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Article

Photoinduced Photocatalyst-Free Cascade Cyclization of Alkynes with Sodium Sulfinates for the Synthesis of Benzothiophenes and Thioflavones

by
Hongqiang Dong
1,*,
Chunli Chen
1,
Jinlei Zhao
2,3,
Yigang Ji
4,* and
Wenchao Yang
5
1
The Open Research Fund of the National and Local Joint Engineering Laboratory of High Efficiency and Superior-Quality Cultivation and Fruit Deep Processing Technology of Characteristic Fruit Trees in South Xinjiang, College of Agriculture, Tarim University, Alaer 843300, China
2
National Engineering Research Center of Low-Carbon Processing and Utilization of Forest Biomass, Nanjing Forestry University, Nanjing 210037, China
3
Jiangsu Surveying and Design Institute of Water Resources Co., Ltd., Yangzhou 225127, China
4
Jiangsu Key Laboratory of Biofuctional Molecules, Department of Life Sciences and Chemistry, Jiangsu Second Normal University, Nanjing 210013, China
5
Guangling College and School of Plant Protection, Yangzhou University, Yangzhou 225009, China
*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(11), 4436; https://doi.org/10.3390/molecules28114436
Submission received: 6 April 2023 / Revised: 19 May 2023 / Accepted: 26 May 2023 / Published: 30 May 2023
(This article belongs to the Special Issue Novel Organic Synthetic Route to Heterocyclic Compounds)
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Versions Notes

Abstract

:
The subject of this investigation is a new method for the construction of sulfonylated heterocycles which overcomes the limitations of classical approaches using a cheap feedstock sulfonylating agent, especially under photocatalyst- and metal-free conditions.

1. Introduction

Sulfonylated heterocycles are important motifs found in many natural products, agrochemicals, and pharmaceuticals, with special physiological and biological activities [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24]. Generally, the oxidation of thioethers is the most popular approach to access sulfones [25,26]. However, in many cases, strong oxidation conditions are not applicable to all functional groups. As a result, developing the efficient and mild synthesis of value-added sulfonylated heterocycles has played a significant role in advancing heterocyclic chemistry, as well as accelerating the discovery of novel agrochemicals [27,28,29,30,31,32,33,34,35,36,37]. Sodium sulfinates, as a common and stable sulfonation raw material, are widely applied in the construction of organic sulfones, including the cascade reaction, direct C–H functionalization, and oxidative coupling, etc., [38,39,40,41]. Among these protocols, radical cascade cyclization of C–C unsaturated bonds has provided a powerful tool for the collection of sulfonylated heterocycles by introducing two different functional groups on the both ends of the alkynes or alkenes in one step [42,43,44,45,46,47,48]. From the point of synthetic chemistry, these radical cascade reactions can be very convenient and efficient to realize direct conversion from relatively inexpensive C–C unsaturated bonds to high-value-added, complex molecular scaffolds with abundant bioactivities. For example, Bi and co-workers realized a silver-catalyzed cascade cyclization of alkynes with sodium sulfinates for the synthesis of 6-methyl sulfonylated phenanthridines, where mechanistic studies indicate the transformation should proceed through an iminyl radical intermediate (Scheme 1a) [42]. Soon afterward, Wu and Jiang’s groups independently utilized sodium sulfinates and 1,6-enynes to achieve the sulfonylated benzofurans’ synthesis by using an AgNO3/K2S2O8 system (Scheme 1b) [43]. Very recently, another radical cascade spiro-cyclization of alkenes with sodium sulfinates for the direct synthesis of sulfonylated spiro[indole-3,3′-pyrrolidines] was reported by Wang’s group (Scheme 1c) [44]. Although significant progress has clearly been made in recent years, most of the traditional transformations usually depend on transition-metal catalysts or harsh reaction conditions. As a result, the development of a practical and green protocol to realize the radical cyclization of alkynes is still an attractive topic.
Over the past few decades, visible-light-induced organic reactions have emerged as an essential tool to construct new chemical bonds, featuring mild reaction conditions such as metal-free, room temperature, and simple operation conditions [49,50,51,52]. In 2015, we reported an example of using sulfinic acids as sulfonation reagents to react with alkyne in the presence of TBHP under visible-light irradiation [10]. However, the sulfonation reagent in this work is prepared from sodium sulfonates, leading to increase reaction steps. With our continuing interest in sustainable and photochemical chemistry [53,54,55,56,57,58], herein we disclose a photo-induced radical cascade cyclization of alkynes with sodium sulfinates for the divergent synthesis of sulfonated benzothiophenes and thioflavones under metal- and photocatalyst-free conditions (Scheme 1d).

