84259-92-7Relevant academic research and scientific papers
Bio-based triacetic acid lactone in the synthesis of azaheterocycles via a ring-opening transformation
Obydennov, Dmitrii L.,El-Tantawy, Asmaa I.,Sosnovskikh, Vyacheslav Ya.
, p. 8943 - 8952 (2018/06/08)
In the present article a new way of converting bio-based triacetic acid lactone (TAL) into azaheterocyclic compounds, such as 4-pyridones, pyrazoles, isoxazolines and isoxazoles, has been found. The main strategy involves the transformation of TAL into re
A novel, two-step synthesis of 4-pyridone-3-carboxamides from 2-cyano-4-pyrones
Obydennov, Dmitrii L.,Sidorova, Ekaterina S.,Usachev, Boris I.,Sosnovskikh, Vyacheslav Ya.
, p. 3085 - 3087 (2013/07/19)
Reactions of 2-cyano-6-(trifluoromethyl)-4-pyrone, 2-cyano-4-pyrone, and 2-cyano-6-methyl-4-pyrone with aliphatic and aromatic amines in ethanol at -20 C for 2-21 days gave 5-amino-3-oxopent-4-enamides in 28-78% yields, which were cyclized with DMF-DMA in toluene under ambient conditions to afford 4-pyridone-3-carboxamides in 31-70% yields.
Synthesis of 6-substituted-4-hydroxy-2-pyridinones via intramolecular ketene trapping of functionalized enamine-dioxinones
Patel, Bhavesh H.,Mason, Andrew M.,Barrett, Anthony G.M.
supporting information; scheme or table, p. 5156 - 5159 (2011/11/29)
The synthesis of various 6-substituted-4-hydroxy-2-pyridinones is reported. The functionalized keto-dioxinones were constructed via a diethylzinc mediated crossed Claisen condensation reaction and subsequent enamine formation, thermolysis, and cyclization
Reactivite de la methyl-6 hydroxy-4 pyrone-2 vis-a-vis des amines primaires : synthese de pyridones-2 N-substituees et d'hexanamides intermediaires
Castillo, Simone,Ouadahi, Hamid,Herault, Valentin
, p. 257 - 261 (2007/10/02)
In the well-documented (1-7) reaction of ammonia or primary amines with 2-pyrones leading to pyridones, the aliphatic intermediates have never been isolated, except for the reaction of 1 with aniline (8).In this work, the reaction of 4-hydroxy-6-methyl-2-pyrone 1 with various primary amines is studied.Three 5-amino-3-oxo-4-hexaneamides 3 are isolated for the first time and characterized by NMR, IR and mass spectra.The corresponding 4-hydroxy-6-methyl-2-pyridones 4 are obtained by heating intermediates 3.Direct attack of 1 by primary amines yields the same compounds 4 and finally leads to 4-alkyl (or phenyl) amino-6-methyl-2-pyridones 5.Thus, compounds of the type 5 are obtained from 4-hydroxy-6-methyl-2-pyrone 1 in for steps including three successive nucleophilic sustitutions by primary amines.
