2-(3-benzamido-4-hydroxyphenyl) propionitrile | 51234-24-3

• 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-(3-benzamido-4-hydroxyphenyl) propionitrile
• 英文别名: 2-(3-benzamido-4-hydroxyphenyl)-propionitrile；3-Benzamido-4-hydroxyphenyl-α-methylacetonitril；Benzamide, N-[5-(1-cyanoethyl)-2-hydroxyphenyl]-；N-[5-(1-cyanoethyl)-2-hydroxyphenyl]benzamide
• CAS: 51234-24-3
• 化学式: C₁₆H₁₄N₂O₂
• 分子量: 266.299
• InChiKey: RRMMMLKTSSCJNL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  73.1
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(3-benzamido-4-hydroxyphenyl) propionitrile 以63%的产率得到
  参考文献：
  名称：

  DUNWELL D. W.; EVANS D.; HICKS T. A.; CASHIN C. H.; KITCHEN A., J. MED. CHEM. , 1975 18, NO 1, 53-58

  摘要：

  DOI：
• 作为产物：
  描述：

  2-(3-氨基-4-羟基苯基)丙腈 、 苯甲酰氯 以 吡啶 为溶剂， 反应 1.33h， 以to yield crude 2-(3-benzamido-4-hydroxyphenyl) propionitrile as an oil的产率得到2-(3-benzamido-4-hydroxyphenyl) propionitrile
  参考文献：
  名称：

  Passiflora plant named ‘Snow Queen’

  摘要：

  一种名为“雪后女王”的西番莲新品种，其特点是由白色花瓣、白色萼片和白色冠丝组成的大型完全白色花朵。 “雪后女王”的花瓣和萼片厚实而有光泽。 “雪后女王”开花量高，适应美国农业部8b区，生长旺盛，叶片浓绿且有韧性。

  公开号：

  USPP029608P3

文献信息

• Esters and amides of substituted fused ring phenyl acetic acids
  申请人：FGN, INC.

  公开号：EP0485173A3

  公开（公告）日：1993-01-27

  Esters and amides of substituted fused ring phenyl acetic acids having the formula wherein Y, together with the ring to which it is fused forms a multi-ring system selected from napthyl, [1]benzopyranol [2, 3-b], pyridine, phenothiazine, carbazole, and benzoxazole ; R1 is lower alkyl or hydrogen ;R2 is one or more independently selected from cyano, nitro, amino, alkylamino, hydrogen, halogen, lower alkyl, lower alkoxy, hydroxy, phenyl or phenyl substituted with halogen, alkyl or alkoxy ;wherein Q is the deprotonated residue of a polymer or macromolecular structure having a molecular weight of at least 1000 containing at least two primary and/or secondary amino groups and/or hydroxy groups ; andn is an integer of at least 2 are useful in treating colonic polyps.

  取代的融合环苯乙酸的酯和酰胺具有下列式其中Y与其融合的环一起形成从萘基、[1]苯并吡喃醇[2,3-b]、吡啶、苯并噻嗪、咔唑和苯并噁唑中选择的多环系统；R1是较低的烷基或氢；R2是一个或多个独立选择自氰基、硝基、氨基、烷基氨基、氢、卤素、较低烷基、较低烷氧基、羟基、苯基或被卤素、烷基或烷氧基取代的苯基；其中Q是具有分子量至少为1000的聚合物或大分子结构的去质子残基，该结构包含至少两个一次和/或二次氨基和/或羟基；n是至少为2的整数，用于治疗结肠息肉。
• Benzoxazole derivatives in treating inflammation, pain and fever
  申请人：Lilly Industries, Ltd.

  公开号：US03962441A1

  公开（公告）日：1976-06-08

  The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclising an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.

  这项发明提供了新颖的5-和6-苯并噁唑基烷酸，可选择在2-位替代，以及具有抗炎、退热和镇痛活性的衍生物。还提供了一种制备这类化合物的方法，通过使适当取代的o-氨基苯酚环化，必要时将产生的苯并噁唑转化为所需的化合物。
• Benzoxazole derivatives as therapeutics
  申请人：Lilly Industries, Ltd.

  公开号：US03962452A1

  公开（公告）日：1976-06-08

  The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclising an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.

  本发明提供了一种新型的5-和6-苯并噁唑基脂肪酸，可选地在2-位取代，并具有抗炎，退热和镇痛活性的衍生物。还提供了一种制备这种化合物的方法，通过使适当取代的o-氨基苯酚环化，必要时将产生的苯并噁唑转化为所需的化合物。
• Cyanomethyl substituted benzoxazoles
  申请人：Eli Lilly Industries Limited

  公开号：US04021440A1

  公开（公告）日：1977-05-03

  The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclizing an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.

  该发明提供了新型的5-和6-苯并噁唑基脂肪酸，可选择在2位取代，并具有抗炎，退热和镇痛活性的衍生物。还提供了一种制备这些化合物的方法，通过使适当取代的o-氨基酚环化，必要时将产生的苯并噁唑转化为所需的化合物。