2. Results and Discussion

Given these considerations, we set out to study this photoinduced cascade cyclization reaction by the treatment of 4-methylbenzenesulfinate and 2-alkynylthioanisoles in the presence of 15-W blue LED. Thankfully, the desired product benzothiophene 3a was obtained with 82% yield using [Ir(dFCF3ppy)2dtbbpy]PF6 as a photocatalyst, KI as an additive, and K2S2O8 as an oxidant (Table 1, entry 1). After the evaluation of various additives such as NaI, NaBr, and KCl, KI was found to be the most effective to promote the reaction (Table 1, Entries 2–4). Then, other oxidants were further investigated, and the yields of the target products were lower than found using K2S2O8 (Table 1, Entries 5–8). We then examined the effect of other photocatalysts to this reaction, including 4CzIPN, 4CzIPN-tBu and Mes-Acr+ClO4 (Table 1, Entries 9–12). It was found that 4CzIPN, 4CzIPN-tBu, and Mes-Acr+ClO4 exhibited a lower catalytic activity than [Ir(dFCF3ppy)2dtbbpy]PF6 and, to our surprise, the sulfonated benzothiophenes could be obtained with considerable yield in the absence of a photocatalyst. This result shows that a photocatalyst is not essential for this reaction system. Finally, no desired product was observed without the irradiation of 15-W blue LED.
After the standard reaction condition was optimized, we tested a variety of sodium sulfinates to explore the reaction scope, and the results are summarized in Scheme 2. The sodium sulfinates with electron-donating and electron-withdrawing groups on the phenyl ring proceeded through this reaction smoothly. For example, sodium sulfinates containing a halogen group (F or Cl) were all favorable, affording the corresponding products with 63% and 75% yields. In addition, sodium sulfinates containing OMe or OEt were also suitable substrates. As shown in Scheme 2, when sodium sulfinates containing a substituent group on the Ar ring were employed for this transformation, 51–79% yields of the products (3g–3i) were obtained.
In order to further prove the practicability and efficiency of the photochemical approach, we further expand the substrate scope on 2-alkynylthioanisoles. As shown in Scheme 3, a variety of substituted 2-alkynylthioanisoles could react with 4-methylbenzenesulfinate to produce the corresponding sulfonated benzothiophenes (3j–3u) with 53–89% yields. The 2-alkynylthioanisoles bearing strong electron-donating groups on the Ar ring were compatible, affording the corresponding products (3m and 3n) with 76% and 62% yields. Moreover, substrates possessing a heteroaromatic ring, such as pyridine and thiophene, could also undergo the reaction smoothly, generating the corresponding products with reasonable yields (3t and 3u). There is no doubt that the bromine-substituted sodium sulfinate could be successfully transformed into the corresponding product 3v, which will allow further complex molecule synthesis via cross-coupling reactions. We next examined the alkynes systems to evaluate their applicability to this transformation, synthesizing and applying aryl ynones as cascade substrates to provide sulfonated thioflavones (5a–5b) with good yields.
In order to elucidate the reaction mechanism of this reaction, a free-radical inhibition experiment was conducted, in which stoichiometric amounts of radical scavengers were added and the reaction was fully suppressed (Scheme 4a). In addition, a well-known free radical accepter N-arylacrylamide, which was widely used in radical tandem reactions, was applied instead of 2-alkynylthioanisoles to give sulfonylated oxindole at a 76% yield (Scheme 4b). These results indicated that the free radical process may be involved in this transformation. A plausible reaction mechanism is outlined in Scheme 4 based on the above observations and previous reports [59]. Initially, I2 is generated from KI by the oxidation of K2S2O8, which would then transfer to the excited state I2* with the irradiation of 15-W blue LEDs. Subsequently, the reaction between I2*, SO4•–, and 4-methylbenzenesulfinate produces a sulfonyl radical, followed by the radical addition of the sulfonyl radical with alkyne in 1a to give a vinyl radical intermediate. After that, the addition of a vinyl radical to the sulfur atom produces the intermediate C. Finally, the corresponding cascade product 3a is obtained via oxidation and demethylation.

3. Materials and Methods

3.1. General Information

All reactions were carried out under a nitrogen atmosphere. 1H NMR 13C NMR, and 19F NMR spectra were measured on a Bruker Avance NMR spectrometer (600 MHz/151 MHz/565 NMR) in CDCl3 as solvent and recorded in ppm relative to the internal tetramethylsilane standard. 1H NMR data are reported as follows: δ, chemical shift; coupling constants (J are given in Hertz, Hz) and integration. Abbreviations to denote the multiplicity of a particular signal are s (singlet), d (doublet), t (triplet), q (quartet), dd (doublet of doublets), and m (multiplet). The 15-W blue LED was purchased from https://item.taobao.com/item.htm?id=524749100016&ali_refid=a3_430673_1006:1121803562:N:FxDVk1sg3f08W8u%2BfdnZUtGvFtTT9lsR:af40c0c0536da02c91473a14c4e25edc&ali_trackid=1_af40c0c0536da02c91473a14c4e25edc&spm=a2e0b.20350158.31919782.21&mt= (accessed on 15 May 2023). Due to the fact that the target compound is known, mass spectrometry analysis for compound characterization was not conducted in the article.

