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Journal of Chemistry
Volume 2013 (2013), Article ID 214617, 5 pages
http://dx.doi.org/10.1155/2013/214617
Research Article

Superparamagnetic Iron Oxide as an Efficient Catalyst for the One-Pot, Solvent-Free Synthesis of 5,5-Disubstituted Hexahydropyrimidines and Their Spiro Analogues

1Department of Chemistry, Faculty of Sciences, Payame Noor University, Mashhad 91735-433, Iran
2Department of Chemistry, School of Sciences, Alzahra University, Vanak, Tehran, Iran

Received 3 September 2012; Revised 27 October 2012; Accepted 10 November 2012

Academic Editor: Saima Q. Memon

Copyright © 2013 Fatemeh Janati et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Superparamagnetic Fe3O4 is shown to act as a very efficient catalyst for the one-pot, three-component synthesis of 5,5-disubstituted hexahydropyrimidines and their spiropiperidines. The catalyst is easily recovered by the use of an external magnet and reused in several reactions without any noticeable loss of activity. The products are obtained in short time and good purity upon separation of the catalyst and evaporation of the volatiles of the reaction mixture.

1. Introduction

Hexahydropyrimidines are biologically important. N,N-Bisarylhexahydropyrimidines are effective against Ehrlichcarcinoma, LK lymphoma, and Staphylococcus aureus [1, 2]. The hexahydropyrimidine skeleton occurs in alkaloids such as verbamethine and verbametrine [3]. N-Substituted hexahydropyrimidines are synthetic intermediates for recently discovered spermidine-nitroimidazole drugs for the treatment of A549 lung carcinoma [4] and structural units in new trypanothion ereductase inhibiting ligands for the regulation of oxidative stress in parasite cells [5]. Benzo-fused hexahydropyrimidines or 1,2,3,4-tetrahydroquinazolines are potential R-adrenergic blockers [6] and possess antiplatelet activity [7]. Hexahydropyrimidines are prepared classically by condensations of substituted propane-1,3-diamines with aldehydes and ketones [8, 9]. Liang and coworkers synthesized this type of compounds using cyclic ketone, amine, and formaldehyde [10]. There are also a few reports in literature describing the synthesis of hexahydropyrimidine derivatives either by using lewis acids and heteropolyacid as catalyst [11, 12]. In recent years multicomponent reactions (MCR) have become a powerful tool for atom efficient and waste-free synthesis of complex building blocks of “drug-like” motifs [13, 14]. Generally MCR strategy affords time and cost advantageous, environmentally benign pathways leading to the synthesis of a library of compounds.

In this letter, we report the multicomponent treaction of 1,3-dicarbonyl compounds, amines, and formaldehyde react in one step in the presence of superparamagnetic Fe3O4 particles at 80°C (Scheme 1). The Fe3O4 NPs were prepared as reported in the literature [15].

214617.sch.001
Scheme 1: Synthesis of hexahydropyrimindines using 1,3-dicarbony compounds/β-keto esters, amines, and formaldehyde.

Although this important carbon-carbon bond forming reaction has witnessed much recent progress, [1620] there are still demands for the development of efficient procedures involving inexpensive, recyclable catalytic systems under solvent-free conditions.

2. Results and Discussion

Table 1 summarizes the results of the Fe3O4-catalyzed reaction of 1,3-dicarbonyl compounds, amines, and formaldehyde. Initial experiments were carried out under solvent-free conditions involving the reaction of ethylacetoacetate,aniline and formaldehyde, at 80°C catalyzed by Fe3O4 (Table 1) [12].

tab1
Table 1: Synthesis of hexahydropyrimidines using 1,3-dicarbonyl compounds/b-keto ester, amines, and formaldehyde.

A series of catalysts were reported with the standard reaction of ethylacetoacetate, aniline, and formaldehyde. The results are depicted in Table 2. Among various Lewis acids including different metal salts [13, 14], Fe3O4 was found to be the best catalyst (yield 90%, Table 1, entry 1) for the reaction.

tab2
Table 2: Comparison of various types of catalysts used for the synthesis of hexahydropyrimidines with our catalyst.

In the presence of strong acid like HCl only trace amount of the product was detected in TLC. This could be due to decomposition of the product in the presence of strong acid. Complete disappearance of the aniline and formation of the product were monitored by TLC. The use of various amounts of the Lewis acid was investigated to optimize the reaction conditions. A catalytic quantity of Fe3O4 (10 mol %) proved to be effective for complete conversion of the starting materials to the desired product 4a within 2.5 h(entry 1). The use of lower amounts of the catalyst (down to 2 mol%) prolonged the reaction time up to 5 h whilst still giving an almost quantitative yield of 4a. Omission of Fe3O4 from the reaction medium led to formation of only trace quantities of 4a after several hours indicating the crucial role of the catalyst. Similar reactions of ethylacetoacetate with other amines were conducted under the same conditions affording high yields of the respective products within the same time period. Other aromatic amines bearing electron-releasing groups reacted equally well with various 1,3-dicarbonyl compounds under the same conditions (entries 2–11). Upon completion of the reactions, the catalyst was recovered from the reaction mixture simply by applying an external permanent magnet and the products were isolated in good purity by removing the volatiles under reduced pressure. Further, the recovered Fe3O4 was reused successfully in 10 subsequent reactions without significant loss of catalytic performance.

