Chitosan Based Heterogeneous Catalyses: Chitosan-Grafted-Poly(4-Vinylpyridne) as an Efficient Catalyst for Michael Additions and Alkylpyridazinyl Carbonitrile Oxidation

Abstract

Chitosan-grafted-poly(4-vinylpyridine) (Cs-PVP) copolymers could be synthesized under heterogeneous conditions in presence of a potassium persulfate and sodium sulfite redox system. The synthesized graft copolymer could be utilized effectively, in the form of beads, as an efficient catalyst for Michael additions of active methylenes to functionally substituted alkenes. Moreover, methyl moiety oxidation in methyl pyridazinyl carbonitriles by H₂O₂ in the presence of chitosan-g-polyvinyl pyridine–supported iron (III) complex, Cs-PVP/Fe, could be affected. A variety of pyrans, naphthopyrans, and thiopyrans could be synthesized efficiently in the presence of these graft copolymer beads by novel catalytic routes. These polymeric catalysts could be used instead of the old toxic commercial organic basic catalysts, piperidine or pyridine, and could be readily isolated from the reaction mixture and recycled several times without significant loss of catalytic activity.

1. Introduction

Recently, biocatalysis and sustainable chemistry researchers are directed to develop new green methodologies that aim to reduce and prevent pollution at its source [1,2,3]. Biocatalysis is a promising technique based on the use of natural renewable biological materials, such as enzymes and polymers, that provide cleaner methodologies with high selectivity and energy-efficient operation under mild conditions in contrast to the traditional chemical catalysts [4,5]. Chitosan (2-acetamido-2-deoxy-β-D-glucose-(N-acetylglucosamine) is a partially deacetylated polymer of chitin and is usually prepared from chitin by reflux with a strong alkaline solution [6,7,8]. Some time ago, the utility of chitosan as an efficient eco-friendly basic biocatalyst for Michael additions was reported and it could already be shown that chitosan can catalyze the addition of bi-functional active methylenes to arylidenemalononitriles and enaminones [9,10,11,12]. This type of reaction, involving simple addition of active methylenes, phenols and naphthols to electron poor functionally substituted alkenes, is an efficient C-C bond forming reaction. Classically these additions have been effected in the presence of homogeneous basic catalysis [13,14,15,16,17]. Recently emphasis has been placed on adopting instead heterogeneous recyclable catalyses [12,18]. So far a diversity of such catalyses were employed [19,20]. Moreover, chitosan, a chiral polysaccharide, has been used as an efficient catalyst for enantioselective syntheses that result in the creation of asymmetric products with chiral center(s) [21,22,23,24,25]. Previously, while using chitosan [9,11], we suffered from some disadvantages of this catalyst namely, that it afforded low yields of products in many of the investigated reactions and it could not easily be recycled because of its high hygroscopicity, leading it to form gels. Herein, we successfully overcome the drawbacks of chitosan and enhance its catalytic activity via heterogeneous grafting with 4-vinyl-pyridine (VP) [26] (Scheme 1), thereby producing a basic, recyclable, eco-friendly biocatalyst that could be used efficiently in Michael additions, especially when a stronger basic catalyst than chitosan, is required. Also, the use of the chitosan-g-polyvinyl pyridine, Cs-PVP in the form of beads is usually required to increase the catalytic activity of the catalyst [18,27,28].

Scheme 1.

Preparation of chitosan-g-PVP catalyst.

In addition, chitosan has been reported to have high affinity for adsorption of metal ions [29,30,31,32]. The adsorption capacity of Fe(III) ions for chitosan/4-vinylpyridine copolymer is higher than that of the original non-grafted chitosan owing to the presence of pyridine moieties in the PVP side chains [33]. Herein, chitosan-g-poly(4-vinylpyridine)-supported iron(III) complex, [Cs-PVP/Fe(III)], could be prepared in the form of beads (Scheme 2) [34] of higher catalytic activity, and effectively used as a powerful recyclable catalyst to oxidize methylpyridazinone in the presence of hydrogen peroxide to afford the corresponding furopyridazinone derivative. The surface adsorption of Fe³⁺ ions on the surface of chitosan involves nitrogen and oxygen atoms of the repeating units of chitosan as shown below [34]:

Cs–NH₂ + Fe³⁺ ↔ [Cs – NH₂ --- Fe --- ]⁺³

Scheme 2.

Probable structure of chelated complexes of chitosan with iron (III) ions.