3.2. Preparation of the Starting Materials

The 2-alkynylthioanisoles (1a) derivatives were prepared according to the reported method [56,60]. The solvents and oxidants including DMF, THF, K2S2O8, DTBP, etc., were purchased from commercial suppliers including Bidepharm (Shanghai, China); functionalized anilines, photocatalysts, and functionalized aryl sulfonyl chlorides were purchased from Energy Chemical (Shanghai, China); petroleum ether and ethyl acetate were purchased from Shanghai Chemical Company (Shanghai, China). All solvents were dried and freshly distilled in N2 prior to use. Products were purified by flash chromatography on a 200–300 mesh silica gel.

3.3. General Procedure for the Synthesis of 3a

A dry 15-mL tube was charged with 2-alkynylthioanisole (1a, 0.20 mmol), sodium sulfinates (2a, 0.40 mmol), CH3CN:H2O (3:1, 2 mL), KI (30 mol%), K2S2O8 (2 equiv), and a magnetic stir bar. Then, the mixture was reacted under a 15-W blue LED light at room temperature and a nitrogen atmosphere for 12 hours. After the reaction, the mixture was concentrated to obtain the crude product, and the crude product was further purified by rapid chromatography (silica gel, petroleum ether (PE)/ethyl acetate (EA) = 30/1 to 15/1) to obtain the required product 3a. The 1H NMR, 13C NMR and 19F NMR spectra of the products can be found in the Supplementary Materials.
Product 3a: 2-phenyl-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3a as a white solid (58 mg, 84% yield). 1H NMR (600 MHz, CDCl3: δ 8.62 (d, J = 8.4 Hz, 1H), 7.76 (d, J = 8.1 Hz, 1H), 7.53 (d, J = 8.3 Hz, 2H), 7.52–7.48 (m, 1H), 7.47–7.43 (m, 1H), 7.43–7.37 (m, 5H), 7.10 (d, J = 8.1 Hz, 2H), 2.30 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 152.5, 143.9, 139.4, 138.2, 136.1, 131.7, 130.5, 130.3, 129.5, 129.4, 127.6, 127.0, 125.9, 125.6, 124.6, 121.8, 21.5.
Product 3b: 2-phenyl-3-(phenylsulfonyl)benzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford the 3b as a white solid (56 mg, 80% yield). 1H NMR (600 MHz, CDCl3): δ 8.64 (d, J = 8.4 Hz, 1H), 7.80 (d, J = 8.0 Hz, 1H), 7.64 (dd, J = 8.4, 1.1 Hz, 2H), 7.55–7.51 (m, 1H), 7.48–7.43 (m, 3H), 7.43–7.39 (m, 4H), 7.33 (t, J = 7.9 Hz, 2H). 13C NMR (151 MHz, CDCl3): δ 152.9, 142.3, 138.1, 136.2, 132.9, 131.6, 130.5, 130.0, 129.5, 128.7, 127.7, 126.9, 126.0, 125.6, 124.6, 121.7.
Product 3c: 3-((4-fluorophenyl)sulfonyl)-2-phenylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3c as a yellow solid (46 mg, 63% yield). 1H NMR (600 MHz, CDCl3): δ 8.65 (d, J = 8.3 Hz, 1H), 7.81 (d, J = 8.0 Hz, 1H), 7.64–7.59 (m, 2H), 7.56–7.51 (m, 1H), 7.49–7.43 (m, 2H), 7.42–7.38 (m, 4H), 7.01–6.94 (m, 2H). 13C NMR (151 MHz, CDCl3): δ 166.0, 164.3, 152.8, 138.3 (d, J = 3.1 Hz), 138.1, 136.0, 131.4, 130.5, 130.0, 129.8, 129.7 (d, J = 22.7 Hz), 126.9 (d, J = 252.1 Hz), 125.7, 124.5, 121.8, 115.9 (d, J = 22.8 Hz).
