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Communication

Efficient Solvent-Free Synthesis of Indolizines Using CuBr Catalyst from Pyridine, Acetophenone, and Electron-Deficient Alkenes

by
Xueguo Zhang
*,
Jianpeng Zhang
,
Zhengyi Liu
,
Wenxuan Bi
,
Jian Shen
and
Guang Li
*
Department of Materials Science and Engineering, Liaocheng University, Liaocheng 252059, China
*
Authors to whom correspondence should be addressed.
Molecules 2024, 29(9), 2061; https://doi.org/10.3390/molecules29092061
Submission received: 26 March 2024 / Revised: 20 April 2024 / Accepted: 28 April 2024 / Published: 29 April 2024
(This article belongs to the Special Issue Novel Organic Synthetic Route to Heterocyclic Compounds)
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Abstract

:
Herein, we have developed a new approach for the synthesis of indolizine via Cu-catalyzed reaction of pyridine, acetophenone, and nitroolefin under mild conditions in high yields. This reaction involved the formation of C–N and C–C bonds and new indolizine compounds with high stereoselectivity and excellent functional group tolerance.

Graphical Abstract

1. Introduction

Indolizine is a heterocyclic organic compound in many pharmaceuticals and natural products, characterized by a fused pyrrole and pyridine ring structure [1,2]. This unique structure gives it a wide range of chemical and biological properties, making it a valuable target for synthetic chemists [3,4]. The pharmaceutical industry has recognized the significance of indolizine-containing compounds and their potential as therapeutic agents. Researchers continue to explore the synthesis of novel indolizine derivatives with enhanced biological activities and improved pharmacokinetic properties [5].
In medicinal chemistry, indolizine derivatives have been found to exhibit significant biological activities, including anti-inflammatory, antimicrobial, antiviral, and anticancer properties [6]. This has led to a surge in research interest in this compound, with scientists seeking to understand its mechanisms of action and to develop new, more effective indolizine-based drugs [7,8,9]. In the field of materials science, indolizine has been studied for its potential use in the development of organic semiconductors and photovoltaic materials [10,11,12]. Its unique electronic properties, combined with its structural versatility, make it a promising candidate for more applications [13,14].
Synthetic chemists have developed numerous strategies to access indolizine derivatives. These methods involve the construction of the fused ring system through cyclization reactions, such as the Tschitschibabin reaction [15]. Additionally, functionalization of the indolizine core enables the introduction of diverse substituents, further expanding the scope of potential applications. Despite the numerous synthetic methods developed for indolizine derivatives, there remain certain hurdles to overcome [16,17,18,19]. For instance, the synthesis method reported by the Kan research group allows the reaction to occur under relatively mild temperature conditions but requires stepwise procedures (Scheme 1) [20]. Boruah’s group synthesized indolizines by using pyridine, bromoacetophenone, and alkyne under microwave conditions [21]. The aforementioned synthesis methods have established a solid foundation for the development and application of indolizine derivatives [22,23,24,25]. However, research on indolizine is still in its early stages. Many of its potential applications are yet to be fully explored, and the synthesis of new indolizine derivatives remains a challenging task. The growing interest in this compound and the promising results obtained so far suggest that indolizine will continue to be a significant focus of research in the coming years [26,27,28].

