Journals / Turkish Journal of Chemistry / 2021 / Cilt: 45 - Sayı: 1

4,4’-trimethylenedipiperidine as a nitrogen heterocycle solvent and/or catalyst: Liquid phase tandem Knoevenagel–Michael condensation

Pages
261–268
Publication Date
2022-11-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Another important result of this work is that the TMDP can be a promising alternative for toxic, volatile, and flammable base reagents such as piperidine and triethylamine in liquid phase organic syntheses owing to its unique properties such as being less toxic, nonflammable, and nonvolatile, and having a low melting point, broad liquid range temperature, high thermal stability, and safe handling and storage.

📌 3 Key Takeaways

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Objective & Hypothesis:Liquid phase tandem Knoevenagel–Michael condensation of various aromatic and heteroaromatic aldehydes with barbituric acid or 2-thiobarbituric acid and malononitrile was studied in a one-pot three-component reaction.
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Key Findings & Data:The reactions were carried out by using greener procedures, including a) the use of TMDP as an N-heterocycle organocatalyst in a green medium including water and ethanol (1:1 v/v) at reflux temperature, and b) the use of TMDP as a dual solvent-catalyst at 65 °C in the absence of any solvent.
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Conclusion & Impact:Another important result of this work is that the TMDP can be a promising alternative for toxic, volatile, and flammable base reagents such as piperidine and triethylamine in liquid phase organic syntheses owing to its unique properties such as being less toxic, nonflammable, and nonvolatile, and having a low melting point, broad liquid range temperature, high thermal stability, and safe handling and storage.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Liquid phase tandem Knoevenagel–Michael condensation of various aromatic and heteroaromatic aldehydes with barbituric acid or 2-thiobarbituric acid and malononitrile was studied in a one-pot three-component reaction. For the first time, TMDP was employed as a safe and efficient solvent and/or catalyst in the liquid and aqueous ethanol medium, respectively, for the practical and eco-friendly Knoevenagel–Michael condensation. The reactions were carried out by using greener procedures, including a) the use of TMDP as an N-heterocycle organocatalyst in a green medium including water and ethanol (1:1 v/v) at reflux temperature, and b) the use of TMDP as a dual solvent-catalyst at 65 °C in the absence of any solvent. High to excellent yields of the desired pyrano[2,3-d] pyrimidinones were obtained under the two earlier mentioned conditions. The current methodologies have advantages, including (a) avoiding hazardous, toxic, volatile, and flammable materials and solvents, (b) avoiding tedious processes, harsh conditions, and multiple steps for the preparation of catalysts, (c) using a less toxic and noncorrosive catalyst, (d) minimizing hazardous waste generation and simple workup process, and (e) high recyclability of TMDP. Another important result of this work is that the TMDP can be a promising alternative for toxic, volatile, and flammable base reagents such as piperidine and triethylamine in liquid phase organic syntheses owing to its unique properties such as being less toxic, nonflammable, and nonvolatile, and having a low melting point, broad liquid range temperature, high thermal stability, and safe handling and storage.

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Cite This Article

GORJIAN, H., KHALIGH, N. G., JOHAN, M. R., ZAHARANI, L. (2022). 4,4’-trimethylenedipiperidine as a nitrogen heterocycle solvent and/or catalyst: Liquid phase tandem Knoevenagel–Michael condensation. Turkish Journal of Chemistry, Cilt: 45 - Sayı: 1, 261–268. https://ajindex.com/articles/601432

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References (10)

  1. Aghahosseini H, Ramazani A, Ślepokura K, Lis T. The first protection-free synthesis of magnetic bifunctional l-proline as a highly active and versatile artificial enzyme: Synthesis of imidazole derivatives. Journal of Colloid and Interface Science 2018
  2. doi: 10.1016/j.jcis.2017.10.020 2. Aghahosseini H, Ramazani A, Jalayer NS, Ranjdoost Z, Souldozi A et al. Vinylphosphonium salt-mediated reactions: A one-pot condensation approach for the highly cis-selective synthesis of N-benzoylaziridines and the green synthesis of 1,4,2-dioxazoles as two important classes of heterocyclic compounds. Organic Letters 2019
  3. 21 (1): 22-26. doi: 10.1021/acs.orglett.8b03388 3. Ahankar H, Ramazani A, Ślepokura K, Lis T, Joo SW. Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation. Green Chemistry 2018
  4. 18 (12): 3582-3593. doi: 10.1039/C6GC00157B 4. Hamidi H, Heravi MM, Tajbakhsh M, Shiri M, Oskooie HA et al. Synthesis and anti-bacterial evaluation of novel thio- and oxazepino[7,6-b] quinolines. Journal of Iranian Chemistry Society 2015
  5. doi: 10.1007/s13738-015-0698-5 5. Ramazania A, Khoobi M, Torkaman A, Nasrabadi FZ, Forootanfar H et al. One-pot, four-component synthesis of novel cytotoxic agents 1-(5-aryl-1,3,4-oxadiazol-2-yl)-1-(1H-pyrrol-2-yl)methanamines. European Journal of Medicinal Chemistry 2014
  6. doi: 10.1016/j.ejmech.2014.03.049 6. Ali EMH, Abdel-Maksoud MS, Oh CH. Thieno[2,3-d]pyrimidine as a promising scaffold in medicinal chemistry: Recent advances. Bioorganic & Medicinal Chemistry 2019
  7. 27 (7): 1159-1194. doi: 10.1016/j.bmc.2019.02.044 7. Haggam RA, Assy MG, Mohamed EK, Mohamed AS. Synthesis of pyrano[2,3‐d]pyrimidine‐2,4‐diones and pyridino[2,3‐d] pyrimidine‐2,4,6,8‐tetraones: Evaluation antitumor activity. Journal of Heterocyclic Chemistry. 2020
  8. 57 (2): 842-850. doi: 10.1002/ jhet.3830 8. Ajmal RB, Rajendra SD, Rupali SS. Potent in vitro antibacterial and antifungal activities of pyrano[2,3-d] pyrimidine derivatives with quantitative yield. International Journal of Pharma and Bio sciences 2014
  9. 5 (1): 422-430. 9. Chabchoub F, Messaad M, Ben Mansour H, Ghdira L, Salem M. Synthesis and antigenotoxic activity of some naphto[2,1-b]pyrano[3,2-e] [1,2,4]triazolo[1,5-c]pyrimidine derivatives. European Journal of Medicinal Chemistry 2007
  10. 42 (5): 715-718. doi: 10.1016/j. ejmech.2006.12.002 10. Shamroukh AH, Zaki M