2-chloro-6-methoxy-4-nitroaniline | 41956-18-7

• 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-chloro-6-methoxy-4-nitroaniline
• 英文别名: 2-chloro-6-methoxy-4-nitro-aniline；2-Chlor-6-methoxy-4-nitro-anilin；2-Chloro-4-nitro-6-methoxyaniline
• CAS: 41956-18-7
• 化学式: C₇H₇ClN₂O₃
• mdl: MFCD18426014
• 分子量: 202.597
• InChiKey: YRAOKFMNBZXHOM-UHFFFAOYSA-N

物化性质

• 熔点：
  122-124 °C(Solv: ethanol, 95% (64-17-5))
• 沸点：
  360.5±37.0 °C(Predicted)
• 密度：
  1.452±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  81.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-chloro-6-methoxy-4-nitroaniline 在 盐酸 、 sodium nitrite 、 copper(l) chloride 作用下， 以 水 为溶剂， 以94%的产率得到2,3-Dichloro-5-nitroanisole
  参考文献：
  名称：

  Computationally-Guided Optimization of a Docking Hit to Yield Catechol Diethers as Potent Anti-HIV Agents

  摘要：

  A 5-mu M docking hit has been optimized to an extraordinarily potent (55 pM) non-nucleoside inhibitor of HIV reverse transcriptase. Use of free energy perturbation (PEP) calculations to predict relative free energies of binding aided the optimizations by identifying optimal substitution patterns for phenyl rings and a linker. The most potent resultant catechol diethers feature terminal uracil and cyanovinylphenyl groups. A halogen bond with Pro95 likely contributes to the extreme potency of compound 42. In addition, several examples are provided illustrating failures of attempted grafting of a substructure from a very active compound onto a seemingly related scaffold to improve its activity.

  DOI：

  10.1021/jm201134m
• 作为产物：
  描述：

  2-甲氧基-4-硝基苯胺 在 盐酸 、 双氧水 作用下， 生成 2-chloro-6-methoxy-4-nitroaniline
  参考文献：
  名称：

  Method for the control of cattle grubs employing a phenylene

  摘要：

  提供了一种控制寄生在反刍动物和其他温血动物身上的踵蝇幼虫的方法，该方法是向这些动物投与一定量未取代或取代的苯基双[亚硫(硫)羰基]二磷(硫)酰胺酸酯。

  公开号：

  US04137310A1

文献信息

• [EN] FUSED IMIDAZOLE COMPOUNDS<br/>[FR] COMPOSÉS D'IMIDAZOLE CONDENSÉS
  申请人：ONO PHARMACEUTICAL CO

  公开号：WO2015115673A1

  公开（公告）日：2015-08-06

  The present invention provides compounds represented by formula (I), pharmaceutically acceptable salts thereof, N-oxides thereof, solvates thereof or prodrugs thereof (wherein the characters are as defined in the description). The compounds represented by formula (I) have affinity and selectivity for the gamma-aminobutyric acid A receptor subunit alpha 5 (GABAA α5) and act as GABAA α5 negative allosteric modulators (GABAA α5 NAM), so that they are useful in the prevention and/or treatment of diseases which are related to the GABAA α5 such as Alzheimer's disease.

  本发明提供了由式(I)表示的化合物，其药学上可接受的盐，N-氧化物，溶剂合物或前药（其中字符如描述中所定义）。由式(I)表示的化合物对γ-氨基丁酸A受体亚单位α5（GABAA α5）具有亲和力和选择性，并作为GABAA α5负向变构调节剂（GABAA α5 NAM）发挥作用，因此它们在预防和/或治疗与GABAA α5相关的疾病，如阿尔茨海默病中是有用的。
• CATECHOL DIETHERS AS POTENT ANTI-HIV AGENTS
  申请人：YALE UNIVERSITY

  公开号：US20140288017A1

  公开（公告）日：2014-09-25

  The present invention is directed to novel catechol diether compounds, pharmaceutical compositions therefrom and methods for inhibiting reverse transcriptase and treating HIV infections, especially included drug resistant strains of HIV 1 and 2 and/or secondary disease states and/or conditions which occur as a consequence of HIV infection.

  本发明涉及新型儿茶酚二醚化合物、其制药组合物以及抑制反转录酶和治疗HIV感染的方法，特别包括抗药性HIV 1和2以及/或作为HIV感染后果的二级疾病状态和/或条件。
• Ink composition for the ink-jet printing process
  申请人：CIBA-GEIGY AG

  公开号：EP0159291A1

  公开（公告）日：1985-10-23

  Ink compositions for the ink jet printing process containing one or more azo dyes of the groups of yellow, magenta and cyan dyes of formulae (1) to (3) are disclosed, which are of use in the production of non-fading coloured and black-and-white images.

  本发明公开了用于喷墨打印工艺的油墨组合物，该组合物含有一种或多种式（1）至（3）的黄色、品红色和青色染料组的偶氮染料，可用于制作不褪色的彩色和黑白图像。
• Fused imidazole compounds
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：US10016439B2

  公开（公告）日：2018-07-10

  The present invention provides compounds represented by formula (I), pharmaceutically acceptable salts thereof, N-oxides thereof, solvates thereof or prodrugs thereof (wherein the characters are as defined in the description). The compounds represented by formula (I) have affinity and selectivity for the gamma-aminobutyric acid A receptor subunit alpha 5 (GABAA α5) and act as GABAA α5 negative allosteric modulators (GABAA α5 NAM), so that they are useful in the prevention and/or treatment of diseases which are related to the GABAA α5 such as Alzheimer's disease.

  本发明提供了式(I)代表的化合物、其药学上可接受的盐、其N-氧化物、其溶液剂或其原药（其中特征如描述中所定义）。式（I）代表的化合物对γ-氨基丁酸A受体亚基α5（GABAA α5）具有亲和性和选择性，可作为GABAA α5负异位调节剂（GABAA α5 NAM），因此可用于预防和/或治疗与GABAA α5相关的疾病，如阿尔茨海默病。
• Quinone Imides. XLIV. The Orientation of Groups in Addition Reactions to Substituted p-Quinonedibenzimides
  作者：Roger Adams、Harry J. Neumiller

  DOI：10.1021/ja01571a050

  日期：1957.7