(3S,4S,5R)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-4-phenylmethoxythiolan-3-ol | 174833-54-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (3S,4S,5R)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-4-phenylmethoxythiolan-3-ol
• CAS: 174833-54-6
• 化学式: C₂₈H₃₄O₃SSi
• 分子量: 478.728
• InChiKey: UROOASPFQXQQKZ-PFBJBMPXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.62
• 重原子数：
  33
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  64
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (3S,4S,5R)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-4-phenylmethoxythiolan-3-ol 在 吡啶 、 4-二甲氨基吡啶 、 二乙胺基三氟化硫 、 sodium methylate 、 三氯化硼 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 8.17h， 生成 (+)-(3S,4S,5R)-5-(tert-butyldiphenylsilanyloxymethyl)-4-fluorotetrahydrothien-3-ol
  参考文献：
  名称：

  Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives

  摘要：

  Novel iso-D-2',3'-dideoxythianucleoside derivatives 1-4 were designed and asymmetrically synthesized as a bioisostere of lamivudine to search for new anti-HIV agents. The information about using sulfur participation occurred on DAST fluorination and Mitsunobu reaction will be of great help in synthesizing sulfur-containing compounds. Final compounds 1-4 were evaluated against HIV-1 and 2, HSV-1 and 2, EMCV, Cox. B3, VSV, FluA (Taiwan), FluA (Johan.), FCV, and FIR Only cytosine analogue 3 showed a potent anti-VSV activity (EC50 = 9.43 mu g/mL). This result implies that iso-2',3'-dideoxy sugar templates might play a role of a sugar surrogate of nucleosides for the development of anti-RNA virus agent. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.09.066
• 作为产物：
  描述：

  5-(hydroxymethyl)-4-phenylmethoxythiolan-3-ol 以71的产率得到(3S,4S,5R)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-4-phenylmethoxythiolan-3-ol
  参考文献：
  名称：

  1-(2-deoxy-2-fluoro-4-thio-beta-D-arabinofuranosyl)cytosine

  摘要：

  本发明涉及具有优异的抗肿瘤活性的1-(2-脱氧-2-氟-4-硫-β-D-阿拉伯呋喃糖基)胞嘧啶，其化学式为[I]：##STR1##其中R表示氢原子或磷酸残基，以及其制备和使用的方法。

  公开号：

  US06147058A1

文献信息

• A Novel Synthesis of 2‘-Modified 2‘-Deoxy-4‘-thiocytidines from <scp>d</scp>-Glucose¹
  作者：Yuichi Yoshimura、Kenji Kitano、Kohei Yamada、Hiroshi Satoh、Mikari Watanabe、Shinji Miura、Shinji Sakata、Takuma Sasaki、Akira Matsuda

  DOI：10.1021/jo9700540

  日期：1997.5.1

  antimetabolites, specifically several 2'-modified 2'-deoxy-4'-thiocytidines, were synthesized as potential new antineoplastic agents. Methyl 3-O-benzylxylofuranoside was converted to a 1,4-anhydro-4-thioarabitol 24. Protection of the primary alcohol of 24 gave a common intermediate (15) which was useful for the synthesis of various 2'-modified 2'-deoxy-4'-thionucleosides. Oxidation of the secondary hydroxyl

