N-phenyl-valeramidine

• 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-phenyl-valeramidine
• 英文别名: N-Phenyl-valeramidin；N'-phenylpentanimidamide
• 化学式: C₁₁H₁₆N₂
• 分子量: 176.261
• InChiKey: DVQQBEFYLKMVCJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  38.4
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  对甲苯磺酰叠氮 、 N-phenyl-valeramidine 、 N-(p-tolyl)propiolamide 在 copper(I) bromide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以71%的产率得到(Z)-3-amino-2-((Z)-N-phenyl-N'-tosylcarbamimidoyl)-N-(p-tolyl)hept-2-enamide
  参考文献：
  名称：

  Construction of Multifunctional 3-Amino-2-carbamimidoylacrylamides and Their Crystalline Channel-Type Inclusion Complexes

  摘要：

  3-Amino-2-carbarmimidoylacrylamides were efficiently prepared via a copper(I)-catalyzed three-component reaction of sulfonylaides, propriolamides, and amidines. The synthesized compounds provided three kinds of crystalline structures based on the position of halogen. Two of them presented channel-type inclusion complexes with ethyl acetate through intermolecular hydrogen bonding, intermolecular C-H center dot center dot center dot pi and pi-pi interactions, and van der Waals forces.

  DOI：

  10.1021/acs.joc.5b00827
• 作为产物：
  描述：

  戊腈 、 苯胺 在 aluminum (III) chloride 作用下， 反应 0.5h， 生成 N-phenyl-valeramidine
  参考文献：
  名称：

  铜催化的β-炔基-N-磺酰基酮丁胺中间体的3-氨基吡唑和4-氨基嘧啶的三组分合成

  摘要：

  通过丁二炔，磺酰叠氮化物，酰肼或酰亚胺酰胺的铜催化三组分反应，可以有效地制备3-氨基吡唑和4-亚氨基嘧啶。通过形成β-炔基-N-磺酰基酮亚胺中间体在区域上选择性地进行反应，该中间体代表有机合成中新的和有效的1，3-二亲电子等效物。

  DOI：

  10.1021/ol502302w

文献信息

• Charlton et al., Journal of the Chemical Society, 1951, p. 485,489, 492
  作者：Charlton et al.

  DOI：——

  日期：——
• A New Regioselective Synthesis of 1,2,5-Trisubstituted 1<i>H</i>-Imidazoles and Its Application to the Development of Eprosartan
  作者：Susan C. Shilcrat、Mohamed K. Mokhallalati、Joseph M. D. Fortunak、Lendon N. Pridgen

  DOI：10.1021/jo971304f

  日期：1997.11.1

  A new method is presented for the preparation of 1,2-disubstitued-1H-imidazole-5-carboxaldehydes by the reaction of N-monosubstituted amidines with 2-halo-3-alkoxy-2-propenals. The reaction is highly regioselective with ratios of 1,2,5:1,2,4-imidazolecarboxaldehydes ranging from 85:15 to 100: 0. This methodology could be extended with similar results to the synthesis of imidazole-g-nitriles by the reaction of 2-bromo-3-methoxy-2-propenenitrile with N-monosubstituted amidines.
• Construction of Multifunctional 3-Amino-2-carbamimidoylacrylamides and Their Crystalline Channel-Type Inclusion Complexes
  作者：Jinjin Wang、Jiyong Liu、Hualong Ding、Jing Wang、Ping Lu、Yanguang Wang

  DOI：10.1021/acs.joc.5b00827

  日期：2015.6.5

  3-Amino-2-carbarmimidoylacrylamides were efficiently prepared via a copper(I)-catalyzed three-component reaction of sulfonylaides, propriolamides, and amidines. The synthesized compounds provided three kinds of crystalline structures based on the position of halogen. Two of them presented channel-type inclusion complexes with ethyl acetate through intermolecular hydrogen bonding, intermolecular C-H center dot center dot center dot pi and pi-pi interactions, and van der Waals forces.
• Copper-Catalyzed Three-Component Synthesis of 3-Aminopyrazoles and 4-Iminopyrimidines via β-Alkynyl-<i>N</i>-sulfonyl Ketenimine Intermediates
  作者：Yanpeng Xing、Binyu Cheng、Jing Wang、Ping Lu、Yanguang Wang

  DOI：10.1021/ol502302w

  日期：2014.9.19

  4-iminopyrimidines were efficiently prepared via copper-catalyzed three-component reactions of butadiynes, sulfonylazides, and hydrazides or imidamides. The reactions were regioselectively approached via the formation of a β-alkynyl-N-sulfonyl ketenimine intermediate which represented a new and effective 1,3-dielectrophilic equivalent in organic synthesis.

  通过丁二炔，磺酰叠氮化物，酰肼或酰亚胺酰胺的铜催化三组分反应，可以有效地制备3-氨基吡唑和4-亚氨基嘧啶。通过形成β-炔基-N-磺酰基酮亚胺中间体在区域上选择性地进行反应，该中间体代表有机合成中新的和有效的1，3-二亲电子等效物。