A greener, efficient approach to Michael addition of barbituric acid to nitroalkene in aqueous diethylamine medium. 2014

Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
Department of Chemistry, College of Science, King Saud University, P. O. Box 2455, Riyadh 11451, Saudi Arabia. hany_33@hotmail.com.

An efficient method for the synthesis of a variety of pyrimidine derivatives 3a-t by reaction of barbituric acids 1a,b as Michael donor with nitroalkenes 2a-k as Michael acceptor using an aqueous medium and diethylamine is described. This 1,4-addition strategy offers several advantages, such as using an economic and environmentally benign reaction media, high yields, versatility, and shorter reaction times. The synthesized compounds were identified by 1H-NMR, 13C-NMR, CHN, IR, and MS. The structure of compound 3a was further confirmed by single crystal X-ray structure determination.

UI MeSH Term Description Entries
D009574 Nitro Compounds Compounds having the nitro group, -NO2, attached to carbon. When attached to nitrogen they are nitramines and attached to oxygen they are NITRATES. Nitrated Compounds
D004048 Diethylamines Diethylamine with the formula CH3CH2NHCH2CH3 and its derivatives.
D001463 Barbiturates A class of chemicals derived from barbituric acid or thiobarbituric acid. Many of these are GABA MODULATORS used as HYPNOTICS AND SEDATIVES, as ANESTHETICS, or as ANTICONVULSANTS.
D012997 Solvents Liquids that dissolve other substances (solutes), generally solids, without any change in chemical composition, as, water containing sugar. (Grant & Hackh's Chemical Dictionary, 5th ed) Solvent
D014867 Water A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Hydrogen Oxide
D055772 Green Chemistry Technology Pollution prevention through the design of effective chemical products that have low or no toxicity and use of chemical processes that reduce or eliminate the use and generation of hazardous substances. Environmentally Friendly Chemical Techniques,Environmentally Friendly Chemical Technology,Environmentally Friendly Chemistry Technology,Green Chemical Techniques,Sustainable Chemistry Technology,Chemical Technique, Green,Chemical Techniques, Green,Chemistry Technologies, Green,Chemistry Technologies, Sustainable,Chemistry Technology, Green,Chemistry Technology, Sustainable,Green Chemical Technique,Green Chemistry Technologies,Sustainable Chemistry Technologies,Technique, Green Chemical,Techniques, Green Chemical,Technologies, Green Chemistry,Technologies, Sustainable Chemistry,Technology, Green Chemistry,Technology, Sustainable Chemistry
D060326 Chemistry Techniques, Synthetic Methods used for the chemical synthesis of compounds. Included under this heading are laboratory methods used to synthesize a variety of chemicals and drugs. Inorganic Synthesis,Inorganic Synthesis Methods,Inorganic Synthesis Techniques,Methods of Inorganic Synthesis,Methods of Organic Synthesis,Methods of Peptide Synthesis,Organic Synthesis,Organic Synthesis Methods,Organic Synthesis Techniques,Peptide Synthesis Methods,Peptide Synthesis Techniques,Peptide Synthesis, Synthetic,Synthetic Chemistry Techniques,Synthetic Peptide Synthesis,Chemistry Technique, Synthetic,Inorganic Syntheses,Inorganic Synthesis Method,Inorganic Synthesis Technique,Method, Inorganic Synthesis,Method, Organic Synthesis,Method, Peptide Synthesis,Methods, Inorganic Synthesis,Methods, Organic Synthesis,Methods, Peptide Synthesis,Organic Syntheses,Organic Synthesis Technique,Peptide Syntheses, Synthetic,Peptide Synthesis Method,Peptide Synthesis Technique,Syntheses, Inorganic,Syntheses, Organic,Syntheses, Synthetic Peptide,Synthesis Method, Inorganic,Synthesis Method, Peptide,Synthesis Methods, Inorganic,Synthesis Methods, Peptide,Synthesis Technique, Inorganic,Synthesis Technique, Organic,Synthesis Technique, Peptide,Synthesis Techniques, Inorganic,Synthesis Techniques, Organic,Synthesis Techniques, Peptide,Synthesis, Inorganic,Synthesis, Organic,Synthesis, Synthetic Peptide,Synthetic Chemistry Technique,Synthetic Peptide Syntheses,Technique, Inorganic Synthesis,Technique, Organic Synthesis,Technique, Peptide Synthesis,Technique, Synthetic Chemistry,Techniques, Inorganic Synthesis,Techniques, Organic Synthesis,Techniques, Peptide Synthesis,Techniques, Synthetic Chemistry

Related Publications

Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
January 1947, The Journal of organic chemistry,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
April 2021, The Journal of organic chemistry,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
April 2022, Molecules (Basel, Switzerland),
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
April 2012, Organic & biomolecular chemistry,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
February 2024, Organic & biomolecular chemistry,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
November 2013, Organic & biomolecular chemistry,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
January 2007, Angewandte Chemie (International ed. in English),
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
July 2023, Organic letters,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
February 2006, Journal of biotechnology,
Hany J Al-Najjar, and Assem Barakat, and Abdullah M Al-Majid, and Yahia N Mabkhot, and Manuel Weber, and Hazem A Ghabbour, and Hoong-Kun Fun
January 2018, Beilstein journal of organic chemistry,
Copied contents to your clipboard!