N2-isobutyroyl-6-isobutyroyloxymethyl-5-(1-benzyl-1,4-dihydronicotinoyl)-5,6,7,8-tetrahydropterin | 1147330-20-8

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: N2-isobutyroyl-6-isobutyroyloxymethyl-5-(1-benzyl-1,4-dihydronicotinoyl)-5,6,7,8-tetrahydropterin
• CAS: 1147330-20-8
• 化学式: C₂₈H₃₄N₆O₅
• 分子量: 534.615
• InChiKey: PKRSCOVFZASHMP-UHFFFAOYSA-N

物化性质

• 密度：
  1.33±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.99
• 重原子数：
  39.0
• 可旋转键数：
  8.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  136.73
• 氢给体数：
  3.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  N2-isobutyroyl-6-isobutyroyloxymethyl-5-(1-benzyl-1,4-dihydronicotinoyl)-5,6,7,8-tetrahydropterin 在 potassium carbonate 作用下， 以 甲醇 为溶剂， 以53%的产率得到6-hydroxymethyl-5-(1-benzyl-1,4-dihydronicotinoyl)-5,6,7,8-tetrahydropterin
  参考文献：
  名称：

  Pteridines CXX. Synthesis and Properties of Tetrahydropterins Coupled to 1,4-Dihydropyridines

  摘要：

  N(2)-Isobutyroyl-5,6,7,8-tetrahydropterins (6-10) have been coupled with nicotinic acid to form the N(5)-nicotinoyl derivatives 11-15. Quaternization at the pyridine moiety led to 19-31 which can be reduced to the corresponding N-substituted 1,4-dihydropyridine dertivatives 35-39. Partial deacylation of the isobutyroyl group afforded the various types of terahydropterins 16-18, 32-34 and 40-42. The newly synthesized 5,6,7,8-tetrahydropterin derivatives have been characterized by pK(a)-determinations, UV- and NMR-spectra as well as elemental analyses.

  DOI：

  10.3987/com-08-s(f)70
• 作为产物：
  描述：

  N2-isobutyroyl-6-isobutyroyloxymethy1-5-(1-benzyInicotinoylium)-5,6,7,8-tetrahydropterin bromide 在 sodium dithionite 、 碳酸氢钠 作用下， 以 水 为溶剂， 反应 1.0h， 以42%的产率得到N2-isobutyroyl-6-isobutyroyloxymethyl-5-(1-benzyl-1,4-dihydronicotinoyl)-5,6,7,8-tetrahydropterin
  参考文献：
  名称：

  Pteridines CXX. Synthesis and Properties of Tetrahydropterins Coupled to 1,4-Dihydropyridines

  摘要：

  N(2)-Isobutyroyl-5,6,7,8-tetrahydropterins (6-10) have been coupled with nicotinic acid to form the N(5)-nicotinoyl derivatives 11-15. Quaternization at the pyridine moiety led to 19-31 which can be reduced to the corresponding N-substituted 1,4-dihydropyridine dertivatives 35-39. Partial deacylation of the isobutyroyl group afforded the various types of terahydropterins 16-18, 32-34 and 40-42. The newly synthesized 5,6,7,8-tetrahydropterin derivatives have been characterized by pK(a)-determinations, UV- and NMR-spectra as well as elemental analyses.

  DOI：

  10.3987/com-08-s(f)70