[1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-acetic acid tert-butyl ester | 189069-50-9

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘧啶核苷
• 英文名称: [1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-acetic acid tert-butyl ester
• CAS: 189069-50-9
• 化学式: C₁₅H₂₂N₂O₈
• 分子量: 358.348
• InChiKey: MDASAZVGBNJCAC-UORFTKCHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.97
• 重原子数：
  25.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  151.08
• 氢给体数：
  4.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  [1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-acetic acid tert-butyl ester 在 三氟乙酸 作用下， 以 吡啶 、 二氯甲烷 为溶剂， 反应 17.0h， 生成 1-(2’,3’,5’-tri-O-acetyl-β-D-ribofuranosyl)-thymine
  参考文献：
  名称：

  Synthesis of Some Hydroxamic Acids Related to Uridine: Potential Inhibitors of Ribonucleoside Diphosphate Reductase

  摘要：

  5-(N-Hydroxy)carboxamidouridine (5) and 5-(N-hydroxy)carboxamidomethyluridine (6) have been synthesized; these hydroxamic acids incorporate a radical trap into a nucleoside structure, and are designed as potential inhibitors of ribonucleotide diphosphate reductase.

  DOI：

  10.1080/07328319708002527
• 作为产物：
  描述：

  (叔丁氧基羰基亚甲基)三苯基磷烷 、 5-羟基尿苷 以 1,4-二氧六环 为溶剂， 反应 9.0h， 以2.59 g的产率得到[1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-acetic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of Some Hydroxamic Acids Related to Uridine: Potential Inhibitors of Ribonucleoside Diphosphate Reductase

  摘要：

  5-(N-Hydroxy)carboxamidouridine (5) and 5-(N-hydroxy)carboxamidomethyluridine (6) have been synthesized; these hydroxamic acids incorporate a radical trap into a nucleoside structure, and are designed as potential inhibitors of ribonucleotide diphosphate reductase.

  DOI：

  10.1080/07328319708002527