2. Results and Discussions

Encouraged by these promising results, we chose pyridine 1a (0.4 mmol), acetophenone 2a (0.4 mmol), and (E)-1-methyl-4-(2-nitrovinyl)benzene 3a (0.2 mmol) as model substrates for the synthesis of indolizines in the presence of CuBr as a catalyst and PIDA as an oxidant. Disappointingly, we detected two new products, which were identified as indolizines compounds 4a and 4a’ after analysis (Table 1, entry 1 and Supplementary Material), and their yields were similar. Unfortunately, the extensive use of nitro compounds has led to the environmental contamination of soil and groundwater [29]. Subsequently, we adjusted the reaction conditions to increase the yield and selectivity of product 4a. Initially, various copper salts were evaluated for this reaction. CuBr still exhibited the highest catalytic efficiency (Table 1, entries 2–4). Next, we examined various types of oxidants separately. (NH4)2S2O8 was proved to be the best oxidant for this process [30]. (NH4)2S2O8 can provide the best oxidation effect when it is maintained at 1 equivalent, but if it exceeds 1 equivalent, the reaction yield will decrease. It was good to see that the yield was not just high, but the effect of denitrification was also noteworthy in the presence of CuBr and (NH4)2S2O8 (Table 1, entries 5–10). Simultaneously, it was established that the reaction temperature and time for this reaction were 130 °C and 5 h, respectively (Table 1, entries 11–18). Finally, using MeCN and DMF as reaction solvents respectively, the yield of the target product was significantly reduced (Table 1, entries 19–20). Therefore, we insisted on conducting the reaction in a solvent-free state. This approach not only enhances the reaction rate but also aligns with the principles of “green chemistry”. Through the screening of reaction conditions, we achieved a satisfactory yield of product 4a using CuBr as the catalyst and (NH4)2S2O8 as an oxidant under solvent-free conditions at 130 °C for 5 h (Table 1, entry 17).
With the optimized conditions in hand, we turned to investigate the indolizines by using a systematic variation of acetophenones, pyridine 1a, and (E)-(2-nitrovinyl)benzene 3b, as shown in Figure 1. From the reaction results, it can be seen that the stronger the electron-withdrawing group of acetophenone, the easier it is to obtain a high-yield product (Figure 1, 4b–4d). When acetophenone was substituted by electron-donating groups methyl, methoxy, and ethyl, the yield decreased slightly (Figure 1, 4e, 4f, and 4i). At the same time, it can also be concluded that the steric hindrance effect of acetophenone has little impact on the reaction (Figure 1, 4g and 4h). After exploring the effect of acetophenone on the reaction, we turned to nitrostyrene. Through these reactions (Figure 1, 4a and 4j–4p), we reached a similar conclusion to the previous one: substrates with electron-withdrawing groups are more likely to promote the progression. In addition, we also investigated the reaction of 4-methyl-substituted pyridine with acetophenone and (E)-(2-nitrovinyl)benzene under standard conditions, and obtained the target product at a yield of 77% (Figure 1, 4q). Finally, we also investigated other electron-deficient alkenes, such as 1-phenyl-2-nitropropene, ethyl acrylate, acrylonitrile, and chalcone, all of which achieved high target yields (Figure 1, 4r–4u). What surprised us was that the reaction yields of two compounds with similar structures, chalcone and cinnamaldehyde, were very different (Figure 1, 4u and 4v). Unfortunately, the target product was not obtained when 1,4-benzoquinone, and trimethylvinylammonium bromide participated in the reaction system (Figure 1, 4w and 4x). This also demonstrates that although the reaction possesses excellent yield and selectivity, it has limitations. The limitation provides direction and theoretical guidance for us to continue to explore this type of reaction.
To understand the reaction process, we carried out a few control experiments. Firstly, we added TEMPO/BHT into the reaction system as radical scavenger under standard conditions (Scheme 2). Luckily, we still managed to produce the desired product 4a. This suggests that the reaction did not include a free radical process. In addition, we introduced ω-bromoacetophenone B into the reaction system with no CuBr catalyst. In this case, we also successfully obtained product 4a (Scheme 2). This indicates that compound B is likely to be an intermediate structure in this transformation process. These experiments offered proof for the verification of the reaction mechanism.
Based on these preliminary experimental results and literature precedents [31,32], we propose a plausible mechanism as shown in Scheme 3. Acetophenone 2a is transformed into 2a’ through enolization, and then it reacts with one molecule of CuBr2 to produce an intermediate A, with HBr as a byproduct. The electron-rich intermediate A interacts with another molecule of CuBr2, leading to the formation of the product ω-bromoacetophenone B. Simultaneously, CuBr would be formed by getting rid of copper ions, which completed the catalytic cycle. ω-Bromoacetophenone B interacts with pyridine to produce an N-ylide intermediate C. The intermediate C reacts with 3a in 1,3-dipolar cycloaddition process to produce intermediate D. Finally, the intermediate compound D is subjected to processes of denitration and aromatization to yield the product 4a [33,34]. Additionally, intermediate D can also be directly converted into product 4a’ through the process of aromatization.

3. Materials and Methods

3.1. Materials

Pyridine, acetophenone, (E)-1-methyl-4-(2-nitrovinyl) benzene, and other raw materials were purchased from Bide Pharmatech Co., Ltd. (Shanghai, China) All commercially available organic and inorganic compounds were used directly without further purification.

