N-(4-溴苯基)-2-甲氧基乙酰胺 | 104703-38-0

• 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: N-(4-溴苯基)-2-甲氧基乙酰胺
• 英文名称: p-bromo-α-methoxyacetanilide
• 英文别名: N-(4-bromophenyl)-2-methoxyacetamide；methoxy-acetic acid-(4-bromo-anilide)；Methoxy-essigsaeure-(4-brom-anilid)
• CAS: 104703-38-0
• 化学式: C₉H₁₀BrNO₂
• mdl: MFCD03138731
• 分子量: 244.088
• InChiKey: UWPRWZGIASZACV-UHFFFAOYSA-N

物化性质

• 熔点：
  82.5 °C
• 沸点：
  372.1±27.0 °C(Predicted)
• 密度：
  1.510±0.06 g/cm3(Predicted)
• 保留指数：
  1739

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.222
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2924299090

反应信息

• 作为产物：
  描述：

  甲氧基乙酸 在 氯化亚砜 作用下， 生成 N-(4-溴苯基)-2-甲氧基乙酰胺
  参考文献：
  名称：

  Optical Crystallographic Studies with the Polarizing Microscope. II. Identification of the Para-bromoanilides of Some Lower Aliphatic Acids¹

  摘要：

  DOI：

  10.1021/ja01278a059

文献信息

• Lincomycin Derivatives and Antimicrobial Agents Comprising the Same as Active Ingredient
  申请人：Umemura Eijirou

  公开号：US20090156512A1

  公开（公告）日：2009-06-18

  This invention provides compounds of formula (I) or its pharmacologically acceptable salt or solvate, wherein A represents aryl or a monocyclic or bicyclic heterocyclic group, R 1 represents a halide, nitro, substituted C 1-6 alkyl, optionally substituted amino, C 1-6 alkyloxycarbonyl, optionally substituted aryl, a heterocyclic group, or heterocyclic carbonyl, R 2 represents a hydrogen atom or C 1-6 alkyl, R 3 represents C 1-6 alkyl, all of R 4 , R 5 , and R 6 represent a hydrogen atom, R 7 represents C 1-6 alkyl, m is 1 or 2, and n is 1. The compounds are novel lincomycin derivatives having a potent activity against resistant pneumococci. The compounds can be used as an antimicrobial agent and are useful for preventing or treating bacterial infectious diseases.

  本发明提供了式（I）的化合物或其药理学上可接受的盐或溶剂，其中A代表芳基或单环或双环杂环基，R1代表卤素、硝基、取代的C1-6烷基、可选取代的氨基、C1-6烷氧羰基、可选取代的芳基、杂环基或杂环羰基，R2代表氢原子或C1-6烷基，R3代表C1-6烷基，R4、R5和R6均代表氢原子，R7代表C1-6烷基，m为1或2，n为1。这些化合物是新型的林可霉素衍生物，对耐药性肺炎球菌具有强大的活性。这些化合物可以用作抗微生物剂，并且对于预防或治疗细菌感染性疾病是有用的。
• LINCOMYCIN DERIVATIVE AND ANTIBACTERIAL AGENT CONTAINING THE SAME AS ACTIVE INGREDIENT
  申请人：Meiji Seika Kaisha, Ltd.

  公开号：EP1970377A1

  公开（公告）日：2008-09-17

  This invention provides compounds of formula (I) or its pharmacologically acceptable salt or solvate, wherein A represents aryl or a monocyclic or bicyclic heterocyclic group, R1 represents a halide, nitro, substituted C1-6 alkyl, optionally substituted amino, C1-6 alkyloxycarbonyl, optionally substituted aryl, a heterocyclic group, or heterocyclic carbonyl, R2 represents a hydrogen atom or C1-6 alkyl, R3 represents C1-6 alkyl, all of R4, R5, and R6 represent a hydrogen atom, R7 represents C1-6 alkyl, m is 1 or 2, and n is 1. The compounds are novel lincomycin derivatives having a potent activity against resistant pneumococci. The compounds can be used as an antimicrobial agent and are useful for preventing or treating bacterial infectious diseases.

  本发明提供了式(I)化合物或其药理学上可接受的盐或溶液，其中 A 代表芳基或单环或双环杂环基团，R1 代表卤化物、硝基、取代的 C1-6 烷基、任选取代的氨基、任选取代的 C1-6 烷氧羰基、任选取代的芳基、杂环基团或杂环羰基，R2 代表氢原子或 C1-6 烷基，R3 代表 C1-6 烷基，R4 代表 C1-6 烷基，R5 代表 C1-6 烷基、C1-6烷氧基羰基、任选取代的芳基、杂环基团或杂环羰基，R2代表氢原子或C1-6烷基，R3代表C1-6烷基，所有R4、R5和R6代表氢原子，R7代表C1-6烷基，m为1或2，n为1。这些化合物是新型的林可霉素衍生物，对耐药性肺炎球菌具有强效活性。这些化合物可用作抗菌剂，用于预防或治疗细菌性传染病。
• 5-PHENYLAZAINDOLE DERIVATIVE HAVING AMPK ACTIVATING EFFECT
  申请人：Shionogi & Co., Ltd

  公开号：EP3421467A1

  公开（公告）日：2019-01-02

  Provided is a compound which is useful as an AMPK activator. A compound represented by formula: wherein X is substituted or unsubstituted monocyclic heterocyclyl or the like; ring A is substituted aryl, substituted heteroaryl, substituted cycloalkyl, substituted cycloalkenyl, or substituted heterocyclyl, wherein the ring A may further have a substituent(s) other than Y; Y is halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl or the like; R4, R5, R6 and R7 are each independently hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylthio, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted acyl, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, or substituted or unsubstituted amino; R8 is hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl or the like; and R9 is hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl or the like, or its pharmaceutically acceptable salt.

  本文提供了一种可用作 AMPK 激活剂的化合物。一种由式表示的化合物： 其中 X 是取代或未取代的单环杂环基或类似物； 环 A 是取代的芳基、取代的杂芳基、取代的环烷基、取代的环烯基或取代的杂环烯基，其中环 A 可进一步具有除 Y 以外的取代基； Y 是卤素、羟基、氰基、硝基、羧基、取代或未取代的烷基、取代或未取代的烯基、取代或未取代的炔基或类似物； R4、R5、R6 和 R7 各自独立地是氢、卤素、羟基、氰基、硝基、羧基、取代或未取代的烷基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的烷氧基、取代或未取代的烷硫基、取代或未取代的烷磺酰基、取代或未取代的酰基、取代或未取代的氨基甲酰基、取代或未取代的氨基磺酰基或取代或未取代的氨基； R8 是氢、卤素、羟基、氰基、硝基、羧基、取代或未取代的烷基、取代或未 取代的烯基、取代或未取代的炔基或类似物；以及 R9 是氢、卤素、羟基、氰基、硝基、羧基、取代或未取代的烷基、取代或未取代的烯基、取代或未取代的炔基或类似物、 或其药学上可接受的盐。
• EP3421467
  申请人：——

  公开号：——

  公开（公告）日：——
• Nicholas, Kumudini U. K. Gamage; Vaughan, Keith, Canadian Journal of Chemistry, 1986, vol. 64, p. 799 - 802
  作者：Nicholas, Kumudini U. K. Gamage、Vaughan, Keith

  DOI：——

  日期：——