Next Article in Journal
In Vivo Anti-Tumor Activity of Polypeptide HM-3 Modified by Different Polyethylene Glycols (PEG)
Previous Article in Journal
Assessment of Acetylcholinesterase Activity Using Indoxylacetate and Comparison with the Standard Ellman’s Method

Int. J. Mol. Sci. 2011, 12(4), 2641-2649; doi:10.3390/ijms12042641

Infrared Assisted Production of 3,4-Dihydro-2(1H)-pyridones in Solvent-Free Conditions
M. Olivia Noguez 1, Vanessa Marcelino 1, Hortensia Rodríguez 2, Osnieski Martín 2, Joel O. Martínez 1, Gabriel A. Arroyo 1, Francisco J. Pérez 3, Margarita Suárez 2 and René Miranda 1,*
Departamento de Ciencias Químicas, Facultad de Estudios Superiores Cuautitlán-UNAM, Estado de México, 54754, Mexico
Laboratorio de Síntesis Orgánica, Facultad de Química, Universidad de la Habana, 10400 Ciudad Habana, Cuba
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Coyoacán, D.F., 04510, Mexico
Author to whom correspondence should be addressed; Tel.: +52-5556232056; Fax: +52-5556232024.
Received: 10 February 2011; in revised form: 14 March 2011 / Accepted: 30 March 2011 / Published: 18 April 2011


: A green approach for the synthesis of a set of ten 4-aryl substituted-5-alcoxy carbonyl-6-methyl-3,4-dihydro-2(1H)-pyridones using Meldrum’s acid has been devised, the absence of solvent and the activation with infrared irradiation in addition to a multicomponent protocol are the main reaction conditions. The transformations proceeded with moderated yields (50–75%) with a reasonable reaction rate (3 h). It is worth noting that two novel molecules of the new class of the bis-3,4-dihydropyridones were also obtained. In addition, a comparison without the use of infrared irradiation was performed.
green approach; infrared irradiation; dihydropyridones; multicomponent reaction; Meldrum’s acid

1. Introduction

One of the main objectives of green chemistry [1] is to carry out reactions using conditions which are not detrimental to the environment [2]. Following this protocol, an ideal synthesis is one in which a target molecule is produced quantitatively in one step, from readily available and inexpensive starting compounds, in an environmentally acceptable process [3]; it is important to note that multicomponent reactions must be considered as appropriate green methods [4].

On the other hand, Meldrum’s acid or 2,2-dimethyl-1,3-dioxane-4,6-dione (1), has attracted considerable attention due to its high acidity and rigid cyclic structure [5]. This versatile molecule is an important substrate in many interesting organic transformations in particular for the production of 4-aryl substituted-5-alcoxycarbonyl-6-methyl-3,4-dihydro-2(1H)-pyridones (DHPDOs). This class of compounds containing the 2(1H)-pyridone moiety are found in nature, and in some cases, useful biological properties for them have been detected [6]. Consequently, the synthesis of DHPDOs is an area of current interest due to the large number of biologically active molecules of this type [79]. In particular, two molecules of commercial interest are Amrinone [10] and Milrinone [1112]. In addition, several natural compounds with this structure have emerged during the last ten years with potent antitumor [1315], antifungal [16], antiviral [17] and psychotherapeutic effects [18], along with a new antibiotic [19]. The DHPDOs are also key intermediates in the synthesis of the corresponding pyridines [20]. The title molecules have been prepared by numerous methods [21], e.g., oxidation of N-substituted pyridinium salts [22], by means of Knoevenagel-type reactions [23] such as the cross-condensation of cyanoacetoamide and β-dicarbonyl compounds with basic catalysts or by the reaction of 2-pyrones with amides. Despite the large number of known methods for their synthesis, the importance of this class of molecules means that new procedures must always be welcomed, in particular using suitable green techniques [2426], in order to be less aggressive to the environment.

As a part of our research program, in particular by the employment of infrared irradiation as the activating mode of the reaction, we have been interested in the production of heterocyclic compounds with important pharmacological effects [2730], mainly using eco-conditions. Thus, the goal of this paper is to present a new mode for the synthesis of a set of ten 3,4-dihidro-2(1H)-pyridones (4a–j), in addition to the two novel bis-3,4-dihydro-2(1H)-pyridones (4k–l), using solvent-free conditions and for the first time the activation with infrared irradiation, for this purpose, as summarized in Schemes 12. This methodology must be considered as a green approach for the production of these classes of molecules, validating the employment of infrared irradiation as a nonclassical heating technique for many organic transformations.

