CAS: 18037-10-0; N-(Trimethylsilyl)-2-((Trimethylsilyl)Oxy)Pyrimidin-4-Amine

该化合物是一种化学化合物,其独特的结构特征是,含有一种以三甲基硅基组物替代的基环,该化合物通常具有有机和有机硅化学的特性,包括由于三甲基硅基物组物的存在,有机溶剂的稳定性和溶性得到加强.三甲基硅基聚物还能够影响化合物的再活动性,使其在各种合成应用中有用,特别是在有机合成领域和化学反应中的保护群体中.此外,氨基亚基质组物的存在可能会给氢联结带来基本性和潜力,从而影响其在生物系统中的相互作用.

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合成工艺路线路线简述

  • 合成目标产物 N-(Trimethylsilyl)-2-[(Trimethylsilyl)Oxy]Pyrimidin-4-Amine 主要起始原料 Cytosine And Hexamethyldisilazane
  • (文献来源)合成步骤主要原料 Cytosine 和 Hexamethyldisilazane
📜胞嘧啶 反应生成N-(三甲基硅基)-2-(三甲基硅氧基)-4-嘧啶胺
参考文献:J. Org. Chem. 1988,53,4786-4789
标题:J. Org. Chem. 1988,53,4786-4789

专利信息


专利号:US-2007042987-A1
优先权日:2004-07-30
标题:Stereoselective synthesis of beta-nucleosides
发明人:LIN KO-CHUNG; LI WENSEN; LIN CHUNHUI; YUNGSHUN WEIN; KUO-HIS KAO
权利人:LIN KO-CHUNG; LI WENSEN; LIN CHUNHUI; YUNGSHUN WEIN; KUO-HIS KAO
摘要:This invention relates to a process of stereoselectively synthesizing an alcohol of the following formula: n n nwherein R 1 , R 2 , R 3 , R 4 , and R 5 are defined in the specification. The process includes reacting (R) 4-formyl-2,2-dimethyldioxolane with α-bromoacetate in the presence of Zn and a Zn activating agent.

专利号:US-7485716-B2
优先权日:2005-05-02
标题:Stereoselective synthesis of β-nucleosides
发明人:LIN KO-CHUNG; LI WENSEN
权利人:PHARMAESSENTIA CORP
摘要:This invention relates to a process for stereoselectively preparing a nucleoside of the following formula: n nwherein R 3 , R 4 , and B are defined herein. The process includes reacting a furanose compound with a nucleobase in the presence of a halide salt. Also disclosed is another process for stereoselectively synthesizing an intermediate that can be used to make the starting compound in the first-mentioned process.

专利号:US-8193339-B2
优先权日:2007-11-06
标 题 :Synthesis of β-nucleosides
发明人:CHU CHI-YUAN; LEE WEI-DER; LI WENSEN; HWANG CHAN KOU
权利人:CHU CHI-YUAN; LEE WEI-DER; LI WENSEN; HWANG CHAN KOU; PHARMAESSENTIA CORP
摘要:This invention relates to a process of stereoselectively synthesizing a β-nucleoside compound of formula (I): n nwherein R 1 , R 2 , and B are as defined in the specification; each of R 3 and R 4 , independently, is H or fluoro. The process includes reacting, in the presence of a transition metal salt, a tetrahydrofuran compound of formula (II):n n nwherein R 1 , R 2 , and L are as defined in the specification, with a nucleobase derivative; and each of R 3 and R 4 , independently, is H or fluoro.

专利号:US-9790252-B2
优先权日:2009-07-01
标 题 :2-fluorinated riboses and arabinoses and methods of use and synthesis
发明人:SAUVE ANTHONY A; CEN YANA
权利人:SAUVE ANTHONY A; CEN YANA; UNIV CORNELL
摘要:Disclosed are halogenated 2-deoxy-lactone, 2′-deoxy-nucleosides, and derivatives thereof, for example, a compound of formula (I). Also disclosed are a composition comprising a pharmaceutically acceptable carrier and at least one compound or salt of the invention, and a method of treating a disorder is selected from the group consisting of an abnormal cellular proliferation, a viral infection, and an autoimmune disorder.

专利号:US-2007015914-A1
优先权日:2005-05-02
标 题:Stereoselective synthesis of beta-nucleosides

专利号:WO-2009061894-A1
优先权日:2007-11-06
标 题 :Novel synthesis of beta-nucleosides

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✅ COA系统入驻 | 共享模式

合成参考文献


摘要:Yamada, H., Science of Synthesis, (2007) 30, 47.
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