2. Results and Discussion

2.1. Preparation of Cs-PVP Catalyst Beads

The investigated basic catalyst, (Cs-PVP), was prepared through heterogeneous grafting of 4-vinylpyridine onto chitosan powder as previously reported by Khalil et al. [26]. The structure of grafted chitosan copolymer was confirmed by FT-IR, ¹H-NMR, ¹³C-NMR and elemental analysis as reported in our previous work [26]. Elemental analysis showed that the nitrogen content of chitosan, N% = 7.1, was increased upon grafting with 4-vinylpyridine to N% = 8.0, which is an evidence for the presence of pyridine moieties. The structure of the grafted copolymer was confirmed by FTIR, that showed a characteristic C=N groups band at 2,197 cm⁻¹ from the poly 4-vinylpyridine chains (Figure 1). Also, the presence of pyridine rings is confirmed in the ¹H-NMR spectrum (Figure 2) by the presence of the peaks at 7.1 and 8.5 ppm in the aromatic range (Figure 2).

Figure 1.

FTIR of (a) Chitosan, (b) chitosan-g-poly(4-vinylpyridine) copolymer 80% G.

Figure 2.

¹H-NMR spectrum of 80% VP grafted chitosan.

The prepared Cs-PVP beads exhibited more basic character (pka = 5.9), as compared to chitosan (pka = 6.4), owing to the presence of pyridine moieties along the chitosan backbone. The cross-linked chitosan graft copolymer is characterized by higher thermal stability as compared to chitosan [26] so it could then be used effectively in higher temperature reactions (TGA was reported previously [26]).

2.2. Applying Cs-PVP Beads as Efficient Basic Heterogeneous Catalyst in Michael Additions

Benzylidene-malononitrile 1 reacted with dimedone to yield the chromene-3-carbonitrile derivative 2 in an excellent yield (>95%), more than that was obtained in presence of the original chitosan (75%), (Scheme 3). The product structure was assigned by using X-ray crystallographic analysis (Figure 3) [35]. These derivatives could be previously prepared in the presence of homogeneous basic catalysts [9,10,11,12,13,14,15,16,17]. As a result of the cross-linking nature of the invented Cs-PVP catalyst, it could be readily isolated by simple filtration and reused again for more than five times without loss of its catalytic activity, after extensive washing with hot ethanol and drying in an oven at 100 °C for 4 h. Similarly, reaction of 1 with cyclohexanone was conducted successfully in the presence of Cs-PVP beads to give a similar product 3 to that was obtained previously [9] in the presence of chitosan (55%) but in much higher yield (~90%). While the reaction of 1 with ethyl acetoacetate has been reported earlier [36] to produce the 2-aminopyran 4 together with the benzene derivative 5, only 4 was formed in a higher yield ~90% when 1 was reacted with ethyl acetoacetate in ethanol in presence of Cs-PVP beads. Again, the produced structure was confirmed by X-ray crystal structure determination (Figure 4). The catalyst could be easily isolated from the reaction media and recycled several times after being washed with ethanol and dried in an oven. α-Naphthol 6 also reacted with 1 to yield 7 in 86% yield.

Scheme 3.

Heterogeneous basic catalyzed Michael additions using Cs-PVP beads.

Figure 3.

X-ray crystal structure of chromene-3-carbonitrile derivative 2.

Figure 4.

X-ray crystal structure of 2-aminopyran derivative 4.

In order to estimate the appropriate catalyst loading, a model reaction of benzylidene-malononitrile 1 (1.54 g, 10 mmol) and dimedone (1.40 g, 10 mmol) was carried out in 25 mL absolute ethanol using 1, 5, 10, 15, and 20% wt. of catalyst under the same conditions. The 10%wt catalyst loading was found to be the optimal quantity (Figure 5). Catalyst was reused four times and the results showed that the chitosan graft copolymer can be reused as such without significant loss in its catalytic activity (Table 1).

Figure 5.

Optimization of the chitosan graft copolymer as basic catalyst.

Table 1.

Recyclability of the chitosan graft copolymer as basic catalyst.

Product	Fresh Catalyst	Recycled (1)	Recycled (2)	Recycled (3)	Recycled (4)
2	95	93	93	92	92

All these products were previously [9,11] obtained in presence of chitosan but in lower yields, and furthermore, with the latter, removal of the product from the catalyst could not be easily accomplished as in each case the catalyst adsorbed part of the reaction media forming a gel mass. The cross-linked graft copolymer beads did not behave similarly and its use in the form of beads has enhanced its catalytic activity to a great extent. The thiopyran 11 could be obtained in a one pot reaction of 8, 9, and 10, (yields: Cs = 80%; Cs-PVP = 95%; cf. Scheme 3). This product has been obtained earlier via addition of cyanothioacetamide to 1. While 1 failed to add to 12 in the presence of chitosan or even piperidine, it reacted smoothly with 12 in the presence of Cs-PVP beads affording the 5-acetyl-2-aminopyran derivative 13 in 80% yield.

Some time ago the formation of dieneamide 15a via reaction of enaminone 14a with malononitrile has been reported from our laboratories [37,38]. We have recently shown that this product can be obtained in better yields by utilizing chitosan as catalyst [11]. Now we report that the dieneamide 15a is also obtainable in higher yield in the presence of grafted chitosan Cs-PVP beads (yields: Cs = 80; Cs-PVP = 90). Moreover, the furanyl derivative 15b could be obtained from 14b (yields: Cs = 78; Cs-PVP = 95). The postulated mechanism of this remarkable transformation is shown below (Scheme 4).