Product 3d: 3-((4-chlorophenyl)sulfonyl)-2-phenylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3d as a yellow solid (57 mg, 75% yield). 1H NMR (600 MHz, CDCl3): δ 8.63 (d, J = 8.4 Hz, 1H), 7.82 (d, J = 8.1 Hz, 1H), 7.54 (t, J = 8.9 Hz, 3H), 7.50–7.44 (m, 2H), 7.43–7.38 (m, 4H), 7.28 (d, J = 8.6 Hz, 2H). 13C NMR (151 MHz, CDCl3): δ 153.1, 140.7, 139.5, 138.1, 136.0, 131.4, 130.5, 129.7, 129.6, 129.0, 128.4, 127.7, 126.1, 125.7, 124.5, 121.8.
Product 3e: 3-((4-(tert-butyl)phenyl)sulfonyl)-2-phenylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3e as a white solid (66 mg, 82% yield). 1H NMR (600 MHz, CDCl3): δ 8.65 (d, J = 8.4 Hz, 1H), 7.81 (d, J = 8.1 Hz, 1H), 7.58 (d, J = 8.6 Hz, 2H), 7.55–7.52 (m, 1H), 7.47–7.43 (m, 2H), 7.43–7.38 (m, 4H), 7.33 (d, J = 8.6 Hz, 2H), 1.26 (s, 9H). 13C NMR (151 MHz, CDCl3): δ 156.7, 152.4, 139.2, 138.1, 136.2, 131.7, 130.4, 129.4, 127.6, 126.9, 125.9, 125.7, 125.5, 124.7, 121.7, 35.1, 31.0.
Product 3f: 3-((4-methoxyphenyl)sulfonyl)-2-phenylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–7/1) to afford 3f as a white solid (58 mg, 77% yield). 1H NMR (600 MHz, CDCl3): δ 8.56 (d, J = 8.4 Hz, 1H), 7.73 (d, J = 8.1 Hz, 1H), 7.50 (d, J = 9.0 Hz, 2H), 7.47–7.43 (m, 1H), 7.41–7.38 (m, 1H), 7.37–7.33 (m, 5H), 6.74–6.69 (m, 2H), 3.71 (s, 3H).13C NMR (151 MHz, CDCl3): δ 162.1, 151.0, 137.1, 135.0, 133.0, 130.7, 129.7, 129.4, 128.3, 128.2, 126.6, 124.8, 124.5, 123.6, 120.7, 112.9, 54.5.
Product 3g: 6-fluoro-2-phenyl-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3g as a brown solid (60 mg, 79% yield). 1H NMR (600 MHz, CDCl3): δ 8.61 (dd, J = 9.2, 5.1 Hz, 1H), 7.50 (d, J = 8.3 Hz, 2H), 7.48–7.44 (m, 2H), 7.41–7.38 (m, 4H), 7.29–7.24 (m, 1H), 7.12 (d, J = 8.2 Hz, 2H), 2.33 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 160.8 (d, J = 247.7 Hz), 152.0 (d, J = 3.3 Hz), 144.0, 139.2 (d, J = 4.4 Hz), 139.1, 132.6, 131.3, 130.5, 130.1, 129.6, 129.4, 127.7, 127.0, 126.1 (d, J = 8.9 Hz), 114.9 (d, J = 23.9 Hz), 107.9 (d, J = 25.4 Hz), 21.5.
Product 3h: 6-chloro-2-phenyl-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3h as a white solid (40 mg, 51% yield). 1H NMR (600 MHz, CDCl3): δ 8.57 (d, J = 8.9 Hz, 1H), 7.78 (d, J = 1.9 Hz, 1H), 7.50–7.46 (m, 4H), 7.40 (d, J = 4.4 Hz, 4H), 7.12 (d, J = 8.2 Hz, 2H), 2.33 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 152.7, 144.1, 139.1, 139.1, 134.6, 131.9, 131.2, 130.5, 130.3, 129.6, 129.4, 127.7, 127.0, 126.8, 125.6, 121.3, 21.5.
Product 3i: 6-bromo-2-phenyl-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3i as a yellow solid (60 mg, 68% yield). 1H NMR (600 MHz, CDCl3): δ 8.51 (d, J = 8.9 Hz, 1H), 7.94 (d, J = 1.8 Hz, 1H), 7.62 (dd, J = 8.9, 1.8 Hz, 1H), 7.48 (t, J = 7.0 Hz, 3H), 7.40 (d, J = 4.4 Hz, 4H), 7.12 (d, J = 8.2 Hz, 2H), 2.33 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 152.7, 144.1, 139.4, 139.1, 135.0, 131.1, 130.5, 130.3, 129.7, 129.4, 129.4, 127.7, 127.0, 125.8, 124.2, 119.7, 21.5.
