Amir Landarani-Isfahani,
Iraj Mohammadpoor-Baltork*,
Valiollah Mirkhani*,
Majid Moghadam
,
Shahram Tangestaninejad
and
Hadi Amiri Rudbari
Department of Chemistry, University of Isfahan, Isfahan, 81746-73441, Iran. E-mail: imbaltork@sci.ui.ac.ir; mirkhani@sci.ui.ac.ir; Fax: +98 031 36689732
First published on 3rd June 2020
Dendrimers are of great interest due to their special structural topology and chemical versatility. Owing to their properties, dendrimers have found practical applications in catalytic processes as efficient nanoreactors. Therefore, we herein report an environmentally attractive strategy and highly efficient route for the synthesis of a wide variety of diaryl sulfides using palladium nanoparticles immobilized on a nano-silica triazine dendritic polymer (Pdnp-nSTDP) as a nanoreactor. In this manner, different diaryl or aryl heteroaryl sulfides and bis(aryl/heteroarylthio)benzene/anthracene/pyridine derivatives were prepared via C–S cross-coupling reactions of aryl halides with diaryl/diheteroaryl disulfides under thermal conditions and microwave irradiation. The catalyst could be easily recovered and reused several times without any significant loss of its activity.
Diarylsulfides are important intermediates in a wide variety of organic synthesis and play a significant role in many biologically and pharmaceutically active compounds.16 These moieties are used for treatment of inflammation,17 cancer,18,19 immunodeficiency virus (HIV),17 and Alzheimer's and Parkinson's diseases.20 Because of their importance and useful properties, different approaches have been developed for the synthesis of diarylsulfides via C–S cross-coupling reactions.21,22 Generally, in these coupling reactions, thiols (ArSH) are reacted with aryl halides or aryl boronic acids as aryl donors in the presence of different catalytic systems including Fe,23–25 Cu,26–28 Ni,29,30 Co,31,32 In (ref. 33) and Pd.34–38
However, thiols have offensive odors and are easily oxidized to the corresponding diaryl disulfides (ArSSAr) in air. Thus, diaryl disulfides are often produced as a by-product in the above mentioned methods.39 To solve this problem and for the effective conversion of thiols to diaryl sulfides, aryl donors are usually used in excess.40 On the contrary, diaryl disulfides are air stable, and easy to handle. Nevertheless, little attention has been paid to the cross-coupling of diaryl disulfides as sulfur nucleophile with aryl donors.41–45 Accordingly, development of convenient methods and catalysts for the synthesis of diaryl sulfides via such a cross-coupling reactions is still critically needed.
Based on the green chemistry concept and principal, synthetic approach and process should be premeditated to use and generate substances which exhibit little or no hazard to human body and the natural environment. Moreover, these chemical transformations are often performed with high yields, at low temperatures, in short reaction times, and in the presence of low amount of the catalyst in water or aqueous media.46
Nano-silica triazine dendritic polymer (nSTDP) can be effectively applied for nanoscale organic transformations. During the course of our research on the application of this nanoreactors47–50 and also our interest in Pd-catalyzed coupling reactions, herein we disclose a convenient method for mono- and di C–S cross-coupling reactions with diaryl or diheteroaryl disulfides using Pdnp-nSTDP (Fig. 1) as an eco-friendly nanoreactor under conventional heating and microwave irradiation (Scheme 1). As far as we know, the use of palladium nanoparticles-based dendritic catalyst for such a coupling reactions is reported for the first time and could be considered as an exclusive feature of nanoscience and green chemistry.
