N-(5-phenylpentyl)-4-(2-aminoethoxy)-3-nitrophenylacetamide | 147497-93-6

• 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: N-(5-phenylpentyl)-4-(2-aminoethoxy)-3-nitrophenylacetamide
• 英文别名: 2-[4-(2-aminoethoxy)-3-nitrophenyl]-N-(5-phenylpentyl)acetamide
• CAS: 147497-93-6
• 化学式: C₂₁H₂₇N₃O₄
• 分子量: 385.463
• InChiKey: SAPIYJFFAHPTHY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  28
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  110
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• [EN] CATALYTIC HYDROGENATION OF NITRILES TO PRODUCE CAPSAICINOID DERIVATIVES AND AMINE COMPOUNDS, AND METHODS FOR PURIFIYING AND OBTAINING THE POLYMORPHS THEREOF<br/>[FR] HYDROGENATION CATALYTIQUE DE NITRILES POUR PRODUIRE DES DERIVES CAPSAICINOIDES ET DES COMPOSES D'AMINES, ET PROCEDES DE PURIFICATION ET D'OBTENTION DE LEURS POLYMORPHES
  申请人：STIEFEL LABORATORIES

  公开号：WO2005068414A1

  公开（公告）日：2005-07-28

  Processes for preparing an amine compound by catalytically hydrogenating a precursor nitrile compound. In a particular aspect, the present hydrogenation process occurs in a dipolar organic solvent in the presence of a palladium/carbon catalyst and a strong anhydrous protic acid. In a further aspect, the preferred embodiment relates to a process for deprotecting a compound to produce an amine compound. In yet a further aspect, the preferred embodiment relates to amine products produced by the present processes. These amine products may be used for a variety of purposes.

  通过在存在钯/碳催化剂和强无水质子酸的情况下，在偶极有机溶剂中催化氢化前体腈化合物的过程。在一个特定方面，目前的氢化过程发生在一个偶极有机溶剂中，在钯/碳催化剂和强无水质子酸的存在下。在另一个方面，首选实施例涉及一种去保护化合物以产生胺化合物的过程。在另一个方面，首选实施例涉及通过目前的过程产生的胺产品。这些胺产品可以用于各种目的。
• Catalytic hydrogenation of nitriles to produce capsaicinoid derivatives and amine compounds, and methods for purifying and obtaining the polymorphs thereof
  申请人：Meckler Harold

  公开号：US20060047171A1

  公开（公告）日：2006-03-02

  Processes for preparing an amine compound by catalytically hydrogenating a precursor nitrile compound. In a particular aspect, the present hydrogenation process occurs in a dipolar organic solvent in the presence of a palladium/carbon catalyst and a strong anhydrous protic acid. In a further aspect, the preferred embodiment relates to a process for deprotecting a compound to produce an amine compound. In yet a further aspect, the preferred embodiment relates to amine products produced by the present processes. These amine products may be used for a variety of purposes.

  通过催化氢化前体腈化合物制备胺化合物的过程。在特定方面，本氢化过程发生在极性有机溶剂中，在钯/碳催化剂和强无水质子酸的存在下。在进一步方面，首选实施例涉及去保护化合物以产生胺化合物的过程。在另一个进一步方面，首选实施例涉及由本过程产生的胺产品。这些胺产品可用于各种用途。
• Novel phenylacetamide derivatives and processes for the preparation thereof
  申请人：KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

  公开号：EP0525360A2

  公开（公告）日：1993-02-03

  The present invention provides novel phenylacetamide derivatives having the following formula wherein: X is a hydrogen, halogen, hydroxy, nitro, amino, R1, NR1R2, NHR1 or OR1 wherein R1 and R2 are an optionally substituted C1 -8 alkyl, cycloalkyl or benzyl group, respectively; Y, which may be the same or different when p is greater than 1, is a hydrogen, halogen, methylenedioxy, hydroxy, trifluoromethyl, R3 or OR3 wherein R3 is an optionally substituted C1 -8 alkyl or benzyl group; n is an integer from 1 to 6; and p is an integer from 1 to 5; and pharmaceutically acceptable salts thereof which have powerful analgesic and anti-inflammatory activities. The invention also provides processes for preparing these compounds and pharmaceutical compositions containing them as an active ingredient.

  本发明提供了具有下式的新型苯乙酰胺衍生物 其中 X是氢、卤素、羟基、硝基、氨基、R1、NR1R2、NHR1或OR1，其中R1和R2分别是任选取代的C1-8烷基、环烷基或苄基；Y（当p大于1时可以相同或不同）是氢、卤素、亚甲基二氧基、羟基、三氟甲基、R3或OR3，其中R3是任选取代的C1-8烷基或苄基； n 是 1 到 6 的整数；以及 p 是 1 至 5 的整数；及其药学上可接受的盐类，具有强大的镇痛和抗炎活性。 本发明还提供了制备这些化合物的工艺以及含有这些化合物作为活性成分的药物组合物。
• CATALYTIC HYDROGENATION OF NITRILES TO PRODUCE CAPSAICINOID DERIVATIVES AND AMINE COMPOUNDS, AND METHODS FOR PURIFIYING AND OBTAINING THE POLYMORPHS THEREOF
  申请人：STIEFEL LABORATORIES, INC.

  公开号：EP1697303A1

  公开（公告）日：2006-09-06
• EP1697303A4
  申请人：——

  公开号：EP1697303A4

  公开（公告）日：2007-07-04