Product 3j: 2-(p-tolyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3j as a white solid (63 mg, 84% yield). 1H NMR (600 MHz, CDCl3): δ 8.59 (d, J = 8.4 Hz, 1H), 7.76 (d, J = 8.0 Hz, 1H), 7.56 (d, J = 8.3 Hz, 2H), 7.51–7.47 (m, 1H), 7.42–7.37 (m, 1H), 7.33 (d, J = 8.0 Hz, 2H), 7.21 (d, J = 7.9 Hz, 2H), 7.12 (d, J = 8.2 Hz, 2H), 2.43 (s, 3H), 2.31 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 153.0, 143.8, 139.6, 139.5, 138.1, 136.2, 130.4, 129.9, 129.4, 128.7, 128.4, 127.0, 125.8, 125.5, 124.5, 121.7, 21.5, 21.5.
Product 3k: 2-(4-ethylphenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3k as a white solid (69 mg, 89% yield). 1H NMR (600 MHz, CDCl3): δ 8.61 (d, J = 8.4 Hz, 1H), 7.74 (d, J = 8.1 Hz, 1H), 7.54 (d, J = 8.3 Hz, 2H), 7.50–7.46 (m, 1H), 7.40–7.36 (m, 1H), 7.34 (d, J = 8.1 Hz, 2H), 7.22 (d, J = 8.0 Hz, 2H), 7.09 (d, J = 8.2 Hz, 2H), 2.71 (q, J = 7.6 Hz, 2H), 2.29 (s, 3H), 1.29 (t, J = 7.6 Hz, 3H). 13C NMR (151 MHz, CDCl3): δ 152.9, 145.8, 143.8, 139.5, 138.1, 136.2, 130.5, 130.0, 129.4, 128.9, 127.2, 127.0, 125.8, 125.5, 124.6, 121.7, 28.8, 21.5, 15.4.
Product 3l: 2-(4-(tert-butyl)phenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3l as a white solid (65 mg, 78% yield). 1H NMR (600 MHz, CDCl3): δ 8.63 (d, J = 8.3 Hz, 1H), 7.78 (d, J = 8.0 Hz, 1H), 7.52–7.48 (m, 3H), 7.43–7.37 (m, 3H), 7.36–7.32 (m, 2H), 7.08 (d, J = 8.1 Hz, 2H), 2.31 (s, 3H), 1.38 (s, 9H). 13C NMR (151 MHz, CDCl3): δ 152.7, 152.6, 143.6, 139.4, 138.1, 136.3, 130.2, 130.0, 129.2, 128.6, 127.1, 125.8, 125.4, 124.6, 124.6, 121.7, 34.8, 31.3, 21.5.
Product 3m: 2-(4-methoxyphenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–7/1) to afford 3m as a white solid (59 mg, 76% yield). 1H NMR (600 MHz, CDCl3): δ 8.60 (d, J = 8.4 Hz, 1H), 7.77 (d, J = 8.0 Hz, 1H), 7.54 (d, J = 8.3 Hz, 2H), 7.52–7.47 (m, 1H), 7.42–7.36 (m, 3H), 7.12 (d, J = 8.2 Hz, 2H), 6.93 (d, J = 8.7 Hz, 2H), 3.88 (s, 3H), 2.32 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 160.6, 152.8, 143.8, 139.5, 138.0, 136.3, 131.9, 129.8, 129.4, 126.9, 125.8, 125.4, 124.5, 123.7, 121.7, 113.1, 55.4, 21.5.
Product 3n: 2-(4-ethoxyphenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–7/1) to afford 3n as a white solid (50 mg, 62% yield). 1H NMR (600 MHz, CDCl3): δ 8.61 (d, J = 8.3 Hz, 1H), 7.77 (d, J = 8.0 Hz, 1H), 7.54 (d, J = 8.3 Hz, 2H), 7.52–7.47 (m, 1H), 7.42–7.38 (m, 1H), 7.38–7.34 (m, 2H), 7.12 (d, J = 8.1 Hz, 2H), 6.94–6.89 (m, 2H), 4.10 (q, J = 7.0 Hz, 2H), 2.32 (s, 3H), 1.46 (t, J = 7.0 Hz, 3H). 13C NMR (151 MHz, CDCl3): δ 160.0, 153.0, 143.7, 139.6, 138.0, 136.3, 131.9, 129.7, 129.3, 126.9, 125.8, 125.4, 124.5, 123.5, 121.6, 113.6, 63.6, 21.5, 14.8.