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Fig. 1 Schematic illustration of preparation of palladium nanoparticles immobilized on nano silica triazine dendritic polymer (Pdnp-nSTDP) catalyst. |
Initially, for screening experiments, the coupling reaction of 4-bromoanisole (1 mmol) with di-p-tolyl disulfide (0.5 mmol) was carried out using Pdnp-nSTDP catalyst for determination of effective factors such as types of base and solvent, temperature, catalyst loading and MW power. The results are shown in Table 1. Primarily, different bases such as NEt3, piperidine, DBU (1,8-diazabicyclo[5.4.0]undec-7-ene), NaOH, Na2CO3, K2CO3 and 20% solution of tetrabutylammonium hydroxide in water (TBAH) were examined. Amongst, TBAH was found as the most effective base in terms of both reaction time and yield. The effect of solvent was also checked in the model reaction and highest yield was obtained in a 1:
1 mixture of H2O–DMF (Table 1, entries 7–12). Next, we investigated the catalyst loading (0.08–0.12 mol% Pd) and 0.1 mol% (8 mg) of the catalyst was found to be the optimum amount for completion of this reaction (Table 1, entries 7, 13 and 14). Finally, the effect of temperature on the activity of this catalyst was studied in the range of 70 to 100 °C. As can be seen in Table 1, by increasing the temperature to 80 °C, the yield of the reaction was improved but its increasing from 80 to 100 °C did not influence the yield of the product. Therefore, 0.1 mol% (8 mg) of the catalyst and TBAH base in a mixture of H2O–DMF (1
:
1) at 80 °C are the most appropriate reaction conditions for this transformation (Table 1, entry 7). It is worth mentioning that aqueous DMF has been used as a green solvent in different organic transformations, especially in cross coupling reactions.52
Entry | Base | Catalyst (mol% Pd) | Solventa | Method | Time (h) | Yieldb (%) | TONc | TOFd (h−1) |
---|---|---|---|---|---|---|---|---|
a The reaction was performed using 1 mL of solvent and 1 mmol of base.b Isolated yield.c TON = turnover numbers.d TOF = turnover frequency.e DBU = 1,8-diazabicyclo[5.4.0]undec-7-ene.f TBAH = 20% tetrabutylammonium hydroxide in water. | ||||||||
1 | Et3N | 0.1 | DMF | 80 °C | 24 | 15 | 150 | 6.25 |
2 | Piperidine | 0.1 | DMF | 80 °C | 24 | 40 | 400 | 16.7 |
3 | DBUe | 0.1 | DMF | 80 °C | 24 | 28 | 280 | 11.7 |
4 | NaOH | 0.1 | DMF | 80 °C | 12 | 64 | 640 | 53.3 |
5 | K2CO3 | 0.1 | DMF | 80 °C | 12 | 60 | 600 | 50.0 |
6 | Na2CO3 | 0.1 | DMF | 80 °C | 12 | 83 | 830 | 69.2 |
7 | TBAHf | 0.1 | H2O/DMF | 80 °C | 5 | 95 | 950 | 190.0 |
8 | TBAH | 0.1 | H2O/EtOH | 75 °C | 12 | 51 | 510 | 42.5 |
9 | TBAH | 0.1 | H2O/DMSO | 80 °C | 12 | 86 | 860 | 71.7 |
10 | TBAH | 0.1 | H2O/dioxane | 80 °C | 12 | 85 | 850 | 70.8 |
11 | TBAH | 0.1 | H2O/toluene | 80 °C | 12 | 30 | 300 | 25.0 |
12 | TBAH | 0.1 | — | 80 °C | 12 | 45 | 450 | 37.5 |
13 | TBAH | 0.08 | H2O/DMF | 80 °C | 5 | 53 | 625 | 125.0 |
14 | TBAH | 0.12 | H2O/DMF | 80 °C | 5 | 95 | 792 | 158.3 |
15 | TBAH | 0.1 | H2O/DMF | 100 °C | 5 | 95 | 950 | 190.0 |
16 | TBAH | 0.1 | H2O/DMF | 70 °C | 8 | 74 | 740 | 92.5 |
17 | TBAH | 0.1 | H2O/DMF | 170 W, 50 °C | 15 min | 85 | 850 | 226.6 |
18 | TBAH | 0.1 | H2O/DMF | 200 W, 70 °C | 10 min | 90 | 900 | 5400 |
19 | TBAH | 0.1 | H2O/DMF | 230 W, 80 °C | 10 min | 95 | 950 | 5700 |
20 | TBAH | 0.15 | H2O/DMF | 230 W, 80 °C | 10 min | 73 | 487 | 2920 |
21 | TBAH | 0.08 | H2O/DMF | 230 W, 80 °C | 10 min | 62 | 775 | 4650 |
In order to evaluate the effect of microwave irradiation (MW) on this transformation, the model reaction was carried out under MW at different conditions (Table 1, entries 17–21). The highest yield was obtained with an applied power of 230 W at 80 °C (Table 1, entry 19).
