3-bromo-5-chloro-2-fluorotoluene | 146948-69-8

• 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: 3-bromo-5-chloro-2-fluorotoluene
• 英文别名: 1-Bromo-5-chloro-2-fluoro-3-methylbenzene
• CAS: 146948-69-8
• 化学式: C₇H₅BrClF
• 分子量: 223.472
• InChiKey: ZULRYKNSOMUWPN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-氯-6-氟甲苯 在 溴 、 铁粉 作用下， 生成 3-溴-2-氯-6-氟甲苯 、 3-bromo-5-chloro-2-fluorotoluene
  参考文献：
  名称：

  Synthesis, Structure−Activity Relationships, and Characterization of Novel Nonsteroidal and Selective Androgen Receptor Modulators

  摘要：

  Herein we describe the discovery of ACP-105 (1), a novel and potent nonsteroidal selective androgen receptor modulator (SARM) with partial agonist activity relative to the natural androgen testosterone. Compound 1 was developed from a series of compounds found in a HTS screen using the receptor selection and amplification technology (R-SAT). In vivo, 1 improved anabolic parameters in a 2-week chronic study in castrated male rats. In addition to compound 1, a number of potent antiandrogens were discovered from the same series of compounds whereof one compound, 13, had antagonist activity at the AR T877A mutant involved in prostate cancer.

  DOI：

  10.1021/jm901149c

文献信息

• Aminophenyl derivatives as selective androgen receptor modulators
  申请人：Schlienger Nathalie

  公开号：US20060160845A1

  公开（公告）日：2006-07-20

  Disclosed herein is a novel class of aminophenyl compounds having the structure: wherein R 1 is cyano or nitro and ring A is a bi- or tricyclic bridged heterocycle and to their use as modulators of androgen receptor for the treatment or prevention of conditions relating thereto.

  本文揭示了一类新颖的氨基苯基化合物，其结构为：其中R1为氰基或硝基，环A为双环或三环桥联杂环，并且它们可用作雄激素受体调节剂，用于治疗或预防相关疾病。
• [EN] 3-[(1H-PYRAZOL-4-YL)OXY]PYRAZIN-2-AMINE COMPOUNDS AS HPK1 INHIBITOR AND USE THEREOF<br/>[FR] COMPOSÉS DE 3-[(1H-PYRAZOL-4-YL)OXY]PYRAZIN-2-AMINE UTILISÉS EN TANT QU'INHIBITEUR DE HPK1 ET LEUR UTILISATION
  申请人：BEIGENE LTD

  公开号：WO2022068848A1

  公开（公告）日：2022-04-07

  Disclosed herein is 3- [ (1H-pyrazol-4-yl) oxy] pyrazin-2-amine compounds of Formula (I), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising thereof. Also disclosed is a method of modulating, e.g., inhibiting or treating HPK1 related disorders or diseases including cancer by using the compound disclosed herein

  本文揭示了化合物3-[(1H-吡唑-4-基)氧基]吡嗪-2-胺的公式(I)或其立体异构体，或其药学上可接受的盐，以及包含它们的制药组合物。还揭示了使用本文所揭示的化合物来调节，例如，抑制或治疗与HPK1相关的疾病或疾病，包括癌症的方法。
• Azoline Compounds for Combating Arthropod Pests
  申请人：Koradin Christopher

  公开号：US20100010058A1

  公开（公告）日：2010-01-14

  The present invention relates to azoline compounds and their salts which are useful for combating arthropod pests. The present invention also relates to a method for combating arthropod pests and to agricultural compositions for combating said pests. It has been found that these objectives can be achieved by azoline compounds of the general formulae Ia or Ib, wherein X is S, O or NR 4 ; Ar is phenyl or a 5 or 6 membered heteroaromatic ring; R 1 is H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, phenyl, a heteroaromatic ring etc.; R 2a , R 2b are H, CN, C 1 -C 6 -alkyl etc.; R 1 together with R 2a may also form a linear C 2 -C 4 -alkandiyl; R 3a-d are H, halogen, C 1 -C 6 -alkyl etc.

  本发明涉及用于对抗节肢动物害虫的噁唑啉化合物及其盐。本发明还涉及一种对抗节肢动物害虫的方法和用于对抗上述害虫的农业组合物。已经发现，通过通式Ia或Ib的噁唑啉化合物可以实现这些目标，其中X为S、O或NR4；Ar为苯基或5或6成员杂芳环；R1为H、C1-C6烷基、C2-C6烯基、苯基、杂芳环等；R2a、R2b为H、CN、C1-C6烷基等；R1与R2a还可以形成线性C2-C4烷二基；R3a-d为H、卤素、C1-C6烷基等。
• AMINOPHENYL DERIVATIVES AS SELECTIVE ANDROGEN RECEPTOR MODULATORS
  申请人：SCHLIENGER NATHALIE

  公开号：US20090270449A1

  公开（公告）日：2009-10-29

  Disclosed herein is a novel class of aminophenyl compounds having the structure: wherein R 1 is cyano or nitro and ring A is a bi- or tricyclic bridged heterocycle and to their use as modulators of androgen receptor for the treatment or prevention of conditions relating thereto.

  本文揭示了一种新的氨基苯基化合物类，具有以下结构：其中R1是氰基或硝基，环A是一个双环或三环的桥接杂环，并且这些化合物可用作雄激素受体调节剂，用于治疗或预防与之相关的疾病。
• Pesticidal Compositions
  申请人：Kordes Markus

  公开号：US20080312085A1

  公开（公告）日：2008-12-18

  The present invention relates to 1-(Azolin-2-yl)-amino-alkane compounds, which are useful for combating insects, arachnids and nematodes. The present invention also relates to a method for combating animal pests selected from insects, arachnids and nematodes, and to agricultural compositions for combating animal pests. It has been found that animal pests can be combated by 1-(Azolin-2-yl)-amino-alkane compounds of the general formula I: wherein A is a radical of the formulae A 1 or A 2 : and wherein X is sulfur or oxygen and W, B and R 1 to R 6 are defined as in the description.

  本发明涉及1-(Azolin-2-yl)-amino-烷基化合物，其可用于对抗昆虫、蜘蛛和线虫。本发明还涉及一种用于对抗昆虫、蜘蛛和线虫等动物害虫的方法，以及用于对抗动物害虫的农业组合物。发现可以通过通式I中的1-(Azolin-2-yl)-amino-烷基化合物对动物害虫进行对抗，其中A是式A1或A2的基团：X是硫或氧，W、B和R1至R6如描述中所定义。