Product 3o: 2-(m-tolyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3o as a white solid (51 mg, 68% yield). 1H NMR (600 MHz, CDCl3): δ 8.63 (d, J = 8.4 Hz, 1H), 7.79 (d, J = 8.1 Hz, 1H), 7.55 (d, J = 8.3 Hz, 2H), 7.54–7.50 (m, 1H), 7.45–7.40 (m, 1H), 7.29 (dd, J = 14.9, 7.5 Hz, 2H), 7.23 (d, J = 7.3 Hz, 1H), 7.17–7.11 (m, 3H), 2.38 (s, 3H), 2.34 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 152.7, 143.8, 139.5, 138.1, 137.2, 136.2, 131.5, 131.0, 130.2, 130.1, 129.3, 127.5, 127.1, 125.8, 125.5, 124.6, 121.7, 21.5, 21.3.
Product 3p: 2-(o-tolyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3p as a white solid (58 mg, 78% yield). 1H NMR (600 MHz, CDCl3): δ 8.66 (d, J = 8.3 Hz, 1H), 7.81 (d, J = 8.1 Hz, 1H), 7.54 (t, J = 8.4 Hz, 3H), 7.47–7.42 (m, 1H), 7.37 (td, J = 7.6, 1.1 Hz, 1H), 7.22 (dd, J = 14.7, 7.2 Hz, 2H), 7.17–7.12 (m, 3H), 2.35 (s, 3H), 2.08 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 151.6, 144.0, 139.2, 138.5, 138.1, 135.8, 131.2, 131.0, 130.2, 129.8, 129.6, 129.4, 127.3, 125.8, 125.5, 124.9, 124.5, 121.8, 21.5, 20.2.
Product 3q: 2-(4-fluorophenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3q as a yellow solid (54 mg, 71% yield). 1H NMR (600 MHz, CDCl3): δ 8.61 (d, J = 8.4 Hz, 1H), 7.80 (d, J = 8.1 Hz, 1H), 7.53 (t, J = 8.0 Hz, 3H), 7.43 (m, J = 8.6, 6.7, 1.4 Hz, 3H), 7.15 (d, J = 8.2 Hz, 2H), 7.10 (t, J = 8.6 Hz, 2H), 2.34 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 162.7, 151.2, 144.0, 139.3, 138.0, 136.0, 132.4 (d, J = 8.4 Hz), 130.6, 129.4, 127.6, 126.9, 126.0, 125.7, 124.6, 121.7, 114.8 (d, J = 21.9 Hz), 21.5.
Product 3r: 2-(4-chlorophenyl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 30/1–15/1) to afford 3r as a yellow solid (55 mg, 70% yield). 1H NMR (600 MHz, CDCl3): δ 8.60 (d, J = 8.4 Hz, 1H), 7.80 (d, J = 8.0 Hz, 1H), 7.55 (t, J = 5.8 Hz, 2H), 7.54–7.51 (m, 1H), 7.46–7.42 (m, 1H), 7.40–7.36 (m, 4H), 7.16 (d, J = 8.2 Hz, 2H), 2.35 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 150.8, 144.1, 139.3, 138.1, 136.0, 135.8, 131.8, 130.7, 130.1, 129.5, 127.9, 127.0, 126.0, 125.8, 124.6, 121.7, 21.5.
Product 3s: 2-(naphthalen-1-yl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–7/1) to afford 3s as a yellow solid (43 mg, 53% yield). 1H NMR (600 MHz, CDCl3): δ 8.60 (d, J = 8.4 Hz, 1H), 7.75 (d, J = 8.0 Hz, 1H), 7.54 (d, J = 8.3 Hz, 2H), 7.51–7.46 (m, 1H), 7.38 (m, J = 8.7, 7.4, 1.6 Hz, 3H), 7.11 (d, J = 8.2 Hz, 2H), 6.94–6.90 (m, 2H), 3.86 (s, 3H), 2.30 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 160.6, 152.9, 143.8, 139.6, 138.0, 136.3, 131.9, 131.4, 130.4, 129.8, 129.4, 126.9, 125.8, 125.4, 124.5, 123.7, 121.7, 113.2, 55.4, 53.5, 31.4, 30.2, 21.5.