The scope and generality of this protocol were then investigated in the C–S cross-coupling of various aryl halides with different diaryl disulfides (Table 2). The reaction of a series of aryl iodides and bromides with different diaryl disulfides proceeded effectively in the presence of Pdnp-nSTDP catalyst under the optimized conditions and the desired diaryl sulfides were produced in 93–96% yields (Table 2, entries 1–11).
Entry | R1 | X | R2 | Thermal | MW | ||
---|---|---|---|---|---|---|---|
Time (h) | Yieldb (%) | Time (min) | Yieldb (%) | ||||
a Reaction conditions: aryl halide (1 mmol), diaryl disulfide (0.5 mmol), TBAH (1 mmol), Pdnp-nSTDP (0.1 mol% Pd, 8 mg), H2O/DMF (1![]() ![]() |
|||||||
1 | 4-Me | I | H | 3 | 96 | 5 | 95 |
2 | 4-Me | I | 4-Me | 3 | 94 | 5 | 95 |
3 | 4-OMe | I | 4-Me | 3 | 96 | 5 | 96 |
4 | 4-Me | I | 4-Ac | 3 | 95 | 5 | 96 |
5 | H | I | 4-Me | 3 | 93 | 5 | 95 |
6 | 4-Me | Br | 4-Ac | 5 | 95 | 10 | 92 |
7 | 4-Me | Br | H | 5 | 95 | 10 | 93 |
8 | H | Br | 4-Me | 5 | 94 | 10 | 89 |
9 | 3-OMe | Br | 4-OMe | 5 | 96 | 10 | 93 |
10 | 4-Me | Br | 4-OMe | 5 | 95 | 10 | 95 |
11 | 4-Me | Br | 4-CHO | 5 | 95 | 10 | 90 |
12 | 4-Me | Cl | 2-Me | 10 | 85 | 25 | 82 |
13 | 4-Me | Cl | 4-CHO | 10 | 90 | 25 | 86 |
14 | 4-Me | Cl | 4-Ac | 10 | 87 | 25 | 90 |
15 | 4-Me | Cl | H | 10 | 83 | 25 | 85 |
The applicability of this palladium-catalyzed C–S cross-coupling reactions was also examined using the less reactive but cheaper and more readily available aryl chlorides instead of their bromide and iodide counterparts. As the data revealed, the cross-coupling of aryl chlorides with diaryl disulfides proceeded smoothly in the presence of Pdnp-nSTDP to afford the corresponding products in 83–90% yields (Table 2, entries 12–15). The results in Table 2 disclose that the dendritic polymer accelerates the C–S cross coupling reactions due to its cavities that isolate the catalytic active sites from the surrounding environment and provide an efficient nanoreactors.
The C–S cross-coupling of these aryl halides with diaryl disulfide was also investigated under microwave irradiation, in which the desired products were provided in 82–96% yields within 5–25 min (Table 2). These results clearly showed that microwave irradiation as an eco-friendly technology has the evident advantage of very short reaction times over the conventional heating mode.
2-(Arylthio)-1,3-benzothiazoles are essential building blocks which are found in a large number of biologically and pharmaceutically active molecules.53,54 Accordingly, we decided to explore the potential of this catalytic system in the synthesis of 2-(arylthio)-1,3-benzothiazoles via C–S cross-coupling of arylbromides with 2,2′-dithiobis(benzothiazole) under conventional heating and microwave irradiation. In this manner, different arylbromides such as bromobenzene, p-tolylbromobenzene and p-methoxybromobenzene were converted to their corresponding sulfides in high to excellent yields (Table 3). One interesting example is 4-(1,3-benzothiazol-2-ylthio)aniline (3d) which is the precursor of cathepsin-D inhibitor. So, this simplified strategy can be potentially utilized for accessing a broad range of pharmaceutically important molecules.55
In order to further broaden the applicability of this method, we studied the one-pot C–S cross-coupling reactions of dibromoarenes with diaryl disulfides or 2,2′-dithiobis(benzothiazole) using this catalytic system. As can be seen, two-fold C–S cross-coupling reaction of 1,4-dibromobenzene, 9,10-dibromoanthracene or 2,6-dibromopyridine with di-p-tolyl disulfide, di-m-methoxyphenyl disulfide or 2,2′-dithiobis(benzothiazole) in the presence of Pdnp-nSTDP catalyst was performed efficiently under conventional heating and microwave irradiation and provided excellent yields of the desired coupling products (Table 4).
