2,6-二氟-3-碘苯甲酸甲酯 | 501433-14-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2,6-二氟-3-碘苯甲酸甲酯
• 英文名称: methyl 2,6-difluoro-3-iodobenzoate
• CAS: 501433-14-3
• 化学式: C₈H₅F₂IO₂
• 分子量: 298.028
• InChiKey: GNFWWJODIGADOC-UHFFFAOYSA-N

物化性质

• 沸点：
  300.2±42.0 °C(Predicted)
• 密度：
  1.888±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2,6-二氟-3-碘苯甲酸甲酯 在 三甲基氯硅烷 、 1,2-二溴乙烷 、 N,N'-羰基二咪唑 、 lithium hydroxide 、 锌 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 6.0h， 生成 methyl 3-(3-(3-chloro-2-fluorobenzyl)-2,6-difluorophenyl)-3-oxopropanoate
  参考文献：
  名称：

  Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors

  摘要：

  A series of new 5-hydroxylquinolone-3-carboxylic acids (HQCAs) with various aryl or benzyl substituents on N-1 position were synthesized and evaluated for their anti-HIV activity in C8166 cell culture. Most of the target compounds displayed activity against wide-type HIV-1 in the low micromolar range in infected C8166 cells. The most active compound 5g exhibited activity against wild-type HIV-1 and HIV-1 mutant virus A17 with an EC50 value of 3.17 and 17.88 mu M, respectively. The biological results and the docking study revealed that the substitution pattern on N-1 position of the quinolone core might contribute to physicochemical properties of HQCAs and resulted in great influence on their antiviral potency. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.07.037
• 作为产物：
  描述：

  1,3-二氟苯 在 potassium tert-butylate 、 2,2,6,6-tetramethylpiperidinyl-lithium 、 碘 、 仲丁基锂 作用下， 以 四氢呋喃 、 正己烷 、 环己烷 为溶剂， 反应 20.0h， 生成 2,6-二氟-3-碘苯甲酸甲酯
  参考文献：
  名称：

  The Basicity Gradient-Driven Migration of Iodine: Conferring Regioflexibility on the Substitution of Fluoroarenes

  摘要：

  DOI：

  10.1002/1099-0690(200210)2002:19<3351::aid-ejoc3351>3.0.co;2-i

文献信息

• [EN] VIRAL POLYMERASE INHIBITORS<br/>[FR] INHIBITEURS DE POLYMÉRASE VIRALE
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2009076747A1

  公开（公告）日：2009-06-25

  Compounds of formula I: wherein X, R2, R3, R3a, R3b,R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

  式I的化合物：其中X，R2，R3，R3a，R3b，R5和R6在此处定义，可用作乙型肝炎病毒NS5B聚合酶的抑制剂。
• Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity
  作者：Qiu-Qin He、Shuang-Xi Gu、Jia Liu、Hai-Qiu Wu、Xuan Zhang、Liu-Meng Yang、Yong-Tang Zheng、Fen-Er Chen

  DOI：10.1016/j.bmc.2011.06.020

  日期：2011.8

  A series of new quinolone-3-carboxylic acids featuring a hydroxyl group at C-5 position were synthesized and evaluated for their in vitro activity against HIV in C8166 cell culture. All the compounds showed anti-HIV-1 activity with low micromolar to submicromolar EC(50) values. The most active compound 2k exhibited activity against wild-type HIV-1 with an EC(50) value of 0.13 mu M. Preliminary structure-activity relationship of the newly synthesized quinolone analogues was also investigated. Further docking study revealed that the anti-HIV activity of these compounds might involve a two-metal chelating mechanism. (C) 2011 Elsevier Ltd. All rights reserved.
• VIRAL POLYMERASE INHIBITORS
  申请人：Beaulieu Pierre L.

  公开号：US20110021486A1

  公开（公告）日：2011-01-27

  Compounds of formula I: wherein X, R 2 , R 3 , R 3a , R 3b , R 5 and R 6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.
• US8476257B2
  申请人：——

  公开号：US8476257B2

  公开（公告）日：2013-07-02
• US8541402B2
  申请人：——

  公开号：US8541402B2

  公开（公告）日：2013-09-24