Scheme 4.

Synthesis of dieneamides by using Cs-PVP basic catalyst.

2.3. Preparation of Cs-PVP/Fe(III) Catalyst Beads

The second goal of our study was the formation of chitosan-PVP/Fe(III) complex, Cs-PVP/Fe(III), using same methodology that published by Ngah et al. [33] and Burke et al. [34]. It is of value to mention that the previously prepared basic catalyst Cs-PVP exhibited higher metal-binding capacity, as compared to the original chitosan, owing to the presence of extra binding nitrogen-atoms with free lone pairs like in NH₂ groups and pyridine moieties. When 50 mg of chitosan or graft chitosan were placed in a 10 nM Fe³⁺ solution at pH = 1.8, for a period of time 5 h, it was found that the adsorption capacity of the graft copolymer, Cs-PVP, was higher than that of the original chitosan, since the amount of adsorbed iron on the graft copolymer was 0.086 mmol Fe³⁺/g while it was 0.077 is for original chitosan. Elemental analysis of Fe(III)-supported chitosan graft copolymer by EDS (Table 2, Figure 6) showed that 32% of Fe(III) wascon the surface as result of the metal complexation with the N-atoms of glucosamine units and pyridine moieties and C-6 hydroxyl group binding sites over the chitosan graft surface.

Table 2.

EDS of chitosan-g-poly(4-vinylpyridine)/Fe³⁺ chelate.

Element	Weight%	Atomic%
C K	17.24	38.89
N K	4.25	8.22
O K	12.25	20.74
Fe K	66.27	32.15
Totals	100.00

Figure 6.

EDS of Fe(III) supported chitosan-poly(4-vinylpyridine) graft, Cs-PVP/Fe³⁺ complex.

The produced Cs-PVP/F(III) complex could be used successfully as an efficient catalyst for oxidation of methyl pyridazinones as shown in the last part of our study. Scanning electron microscopy exhibited great differences in the surface morphology upon grafting and complexation with Fe³⁺ ions (Figure 7). From the SEM the fibrous nature of chitosan is lost upon grafting and regular geometric shapes appeared that were attributed to the coordination with Fe³⁺ ions. The suggested structure of chitosan Fe(III) chelates is supposed [39] to occur as follows (Scheme 4).

Figure 7.

Scanning electron microscope for (a) Chitosan Cs, (b) Cs-PVP 80%G, (c) Cs-PVP/Fe³⁺ complex.

2.4. Utility of Cs-PVP/Fe(III) beads as an Efficient Catalyst for Oxidation of Methyl Pyridazinones

One of the major challenges for organic synthesis is how to effect controlled oxidation of non-activated alkyl functions. Several approaches exist among which Fe (III) Chitosan-PVP copolymer catalysts are of utility. We would like here to report first successful controlled oxidation of the methyl function in 16 utilizing Cs-PVP/Fe (III) chelates. Thus refluxing 16a,b with Cs-PVP/Fe (III) complex in the presence of excess hydrogen peroxide afforded 17a,b. The potential utility of 17a,b as precursors to phthalazines via addition of electron poor alkenes, thus replacing thienopyridazines classically utilized by Elnagdi et al. for this purpose will be subject of further communication (Scheme 5).

Scheme 5.

Selective oxidation of methylpyridazinones in presence of chitosan-based iron (III) catalyst, Cs-PVP/Fe(III).

3. Experimental

3.1. General

Melting points were recorded on Gallenkamp apparatus and are reported uncorrected. The Fourier Transform infrared (FTIR) spectra were recorded in KBr pellets on a JASCO FT-IR-6300 system at a resolution of 4 cm⁻¹ in the 400–4000 cm⁻¹ range. ¹H-NMR measurements were determined on a Bruker DPX spectrometer, at 400 MHz for ¹H-NMR and 100 MHz for ¹³C-NMR, in DMSO-d₆ as solvent using TMS as internal standard. Solid NMR spectra were recorded on a 600MHz Bruker Avance II spectrometer, operating at 150 MHz for ¹³C-NMR. Mass spectra were measured on a GC-MS DFS-Thermo spectrometer, using 70 eV EI. Elemental analyses were measured by means of an Elementar-Vario Microcube Elemental Analyzer. The scanning electron microscopy (SEM) was conducted using a JEOL JSM-630 J scanning electron microscope operated at 20 kV. (TGA data was reported previously [26]) Single crystal X-ray crystallographic analysis was performed using a Rigaku Rapid II instrument. Copies of original data can be provided upon request.