The stoichiometric ratio of 1 : 2 : 3 (1,3-dicarbonyl compound: amine: formaldehyde) in the presence of 10 mol % of Fe3O4 in solvent-free condition at 80°C was found to be the optimum condition for the maximum yield of hexahydropyrimidines. Under these reaction conditions, the product 4a was obtained in a very good yield of 90% in 2.5 h. After the standardization of the reaction condition, a variety of b-keto esters and 1,3-dicarbonyl compounds like methylacetoacetate, ethylacetoacetate, allylacetoacetate, and 1-benzoyl acetone were used.

A tentative mechanism for the reaction is proposed in Scheme 2. The 1,3-diketone or β-keto ester undergoes twice α-aminomethylation reactions in succession on the same α-carbon of carbonyl-catalyzed by Fe3O4. The condensation of the resulting substituted propane- 1,3-diamine with formaldehyde furnishes the desired spirohexahydropyrimidine. Using Mannich bases instead of β-keto estersas reactants can also generate the desired products. Here the acidic nature of Fe3O4 may facilitate both the enolization steps of the 1,3-diketone or β-ketoestr.

214617.sch.002
Scheme 2: Probable mechanism of hexahydropyrimidine formation

When dimedone was used as 1,3-dicarbonyl compound instead of hexahydropyrimidines, spiro-substituted piperidines were obtained (Scheme 3) with the same methodology. One of the advantages of this methodology is that 3-methylaniline also gives the desired product (Table 3, entry 2) which was not possibly using the methodology of Kozlov and Kadutskii [21]. This may happen due to the high reactivity of dimedone. Here maximum yield of the piperidine compound was obtained when dimedone, aromatic amine, and formaldehyde were taken in the ratio of 2 : 1 : 3. Probable mechanism for the formation of the bisspiropiperidine is outlined in Scheme 4.

tab3
Table 3: Synthesis of bis-spiropiperidines using dimedone, aromatic amines, and formaldehyde.
214617.sch.003
Scheme 3: Synthesis of bis-spiropiperidines using dimedone, aromatic amines, and formaldehyde.
214617.sch.004
Scheme 4: Probable mechanism of bis-spiropiperidines formation.

3. Experimental Section

3.1. General Procedure for the Synthesis of Hexahydropyrimidines and Their Spiro Analogue

A mixture of β-keto ester (1 mmol), aniline (2 mmol), formaldehyde (3 mmol, 37–41% aqueous solution), and a catalytic amount of Fe3O4 (10 mol %) was stirred at 80°C for 2.5 hours. The progress of the reaction was monitored by TLC. Upon completion of the reactions, the catalyst was recovered from the reaction mixture simply by applying an external permanent magnet and the products were purified by column chromate-graphy. All products are known compounds. The identity of the products was confirmed by comparison of their spectroscopic data with literature data. The isolated yields of the products were 70–94%.

3.2. General Procedure for the Synthesis of Spiropiperidines

A mixture of dimedone (2 mmol), aniline (1 mmol), formaldehyde (3 mmol, 37–41% aqueous solution), and a catalytic amount of Fe3O4 (10 mol %) in solvent-free condition was stirred at 80°C for 3 hours. The progress of the reaction was monitored by TLC. After the completion of the reaction Fe3O4 was removed from the reaction mixture by external magnet The solvent was removed under reduced pressure. The crude product mixture was then purified directly by crystallization from etylacetate.

Spectroscopie and analytical data of several compounds have been reported.

4. The Spectral and Analytical Data of a Few Compounds Reported in Tables 1 and 3

4.1. 5-Acetyl-1,3-bis-(4-nitrophenyl)-hexahydropyrimidine-5-carboxylic Acid Ethyl Ester (4l)

