N3-benzyl 5-fluorouracil | 77384-89-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: N3-benzyl 5-fluorouracil
• 英文别名: 3-Benzyl-5-fluoropyrimidine-2,4(1H,3H)-dione；3-benzyl-5-fluoro-1H-pyrimidine-2,4-dione
• CAS: 77384-89-5
• 化学式: C₁₁H₉FN₂O₂
• 分子量: 220.203
• InChiKey: QWYRVCJZUMRTJJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  49.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  cis-2-fluoro-trans-3-(benzyloxymethyl)cyclobutyl-mesylate 、 N3-benzyl 5-fluorouracil 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 氯苯 为溶剂， 反应 24.0h， 以44.7%的产率得到N3-benzyl-5-fluoro-1-[trans-2-fluoro-cis-3-(benzyloxymethyl)cyclobutyl]uracil
  参考文献：
  名称：

  WO2006/63281

  摘要：

  公开号：
• 作为产物：
  描述：

  3-benzyl-6-chloro-5-fluoro-1H-pyrimidine-2,4-dione 在 palladium on activated charcoal sodium hydroxide 、 氢气 作用下， 以 乙醇 为溶剂， 反应 4.0h， 以87%的产率得到N3-benzyl 5-fluorouracil
  参考文献：
  名称：

  A NOVEL ROUTE TO 5-FLUOROURACILS FROM CHLOROTRIFLUOROETHENE

  摘要：

  二乙基氟代苹果酸酯是通过氯三氟乙烯和三氟丙烯酸锂盐一锅法制备的，产率为79%。二乙基氟代苹果酸酯易于转化为5-氟-6-氯尿嘧啶，随后还原可获得产率良好的5-氟尿嘧啶。

  DOI：

  10.1246/cl.1984.1573

文献信息

• Studies of antitumor-active 5-fluorouracil derivatives. I. Synthesis of N-phthalidyl 5-fluorouracil derivatives.
  作者：SUSUMU KAMATA、NOBUHIRO HAGA、TAKEAKI MATSUI、WATARU NAGATA

  DOI：10.1248/cpb.33.3160

  日期：——

  Several 5-fluorouracil derivatives in which the phthalidyl (1, 3-dihydro-3-oxoisobenzofuran-1-yl) group, appropriately substituted on its benzene ring, is substituted at the N (1)-or N (3)-position or at both positions were synthesized, and their antitumor activities were evaluated. Among these compounds, 1-(1, 3-dihydro-3-oxoisobenzofuran-1-yl)-5-fluorouracil (3a, 590-S) was shown to be markedly active against several experimental tumor systems. Several methods for a simple and efficient large-scale preparation of 3a were examined. The large-scale preparation of 3a was effected most efficiently by the condensation of 5-fluorouracil with the quaternary ammonium salt of 3-bromophthalide in the presence of a base. The synthesis of (+)- and (-)-3a is also described.

  合成了几种5-氟尿嘧啶衍生物，其中苯并二氢呋喃酮（1,3-二氢-3-氧异苯并呋喃-1-基）基团在其苯环上适当取代，并在N(1)或N(3)位或两个位置上进行取代，并评估了它们的抗肿瘤活性。在这些化合物中，1-(1,3-二氢-3-氧异苯并呋喃-1-基)-5-氟尿嘧啶（3a，590-S）显示出对几种实验性肿瘤系统有显著的活性。研究了几种简单高效的3a大规模制备方法。通过5-氟尿嘧啶与3-溴邻苯二甲酰亚胺的季铵盐在碱存在下缩合，最有效地实现了3a的大规模制备。还描述了(+)-和(-)-3a的合成。
• Application of the Benzyloxycarbonyloxymethyl Moiety to a Protective Group of 5-Fluorouracil. Selective Alkylation of Amide Nitrogen of the Uracil Ring
  作者：Toshio Nagase、Kanzo Seike、Kazuto Shiraishi、Yutaka Yamada、Shoichiro Ozaki

  DOI：10.1246/cl.1988.1381

  日期：1988.8.5

  Selective alkylation of 5-fluorouracil using the benzyloxycarbonyloxymethyl moiety as a protective group of amide nitrogen of the uracil ring is described. Protection, alkylation and deprotection were carried out in high yields.

  描述了使用苄氧羰基氧甲基部分作为尿嘧啶环的酰胺氮保护基团的 5-氟尿嘧啶的选择性烷基化。以高产率进行保护、烷基化和脱保护。
• Ozaki, Shoichiro; Watanabe, Yutaka; Fujisawa, Hiroshi, Heterocycles, 1984, vol. 22, # 3, p. 527 - 530
  作者：Ozaki, Shoichiro、Watanabe, Yutaka、Fujisawa, Hiroshi、Hoshiko, Tomonori

  DOI：——

  日期：——
• Benzhydryl as an Efficient Selective Nitrogen Protecting Group for Uracils
  作者：Fan Wu、Musole G. Buhendwa、Donald F. Weaver

  DOI：10.1021/jo0485076

  日期：2004.12.1

  Regioselective N-substitution of the less active nitrogen within uracil analogues has been achieved following preliminary N-protection at the more active N-position with a benzhydryl protecting group. This protecting group is stable to concentrated HCl (aqueous) at reflux temperature, TFA at room temperature, and Pd-C-catalyzed normal pressure hydrogenation at room temperature; the benzhydryl group can be removed quantitatively and selectively with a 10% triflic acid solution in TFA at 0 degreesC.
• OZAKI, SHOICHIRO;WATANABE, YUTAKA;FUJISAWA, HIROSHI;HOSHIKO, TOMONORI, HETEROCYCLES, 1984, 22, N 3, 527-530
  作者：OZAKI, SHOICHIRO、WATANABE, YUTAKA、FUJISAWA, HIROSHI、HOSHIKO, TOMONORI

  DOI：——

  日期：——