3.2. Samples

Chitosan, with degree of deacetylation (DDA) = 77.8%, was kindly supplied by Professor Furuhata of Tokyo Institute of Technology (T. I. Tech.). 4-Vinylpyridine, initiators (K₂S₂O₇ and NaHSO₃), and all solvents were purchased from Sigma-Aldrich Chemicals (Germany) and used without any further purification.

3.3. Materials

3.3.1. Preparation of Chitosan Beads Cs

Chitosan beads were prepared according to the published procedure of Ngah et al. [30]. Chitosan solution was prepared by dissolving chitosan powder (2.00 g) in 5% (v/v) acetic acid solution (60 mL). The chitosan solution was sprayed into 0.50 M NaOH solution (500 mL) as a precipitation bath, which neutralized the acetic acid within the chitosan gel and thereby coagulated the chitosan gel as uniform spherical chitosan gel beads. A magnetic stirrer was used to stir the aqueous NaOH solution. The wet chitosan gel beads (hereafter called chitosan beads) were extensively rinsed with distilled water to remove any NaOH, filtered and finally air-dried to remove the water from the pores of the structure. The beads were then stored in distilled water and ready for use.

3.3.2. Preparation of Basic Catalyst Chitosan-g-poly(vinylpyridine)(Cs-PVP) Beads

3.3.2.1. Heterogeneous Grafting of 4-Vinylpyridine onto Chitosan

The grafting of 4-vinylpyridine onto chitosan was conducted using the same procedure reported in the literature [21], a typical heterogeneous method in which chitosan powder (1.00 g) was suspended in distilled water (50 mL) and mixed with 3 × 10⁻³ M of redox initiator mixture (1:0.75) K₂S₂O₇ and NaHSO₃, respectively. 4-Vinylpyridine monomer (1.05 g, 10 mmol) was added and the reaction was conducted at 55 °C for 3 h. At the end of reaction time, the graft copolymer was filtered off and washed with water and was then extensively purified with hot ethanol using the Soxhlet extraction technique to get rid of the unreacted monomer. Finally the graft copolymer (Cs-PVP), was dried. An 80% graft was obtained. The used amount in all reaction was 10% wt of the Cs-PVP catalyst.

3.3.2.2. Preparation of Chitosan/PVP Copolymer Beads

Applying the same reported methodology [30], freshly prepared Cs-PVP copolymer was converted into spherical beads by dissolving graft copolymer (1.00 g) in 5% (v/v) acetic acid solution (50 mL). The graft copolymer solution was treated as usual and thereby the gel beads were coagulated. The wet grafted chitosan beads were extensively washed with distilled water to be ready for use.

3.3.3. Preparation of Cs-PVP—Supported Iron(III) Complex by Adsorption of Fe³⁺ Ions on Cs-PVP Grafted Chitosan Beads Using Fe(NO₃)₃ [34]

The degree of adsorption was calculated based on the difference of Fe³⁺ concentration in aqueous solution before and after adsorption at a wavelength of 248 nm using an atomic absorption spectrophotometer (Perkin-Elmer 3100 Model). For Fe(III) adsorption onto Cs-PVP, a contact time of 5 h at pH 1.8 was used for stirred mixture of Cs-PVP beads (0.05 g) and Fe(III) solution (100 mL, 10 mM) in a 250 mL beaker. The amount adsorbed on the beads was calculated according to the following equation:

where C₀ is the initial Fe(III) concentration (ppm), C_e is the final concentration of Fe(III) after the adsorption time, V is the volume of Fe(III) solution (mL) and W is the used weight of graft copolymer Cs-PVP beads (g). The yellowish-colored beads adsorbed Fe³⁺ were washed thoroughly with distilled water and stored in distilled water for further use. Under the previous conditions, the maximum adsorption capacity was obtained as 0.089 mmol Fe³⁺/g chitosan.

3.3.4. Reaction of Benzylidene-Malononitrile 1 with Dimedone and Cyclohexanone

A mixture of benzylidene-malononitrile 1 (1.54 g, 10.0 mmol) with either dimedone or cyclohexanone (10.0 mmol) in absolute ethanol (50 mL) was refluxed for 3 h in the presence of a catalytic amount (10%wt.) of the catalyst (Method A using Cs beads and Method B using Cs-PVP beads). The solid product, so formed, was filtered of and recrystallized from ethanol.

2-Amino-7,7-dimethyl-5-oxo-4-phenyl-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (2). Colorless crystals; % Yields: Method A (Cs beads = 75%), Method B (Cs-PVP beads = 95%); Mp 234 °C, lit. 233–235 °C [40]; IR (KBr): υ = 1708 (C=O), 2198 (CN), 3341, 3420 (NH₂) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 0.96 (s, 3H, CH₃), 1.05 (s, 3H, CH₃), 2.09–2.24 (s, 2H, CH₂), 2.47 (s, 2H, CH₂), 4.20 (s, 1H, CH, C-4 pyran), 7.01 (s, 2H, NH₂), 7.15–7.28 (m, 5H, phenyl-H); ¹³C-NMR (DMSO-d₆): δ = 26.9 (CH₃), 28.5 (CH₃), 31.9 (C(CH₃)₂), 35.7 (C-4, pyran), 50.1 (CH₂), 58.5 (CH₂), 119.8 (CN), 112.9, 126.7, 127.3, 128.5, 144.8, 158.6, 162.7 (aromatic carbons); MS, m/z (%), 294.1 (M⁺, 29), 217.1 (66), 55.1 (100). Anal. Calcd. for C₁₈H₁₈N₂O₂: C, 73.45; H, 6.16; N, 9.52. Found: C, 73.36; H, 6.10; N, 16.43.

