5-bromo-2-(2-chloro-phenoxy)-thiazole | 1354526-49-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 5-bromo-2-(2-chloro-phenoxy)-thiazole
• 英文别名: 5-Bromo-2-(2-chlorophenoxy)-1,3-thiazole
• CAS: 1354526-49-0
• 化学式: C₉H₅BrClNOS
• 分子量: 290.568
• InChiKey: IIMFRBKPYGLSLR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  50.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-chloro-N-(2-methylbut-3-yn-2-yl)benzamide 、 5-bromo-2-(2-chloro-phenoxy)-thiazole 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以59%的产率得到4-chloro-N-(4-(2-(2-chlorophenoxy)thiazol-5-yl)-2-methylbut-3-yn-2-yl)benzamide
  参考文献：
  名称：

  Synthesis and Bioactivities of NovelN-(4-(2-Aryloxythiazol-5-yl)but-3-yn-2-yl)benzamides

  摘要：

  AbstractA series of novel N‐(4‐(2‐aryloxythiazol‐5‐yl)but‐3‐yn‐2‐yl)benzamide derivatives were designed and synthesized. Their structures were identified by 1H NMR and elemental analyses. Preliminary bioassays indicated that some title compounds provided >80% control of Sclerotinia sclerotiorum at 50 µg/mL and >70% herbicidal activities against B. campestris at 100 µg/mL. Their structure‐activities relationships were also discussed.

  DOI：

  10.1002/cjoc.201200824

文献信息

• [EN] THIAZOLE COMPOUNDS USEFUL AS ACETYL-COA CARBOXYLASE (ACC) INHIBITORS<br/>[FR] COMPOSÉS THIAZOLES UTILES COMME INHIBITEURS DE L'ACÉTYL-CoA CARBOXYLASE (ACC)
  申请人：JUBILANT BIOSYS LTD

  公开号：WO2012090219A2

  公开（公告）日：2012-07-05

  The present invention provides thiazole compounds of Formula I or its pharmaceutically acceptable salts, prodrugs, solvates, N-oxide thereof; solvates of pharmaceutically acceptable salts and N-oxides; pharmaceutically acceptable salts of N-oxides, or prodrugs; or combination or mixtures thereof; (I) The present invention further provides a method for preventing or treating a condition that responds to an Acetyl-CoA Carboxylase (ACC) inhibitor by using compounds of formula (I) or ), its pharmaceutically acceptable salts, prodrugs, solvates, N-oxide thereof; solvates of pharmaceutically acceptable salts and N-oxides; pharmaceutically acceptable salts of N-oxides, or prodrugs; or combination or mixtures thereof.
• Synthesis and Bioactivities of Novel<i>N</i>-(4-(2-Aryloxythiazol-5-yl)but-3-yn-2-yl)benzamides
  作者：Youquan Zhu、Pei Liu、Danyang Wang、Jin Zhang、Jie Cheng、Yuan Ma、Xiaomao Zou、Huazheng Yang

  DOI：10.1002/cjoc.201200824

  日期：2013.2

  AbstractA series of novel N‐(4‐(2‐aryloxythiazol‐5‐yl)but‐3‐yn‐2‐yl)benzamide derivatives were designed and synthesized. Their structures were identified by 1H NMR and elemental analyses. Preliminary bioassays indicated that some title compounds provided >80% control of Sclerotinia sclerotiorum at 50 µg/mL and >70% herbicidal activities against B. campestris at 100 µg/mL. Their structure‐activities relationships were also discussed.