3.2. Methods

3.2.1. Test Methods

1H NMR spectra were recorded at 400 MHz or 500 MHz in CDCl3 and 13C NMR spectra were recorded on 101 MHz or 126 MHz in CDCl3, using TMS as the internal standard. The chemical shifts (δ) were measured in ppm and with the solvents as references (for CDCl3, 1H: δ = 7.26 ppm, 13C: δ = 77.0 ppm). All compounds were further characterized by HRMS; copies of their 1H NMR and 13C NMR spectra are provided. Products were purified by flash chromatography on 200–300 mesh silica gels. All melting points were determined on a microscopic apparatus without correction.

3.2.2. Synthesis Methods

The general procedure for the synthesis of phenyl(2-(p-tolyl)indolizin-3-yl)methanone 4a and (1-nitro-2-(p-tolyl)indolizin-3-yl)(phenyl)methanone 4a’ was as follows:
1a (0.8 mmol), 2a (0.4 mmol), 3a (0.2 mmol), (NH4)2S2O8 (1.0 equiv), and CuBr (0.3 equiv) were heated at 130 °C for 5 h in a sealed tube. When the reaction was completed (detected by TLC), the mixture was cooled to room temperature. The product 4a and 4a’ was purified by column chromatography on silica gel (petroleum ether/EtOAc = 6:1).
phenyl(2-(p-tolyl)indolizin-3-yl)methanone (4a) yellow solid; mp 109–110 °C
1H NMR (500 MHz, CDCl3) δ 9.79 (d, J = 7.1 Hz, 1H), 7.53 (d, J = 8.8 Hz, 1H), 7.41 (dd, J = 8.1, 1.1 Hz, 2H), 7.15 (dd, J = 10.9, 4.8 Hz, 2H), 7.01 (t, J = 7.7 Hz, 2H), 6.96 (d, J = 8.0 Hz, 2H), 6.88 (td, J = 7.0, 1.3 Hz, 1H), 6.81 (d, J = 7.9 Hz, 2H), 6.56 (s, 1H), 2.20 (s, 3H). 13C NMR (126 MHz, CDCl3) δ 186.77, 140.15, 139.80, 137.57, 136.23, 132.88, 130.38, 129.90, 129.56, 128.21, 128.14, 127.29, 124.03, 120.01, 118.25, 113.34, 103.99, 20.97. HRMS (ESI): m/z calcd for C22H18NO (M + H)+ 312.1388; found: 312.1385.
(1-nitro-2-(p-tolyl)indolizin-3-yl)(phenyl)methanone (4a’) yellow solid; mp 138–140 °C
1H NMR (500 MHz, CDCl3) δ 9.53–9.40 (m, 1H), 8.65 (dt, J = 9.1, 1.1 Hz, 1H), 7.64 (ddd, J = 9.0, 6.9, 1.0 Hz, 1H), 7.38 (dd, J = 8.2, 1.2 Hz, 2H), 7.24–7.20 (m, 1H), 7.17 (td, J = 7.0, 1.4 Hz, 1H), 7.09–7.00 (m, 4H), 6.84 (d, J = 7.8 Hz, 2H), 2.18 (s, 3H). 13C NMR (126 MHz, CDCl3) δ 188.49, 138.23, 137.99, 134.62, 134.16, 131.58, 130.94, 130.19, 129.21, 128.10, 128.06, 127.70, 127.62, 121.39, 119.34, 116.30, 21.09. HRMS (ESI): m/z calcd for C22H17N2O3 (M + H)+ 357.1239; found: 357.1236.

4. Conclusions

In conclusion, the reaction of pyridine, acetophenone, and nitroolefin under the catalysis of CuBr and (NH4)2S2O8 as the oxidant is a crucial process in the synthesis of indolizine. This reaction showcases the importance of catalysts and oxidants in facilitating chemical transformations and the production of valuable organic compounds. At the same time, the reaction occurs under solvent-free conditions, reflecting environmental friendliness. Further studies on the mechanistic details and synthetic applications of this method are in progress in our group. It is believed that with the progress of science and technology, more potential applications of indolizine will be found.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/molecules29092061/s1. NMR spectra, melting points, and HRMS of (4a–4u) detailed data are available as Supplementary Materials.

Author Contributions

X.Z. contributed to the conception of the study; J.Z. and Z.L. performed the experiment; W.B. and J.S. contributed significantly to analysis and manuscript preparation; G.L. helped perform the analysis with constructive discussions. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Natural Science Foundation of Shandong Province, China, grant number: ZR2022QB240 and ZR2021ME149 and Research Foundation of Liaocheng University (No. 318052125).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article and Supplementary Materials.