Product 3t: 2-(thiophen-2-yl)-3-tosylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 3t as a yellow solid (56 mg, 77% yield). 1H NMR (600 MHz, CDCl3): δ 8.67 (d, J = 8.4 Hz, 1H), 7.77 (d, J = 8.1 Hz, 1H), 7.59 (d, J = 8.3 Hz, 2H), 7.53–7.49 (m, 3H), 7.44–7.40 (m, 1H), 7.17–7.11 (m, 3H), 2.33 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 144.6, 143.9, 139.1, 138.2, 136.5, 132.2, 131.0, 130.7, 129.4, 129.3, 127.4, 126.9, 126.0, 125.8, 124.8, 121.5, 21.5.
Product 3u: 2-(3-tosylbenzo[b]thiophen-2-yl)pyridine. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 3u as a white solid (59 mg, 82% yield). 1H NMR (600 MHz, CDCl3): δ 8.71–8.68 (m, 1H), 8.45 (d, J = 8.3 Hz, 1H), 7.85–7.79 (m, 5H), 7.51–7.46 (m, 1H), 7.43–7.40 (m, 1H), 7.40–7.37 (m, 1H), 7.20 (d, J = 8.2 Hz, 2H), 2.32 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 151.1, 150.8, 149.0, 144.0, 138.9, 138.6, 135.8, 135.6, 130.3, 129.6, 127.3, 126.9, 125.9, 125.9, 124.5, 123.9, 122.0, 21.5.
Product 3v: 3-((4-bromophenyl)sulfonyl)-2-phenylbenzo[b]thiophene. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 3v as a white solid (65 mg, 76% yield). 1H NMR (600 MHz, CDCl3): δ 8.62 (d, J = 6 Hz, 1H), 7.81 (d, J = 6 Hz, 1H), 7.55–7.53 (m, 1H), 7.48–7.43 (m, 6H), 7.42–7.39 (m, 4H). 13C NMR (151 MHz, CDCl3): δ 153.1, 141.2, 138.1, 136.0, 132.7, 132.0, 131.4, 130.5, 129.7, 128.5, 128.1, 127.7, 126.1, 125.7, 124.5, 121.8.
Product 5a: 2-phenyl-3-tosyl-4H-thiochromen-4-one. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 5a as a white solid (58 mg, 75% yield). 1H NMR (600 MHz, CDCl3): δ 8.20 (d, J = 7.9 Hz, 1H), 7.84–7.73 (m, 2H), 7.61–7.54 (m, 1H), 7.52–7.34 (m, 7H), 7.19 (d, J = 7.7 Hz, 2H), 2.30 (s, 3H). 13C NMR (151 MHz, CDCl3): δ 175.9, 162.4, 144.0, 138.9, 135.7, 134.9, 132.8, 132.5, 131.6, 130.1, 128.9, 128.7, 128.5, 128.0, 127.9, 125.3, 21.3.
Product 5b: 3-((4-chlorophenyl)sulfonyl)-2-phenyl-4H-thiochromen-4-one. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 5b as a yellow solid (66 mg, 80% yield). 1H NMR (600 MHz, CDCl3): δ 8.28 (dd, J = 8.1, 1.0 Hz, 1H), 7.91–7.86 (m, 2H), 7.58 (td, J = 8.0, 1.4 Hz, 1H), 7.50–7.42 (m, 7H), 7.38–7.34 (m, 2H). 13C NMR (151 MHz, CDCl3): δ 176.0, 163.2, 140.2, 139.6, 135.7, 134.5, 132.7, 132.6, 131.6, 130.5, 130.3, 129.2, 128.9, 128.7, 128.2, 128.1, 125.3.
Product 6: 1,3-dimethyl-3-(tosylmethyl)indolin-2-one. The sulfonylation product was purified by flash column chromatography on silica gel (PE/AcOEt: 15/1–5/1) to afford 6 as a white solid (50 mg, 76% yield). 1H NMR (600 MHz, CDCl3): δ: 7.38–7.37 (m, 2H), 7.30–7.27 (m, 1H), 7.16 (d, J = 6 Hz, 2H), 7.07 (d, J = 6 Hz, 1H), 6.93–6.90 (m, 1H), 6.84 (d, J = 6 Hz, 1H), 3.85 (d, J = 12 Hz, 1H), 3.67 (d, J = 18 Hz, 1H), 3.16 (s, 3H), 2.39 (s, 3H), 1.38 (s, 3H); 13C NMR (151 MHz, CDCl3): δ 177.6, 144.3, 143.2, 137.0, 129.6, 129.5, 128.5, 127.8, 124.1, 122.4, 108.3, 61.9, 45.6, 26.5, 25.5, 21.5.