2-Amino-4-phenyl-4a,5,6,7-tetrahydronaphthalene-1,3,3(4H)-tricarbonitrile (3). Yellow crystals; % Yields: Method A (Cs beads = 55%), Method B (Cs-PVP beads = 90%); Mp 252 °C; Lit. Mp 253 °C [9]; IR (KBr): υ = 1650 (olefinic C=C), 2211 (CN), 2254 (CN) 3341, 3420 (NH₂) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 0.84 (m, 1H, 5-H), 1.44 (m, 2H, 5-H, 6-H), 1.66 (m, 1H, 6-H), 2.04 (m, 1H, 7-H), 2.17 (m, 1H, 7-H), 2.80 (m, 1H, 4a-H), 3.52 (d, 3J = 12.3 Hz, 1H, 4-H), 5.72 ("s", 1H, 8-H), 7.37 (s, 2H, NH₂), 7.41 (m, 3H, m-H, p-H, Phenyl), 7.48 (m, 1H, o-H, Phenyl), 7.59 (m, 1H, o-H, Phenyl); ¹³C-NMR (DMSO-d₆): δ = 21.0 (C-6), 24.9 (C-7), 27.0 (C-5), 33.8 (C-4a), 42.9 (C-3), 50.5 (C-4), 81.5 (C-1), 112.4 (3-CN), 112.6 (3-CN), 116.2 (1-CN), 120.3 (C-8), 126.9 (o-C, Phenyl), 128.6 (m-C, Phenyl), 128.8 (C-8a), 128.9 (p-C, Phenyl), 132.4 (o-C, Phenyl), 134.6 (i-C, Phenyl), 143.6 (C-2); MS, m/z (%), 300.2 (M⁺, 100), 209.1 (43), 91.1 (54).

3.3.5. Reaction of Arylidene-Malononitrile with Ethyl Acetoacetate

A mixture of the arylidenemalononitrile derivative (phenyl, p-chlorophenyl or p-methoxyphenyl) (10.0 mmol) with ethyl acetoacetate (10.0 mmol) in absolute ethanol (50 mL) was refluxed for 3 h in the presence of catalytic amount (10%wt.) of the catalyst (Method A using Cs beads and Method B using Cs-PVP beads). The solid product, so formed, was filtered off and recrystallized from ethanol.

Ethyl 6-amino-5-cyano-2-methyl-4-phenyl-4H-pyran-3-carboxylate (4a). Colorless crystals; % Yields: Method A (Cs beads = 59%), Method B (Cs-PVP = 90%); Mp 194 °C; Lit. Mp 194–195 °C [41]; IR (KBr): υ = 1691 (C=O), 2190 (CN), 3329, 3385 (NH₂) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 1.03 (t, J = 7.0 Hz, 3H, ester CH₃), 2.32 (s, 3H, pyran-CH₃), 3.98 (AB of ABX₃, J = 7.0 Hz, 2H, OCH₂), 4.32 (s, 1H, H-4), 6.93 (br. s, 2H, NH₂), 7.16–7.34 (m, 5H, Phenyl); ¹³C-NMR (DMSO-d₆): δ = 13.7 (CH₃, ester), 18.1 (CH₃), 38.8 (C-4), 57.3 (C-3), 60.1 (CH₂, ester), 107.3 (C-5), 119.6 (CN), 126.8 (C-4', Phenyl), 127.1 (C-2', Phenyl), 128.4 (C-3', Phenyl), 144.8 (C-1', Phenyl), 156.5 (C-6), 158.5 (C-2), 165.4 (C=O); MS, m/z (%), 284.1 (M⁺, 70), 207.1 (100). Anal. Calcd. for C₁₆H₁₆N₂O₃: C, 67.59; H, 5.67; N, 9.85. Found: C, 67.44; H, 5.61; N, 9.70.

