2-chloro-6-(2-chloro-8-methyl-4H-1,3,2-benzodioxaphosphinin-6-yl)-8-methyl-4H-1,3,2-benzodioxaphosphinine | 1160003-70-2

• 分子结构分类: 有机化合物 - 苯类化合物
• 英文名称: 2-chloro-6-(2-chloro-8-methyl-4H-1,3,2-benzodioxaphosphinin-6-yl)-8-methyl-4H-1,3,2-benzodioxaphosphinine
• CAS: 1160003-70-2
• 化学式: C₁₆H₁₄Cl₂O₄P₂
• 分子量: 403.138
• InChiKey: PHUZSGAGQWTLDY-UHFFFAOYSA-N

物化性质

• 沸点：
  479.9±55.0 °C(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  24
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  36.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-chloro-6-(2-chloro-8-methyl-4H-1,3,2-benzodioxaphosphinin-6-yl)-8-methyl-4H-1,3,2-benzodioxaphosphinine 、 司他夫定 在 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 反应 1.0h， 生成
  参考文献：
  名称：

  Doubly Loaded cycloSaligenyl-Pronucleotides – 5,5′-Bis-(cycloSaligenyl-2′,3′-dideoxy-2′,3′-didehydrothymidine Monophosphates)

  摘要：

  Recently, we reported on 3,3'-bis-(cycloSaligenyl-2',3'-dideoxy-2',3'-didehydrothymidine monophosphates) (3,3'-bis-(cycloSal-d4TMPs) 4) as the first pronucleotides with a mask-to-drug ratio of 1:2 that is still a novelty in the field of pronucleotides. Here, we report on a new set of compounds of these unique type of cycloSaligenyl prodrugs 5 that bear a biaryl axis at the 5-position of the cycloSal residue. All compounds 5 showed pronounced in vitro activity against HIV-1 and HIV-2 in wild-type CEM cell cultures and better retained their antiviral activities in thymidine kinase-deficient CEM cells than the compound 4 series. Moreover, compound 5b is the first bis-(cycloSal-d4TMP) that even showed complete retention of antiviral activity in TK-deficient CEM cells. The complex hydrolysis behavior of 5 was investigated, and the proposed hydrolysis mechanism was proven by means of P-31 NMR spectroscopy and HPLC analysis.

  DOI：

  10.1021/jm900164g
• 作为产物：
  描述：

  3,3'-bis-(hydroxymethyl)-5,5'-dimethyl-biphenyl-4,4'-diol 在 三氯化磷 、 吡啶 作用下， 以 四氢呋喃 、 乙醚 为溶剂， 反应 0.17h， 生成 2-chloro-6-(2-chloro-8-methyl-4H-1,3,2-benzodioxaphosphinin-6-yl)-8-methyl-4H-1,3,2-benzodioxaphosphinine
  参考文献：
  名称：

  Doubly Loaded cycloSaligenyl-Pronucleotides – 5,5′-Bis-(cycloSaligenyl-2′,3′-dideoxy-2′,3′-didehydrothymidine Monophosphates)

  摘要：

  Recently, we reported on 3,3'-bis-(cycloSaligenyl-2',3'-dideoxy-2',3'-didehydrothymidine monophosphates) (3,3'-bis-(cycloSal-d4TMPs) 4) as the first pronucleotides with a mask-to-drug ratio of 1:2 that is still a novelty in the field of pronucleotides. Here, we report on a new set of compounds of these unique type of cycloSaligenyl prodrugs 5 that bear a biaryl axis at the 5-position of the cycloSal residue. All compounds 5 showed pronounced in vitro activity against HIV-1 and HIV-2 in wild-type CEM cell cultures and better retained their antiviral activities in thymidine kinase-deficient CEM cells than the compound 4 series. Moreover, compound 5b is the first bis-(cycloSal-d4TMP) that even showed complete retention of antiviral activity in TK-deficient CEM cells. The complex hydrolysis behavior of 5 was investigated, and the proposed hydrolysis mechanism was proven by means of P-31 NMR spectroscopy and HPLC analysis.

  DOI：

  10.1021/jm900164g

文献信息

• Doubly Loaded <i>cyclo</i>Saligenyl-Pronucleotides – 5,5′-Bis-(<i>cyclo</i>Saligenyl-2′,3′-dideoxy-2′,3′-didehydrothymidine Monophosphates)
  作者：Nicolas Gisch、Jan Balzarini、Chris Meier

  DOI：10.1021/jm900164g

  日期：2009.6.11

  Recently, we reported on 3,3'-bis-(cycloSaligenyl-2',3'-dideoxy-2',3'-didehydrothymidine monophosphates) (3,3'-bis-(cycloSal-d4TMPs) 4) as the first pronucleotides with a mask-to-drug ratio of 1:2 that is still a novelty in the field of pronucleotides. Here, we report on a new set of compounds of these unique type of cycloSaligenyl prodrugs 5 that bear a biaryl axis at the 5-position of the cycloSal residue. All compounds 5 showed pronounced in vitro activity against HIV-1 and HIV-2 in wild-type CEM cell cultures and better retained their antiviral activities in thymidine kinase-deficient CEM cells than the compound 4 series. Moreover, compound 5b is the first bis-(cycloSal-d4TMP) that even showed complete retention of antiviral activity in TK-deficient CEM cells. The complex hydrolysis behavior of 5 was investigated, and the proposed hydrolysis mechanism was proven by means of P-31 NMR spectroscopy and HPLC analysis.