Dibromoarene | Product | Yieldb (%) (time) | |
---|---|---|---|
Thermal | MW | ||
a Reaction conditions: dibromoarene or 2,6-dibromopyridine (1 mmol), diaryl or 2,2′-dibenzothiazyl disulfide (1 mmol), TBAH (2 mmol), Pdnp-nSTDP (0.2 mol% Pd, 16 mg), H2O/DMF (1![]() ![]() |
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85 (10 h) | 81 (10 min) |
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82 (6 h) | 90 (45 min) |
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81 (8 h) | 85 (15 min) |
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90 (6 h) | 94 (12 min) |
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90 (6 h) | 93 (10 min) |
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75 (6 h) | 89 (10 min) |
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85 (6 h) | 85 (10 min) |
The products were characterized by different analytical tools such FT-IR, 1H NMR, and 13C NMR and elemental analysis. In addition, the compound 5D was characterized by X-ray crystallographic analysis (CCDC 1029634,† Fig. 2).
The recovery and reuse of a catalyst is of practical importance and is economically as well as environmentally attractive. In this manner, the recovery of Pdnp-nSTDP was investigated in model reaction. After completion of the reaction, ethyl acetate was added and the catalyst was separated by centrifugation. The recovered catalyst was washed with DMF, dried and reused for subsequent reactions. As shown in Fig. 3, Pdnp-nSTDP could be recycled and reused at least five times without any significant loss of its activity. The yields of the desired product after six consecutive runs were 93 and 89% under conventional heating and MW irradiation, which show the high efficiency of this method. Moreover, the amount of palladium leached from Pdnp-nSTDP catalyst, measured by ICP-OES, indicated very low leaching of palladium.
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Fig. 3 Reusability of the Pdnp-nSTDP catalyst in the C–S cross coupling reaction of 4-bromoanisole and di-p-tolyl disulfide. |
In addition, little increase in the yield of product in the hot filtration test confirmed the low leaching of the Pd species. This means that the leached Pd species are restabilized by the dendritic polymer. Therefore, it seems that the reaction mechanism is identical as a “Cocktail” of catalysts in which the Pd species are leached into the reaction medium, and then C–S coupling reaction occurs in the solution phase. After the corresponding product forms via reductive elimination, the leached Pd species are restabilized on the surface of the dendritic polymer.56–58
Based on these findings, the C–S cross-coupling mechanism is shown in Scheme 2. First, the aryl halide (ArX) is added to palladium nanoparticles via an oxidative-addition pathway to form the organopalladium species 1. Then, aromatic disulfide is added to intermediate 1 to produce the intermediate 2 and released X2.58 Finally, the desired C–S cross-coupling product 3 is formed by a reductive-elimination process and restores the Pdnp-nSTDP catalyst for the next cycle.
The structure of the catalyst after the final run was also investigated by SEM and compared with the fresh Pdnp-nSTDP catalyst. As shown in Fig. 4, the shape and morphology of Pdnp-nSTDP did not show any significant change after 6th run.
The applicability and reactivity of Pdnp-nSDTP catalyst was also compared with some other previously reported catalysts. As presented in Table 5, the Pdnp-nSDTP catalyst is superior in terms of TOF (h−1), reaction times and amount of catalyst.
Catalyst and conditions | Aryl halide | Yield (%) | TOF (h−1) | Ref. |
---|---|---|---|---|
Cu2S (1 mol%), Fe, K2CO3, DMSO, 110 °C, 18 h | ![]() |
95 | 5.28 | 45 |
CuFe2O4 (5 mol%), Cs2CO3, DMSO, 100 °C, 24 h | ![]() |
90 | 0.75 | 44 |
PdCl2(dppf) (5 mol%), Zn, THF, reflux, 24 h | ![]() |
68 | 0.57 | 43 |
Pdnp-nSDTP (0.1 mol%), TBAH, DMF/H2O, 80 °C, 3–5 h | ![]() |
93 | 310 | Present work |
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94 | 188 |
Footnote |
† Electronic supplementary information (ESI) available: Experimental procedures and spectrum. CCDC 1029634. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d0ra00719f |
This journal is © The Royal Society of Chemistry 2020 |