2. Results and Discussion

The results of this new and ecologically sound method for the production of this series of twelve 4-aryl substituted-5-alcoxycarbonyl-6-methyl-3,4-dihydro-2(1H)-pyridones, are summarized in Table 1.

As it can be seen, a wide range of aldehydes undergo this reaction with moderate yields (50–75%) of the corresponding products. The known molecules (4a–j) (Scheme 1) were identified by correlating the corresponding physical and spectroscopic data with literature values [3136]. Moreover, this procedure must be considered as a new and simple method with an appropriately green approach, since no solvent was employed, in addition to the use of infrared irradiation to give a clean and rapid activation of this multicomponent reaction.

In addition, an appropriate comparison with the corresponding thermal reactions was also performed using a heating mantle (neat, same time and temperature); no more than 40% of substrate transformation was achieved, maybe because heat transference by the thermal method is less effective.

The molecules were structurally confirmed by NMR and MS studies. The 1H-NMR spectra of these compounds show the two proton on C-3 confirmed by a doublet of doublets at δ 4.4–4.7 corresponding to the proton on C-4 subject to the splitting by coupling with the protons C-3a,b. It is important to note that, in general, the corresponding signal of the proton C-4 appears as a doublet due to weak coupling with one of the protons C-3a, b (J3b,4 = 1.9 Hz and J3a,4 = 8.3 Hz). In this sense, the signals of the protons C-3 correspond to a doublet of doublets between δ 2.8–3.2. The 13C-NMR spectra of the title compounds show the signals of the olefinic carbons at 104 and 148 assigned to C-5 and C-6, respectively. Other characteristic signals were observed at δ ≈ 169 and δ ≈ 166 corresponding to C-2 and C-8, respectively [35].

Along with the assignment of the MS data of the compounds studied, the corresponding molecular ions M+ were observed with significant relative abundances (25–83). In addition, a series of common fragments were observed, including [M-CH3]+, [M-OCH3]+ and [M-OCH2CH3]+. Moreover, it is important to note that structures of the new bis-3,4-dihydropyridones (4k–l) (Scheme 2) were also confirmed by their high resolution mass spectrometry data.

3. Experimental Section

The aldehydes, used as substrates, are commercially available (Sigma-Aldrich Chemical Co.) and were employed without further purification. The reactions were monitored by tlc on percolated (0.25 mm) Merck silica-gel 60-F254 aluminum sheets. In general, the product visualization was done using a 254 and 365 nm UV lamp, I2 or CeSO4·H2SO4 1%. Melting points, uncorrected, were measured using a Fisher Scientific apparatus. The mass spectrometric analyses (EIMS, HRMS) were performed using a JEOL MStation JMS-700 mass spectrometer with a source temperature of 230 °C, an ionization energy of 70 eV and an ionization trap current of 300 μA. In the HRMS studies, perfluorokerosene was used as internal mass reference. The corresponding range of mass measurements was set so as to include the two standard peaks that encompassed the sample peak of interest, in addition the mass resolution and scan speed used were 30,000 (10% valley) and 60 s/decade, respectively. The accurate mass was calculated as the average of the values measured in 5–10 scans, determined from the mass centroids of the M+• ion and the other peaks. The corresponding elemental composition data was calculated within a mass window of ±10 ppm from the measured accurate mass using the program installed in the data system. Thus the elemental composition with a mass that best fitted the measured value and that made chemical sense was assigned to the ion of interest. NMR experiments were carried out using a Varian Mercury-300 at 300 MHz and 75 MHz for hydrogen and carbon respectively, the solvents used were DMSO-d6 and CDCl3; TMS was employed as the internal reference. The infrared irradiation was performed using a Phillips IR lamp (375 W/220 V) integrated to an infrared reactor [2728], designed by our research group [2930] and validated by a wide number of applications summarized in a recent review [31].

General Method: (Table 1, entry 4a–j) A mixture of Meldrum’s acid, methyl or ethyl acetoacetate, substituted benzaldehyde and ammonium acetate (1 mmol of each reagent), were thoroughly mixed in a round-bottomed flask (50 mL), equipped with a condenser. This mixture was exposed to infrared irradiation for 3 h. The reactions were monitored by tlc using n-hexane: ethyl acetate (80:20 or 60:40) as eluent. The purification of the products was carried out by means of preparative chromatography, using n-hexane/ethyl acetate (80:20 or 60:40) as eluent; the product was dissolved in acetone and then supported on percolated Merck silica-gel 60-F230 glass sheets. For the production of 4k–l were employed 2 mmol of Meldrum’s acid, methyl or ethyl acetoacetate, ammonium acetate and 1 mmol of the para-dialdehyde.