(Table 1, entry 13) Brown viscous liquid; νmax (KBr)/cm-1 3029, 2948, 2825, 2824, 1716, 1592, 1488, 1440, 1350, 1229, 1075, 1022, 990, and 815; 1H NMR (300 MHz, CDCl3) : 8.15 (4H, d,  Hz, ArH), 7.54 (4H, d,  Hz, ArH), 4.46 (1H, d,  Hz, equatorial N–CH–N), 4.32 (1H, d,  Hz, axial N–CH–N), 4.05 (2H, q,  Hz, O–CH2), 3.88 (2H, d,  Hz, N–CH2), 3.74 (2H, d,  Hz, N–CH2), 2.26 (3H, s, CH3–CO), 1.17 (3H, t,  Hz, O–CH2–CH3); 13C NMR (75 MHz, CDCl3) δC: 194.2 (C, CH3–CO–), 168.0 (C, COOEt), 152.6 (C, C aromat), 128.6 (CH, C aromat), 127.76 (CH, C aromat), 116.2 (CH, C aromat), 67.3 (N–CH2–N), 62.8 (CH2, COO–CH2), 60.2 (C, C5), 54.1 (CH2–N), 27.8 (CH3–CO), 15.9 (CH3, COOCH2CH3); Anal. calcd. for C21H22N4O7; C: 57.09; H: 4.87; N: 12.61; Found: C: 57.29; H: 4.91; N: 12.57%.

4.2. 5-Acetyl-1,3-bis-(4-chloro-phenyl)-hexahydropyrimidine-5-carboxylic Acid Methyl Ester (4m)

(Table 1, entry 14) Brown viscous liquid; νmax (KBr)/cm-3010, 2944, 2848, 2800, 2701, 1702, 1615, 1459, 1441, 1346, 1209, 1121, 1068, 918 and 810 1H NMR (300 MHz, CDCl3) δH: 7.12 (4H, d,  Hz, ArH), 6.85 (4H, d,  Hz, ArH), 4.33 (1H, d,  Hz, equatorial N–CH–N), 4.22 (1H, d,  Hz, axial N–CH–N), 3.35 (4H, s, N–CH2), 3.59 (3H, s, OMe), 2.13 (3H, s, CH3–CO); 13C NMR (75 MHz, CDCl3) δC: 200.7 (C, CH3–CO–), 168.3 (C, COOMe), 146.7 (C, Caromat), 129.5 (C, Caromat), 128.6 (CH, Caromat), 117.0 (CH, Caromat), 69.5 (O–CH3), 59.6 (C, C5), 53.7 (N–CH2–N), 50.5 (CH2–N), 29.6 (CH3–CO), Anal. calcd. for C20H20N2O3Cl2; C: 60.62; H: 5.10; N: 7.14; Found: C: 60.57; H: 5.15; N: 7.05%.

4.3. 5-Acetyl-1,3-di-p-boromo-hexahydropyrimidine-5-carboxylic Acid Ethyl Ester (4n)

(Table 2, entry 2) Brown viscous liquid; νmax (KBr)/cm-1 2980, 2930, 2863, 2804, 1712, 1620, 1580, 1500, 1440, 1382, 1295, 1230, 1129, 1060, 1025, 950 and 820; 1H NMR (300 MHz, CDCl3) δH: 7.09 (4H, d,  Hz, ArH), 7.03 (4H, d,  Hz, ArH), 4.47 (1H, d,  Hz, equatorial N–CH–N), 4.30 (1H, d, axial N–CH–N), 4.01 (2H, q,  Hz, O–CH2), 3.74 (2H, d,  Hz, N–CH2), 3.60 (2H, d, N–CH2), 2.23 (3H, s, CH3–CO), 1.21 (3H, t  Hz, O–CH2–CH3); 13C NMR (75 MHz, CDCl3) δC: 203.0 (C, CH3–CO–), 169.0 (C, COOEt), 147.2 (C, Caromat), 130.6 (CH, Caromat), 129.76 (CH, Caromat), 118.2 (CH, Caromat), 69.3 (N–CH2–N), 61.8 (CH2, COO–CH2), 59.9 (C, C5), 54.1 (CH2–N), 26.8 (CH3–CO), 13.9 (CH3, COOCH2CH3).

4.4. Spectral Data of the Spiropiperidines Tetramethyl-15-(4-chlorophenyl)-15-azadispiro [5.1.5.3] Hexadecane-1,5,9,13-tetrone (5d)

(Table 3, entry 4) m.p.: 198–200°C. IR (KBr): 2959, 2949, 2922, 1732, 1721, 1703, 1689, 1590, 1492, 1250, 1223, 1078, 826, 516 cm_1. 1H NMR (500 MHz, CDCl3): d = 0.96 (s, 6H), 0.97 (s, 6H), 2.46 (s, 2H), 2.61 (d,  Hz, 4H), 2.79 (d,  Hz, 4H), 3.38 (s, 4H), 6.95 (d,  Hz, 2H), 7.30 (d,  Hz, 2 H). 13C NMR (100 MHz, CDCl3): d 28.20, 28.50, 30.66, 32.01, 51.05, 54.43, 65.36, 113.67, 120.21, 131.80, 150.38, 205.76.

Acknowledgment

The authors are thankful to Payame Noor University Research Council for financial support.

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