Enaminones in Heterocyclic Synthesis: A Novel Route to Tetrahydropyrimidines, Dihydropyridines, Triacylbenzenes and Naphthofurans under Microwave Irradiation

Molecules

Saleh Mohammed Al-Mousawi¹  Morsy Ahmed El-Apasery¹ 

[1]Department of Chemistry, Faculty of Science

[2] Kuwait University, P.O. Box 5969 Safat, 13060, Kuwait

关键词: enaminones;    Biginelli's condensation;    naphthofuran;    zeolites;    microwave irradiation with simultaneous cooling;   

DOI  :  10.3390/molecules15010058

来源: mdpi

【 摘 要 】

Condensation of phthalimidoacetone (1) with DMFDMA (N,N-Dimethylformamide dimethyl acetal) has afforded enaminone 2. Refluxing 2 with equimolecular amounts of benzaldehyde and urea in acetic acid afforded a mixture of tetrahydropyrimidine 5 and the dihydropyridine 6. Compound 2 undergoes self-condensation on heating in acetic acid or under microwave irradiation in presence of acidic zeolite to give 1,3,5-triacylbenzene 9. Reacting enaminone 11a with naphthoquinone 15 afforded the naphthofuran 18. The possible formation of the aldehyde 19 was excluded based on an HMQC experiment, which revealed that the carbonyl carbon is not linked to any hydrogen.

【 授权许可】

CC BY   
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.