4-(4’-Fluorophenyl)-5-methoxycarbonyl-6-methyl-3,4-dihydro-2(1H)-pyridone (4c)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.95 (s, 1H, NH); 7.31–7.06 (m, 4H, Ar); 4.72 (d, 1H, H-4, J = 8.1 Hz); 4.20 (s, 3H, OCH3-9); 2.93 (dd, 1H, H-3a, J = 16.3 Hz, J = 8.1 Hz), 2.69 (d, 1H, H-3b); 2.33 (s, 3H, CH3-7).

13C-NMR (CDCl3-d6/TMS, δ ppm): 169.7 (C-2); 166.9 (C=O); 164.8 (C-4’); 148.8 (C-6); 138.5; 131.8; 128.4 (C-Ar); 106.6 (C-5); 52.1 (CH3-9); 38.3 (C-3); 36.6 (C-4); 18.9 (C-7).

EI-MS m/z (relative abundance %): ·263(25) M+; 204(100); 149(80) [M-114]+; 122(50) [M-141]+.

5-Ethoxycarbonyl 4-(4’-fluorophenyl)-6-methyl-3,4-dihydro-2(1H)-pyridone (4d)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.93 (s, 1H, NH); 7.21–7.06 (m, 4H, Ar); 4.12 (dd, 1H, H-4, J = 7.4 Hz); 4.01 (q, 2H, CH2-9); 2.93(dd, 1H, H-3a, J = 16.0 Hz, J = 7.4 Hz), 2.70 (dd, 1H, H-3b, J = 16.0 Hz); 2.31 (s, 3H, CH3-7); 1.09 (t, 3H, CH3-10).

13C-NMR (DMSO-d6/TMS, δ ppm): 169.6 (C-2); 166.4 (C-8); 148.3 (C-6); 138.9 (C-4’); 128.4; 115.4; 115.0 (C-Ar); 104.9 (C-5); 59.4 (CH3-9); 38.2 (C-3), 36.7 (C-4); 18.3 (C-7); 14.1 (C-10).

EI-MS m/z (relative abundance %): 277(75) M+; 248(85)[M-29]+; 231(55) [M-46]+; 204(100).

6-Methyl-4-(2’-methylphenyl)-5-methoxycarbonyl-3,4-dihydro-2(1H)-pyridone (4g)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.95 (s, 1H, NH); 7.18–6.88 (m, 4H, Ar); 4.31 (d, 1H, H-4, J = 8.2 Hz); 3.49 (s, 3H, CH3-9); 2.95 (dd, 1H, H-3a, J = 16.3Hz; J = 8.2 Hz); 2.45 (d, 1H, H-3b, J = 16.3 Hz); 2.36(s, 3H, CH3-2’); 2.34 (s, 3H, CH3-7).

13C-NMR (DMSOd6, δ ppm): 169.5 (C-2); 169.9 (C-8); 148.9 (C-6); 140.4; 134.9; 130.8; 126.6; 126.2; 125.1 (C-Ar); 104.8 (C-5); 51.1 (CH3-9); 36.9 (C-3); 33.9 (C-4); 18.9(CH3-C-2’); 18.1 (C-7).

EI-MS m/z (relative abundance %): 259(55) M+; 244(10) [M-15]+; 200(65); 115(40) [M-114]+; 43(100) [M-216]+.

5-Ethoxycarbonyl-6-methyl-4-(2’-methylphenyl)-3,4-dihydro-2(1H)-pyridone (4h)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.94 (s, 1H, NH); 7.20–6.89 (m, 4H, Ar); 4.32 (dd, 1H, H-4, J = 8.2 Hz); 3.93 (q, 3H, OCH2-9); 2.94 (dd, 1H, H-3a, J = 16.4 Hz, J = 8.2 Hz), 2.40 (dd, 1H, H-3b, J = 16.4 Hz); 2.36 (s,3H, CH3-C2’); 2.34 (s, 3H, CH3-7); 1.39 (t, 3H, CH3-10).

13C-NMR. (DMSO-d6/TMS, δ ppm): 169.4 (C-2); 166.4 (C-8); 148.5 (C-6); 140.7; 134.8; 130.7; 126.5; 126.2; 125.1 (C-Ar); 105.1 (C-5); 59.4 (CH2-9); 38.2 (C-3); 33.8 (C-4); 18.9 (CH3-C2’); 18.2 (C-7); 14.0 (C-10).