Ethyl 6-amino-4-(4-chlorophenyl)-5-cyano-2-methyl-4H-pyran-3-carboxylate (4b). Pale yellow crystals; % Yields: Method A (Cs beads = 68%), Method B (Cs-PVP = 87%); Mp 162 °C; IR (KBr): υ = 1695 (C=O), 2210 (CN), 3330, 3400 (NH₂) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 1.10 (t, J = 7.1 Hz), 3H, ester CH₃), 2.39 (s, 3H, pyran-CH₃), 4.14 (AB of ABX₃, J = 7.1 Hz), 2H, OCH₂), 4.34 (s, 1H, 4-H), 7.01 (br. s, 2H, NH2), 7.08 (d, 2H, o-H, J = 8 Hz, aryl), 7.37 (d, 2H, m-H, J = 8 Hz, aryl); ¹³C-NMR (DMSO-d₆): δ = 14.1 (CH₃ of CO₂C₂H₅), 19.2 (CH₃), 37.0 (C-4), 56.1 (C-5), 61.3 (O-CH₂), 106.5 (C-3), 118.6 (CN), 125.8, 128.7, 129.6, 146.4, 154.2, 156.8 (C-2, C-6), 167.0 (C=O); MS, m/z (%), 318.1 (M⁺, 37), 207.1 (100). Anal. Calcd. for C₁₆H₁₅ClN₂O₃: C, 60.29; H, 4.74; Cl, 11.12; N, 8.79. Found: C, 60.13; H, 4.66; Cl, 10.94; N, 8.57.

Ethyl 6-amino-5-cyano-4-(4-methoxyphenyl)-2-methyl-4H-pyran-3-carboxylate (4c). Colorless crystals; % Yields: Method A (Cs beads = 70%), Method B (Cs-PVP = 90%); Mp. 145 °C; Mp 144–145 °C [41]; IR (KBr): υ = 1684 (C=O), 2188 (CN), 3325, 3395 (NH₂) cm^-1; ¹H-NMR (DMSO-d₆): δ = 1.12 (t, J = 7.1 Hz, 3H, ester CH₃), 2.36 (s, 3H, pyran-CH₃), 3.79 (s, 3H, O-CH₃), 3.99 (AB of ABX₃, J = 7.1 Hz, 2H, ester CH₂), 4.38 (s, 1H, H-4), 4.54 (br. s, 2H, NH₂), 6.85 (d, 2H, H-3', J = 8 Hz, aryl), 7.16 (d, 2H, H-2', J = 8 Hz, aryl); ¹³C-NMR (DMSO-d₆): δ = 18.1 (CH₃ of ester), 37.7 (C-4), 55.0 (O-CH₃), 60.3 (CH₂ of ester), 62.4 (C-3), 108.1 (C-5), 114.1 (C-3'), 118.8 (CN), 128.7 (C-2'), 136.0 (C-1'), 156.4 (C-4'), 157.4 (C-6), 158.5 (C-2), 160.3 (C=O); MS, m/z (%), 314.1 (M⁺, 9), 184.1 (100). Anal. Calcd. for C₁₇H₁₈N₂O₄: C, 64.96; H, 5.77; N, 8.91. Found: C, 64.58; H, 5.62; N, 8.78.

3.3.6. Reaction of 1 with α-Naphthol

A mixture of benzylidene-malononitrile 1 (1.54 g, 10.0 mmol) with α-naphthol (10.0 mmol) in absolute ethanol (50 mL) was refluxed for 4 h in the presence of a catalytic amount (10% wt.) of the catalyst (Method A using Cs beads and Method B using Cs-PVP beads). The solid product, so formed, was filtered off and recrystallized from ethanol.

2-Amino-4-phenyl-4H-benzo[h]chromene-3-carbonitrile (7). This compound was obtained as yellow crystals [42]; % Yields: Method A (Cs beads = 71%), Method B (Cs-PVP = 86%); Mp 210 °C; IR (KBr): υ = 1605 (Ar C=C), 1656 (olefinic C=C), 2205 (CN), 3303, 3448 (NH₂) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 4.90 (s, 1H, 4-H), 7.11 (d, 3J = 8.5 Hz, 1H, 5-H), 7.56 m, 2H/7.64, t, 1H/7.88, d, 1H/8.27, d, 1H (6-H, 7-H, 8-H, 9-H, 10-H), 7.18 (s, 2H, NH₂), 7.24 (m, 1H, p-H, Phenyl), 7.25 (m, 2H, o-H, Phenyl), 7.32 (m, 2H, m-H, Phenyl); ¹³C-NMR (DMSO-d₆): δ = 40.9 (C-4), 56.3 (C-3), 117.9, 120.7, 122.7, 123.9, 126.2, 126.6, 126.7, 126.9, 127.6, 132.7 (C-4a, C-5, C-6, C-6a, C-7, C-8, C-9, C-10, C-10a, p-C, Phenyl), 120.4 (CN), 127.6 (o-C, Phenyl), 128.7 (m-C, Phenyl), 142.7, 145.6 (C-10b, i-C, Phenyl), 160.1 (C-2); MS, m/z (%), 298.1 (M⁺, 75), 221.1 (100), 77 (10). Anal. Calcd. for C₂₀H₁₄N₂O: C, 80.52; H, 4.73; N, 9.39. Found: C, 80.19; H, 4.64; N, 8.17.

