYP51 Inhibitors

  摘要：

  In a program aimed at the design and synthesis of novel azole inhibitors of Candida albicans CYP51 (CA-CYP51), a series of azole 1,4-benzothiazines (BT) and 1,4-benzoxazines (BO) were recently synthesized. A morphological study of the enzyme active site highlighted a hydrophobic access channel, and a docking study pointed out that the C-2 position of the BT or BO nucleus was oriented toward the access channel. Here, we report the design, synthesis, and microbiological evaluation of C-2-alkyl BT and BO compounds. In both series, introduction of the alkyl chain maintained and in some cases improved the anti-Candida in vitro activity; however, there was not always a strict correlation between in vitro and in vivo activity for several compounds.

  DOI：

  10.1021/jm050685j
• 作为产物：
  描述：

  二氯乙酰氯 、 1-(3-氨基-4-羟基苯基)乙酮 以 四氢呋喃 为溶剂， 反应 1.0h， 以80%的产率得到N-(5-acetyl-2-hydroxyphenyl)-2,2-dichloroacetamide
  参考文献：
  名称：

  Design, Synthesis, and Microbiological Evaluation of New Candida albicans CYP51 Inhibitors

  摘要：

  In a program aimed at the design and synthesis of novel azole inhibitors of Candida albicans CYP51 (CA-CYP51), a series of azole 1,4-benzothiazines (BT) and 1,4-benzoxazines (BO) were recently synthesized. A morphological study of the enzyme active site highlighted a hydrophobic access channel, and a docking study pointed out that the C-2 position of the BT or BO nucleus was oriented toward the access channel. Here, we report the design, synthesis, and microbiological evaluation of C-2-alkyl BT and BO compounds. In both series, introduction of the alkyl chain maintained and in some cases improved the anti-Candida in vitro activity; however, there was not always a strict correlation between in vitro and in vivo activity for several compounds.

  DOI：

  10.1021/jm050685j

文献信息

• Design, Synthesis, and Microbiological Evaluation of New <i>Candida albicans </i>CYP51 Inhibitors
  作者：Fausto Schiaffella、Antonio Macchiarulo、Lara Milanese、Anna Vecchiarelli、Gabriele Costantino、Donatella Pietrella、Renata Fringuelli

  DOI：10.1021/jm050685j

  日期：2005.12.1

  In a program aimed at the design and synthesis of novel azole inhibitors of Candida albicans CYP51 (CA-CYP51), a series of azole 1,4-benzothiazines (BT) and 1,4-benzoxazines (BO) were recently synthesized. A morphological study of the enzyme active site highlighted a hydrophobic access channel, and a docking study pointed out that the C-2 position of the BT or BO nucleus was oriented toward the access channel. Here, we report the design, synthesis, and microbiological evaluation of C-2-alkyl BT and BO compounds. In both series, introduction of the alkyl chain maintained and in some cases improved the anti-Candida in vitro activity; however, there was not always a strict correlation between in vitro and in vivo activity for several compounds.