EI-MS m/z (relative abundance %): 273(80) M+; 258(10) [M-15]+; 244(50) [M-29]+; 212(80) [M-61]+; 200(100).

Phenylene-1’,4’-di-(4-(6-methyl-5-methoxycarbonyl-3,4-dihydro-2(1H)-pyridone)) (4k)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.97 (s, 1H, NH); 7.41–6.93 (m, 4H, Ar); 4.17–3.94 (m, 6H, H-4, OCH2-9); 2.51 (dd, 1H, H-3a); 2.21 (s, 3H, CH3-7); 1.07 (t, 3H, CH3-10).

13C-NMR. (DMSO-d6/TMS, δ ppm): 169.6 (C-2); 163.7 (C-8); 148.0 (C-6); 140.9; 134.8; 128.2; 127.0; 126.7; (C-Ar); 104.9 (C-5); 59.3 (CH2-9); 38.6 (C-3); 37.3 (C-4); 18.9 (CH3-C2’); 18.2 (C-7); 14.1 (C-10).

EI-MS m/z (relative abundance %): 412(0) M+; 381(5) [M-31]+; 354(7) [M-61]+; 245(20) [C14H15O3N]+; 169(15)[C8H10O2N]+.

HR-MS: observed 412.1628, expected 412.1634, C22H24N2O6.

Phenylene-1’,4’-di-(4-(5-ethoxycarbonyl-6-methyl-3,4-dihydro-2(1H)-pyridone)) (4l)

¹H-NMR (DMSO-d6/TMS, δ ppm): 9.84 (s, 1H, NH); 7.40–6.90 (m, 4H, Ar); 4.20–3.90 (m, 6H, H-4, OCH2-9); 2.94 (dd, 1H, H-3a); 2.25 (s, 3H, CH3-7); 1.05 (t, 3H, CH3-10).

13C-NMR. (DMSO-d6/TMS, δ ppm): 169.7 (C-2); 167.5 (C-8); 148.0 (C-6); 140.9; 134.8; 128.3; 127.0; 126.7; (C-Ar); 104.9 (C-5); 59.4 (CH2-9); 38.3 (C-3); 36.9 (C-4); 18.9 (CH3-C2’); 18.2 (C-7); 14.1 (C-10).

EI-MS m/z (relative abundance %): 440(5) M+; 396(4) [M-OEt]+; 367(5) [M-CO2Et]+; 259(10) [M-C9H12O2N]+; 182(5)[C9H12O2N]+.

HR-MS: observed 440.1941, expected 440.1947, C24H28N2O6.

4. Conclusions

This procedure for the production of 3,4-dihydro-2(1H)-pyridones should be regarded as a new and simple method with an appropriately green approach, since no solvent was employed. This, in addition to the use of infrared irradiation, provides a clean and rapid mode for the activation of this multicomponent reaction. Finally, this work is another contribution detailing the employment of infrared irradiation as a nonclassical heating technique for the transformation of many organic molecules.


To DGAPA-UNAM grant PAPIIT IN228010 for financial support; O. Noguez to CONACyT for a PHD scholarship (grant-191585) and to Red Macro Universidades for a scholarship to Osnieski Martin.


