7-Methyl-3-phenyl-5,6,7,8-tetrahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidine-2,4-dione

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并嘧啶酮衍生物
• 英文名称: 7-Methyl-3-phenyl-5,6,7,8-tetrahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidine-2,4-dione
• 英文别名: 7-methyl-3-phenyl-5,6,7,8-tetrahydro-1H-[1]benzothiolo[2,3-d]pyrimidine-2,4-dione
• 化学式: C₁₇H₁₆N₂O₂S
• 分子量: 312.392
• InChiKey: DHIOJGJKPRANAJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  77.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  7-Methyl-3-phenyl-5,6,7,8-tetrahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidine-2,4-dione 在 aluminum(III) sulfate 、 四氯化锡 、 六甲基二硅氮烷 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 16.0h， 生成 1-(2',3',5'-tri-O-Benzoyl-D-ribofuranosyl)-5,6,7,8-tetrahydro-7-methyl-3-phenylbenzothieno<2,3-d>pyrimidin-2,4(1H,3H)-dion
  参考文献：
  名称：

  Heterocyclische ?-Enaminoester. 57. Studien zur N-Glycosidierung heterokondensierter Uracile

  摘要：

  N-Glycosylations of various heterocondensed uracils of the general type 4 are described. The thieno[2,3-d]pyrimidines (9a-e) afford with 1-0-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose (7) the corresponding 1-ribosides (10a-e) in a modified Hilbert-Johnson-Birkofer synthesis; from these 10a was smoothly saponified to give the free riboside 11a. - In a more generally applicable stereospecific sodium salt glycosylation procedure employing alpha-acetobromglucose, the 1-glucosides 12-16 and with beta-(trimethylsilyl)ethoxymethyl chloride (SEM-Cl) a variation of acyclonucleosides 17-22 have been obtained. The structure of 18a has been confirmed by X-ray analysis.

  DOI：

  10.1002/prac.19943360206

文献信息

• Heterocyclische ?-Enaminoester. 57. Studien zur N-Glycosidierung heterokondensierter Uracile
  作者：H. Wamhoff、W. Wambach、S. Herrmann、M. Jansen、B. Br�hne

  DOI：10.1002/prac.19943360206

  日期：——

  N-Glycosylations of various heterocondensed uracils of the general type 4 are described. The thieno[2,3-d]pyrimidines (9a-e) afford with 1-0-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose (7) the corresponding 1-ribosides (10a-e) in a modified Hilbert-Johnson-Birkofer synthesis; from these 10a was smoothly saponified to give the free riboside 11a. - In a more generally applicable stereospecific sodium salt glycosylation procedure employing alpha-acetobromglucose, the 1-glucosides 12-16 and with beta-(trimethylsilyl)ethoxymethyl chloride (SEM-Cl) a variation of acyclonucleosides 17-22 have been obtained. The structure of 18a has been confirmed by X-ray analysis.