2-(benzyloxy)-6-fluorobenzamide | 160564-66-9

• 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: 2-(benzyloxy)-6-fluorobenzamide
• 英文别名: 2-benzyloxy-6-fluorobenzamide；2-fluoro-6-phenylmethoxybenzamide
• CAS: 160564-66-9
• 化学式: C₁₄H₁₂FNO₂
• 分子量: 245.253
• InChiKey: WRPUGUVJZWWEJI-UHFFFAOYSA-N

物化性质

• 沸点：
  360.2±37.0 °C(Predicted)
• 密度：
  1.244±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  52.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(benzyloxy)-6-fluorobenzamide 在 sodium hydroxide 、 sodium hypochlorite 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 1.0h， 以90%的产率得到2-苄氧基-6-氟苯基胺
  参考文献：
  名称：

  [EN] N-ARYL-2-OXAZOLIDINONE-5-CARBOXAMIDES AND THEIR DERIVATIVES AND THEIR USE AS ANTIBACTERIALS
  [FR] N-ARYL-2-OXAZOLIDINONE-5-CARBOXAMIDES ET LEURS DERIVES ET UTILISATION DE CES COMPOSES COMME ANTIBACTERIENS

  摘要：

  公式为B-C-A-CO-NH-R1的化合物，其中A是结构i、ii或iii：公式(I)、(II)、(III)。C是可选择取代的芳基或杂环芳基，而B是特定的环状基团，或者C和B一起是一个杂双环基团，可用作抗菌剂。

  公开号：

  WO2003072553A1
• 作为产物：
  描述：

  2-苄氧基-6-氟苯甲腈 在 双氧水 、 potassium carbonate 作用下， 以 二甲基亚砜 为溶剂， 生成 2-(benzyloxy)-6-fluorobenzamide
  参考文献：
  名称：

  Discovering Potent Small Molecule Inhibitors of Cyclophilin A Using de Novo Drug Design Approach

  摘要：

  This work describes an integrated approach of de novo drug design, chemical synthesis, and bioassay for quick identification of a series of novel small molecule cyclophilin A (CypA) inhibitors (1-3). The activities or the two most potent CypA inhibitors (3h and 3i) are 2.59 and 1.52 nM, respectively, which are about 16 and 27 times more potent than that of cyclosporin A. This study clearly demonstrates the power of our de novo drug design strategy and the related program LigBuilder 2.0 in drug discovery.

  DOI：

  10.1021/jm9008295

文献信息

• N-aryl-2-oxazolidinone-5-carboxamides and their derivatives
  申请人：——

  公开号：US20040147760A1

  公开（公告）日：2004-07-29

  The present invention provides antibacterial agents having the formulae I, II, and III described herein.

  本发明提供了具有以下式I、II和III的抗菌剂。
• Process for preparing amines
  申请人：——

  公开号：US05410082A1

  公开（公告）日：1995-04-25

  Process for preparing amines by reacting amides in aqueous-alkaline solutions and/or suspensions with halogens or hypohalites in the presence of alcohols, and converting the reaction products into the amines by hydrolysis, hydrogenation or reductive methods.

  通过在含有醇的水性碱性溶液和/或悬浮液中与卤素或次卤酸盐反应，制备胺基化合物，然后通过水解、加氢或还原方法将反应产物转化为胺基化合物的过程。
• Diaminopyrimidinecarboxa mide derivative
  申请人：Nagashima Shinya

  公开号：US20050272753A1

  公开（公告）日：2005-12-08

  A compound which may be used for the prevention or treatment of respiratory diseases in which STAT 6 is concerned, particularly asthma, chronic obstructive pulmonary disease and the like is provided. A pyrimidine derivative or a salt thereof, which has an arylamino or arylethylamino group which may be substituted with a specified substituent, at the 2-position, amino group substituted with benzyl group or the like, at the 4-position, and carbamoyl group which may be substituted, at the 5-position, is provided.

  提供了一种可用于预防或治疗呼吸道疾病，特别是哮喘、慢性阻塞性肺病等与STAT 6有关的化合物。该化合物是一种嘧啶衍生物或其盐，其在2位具有可以被指定取代基取代的芳基氨基或芳基乙基氨基，4位具有被苄基基团或类似基团取代的氨基，5位具有可以被取代的氨基甲酰基。
• N-Aryl-2-oxazolidinone-5-carboxamides and their derivatives
  申请人：——

  公开号：US20040044052A1

  公开（公告）日：2004-03-04

  The present invention provides antibacterial agents having the formulae I, II, and III described herein.

  本发明提供了具有以下公式I、II和III的抗菌剂。
• Diaminopyrimidinecarboxamide Derivative
  申请人：Nagashima Shinya

  公开号：US20090281072A1

  公开（公告）日：2009-11-12

  A compound which may be used for the prevention or treatment of respiratory diseases in which STAT 6 is concerned, particularly asthma, chronic obstructive pulmonary disease and the like is provided. A pyrimidine derivative or a salt thereof, which has an arylamino or arylethylamino group which may be substituted with a specified substituent, at the 2-position, amino group substituted with benzyl group or the like, at the 4-position, and carbamoyl group which may be substituted, at the 5-position, is provided.

  提供了一种可用于预防或治疗呼吸系统疾病，特别是哮喘、慢性阻塞性肺疾病等与STAT 6有关的化合物。该化合物为嘧啶衍生物或其盐，其在2位具有可被取代的芳基氨基或芳基乙基氨基基团，4位具有氨基取代的苯甲基基团或类似基团，5位具有可被取代的氨基甲酰基团。