4. Conclusions

In summary, we have reported a straightforward strategy for the synthesis of sulfonated benzothiophenes and thioflavones from 2-alkynylthioanisoles and sodium sulfinates via visible-light-induced cascade cyclization reaction under metal- and photocatalyst-free conditions. This approach features good functional group tolerance, simple operation, and mild conditions. The further synthetic application of this strategy is underway in our laboratory.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28114436/s1. References [61,62,63,64] are cited in the supplementary materials.

Author Contributions

H.D. and C.C. performed the experiments, and J.Z. analyzed the data. Y.J. and W.Y. conceived the concept, and the manuscript was written through contributions of all authors. All authors have read and agreed to the published version of the manuscript.

Funding

We acknowledge financial support from the Open Research Fund of the National and Local Joint Engineering Laboratory of High Efficiency and Superior-Quality Cultivation and Fruit Deep Processing Technology of Characteristic Fruit Trees in South Xinjiang (No. FE202203) and the Postgraduate Research and Innovation Project of Tarim University (XJ2022G244).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not applicable.

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Molecules 28 04436 g001 550
Scheme 1. Selected reactions using sodium sulfinates as sulfonylation reagents (a–c) and our work (d).
Scheme 1. Selected reactions using sodium sulfinates as sulfonylation reagents (a–c) and our work (d).
Molecules 28 04436 g001
Molecules 28 04436 g002 550
Scheme 2. Substrate scope of sodium sulfinates: 1 (0.20 mmol), sodium sulfinates (2, 2.0 equiv), KI (30 mol%), K2S2O8 (2 equiv), CH3CN/H2O (3:1, 2.0 mL), N2, 15-W blue LED at room temperature for 12 h; isolated yield of the product based on 1, reaction progress is monitored through TLC.
Scheme 2. Substrate scope of sodium sulfinates: 1 (0.20 mmol), sodium sulfinates (2, 2.0 equiv), KI (30 mol%), K2S2O8 (2 equiv), CH3CN/H2O (3:1, 2.0 mL), N2, 15-W blue LED at room temperature for 12 h; isolated yield of the product based on 1, reaction progress is monitored through TLC.
Molecules 28 04436 g002
Molecules 28 04436 g003 550
Scheme 3. Substrate scope of 2-alkynylthioanisoles: Unless otherwise noted, all reactions were performed with 1 (0.20 mmol), sodium sulfinates (2, 2.0 equiv), KI (30 mol%), K2S2O8 (2 equiv), CH3CN/H2O (3:1, 2.0 mL), N2, 15-W blue LED at room temperature for 12 h; isolated yield of the product based on 1, reaction progress is monitored through TLC.
Scheme 3. Substrate scope of 2-alkynylthioanisoles: Unless otherwise noted, all reactions were performed with 1 (0.20 mmol), sodium sulfinates (2, 2.0 equiv), KI (30 mol%), K2S2O8 (2 equiv), CH3CN/H2O (3:1, 2.0 mL), N2, 15-W blue LED at room temperature for 12 h; isolated yield of the product based on 1, reaction progress is monitored through TLC.
Molecules 28 04436 g003
Molecules 28 04436 g004 550
Scheme 4. The controlled experiments (a,b) and proposed mechanism (c).
Scheme 4. The controlled experiments (a,b) and proposed mechanism (c).
Molecules 28 04436 g004
Table
Table 1. Optimization of the reaction conditions a.
Table 1. Optimization of the reaction conditions a.
Molecules 28 04436 i001
EntryPhotocatalystOxidantAdditiveYield (%) b
1[Ir(dFCF3ppy)2dtbbpy]PF6K2S2O8KI82
2[Ir(dFCF3ppy)2dtbbpy]PF6K2S2O8NaI47
3[Ir(dFCF3ppy)2dtbbpy]PF6K2S2O8NaBr29
4[Ir(dFCF3ppy)2dtbbpy]PF6K2S2O8KCl35
5[Ir(dFCF3ppy)2dtbbpy]PF6Na2S2O8KI67
6[Ir(dFCF3ppy)2dtbbpy]PF6O2KItrace
7[Ir(dFCF3ppy)2dtbbpy]PF6DTBPKI15
8[Ir(dFCF3ppy)2dtbbpy]PF6TBHPKI23
94CzIPNK2S2O8KI41
104CzIPN-tBuK2S2O8KI47
11Mes-Acr+ClO4K2S2O8KI65
12--K2S2O8KI84
13--K2S2O8--30
14------24
Reaction conditions: a 1a (0.20 mmol), 2a (0.4 mmol), photocatalyst (1 mol%), additive (30 mol%), oxidant (2 equiv), CH3CN/H2O (3:1, 2.0 mL), N2, 15-W blue LED at room temperature for 12 h; b isolated yield of the product based on 1, reaction progress is monitored through TLC.
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Dong, H.; Chen, C.; Zhao, J.; Ji, Y.; Yang, W. Photoinduced Photocatalyst-Free Cascade Cyclization of Alkynes with Sodium Sulfinates for the Synthesis of Benzothiophenes and Thioflavones. Molecules 2023, 28, 4436. https://doi.org/10.3390/molecules28114436

AMA Style

Dong H, Chen C, Zhao J, Ji Y, Yang W. Photoinduced Photocatalyst-Free Cascade Cyclization of Alkynes with Sodium Sulfinates for the Synthesis of Benzothiophenes and Thioflavones. Molecules. 2023; 28(11):4436. https://doi.org/10.3390/molecules28114436

Chicago/Turabian Style

Dong, Hongqiang, Chunli Chen, Jinlei Zhao, Yigang Ji, and Wenchao Yang. 2023. "Photoinduced Photocatalyst-Free Cascade Cyclization of Alkynes with Sodium Sulfinates for the Synthesis of Benzothiophenes and Thioflavones" Molecules 28, no. 11: 4436. https://doi.org/10.3390/molecules28114436

APA Style

Dong, H., Chen, C., Zhao, J., Ji, Y., & Yang, W. (2023). Photoinduced Photocatalyst-Free Cascade Cyclization of Alkynes with Sodium Sulfinates for the Synthesis of Benzothiophenes and Thioflavones. Molecules, 28(11), 4436. https://doi.org/10.3390/molecules28114436

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