  1. Tundo, P; Anastas, P; Black, DC; Breen, J; Collins, T; Memoli, S; Miyamoto, J; Polyakoff, M; Tumas, W. Synthetic pathways and processes in green chemistry. Introductory overview. Pure Appl. Chem 2000, 72, 1207–1228. [Google Scholar]
  2. Anastas, PT; Williamson, TC. Green Chemistry, Frontiers in Benign Chemical Syntheses and Processes; Oxford University Press: Great Britain, UK, 1998; p. 2. [Google Scholar]
  3. Wender, PA; Handy, ST; Wright, DL. Towards the ideal synthesis. Chem Ind 1997, 765–769. [Google Scholar]
  4. Zhu, J; Bienaymé, H. Multicomponent Reactions; Wiley-VCH: Weinheim, Germany, 2004. [Google Scholar]
  5. Pihlaja, K; Seilo, M. The acidity and general base catalyzed hydrolysis of Meldrum’s acid and its methyl derivates. Acta Chem. Scand 1969, 23, 3003–3010. [Google Scholar]
  6. Ochoa, E; Suárez, M; Verdecia, Y; Pita, B; Matín, N; Quinteiro, M; Seoane, C; Soto, JL; Duque, J; Pomés, R. Structural study of 3,4-dihydropyridones and furo[3,4-b]-2(1H)-pyridones as potentional calcium channel modulators. Tetrahedron 1998, 54, 12409–12420. [Google Scholar]
  7. Smith, D; Sammes, PG. Comprehensive Organic Chemistry; Pergamon: Oxford, UK, 1979; Volume 4, p. 3. [Google Scholar]
  8. Bayley, T; Goe, G; Scriven, E. Heterocyclic Compounds; Newkome, GRW, Ed.; Wiley: New York, NY, USA, 1984; Volume 14, p. 1. [Google Scholar]
  9. McKillop, A. Comprehensive Heterocyclic Chemistry; McKillop, A, Boulton, A, Eds.; Pergamon: Oxford, UK, 1984; Volume 2, p. 67. [Google Scholar]
  10. Bristol, JA; Sircar, I; Moos, WH; Evans, DB; Weishaar, RE. Cardiotonic agents 1.4,5-dyhidro-6-[4-(1H-imidazol-1-yl)phenyl]-3(2H)-pyridazinones: Novel positive inotropic agents for the treatment of congestive heart failure. J. Med. Chem 1984, 27, 1099–1101. [Google Scholar]
  11. Lemke, JV. New inotropic drugs: amrinone and milrinone. J. Med. Assoc. Ga 1987, 76, 854–857. [Google Scholar]
  12. Iven, H; Brasch, M; Armah, BI. Electrophysiologic effects of saterinone and milrinone in the isolated guinea pig myocardium. Arneim. Forcg. Drugs Res 1988, 38, 1298–1302. [Google Scholar]
  13. Schultz, AG. Camptothecin. Chem. Rev 1973, 73, 385–405. [Google Scholar]
  14. Kelly, TR; Bell, SH; Osashi, N; Armstrong-Chong, RJ. Synthesis of (+)-fredericamycin A. J. Am. Chem. Soc 1988, 110, 6471–6480. [Google Scholar]
  15. Curran, DP; Liu, H. New 4 + 1 radical annulations. A formal total synthesis of (+)-camptothecin. J. Am. Chem. Soc 1992, 114, 5863–5864. [Google Scholar]
  16. Cox, RJ; O’Hagan, D. Synthesis of isotopically labelled 3-amino-2-phenylpropionic acid and its role as a precursor in the biosynthesis of tenellin and tropic acid. J. Chem. Soc. Perkin Trans 1991, 1, 2537–2540. [Google Scholar]
  17. Williams, D; Lowder, P; Gu, YG. Studies toward funiculosin. Intramolecular carbonyl condensations using carboxamidimidazolide intermediates. Tetrahedron Lett 1997, 38, 327–330. [Google Scholar]
  18. Kozikowski, AP; Campiani, G; Sun, LQ; Wang, S; Saxena, A; Doctor, BP. Identification of a more potent analogue of the naturally occurring alkaloid Huperzine a. Predictive molecular modeling of its interactions with ACLE. J. Am. Chem. Soc 1996, 118, 11357–11362. [Google Scholar]
  19. Brickner, S. Multidrug-resistant bacterial infections: Driving the search for new antibiotics. Chem Ind 1997, 131–135. [Google Scholar]
  20. Murray, T; Zimmerman, S. 7-amido-1,8-naphthyridines as hydrogen bonding units for the complexation of guanine derivates. The role of 2-alkoxyl groups in decreasing binding affinity. Tetrahedron Lett 1995, 36, 7627–7630. [Google Scholar]
  21. Jones, G; Katritzky, A; Rees, CW; Scriven, EF. Comprehensive Heterocyclic Chemistry II; Pergamon Press: Oxford, UK, 1996. [Google Scholar]
