Magnesium Bromide and Magnesium Chloride Hexahydrate Catalyzed One-Pot Synthesis of Dihydropyrimidines via Biginelli Reaction under Solvent-Free Conditions
| dc.contributor.author | Gulten, Sirin | |
| dc.date.accessioned | 2025-01-27T20:17:07Z | |
| dc.date.available | 2025-01-27T20:17:07Z | |
| dc.date.issued | 2013 | |
| dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
| dc.description.abstract | Biologically important 12 new important 3,4-dihydropyrimidin-2-(1H)-ones (-thiones) were synthesized with in one-pot three-component Biginelli reaction from the corresponding aromatic aldehydes (5-methyl-2-thiophenecarboxaldehyde and 2-chloro-5-nitrobenzaldehyde), -keto esters (ethylacetoacetate, allylacetoacetate, and t-butylacetoacetate), and urea/thiourea in the presence of catalytic amount of magnesium bromide and magnesium chloride hexahydrate as nontoxic, inexpensive, and easily available catalysts under solvent-free conditions at 80 and 100 degrees C. Compared with the catalyst-free three-component Biginelli reaction conditions, this method consistently has the advantage of short reaction time (45100 min) and good to excellent yields (7591%). | |
| dc.description.sponsorship | Canakkale Onsekiz Mart University [BAP 2008/28] | |
| dc.description.sponsorship | The author thanks to Canakkale Onsekiz Mart University (BAP 2008/28) for financial support. The author also thanks to NMR Analysis Laboratory of Hacettepe University for recording NMR spectra and Central Laboratory of Pharmacy, Ankara University, for the measurement of the mass spectra and elemental microanalyses. | |
| dc.identifier.doi | 10.1002/jhet.980 | |
| dc.identifier.endpage | 395 | |
| dc.identifier.issn | 0022-152X | |
| dc.identifier.issn | 1943-5193 | |
| dc.identifier.issue | 2 | |
| dc.identifier.scopus | 2-s2.0-84876938396 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.startpage | 391 | |
| dc.identifier.uri | https://doi.org/10.1002/jhet.980 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12428/21493 | |
| dc.identifier.volume | 50 | |
| dc.identifier.wos | WOS:000318293000034 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Wiley | |
| dc.relation.ispartof | Journal of Heterocyclic Chemistry | |
| dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WoS_20250125 | |
| dc.subject | Calcium-Channel Blockers | |
| dc.subject | Small-Molecule Inhibitor | |
| dc.subject | Acid-Esters | |
| dc.subject | Conformational-Analysis | |
| dc.subject | Mitotic Kinesin | |
| dc.subject | Efficient | |
| dc.subject | Derivatives | |
| dc.subject | Facile | |
| dc.subject | 3,4-Dihydropyrimidin-2-(1h)-Ones | |
| dc.subject | 3-Component | |
| dc.title | Magnesium Bromide and Magnesium Chloride Hexahydrate Catalyzed One-Pot Synthesis of Dihydropyrimidines via Biginelli Reaction under Solvent-Free Conditions | |
| dc.type | Article |