3.3.7. One Pot Reaction of benzaldehyde and malononitrile with 2-cyanothioacetamide (11)

A mixture of benzaldehyde (1.06 g, 10.0 mmol), malononitrile (0.66 g, 10.0 mmol) and 2-cyanothioacetamide (1.00 g, 10.0 mmol) in absolute ethanol (50 mL) was refluxed for 4 h in the presence of a catalytic amount (10% wt.) of both catalysts (Method A using Cs beads and Method B using Cs-PVP beads). The solid product was filtered off and recrystallized from ethanol.

2,6-Diamino-4-phenyl-4H-thiopyran-3,5-dicarbonitrile (11). Yellow crystals; % Yields: Method A (Cs beads = 80%), Method B (Cs-PVP = 95%); Mp 191–192 °C [36]; IR(KBr): υ = 2192 (broad band, two CN groups), 3300–3450 (two NH₂ groups) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 4.24 (s, 1H,4-H), 6.86–6.89 (s, 4H, two NH₂ groups), 7.22–7.34 (m, 5H, Phenyl); ¹³C-NMR (DMSO-d₆): δ = 43.4 (C-4), 72.0 (C-3), 118.6 (two CN), 126.7, 127.2, 128.9, 143.2 (Phenyl), 151.0 (C-2, thiopyran); MS, m/z (%), 254.1 (M⁺, 12), 228.1 (41), 77.1 (100). Anal. Calcd. for C₁₃H₁₀N₄S: C, 61.40; H, 3.96; N, 22.03; S, 12.61. Found: C, 61.13; H, 3.88; N, 21.87; S, 12.52.

3.3.8. Reaction of 1 with 4,4-Dimethoxybutan-2-one

A mixture of benzylidene-malononitrile 1 (1.54 g, 10.0 mmol) with acetylacetaldehyde, dimethyl acetal (AADMA, 10.0 mmol) in absolute ethanol (50 mL) was refluxed for 4 h in the presence of a catalytic amount (10%wt.) of the catalyst (Method A using Cs beads and Method B using Cs-PVP beads). The solid product, so formed, was filtered off and recrystallized from ethanol.

5-Acetyl-2-amino-4-phenyl-4H-pyran-3-carbonitrile (13). Yellow powder; % Yields: Method A (Cs beads = 0%), Method B (Cs-PVP = 70%); 198 °C; IR (KBr): υ = 1701 (C=O), 2205 (CN), 3320–3400 (NH₂ groups) cm⁻¹; ¹H-NMR (DMSO-d₆): δ = 2.32 (s, 3H, CH₃), 4.29 (s, 1H, C-2 pyran), 6.94 (s, 2H, NH₂), 7.14–7.33 (m, 5H, Phenyl); ¹³C-NMR (DMSO-d₆): δ = 19.4 (CH₃), 38.6 (C-4, pyran), 60.9 (C-3, pyran), 114.2 (C-5, pyran), 116.8 (CN), 122.1, 128.4, 129.0, 138.6, (phenyl), 152.9, 157.3 (C-2, C-6 pyran), 183.9 (C=O); MS, m/z (%), 240.1 (M⁺, 24), 197.1 (92), 163.1 (100). Anal. Calcd. for C₁₄H₁₂N₂O₂: C, 69.99; H, 5.03; N, 11.66. Found: C, 69.78; H, 4.92; N, 11.49.

3.3.9. Reaction of Enaminones 14a,b with Malononitrile

A mixture of (10.0 mmol) of enaminone 14a,b with malononitrile (0.66 g, 10.0 mmol), in absolute ethanol (50 mL) was refluxed for 3 h in the presence of catalytic amounts (10%wt.) of the catalyst (Method A using Cs beads and Method B using Cs-PVP beads). The solid product, so formed, was filtered off and recrystallized from ethanol.

2-Cyano-5-(dimethylamine)-5-phenylpenta-2,4-dienamide (15a). Yellow crystals; % Yields: Method A (Cs beads = 80%), Method B (Cs-PVP = 90%); Mp: 257 °C; IR (KBr, cm^-1): ν = 1667 (CO), 2191 (CN), 3330 and 3395 (NH₂); ¹H-NMR (400 MHz, DMSO_-d₆) δ = 2.77 (s, 3H, CH₃), 3.16 (s, 3H, CH3), 5.63 (d, 1H, J = 12.6 Hz, H-4), 6.84 (s, 2H, NH₂), 6.98 (d, 1H, J = 12.6 Hz, H-3), 7.26–7.29 (m, 2H, phenyl-H), 7.38–7.41 (m, 3H, phenyl-H). ¹³C-NMR (125 MHz, DMSO-d₆), δ = 39.8 (N(CH₃)₂), 87.6, 96.9, 118.8 (CN), 128.6, 129.6, 134.0 (aromatic carbons), 153.3 (C-3), 164.6 (C-5), 165.11 (C=O). MS (m/z (%)): 241.1 (M⁺, 100), 179.1(76). Anal. Calcd. for C₁₄H₁₅N₃O: C, 69.69; H, 6.27; N, 17.41. Found: C, 69.56; H, 6.27; N, 17.29.