  22. Mohrle, H; Weber, H. Oxidation von 1-methyl-und 1,3-dimethylpyridium salzen: überpyridone—I. Tetrahedron 1970, 26, 2953–2958. [Google Scholar]
  23. Jones, G. The Knoevenagel condensation. Org. React 1967, 15, 204–582. [Google Scholar]
  24. Alberola, A; Calvo, LA; González-Ortega, A; Sañudo Ruíz, MC; Yustos, P; García, S; García-Rodríguez, E. Regioselective synthesis of 2(1H)-pyridones from β–aminoenones and malonitrile. Reaction mechanism. J. Org. Chem 1999, 64, 9493–9498. [Google Scholar]
  25. Brun, E; Gil, S; Mestres, R; Parra, M. A new synthetic method to 2-pyridones. Synthesis 2000, 2000, 273–280. [Google Scholar]
  26. Paulvannan, K; Chen, T. Solid-phase synthesis of 1,2,3,4-tetrahydro-2 pyridones via aza-annulation of enamines. J. Org. Chem 2000, 65, 6160–6166. [Google Scholar]
  27. Gómez-Pliego, R; Ramírez-San, JE; Miranda, R; Villalobos-Molina, R; Delgado, F; Osnaya, R; Trujillo-Ferrara, JG. Vasodilator effects of bis-dihydropyridines structurally related to nifedipine. Med. Chem 2006, 2, 527–534. [Google Scholar]
  28. Velasco-Bejarano, B; Trujillo-Ferrara, J; Miranda, R. Preparation of apoptotic inducer, 2,2-diphrnyl-1,3,2-oxazaborolidin-5-ones, under alkaline conditions. Synlett 2007, 6, 921–924. [Google Scholar]
  29. Velasco, B; Trujillo-Ferrara, JG; Fabila Castillo, LH; Miranda, R; Sánchez-Torres, LE. In vitro apoptotic activity of 2,2-diphenyl-1,3,2-oxazaborolidin-5-ones in L58178Y cells. Life Sci 2007, 80, 1007–1013. [Google Scholar]
  30. Noguez, O; García, A; Ibarra, C; Cabrera, A; Aceves, JM; Miranda, R. Green synthesis of bis-Biginelli esters, with vasodilatory effects, their mass spectrometric and physical. Trends Org. Chem 2009, 13, 75–82. [Google Scholar]
  31. Miranda, R; Noguez, O; Velasco, B; Arroyo, G; Penieres, G; Martínez, JO; Delgado, F. Irradiación infrarroja una alternativa para la activación de reacciones y su contribución a la química verde. Educ. Quím 2009, 20, 421–425. [Google Scholar]
  32. Suárez, M; Verdecia, Y; Ochoa, E; Salfrán, E; Morán, L; Martín, N; Martínez, R; Quinteiro, M; Seoane, C; Soto, JL; Novoa, H; Blaton, N; Peeters, OM; de Ranter, C. Synthesis and structural study of 3,4-dihydro-2(1H)-pyridones and isoxazolo[5,4-b]pyridin-6(7H)-ones. Eur J Org Chem 2000, 2079–2088. [Google Scholar]
  33. Martínez, R; Suárez, M; Martín, N; Ochoa, E; Seoane, C; Verdecia, Y. Mass spectral fragmentation patterns of new 5-acetyl-4-aryl-6-methyl-2(1H) pyridones. Rapid Commun. Mass Espectrom 1999, 13, 2180–2182. [Google Scholar]
  34. Suárez, M; Martínez-Álvarez, R; Martín, N; Verdecia, Y; Ochoa, E; Alba, L; Seoane, C; Kayali, N. Electrospray ionisation and ion-trap fragmentation of substituted 3,4-dihydro-2(1H)-pyridin-2-ones. Rapid Commun. Mass Espectrom 2002, 16, 740–754. [Google Scholar]
  35. Molero, D; Suárez, M; Martínez-Álvarez, R; Verdecia, Y; Martín, N; Seoane, C; Ochoa, E. 1H and 13C spectral assignment of 2(1H)-pyridin-2-ones derivates. Magn. Reson. Chem 2004, 42, 704–708. [Google Scholar]
  36. Morales, A; Ochoa, E; Suárez, M; González, L; Verdecia, Y; Martín, N; Quinteiro, M; Seoane, C; Soto, JL. Novel hexahydrofuro [3,4-b]-2(1H)-pyridones from 4-aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones. J. Heterocyclic Chem 1996, 33, 103–107. [Google Scholar]
Scheme 1.
Scheme 1.
Ijms 12 02641f1 1024
Scheme 2.
Scheme 2.
Ijms 12 02641f2 1024
Table 1. Dihydropyridones (4a–j) produced under infrared irradiationa.
Table 1. Dihydropyridones (4a–j) produced under infrared irradiationa.
CompoundMelting point[b] (°C)Yield[c]%
4a197–198(197–198) [12,28]75
4c206–208(207–209) [12,28]75
4d184–186(184–186) [29]70
4e200–202(201–201) [29]75

[a]3 hours[b]Experimental[c]Isolated pure product.

Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert