3-Phenyl-4-propionylpyrrole | 131911-07-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 3-Phenyl-4-propionylpyrrole
• 英文别名: 1-(4-phenyl-1H-pyrrol-3-yl)propan-1-one
• CAS: 131911-07-4
• 化学式: C₁₃H₁₃NO
• 分子量: 199.252
• InChiKey: UNAZFNPBGGRDBE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.27
• 重原子数：
  15.0
• 可旋转键数：
  3.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  32.86
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  3-Phenyl-4-propionylpyrrole 在 sodium ethanolate 、 potassium carbonate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 2.5h， 生成 ethyl 4-(1-(4-fluorobenzyl)-4-phenyl-1H-pyrrol-3-yl)-2-hydroxy-3-methyl-4-oxobut-2-enoate
  参考文献：
  名称：

  Structure–Activity Relationship of Pyrrolyl Diketo Acid Derivatives as Dual Inhibitors of HIV-1 Integrase and Reverse Transcriptase Ribonuclease H Domain

  摘要：

  The development of HIV-1 dual inhibitors is a highly innovative approach aimed at reducing drug toxic side effects as well as therapeutic costs. HIV-1 integrase (IN) and reverse transcriptase-associated ribonuclease H (RNase H) are both selective targets for HIV-1 chemotherapy, and the identification of dual IN/RNase H inhibitors is an attractive strategy for new drug development. We newly synthesized pyrrolyl derivatives that exhibited good potency against IN and a moderate inhibition of the RNase H function of RT, confirming the possibility of developing dual HIV-1 IN/RNase H inhibitors and obtaining new information for the further development of more effective dual HIV-1 inhibitors.

  DOI：

  10.1021/jm501799k
• 作为产物：
  描述：

  cis-β-Aminovinyl-ethylketon 在 sodium ethanolate 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 2.5h， 生成 3-Phenyl-4-propionylpyrrole
  参考文献：
  名称：

  β-氨基烯酮和3-二甲基氨基丙烯醛对α-氨基衍生物的差异反应性

  摘要：

  未取代的β-氨基烯酮通过一种完善的途径与α-氨基衍生物反应，这意味着快速的氨基转移过程-1,4-加成，然后消除-并将中间体环脱水为3-官能化的吡咯。相反，使3-二甲基氨基丙烯醛进行1，2-加成，然后环化，得到最终的2-取代的吡咯。中间体的分离为每种反应提供了建议的机理。

  DOI：

  10.1039/p19900002681

文献信息

• ALBEROLA, ANGEL;ANDRES, JOSE M.;GONZALEZ, ALFONSO;PEDROSA, RAFAEL;VICENTE+, J. CHEM. SOC. PERKIN TRANS. PT 1,(1990) N0, C. 2681-2685
  作者：ALBEROLA, ANGEL、ANDRES, JOSE M.、GONZALEZ, ALFONSO、PEDROSA, RAFAEL、VICENTE+

  DOI：——

  日期：——
• Differential reactivity of β-amino enones and 3-dimethylaminoacrylaldehyde towards α-amino derivatives
  作者：Angel Alberola、José M. Andrés、Alfonso González、Rafael Pedrosa、Martina Vicente

  DOI：10.1039/p19900002681

  日期：——

  Unsubstituted β-amino enones react with α-amino derivatives by a well established route which implies a fast transamination process — 1,4-addition followed by elimination — and cyclodehydration of the intermediate to 3-functionalized pyrroles. In contrast, 3-dimethylaminoacrylaldehyde undergoes 1,2-addition followed by cyclization to give the final 2-substituted pyrroles. Isolation of the intermediates

  未取代的β-氨基烯酮通过一种完善的途径与α-氨基衍生物反应，这意味着快速的氨基转移过程-1,4-加成，然后消除-并将中间体环脱水为3-官能化的吡咯。相反，使3-二甲基氨基丙烯醛进行1，2-加成，然后环化，得到最终的2-取代的吡咯。中间体的分离为每种反应提供了建议的机理。
• Structure–Activity Relationship of Pyrrolyl Diketo Acid Derivatives as Dual Inhibitors of HIV-1 Integrase and Reverse Transcriptase Ribonuclease H Domain
  作者：Giuliana Cuzzucoli Crucitti、Mathieu Métifiot、Luca Pescatori、Antonella Messore、Valentina Noemi Madia、Giovanni Pupo、Francesco Saccoliti、Luigi Scipione、Silvano Tortorella、Francesca Esposito、Angela Corona、Marta Cadeddu、Christophe Marchand、Yves Pommier、Enzo Tramontano、Roberta Costi、Roberto Di Santo

  DOI：10.1021/jm501799k

  日期：2015.2.26

  The development of HIV-1 dual inhibitors is a highly innovative approach aimed at reducing drug toxic side effects as well as therapeutic costs. HIV-1 integrase (IN) and reverse transcriptase-associated ribonuclease H (RNase H) are both selective targets for HIV-1 chemotherapy, and the identification of dual IN/RNase H inhibitors is an attractive strategy for new drug development. We newly synthesized pyrrolyl derivatives that exhibited good potency against IN and a moderate inhibition of the RNase H function of RT, confirming the possibility of developing dual HIV-1 IN/RNase H inhibitors and obtaining new information for the further development of more effective dual HIV-1 inhibitors.