Conflicts of Interest

The authors declare no conflicts of interest.

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Molecules 29 02061 sch001
Scheme 1. Synthesis of indolizines derivatives.
Scheme 1. Synthesis of indolizines derivatives.
Molecules 29 02061 sch001
Molecules 29 02061 g001
Figure 1. Scope of electron-deficient alkenes a,b. a Reaction conditions: 1 (0.8 mmol), 2 (0.4 mmol), 3a (0.2 mmol), CuBr, (NH4)2S2O8, sealed tube, at 130 °C in an oil bath for 5 h, unless otherwise specified. b Isolated yields. n.d.: not detected.
Figure 1. Scope of electron-deficient alkenes a,b. a Reaction conditions: 1 (0.8 mmol), 2 (0.4 mmol), 3a (0.2 mmol), CuBr, (NH4)2S2O8, sealed tube, at 130 °C in an oil bath for 5 h, unless otherwise specified. b Isolated yields. n.d.: not detected.
Molecules 29 02061 g001
Molecules 29 02061 sch002
Scheme 2. Control experiments.
Scheme 2. Control experiments.
Molecules 29 02061 sch002
Molecules 29 02061 sch003
Scheme 3. Proposed mechanism.
Scheme 3. Proposed mechanism.
Molecules 29 02061 sch003
Table 1. Optimization of reaction conditions a.
Table 1. Optimization of reaction conditions a.
Molecules 29 02061 i001
EntryCat.Oxidant (x Equiv)T (°C)t (h)Yield [%] b
4a (4a’)
1CuBrPIDA (2.0)1101234 (30)
2CuClPIDA (2.0)1101226 (20)
3Cu2OPIDA (2.0)1101224 (22)
4Cu2SPIDA (2.0)1101224 (25)
5CuBrO21101236 (30)
6CuBrIBX (2.0)1101235 (31)
7CuBr(NH4)2S2O8 (2.0)1101265 (14)
8CuBr(NH4)2S2O8 (1.0)1101271 (15)
9CuBr(NH4)2S2O8 (3.0)1101263
10CuBr(NH4)2S2O8 (4.0)1101256
11CuBr(NH4)2S2O8 (1.0)1201272
12CuBr(NH4)2S2O8 (1.0)1301276
13CuBr(NH4)2S2O8 (1.0)1401273
14CuBr(NH4)2S2O8 (1.0)1301075
15CuBr(NH4)2S2O8 (1.0)130876
16CuBr(NH4)2S2O8 (1.0)130678
17CuBr(NH4)2S2O8 (1.0)130580 (<5)
18CuBr(NH4)2S2O8 (1.0)130478
19 cCuBr(NH4)2S2O8 (1.0)130576
20 dCuBr(NH4)2S2O8 (1.0)130555
a Reaction conditions: 1a (0.4 mmol), 2a (0.4 mmol), 3a (0.2 mmol), copper catalyst (0.3 equiv), oxidant, solvent-free sealed tube in an oil bath, unless otherwise specified. b Isolated yields. c Reacting solvent was MeCN. d Reacting solvent was DMF. PID: phenyliodine(III) diacetate. IBX: 2-Iodoxybenzoic acid. DMF: N,N- dimethylformamide.
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Zhang, X.; Zhang, J.; Liu, Z.; Bi, W.; Shen, J.; Li, G. Efficient Solvent-Free Synthesis of Indolizines Using CuBr Catalyst from Pyridine, Acetophenone, and Electron-Deficient Alkenes. Molecules 2024, 29, 2061. https://doi.org/10.3390/molecules29092061

AMA Style

Zhang X, Zhang J, Liu Z, Bi W, Shen J, Li G. Efficient Solvent-Free Synthesis of Indolizines Using CuBr Catalyst from Pyridine, Acetophenone, and Electron-Deficient Alkenes. Molecules. 2024; 29(9):2061. https://doi.org/10.3390/molecules29092061

Chicago/Turabian Style

Zhang, Xueguo, Jianpeng Zhang, Zhengyi Liu, Wenxuan Bi, Jian Shen, and Guang Li. 2024. "Efficient Solvent-Free Synthesis of Indolizines Using CuBr Catalyst from Pyridine, Acetophenone, and Electron-Deficient Alkenes" Molecules 29, no. 9: 2061. https://doi.org/10.3390/molecules29092061

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