2-Cyano-5-(dimethylamino)-5-(furan-2-yl)penta-2,4-dienamide (15b). Reddish brown crystals; % Yields: Method A (Cs beads = 78%), Method B (Cs-PVP = 95%); M.p. 245 °C; IR (KBr, cm⁻¹): ν = 1669 (CO), 2189 (CN), 3340 and 3305 (NH₂); ¹H-NMR (400 MHz, DMSO-d₆), δ = 2.97 (s, 6H, N(CH₃)₂), 5.59 (d, 1H, J = 12.5 Hz, H-4), 6.72 (d, 1H, J = 5.0 Hz, furyl H-3), 6.78 (d, 1H, J = 5.0 Hz, furyl H-5), 7.02 (s, 2H, NH₂), 7.56 (d, 1H, J = 12.5 Hz, H-3), 7.99 (t, 1H, J = 5.0 Hz, furyl H-4); ¹³C-NMR (125 MHz, DMSO-d₆): δ = 40.77, 90.40, 98.31, 111.53, 115.75, 118.38, 144.80, 145.37, 151.73, 153.40 (C-5), 164.49 (CONH₂). MS (m/z (%)): 231.1 (M⁺, 21), 179.1(100). Anal. Calcd. for C₁₂H₁₃N₃O₂: C, 62.33; H, 5.67; N, 18.17. Found: C, 62.19; H, 5.57; N, 17.58.

3.3.10. Oxidation of Methyl Pyridazinone with Cs-PVP-Fe(III) Complex

Hydrogen peroxide solution (10 mmol, 30%) was added carefully to a preheated solution of methylpyridazinones 16a,b (2 mmol) in glacial acetic acid (5 mL). The reaction mixture was then refluxed in the presence of 10%wt of Cs-PVP/Fe catalyst until thin layer chromatography indicated that the reaction was completed. The solid crude product, so formed, was poured into ice/water mixture (20 mL) and stirred for 30 min. The product so formed was extracted using CH₂Cl₂. The organic layer was dried over anhydrous Na₂SO₄ and then concentrated under reduced pressure to yield analytically pure products 17a,b. The used Cs-PVP/Fe(III) catalyst could be regenerated and used for 5 times without appreciable loss of activity.

7-Amino-2-phenylfuro[3,4-d]pyridazin-1(2H)-one (17a). Yellow powder; M.p. 198 °C; IR (KBr, cm^-1): ν = 1660 (CO), 3330 and 3390 (NH₂); ¹H-NMR (400 MHz, DMSO-d₆), δ = 6.07 (s, 2H, NH₂), 7.46 (s, 1H, pyridazinone), 7.51 (m, 5H, phenyl), 8.14 (s, 1H, furan); ¹³C-NMR (125 MHz, DMSO-d₆), δ = 114.1, 121.6, 126.8, 130.7, 131.2, 139.9, 140.8, 144.0, 147.2 (aromatic carbons), 168.2 (C=O). MS (m/z (%)): 227.1 (M⁺, 12), 77.1 (100). Anal. Calcd. for C₁₂H₉N₃O₂: C, 63.43; H, 3.99; N, 18.49. Found: C, 63.28; H, 3.78; N, 18.29.

7-Amino-2-(4-chlorophenyl)furo[3,4-d]pyridazin-1(2H)-one (17b). Pale yellow powder. (M.p. 216 °C); IR (KBr, cm⁻¹): ν = 1668 (CO), 3360 and 3330 (NH₂); ¹H-NMR (400 MHz, DMSO-d₆), δ = 6.29 (s, 2H, NH₂), 7.25 (d, 2H, o-H, J = 8 Hz, aryl), 7.69 (d, 2H, m-H, J = 8 Hz, aryl), 8.26 (s, 1H, furan); ¹³C-NMR (125 MHz, DMSO-d₆) δ = 113.1, 124.4, 126.9, 128.6, 129.0, 133.1, 139.1, 151.7, 155.9 (aromatic carbons), 171.9 (C=O). MS (m/z (%): 261.1 (M+, 4), 111.1 (100). HRMS; 261.0298 (C₁₂H₈O₂N₃Cl₁).

4. Conclusions

We could clearly show that chitosan-g-PVP beads can be used as an efficient basic, recyclable, environmentally friendly biocatalyst for Michael additions while its supported iron (III) complex is a promising catalyst for controlled oxidation of alkyl functions. The novel catalysts, Cs-PVP and Cs-PVP/Fe(III) beads, could be regenerated and reactivated at least five times, without appreciable loss of activity.

Conflicts of Interest

The authors declare no conflict of interest.