Journals / Turkish Journal of Chemistry / 1999 / Cilt: 23 - Sayı: 4

Reactions of N-Aminopyrimidine Derivatives with 1,3-Dicarbonyl Compounds

Pages
401–405
Publication Date
2022-11-05
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)

The molecular structures of all the prepared compounds were determined by 1H-nmr, 13C-nmr, i.r. spectra and elemental analyses, and were drawn by taking imine-enamine tautomerism into account.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The reactions of 1-Amino-pyrimidine derivatives (1) and some 1,3-dicarbonyl compounds (2) were realized in the presence of p-toluensulfonic acid catalyst to give convenient enamine (3) and/or imine derivatives (4).
📊
Key Findings & Data:In the same way, the enamine (5) and/or imine derivatives (6) were synthesized using (1) and 1,3-indanedione which is one of the different 1,3-dicarbonyl compounds.
💡
Conclusion & Impact:The molecular structures of all the prepared compounds were determined by 1H-nmr, 13C-nmr, i.r. spectra and elemental analyses, and were drawn by taking imine-enamine tautomerism into account.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Enamine · Imine · 3-Diketone

Abstract

The reactions of 1-Amino-pyrimidine derivatives (1) and some 1,3-dicarbonyl compounds (2) were realized in the presence of p-toluensulfonic acid catalyst to give convenient enamine (3) and/or imine derivatives (4). In the same way, the enamine (5) and/or imine derivatives (6) were synthesized using (1) and 1,3-indanedione which is one of the different 1,3-dicarbonyl compounds. The molecular structures of all the prepared compounds were determined by 1H-nmr, 13C-nmr, i.r. spectra and elemental analyses, and were drawn by taking imine-enamine tautomerism into account.

Özet

The reactions of 1-Amino-pyrimidine derivatives (1) and some 1,3-dicarbonyl compounds (2) were realized in the presence of p-toluensulfonic acid catalyst to give convenient enamine (3) and/or imine derivatives (4). In the same way, the enamine (5) and/or imine derivatives (6) were synthesized using (1) and 1,3-indanedione which is one of the different 1,3-dicarbonyl compounds. The molecular structures of all the prepared compounds were determined by 1H-nmr, 13C-nmr, i.r. spectra and elemental analyses, and were drawn by taking imine-enamine tautomerism into account.

🔖

Cite This Article

ÖNAL, Z., ALTURAL, B. (2022). Reactions of N-Aminopyrimidine Derivatives with 1,3-Dicarbonyl Compounds. Turkish Journal of Chemistry, Cilt: 23 - Sayı: 4, 401–405. https://ajindex.com/articles/602471

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...