  合成了新型的2'-脱氧胞苷抗代谢物，特别是几种2'-修饰的2'-脱氧-4'-硫胞苷，作为潜在的新型抗肿瘤药。将3-O-苄基木呋喃糖苷甲基转化为1,4-脱水-4-硫代阿拉伯糖醇24。保护伯醇24得到通用中间体（15），该中间体可用于合成各种2'-修饰的2'-脱氧4'-硫代核苷。氧化15个仲羟基，然后进行Wittig反应或用（二乙基氨基）三氟化硫（DAST）处理，生成2-脱氧-2-亚甲基（26）和2-脱氧-2,2-二氟（34）衍生物， 分别。相应的亚砜和三甲基甲硅烷基化的N（4）-乙酰胞嘧啶之间的唯一Pummerer型糖基化反应产生2'-deoxy-2'-亚甲基-（10）和2'-deoxy-2'，2' -二氟-4'-硫胞苷（11）。另一方面，用DAST处理15引入了一个氟原子，保留了2'-立体化学，得到40。相反，使用5步从15获得的3-O-苯甲酰基衍生物53的Mitsunobu反应二苯基磷酰
• 1-(2-deoxy-2-fluoro-4-thio-beta-D-arabinofuranosyl)cytosine
  申请人：Yamasa Corporation

  公开号：US06147058A1

  公开（公告）日：2000-11-14

  The present invention relates to 1-(2-deoxy-2-fluoro-4-thio-beta-D-arabinofuranosyl)cytosines having excellent antitumor activity, represented by formula [I]: ##STR1## wherein R represents a hydrogen atom or a phosphoric acid residue, and to a process for the production and use thereof.

  本发明涉及具有优异的抗肿瘤活性的1-(2-脱氧-2-氟-4-硫-β-D-阿拉伯呋喃糖基)胞嘧啶，其化学式为[I]：##STR1##其中R表示氢原子或磷酸残基，以及其制备和使用的方法。
• Design, Enantiopure Synthesis, and Biological Evaluation of Novel ISO-D-2′,3′-Dideoxy-3′-Fluorothianucleoside Derivatives as a bioisostere of Lamivudine
  作者：Kyung Ran Kim、Ah-Young Park、Hyung Ryong Moon、Moon Woo Chun、Lak Shin Jeong

  DOI：10.1080/15257770701506426

  日期：2007.11.26

  Novel isoD-2',3'-dideoxythianucleoside derivatives 1-3 were designed and asymmetrically synthesized to search for new anti-HIV agents. Final compounds 1-3 were evaluated against a variety of viruses including HIV-1 and 2. Only cytosine analog 3 showed a potent anti-VSV activity (EC50 = 9.43 mu g/mL). This result implies that iso 2',3'-dideoxy sugar templates might play a role of a sugar surrogate of nucleosides for the development of anti-RNA virus agent.
• Synthesis of Novel Iso-4‘-thionucleosides Using the Mitsunobu Reaction
  作者：Kohei Yamada、Shinji Sakata、Yuichi Yoshimura

  DOI：10.1021/jo980667s

  日期：1998.10.1

  A novel class of isomeric 4'-thionucleosides with the base moiety at the 2'-position was synthesized from D-glucose. The coupling of 1,4-anhydro-4-thioarabitol (13) with various nucleobases using the Mitsunobu reaction was investigated. With both purines and N-3-benzoyluracils, the reaction predominantly gave beta-isomers, suggesting that these were produced via an episulfonium intermediate. The beta-anomers produced by the reaction of N-3-benzoyluracils included both N- and O-alkylated derivatives. Interestingly, only the reaction of N-3-benzoyluracil gave a mixture of N-alkylated adduct (20d) and O-alkylated bipyrimidinyl adduct (22), the structure of which was unambiguously determined by NMR spectroscopic data including HMBC and NOE. Deprotection of the Mitsunobu reaction products gave the desired iso-4'-thionucleosides.
• Synthetic Studies on 2′-Substituted-4′-thiocytidine Derivatives as Antineoplastic Agents
  作者：Yuichi Yoshimura、Mikari Endo、Kenji Kitano、Kohei Yamada、Shinji Sakata、Shinji Miura、Haruhiko Machida

  DOI：10.1080/15257779908041569

  日期：1999.4

  As potential antineoplastic agents, we have synthesized 4'-thioFAC and 4'-thiocytarazid by developing an alternative synthetic method. 4'-ThioFAC showed potent antineoplastic activities in vivo as well as in vitro.