Journals / Hacettepe Journal of Biology and Chemistry / 2015 / Cilt: 43 - Sayı: 2

Efficient and Green Synthesis of Mono- and Disubstituted 2,3-Dihydroquinazolin-4 1H -Ones Using Squaric Acid as a New Organocatalyst in Water

Yeni Sulu Organokatalizör Skuarik Asit Varlığında Mono ve Disübstitüye 2,3-Dihidroksikuinazolin- 4 1H -Ones’un Etkin ve

Pages
127–132
Publication Date
2015-06-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

These catalytic condensation reactions represent green chemical processes and the squaric acid organocatalyst is air-stable, cost-effective, easy to handle, and easily removed from the reaction.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Asimple and facile synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4 1H -one derivatives has been successfully developed by treatment of aldehydes, ammonium acetate, and isatoic anhydride under reflux conditions in the presence of a squaric acid organocatalyst.
📊
Key Findings & Data:Asimple and facile synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4 1H -one derivatives has been successfully developed by treatment of aldehydes, ammonium acetate, and isatoic anhydride under reflux conditions in the presence of a squaric acid organocatalyst.
💡
Conclusion & Impact:These catalytic condensation reactions represent green chemical processes and the squaric acid organocatalyst is air-stable, cost-effective, easy to handle, and easily removed from the reaction.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Yeşil kimya · organokatalitik · skuarik asit

Abstract

Asimple and facile synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4 1H -one derivatives has been successfully developed by treatment of aldehydes, ammonium acetate, and isatoic anhydride under reflux conditions in the presence of a squaric acid organocatalyst. These catalytic condensation reactions represent green chemical processes and the squaric acid organocatalyst is air-stable, cost-effective, easy to handle, and easily removed from the reaction.

Özet

A ldehitler, amonyum asetat ve izotaktik anhidrit muameleleriyle skuarik asit organokatalizörü varlığında geri soğutucu altında, mono ve disübstitiye 2,3-dihidrokinazolin -4 1H türevlerinin sentezi başarılı bir şekilde gerçekleştirilmiştir. Bu katalitik yoğuşma tepkimeleri yeşil kimya süreçlerini kapsamaktadır. Skuarik asit organokatalizörü havada kararlı, uygun maliyetli ve kullanımı kolaydır. Ayrıca tepkime ortamından kolaylıkla uzaklaştırılabilir

🔖

Cite This Article

KHAKSAR, S., ARSHADİ, S., GHANBARİ, F. (2015). Efficient and Green Synthesis of Mono- and Disubstituted 2,3-Dihydroquinazolin-4 1H -Ones Using Squaric Acid as a New Organocatalyst in Water. Hacettepe Journal of Biology and Chemistry, Cilt: 43 - Sayı: 2, 127–132. https://ajindex.com/articles/255896

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Y.S. Sadanadam, R.M. Reddy, A. Bhaskar, Eur. J. Med. Chem., 169 (1987) 22. G. Bonola, E. Sianesi, J. Med. Chem., 329 (1970) 13. M.L. Hour, L. Huang, S. Kuo, Y. Xia, K. Bastow, Y. Nakanishi, E. Hamel, K. Lee, J. Med. Chem., 4479 (2000) 43. S. H. Lee, S. Y. Jung, H. A. Park, H. B. Kang, J. Kim, D. J. Choo, A. Handforth, J. Y. Lee, Bull. Korean. Chem. Soc., 2451 (2010) 31. P. A. Ple, T. P.Green, L. F. Hennequin, J. Curwen, M. Fennell, J. Allen, Brempt, C. L. Costello, G. J. Med. Chem., 871 (2004) 47. H. N. Seo, J. Y. Choi, Y. J. Choe, Y. Kim, H. Rhim, S. H. Lee, J. Kim, D. J. Joo and J. Y. Lee, Bioorg. Med. Chem. Lett., 5740 (2007) 17. 7. M. Baghbanzadeh, P. Salehi, M. Dabiri, G. Kozehgarya, Synthesis, (2006) 344. Kozehgarya, A. A. Mohammadi, Tetrahedron Lett., 6123 (2005) 46. P. Salehi, M. Dabiri, M. Baghbanzadeh, M. Bahramnejad, Synth.Commun., 2287 (2006) 36. J. X. Chen, W. K. Su, H. Y. Wu, M. C. Liu, C. Jin. Green Chem., 972 (2007) 9. J. Chen, D. Wu, F. He, M. Liu, H. Wu, J. Ding, W. Su. Tetrahedron Lett., 3814 (2008) 49. P. Salehi, M. Dabiri, M. A. Zolfigol, M. Baghbanzadeh, Synlett., (2005) 1155. H. L. J. Yale, Heterocycl. Chem., 1357 (1977), 14. M. R. Mousavi, M. T. Maghsoodlou, J. Iranian. Chem. Soc., 743 (2015) 12. A. Chanda, V. V. Fokin, Chem. Rev., 725 (2009) 109. S. Minakata, M. Komatsu, Chem. Rev., 711 (2009) 109. G. V. Oshovsky, D. N. Reinhoudt, W. Verboom, Angew. Chem. Int. Ed., 2366 (2007) 46. C.J. Li, Chem. Rev., 3095 (2005) 105. V. M. Dong, D. Fiedler, B. Cari, R. G. Bergmann, K. N. Raymond, J. Am. Chem. Soc., 14464 (2006) 128. P.I. Dalko, L. Moisan, Angew. Chem. Int. Ed., 3726 (2001),40. P.I. Dalko, L. Moisan, Angew. Chem. Int. Ed., 5138 (2004),43. Ed., 1570 (2007) 46. N. Azizi, A. Davoudpour, F. Eskandari, E. Batebi, Monatsh. Chem., 405 (2013) 144. N. Azizi, E. Saki, M. Edrisi, C R Chimie., 973 (2011) 14. N. Azizi, A. Davoudpour, Catalysis Lett., 1506 (2011) 141. R. I. Storer, C. Aciroa, L. H. Jones, Chem. Soc. Rev., 40 (2011) 2330. S. Khaksar, M. Yaghoobi, J. Fluorine. Chem., 41, (2012), 142. S. Khaksar, A. Rouhollahpour, S.M. Talesh, J. Fluorine. Chem., 11 (2012) 141. S. Khaksar, M. Tajbakhsh, M. Gholami, F. Rostamnezhad, Chin.Chem.Lett., 1287 (2014) 25.