tertbutyldiphenyl(2,3,4-trifluorobenzyloxy)silane | 361345-65-5

• 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: tertbutyldiphenyl(2,3,4-trifluorobenzyloxy)silane
• 英文别名: tert-butyl-diphenyl-(2,3,4-trifluoro-benzyloxy)-silane；tert-butyldiphenyl(2,3,4-trifluorobenzyloxy)silane；tert-butyl-diphenyl-[(2,3,4-trifluorophenyl)methoxy]silane
• CAS: 361345-65-5
• 化学式: C₂₃H₂₃F₃OSi
• 分子量: 400.516
• InChiKey: YHNAHYDQLPXBHK-UHFFFAOYSA-N

物化性质

• 沸点：
  415.8±45.0 °C(Predicted)
• 密度：
  1.15±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.18
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  tertbutyldiphenyl(2,3,4-trifluorobenzyloxy)silane 在 potassium tert-butylate 、 仲丁基锂 作用下， 以 四氢呋喃 、 环己烷 为溶剂， 反应 12.33h， 生成 (6,7-difluoro-3-methyl-1,2-benzisoxazol-5-yl)methanol
  参考文献：
  名称：

  Novel DNA Gyrase Inhibiting Spiropyrimidinetriones with a Benzisoxazole Scaffold: SAR and in Vivo Characterization

  摘要：

  The compounds described herein with a spirocyclic architecture fused to a benzisoxazole ring represent a new class of antibacterial agents that operate by inhibition of DNA gyrase as corroborated in an enzyme assay and by the inhibition of precursor thymidine into DNA during cell growth. Activity resided in the configurationally lowest energy (2S,4R,4aR) diastereomer. Highly active compounds against Staphylococcus aureus had sufficiently high solubility, high plasma protein free fraction, and favorable pharmacokinetics to suggest that in vivo efficacy could be demonstrated, which was realized with compound (-)-1 in S. aureus mouse infection models. A high drug exposure NOEL on oral dosing in the rat suggested that a high therapeutic margin could be achieved. Importantly, (-)-1 was not cross-resistant with other DNA gyrase inhibitors such as fluoroquinolone and aminocoumarin antibacterials. Hence, this class shows considerable promise for the treatment of infections caused by multidrug resistant bacteria, including S. aureus.

  DOI：

  10.1021/jm501174m
• 作为产物：
  描述：

  2,3,4-三氟苯甲醇 、 叔丁基二苯基氯硅烷 在 咪唑 作用下， 以 二氯甲烷 为溶剂， 反应 17.0h， 以68.5%的产率得到tertbutyldiphenyl(2,3,4-trifluorobenzyloxy)silane
  参考文献：
  名称：

  5-Amide substituted diarylamines as mex inhibitors

  摘要：

  Diarylanines，例如式（I）或式（II）中的5-酰胺取代的二芳胺，其中A是羟基、C1-6烷氧基或NR6OR7；X是OR12、NR13R12或NR14；MEK的抑制剂，在治疗各种增殖性疾病状态方面非常有用，例如与MEK过度活跃有关的疾病，以及由MEK级联调节的疾病。

  公开号：

  US20030225076A1

文献信息

• 5-Amide substituted diarylamines as mex inhibitors
  申请人：——

  公开号：US20030225076A1

  公开（公告）日：2003-12-04

  Diarylanines, such as 5-amide substituted diarylamines of formula (I) or formula (II) wherein A is hydroxy, C 1-6 alkoxy, or NR 6 OR 7 ; X is OR 12 , NR 13 R 12 , or NR 14 ; inhibitors of MEK and are useful in the treatment of a variety of proliferative disease states, such as conditions related to the hyperactivity of MEK, as well as diseases modulated by the MEK cascade.

  Diarylanines，例如式（I）或式（II）中的5-酰胺取代的二芳胺，其中A是羟基、C1-6烷氧基或NR6OR7；X是OR12、NR13R12或NR14；MEK的抑制剂，在治疗各种增殖性疾病状态方面非常有用，例如与MEK过度活跃有关的疾病，以及由MEK级联调节的疾病。
• [EN] FUSED, SPIROCYCLIC HETEROAROMATIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS<br/>[FR] COMPOSÉS HÉTÉROAROMATIQUES SPIROCYCLIQUES FUSIONNÉS POUR TRAITER LES INFECTIONS BACTÉRIENNES
  申请人：ASTRAZENECA AB

  公开号：WO2010043893A1

  公开（公告）日：2010-04-22

  The present invention relates to compounds of Formula (I); to pharmaceutically acceptable salts thereof, to methods of using them to treat bacterial infections, and to methods for their preparation.

  本发明涉及式(I)的化合物；其药学上可接受的盐；使用它们治疗细菌感染的方法；以及它们的制备方法。
• FUSED, SPIROCYCLIC HETEROAROMATIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS
  申请人：Barvian Kevin

  公开号：US20110245224A1

  公开（公告）日：2011-10-06

  The present invention relates to compounds of Formula (I); to pharmaceutically acceptable salts thereof, to methods of using them to treat bacterial infections, and to methods for their preparation.

  本发明涉及式(I)的化合物；其药学上可接受的盐；使用它们治疗细菌感染的方法；以及它们的制备方法。
• Fused, spirocyclic heteroaromatic compounds for the treatment of bacterial infections
  申请人：Barvian Kevin

  公开号：US08658641B2

  公开（公告）日：2014-02-25

  The present invention relates to compounds of Formula (I); to pharmaceutically acceptable salts thereof, to methods of using them to treat bacterial infections, and to methods for their preparation.

  本发明涉及以下式（I）的化合物；其药学上可接受的盐；使用它们治疗细菌感染的方法；以及它们的制备方法。
• CHEMICAL COMPOUNDS 542
  申请人：ASTRAZENECA AB

  公开号：US20140128371A1

  公开（公告）日：2014-05-08

  The present invention relates to compounds of Formula (I): to pharmaceutically acceptable salts thereof, to methods of using them to treat bacterial infections, and to methods for their preparation.

  本发明涉及式（I）的化合物，其中：制备这些化合物的方法，以及将其用于治疗细菌感染的方法和其制备方法的药学上可接受的盐。