An Efficient Synthesis of Aryl-Substituted Pyrroles by the Suzuki⁻Miyaura Coupling Reaction of SEM-Protected Pyrroles.

An efficient arylation of SEM-protected pyrroles by the Suzuki-Miyaura coupling reaction has been developed. The reaction can be carried out under mild conditions to provide aryl-substituted pyrroles in moderate to excellent yields. The scope and limitations of the methodology were evaluated, and the reaction was tolerant of a wide range of functionalities. Compared to the reported methods, the protocol has some advantages, such as commercially available materials, no debrominated by-products being formed, and the amine-protecting group being stable under the reaction conditions. The synthetic utility of the product has also been demonstrated, with several common transformations of the aryl-substituted pyrrole product being conducted. This protocol will offer the opportunity to explore other metal-catalyzed cross-coupling reactions employing SEM-protected pyrroles.

1. Introduction

Aryl-substituted pyrroles are an important structural motif in both pharmaceuticals and natural products alike, and display a wide range of interesting biological activities [1]. Aryl pyrroles bearing an ester functional group are commonly used in organic synthesis and medicinal chemistry as synthetic intermediates [2,3,4,5,6]. There are a great deal of methods for the preparation of aryl-substituted pyrroles with this pendant ester group, and generally, the pyrrole core is formed from functionalized precursors with complex structures employing various catalysts and ligands [7,8,9,10,11,12,13,14]. As our aim was to construct a small library of aryl-substituted pyrroles for biological activity assays, we found that it was inefficient to build these required pyrrole structures from some non-commercial starting materials. If the aryl-substituted pyrroles could be synthesized from commercially available pyrrole compounds, the approach will be simple, straightforward, and efficient. The coupling reaction is a powerful method in the formation of C(sp2)–C(sp2) bonds, and the aryl-substituted pyrroles could be synthesized by the Stille–Migita cross-coupling reaction [15,16], decarboxylative coupling reaction [16,17], metal-catalyzed desulfitative coupling reaction [18], and Suzuki–Miyaura coupling reaction [16]. Considering the availability of materials and the operability of the reaction, the Suzuki–Miyaura coupling reaction may be the most suitable method to prepare aryl pyrroles from arylboronic acids and bromopyrroles. However, without protection of the nitrogen of the pyrrole moiety, debromination readily occurs, and the debrominated compounds are generally obtained in a large percentage [19,20]. A t-butyloxy carbonyl (BOC) group is the traditional choice for an amine-protecting group; however, it is well known that these groups are often unstable under general Suzuki–Miyaura coupling reaction conditions [3,19,21]. Therefore, the development of a high-throughput synthesis of aryl-substituted pyrroles with protection for subsequent application via a Suzuki–Miyaura coupling reaction is highly desirable. SEM (2-(trimethylsilyl)ethoxymethyl) represents a versatile and robust protecting group for nitrogen heterocycles that can readily be removed under a variety of deprotection conditions [22,23,24,25,26,27]. Herein, we present a method that allows for the efficient arylation of SEM-protected pyrroles via the Suzuki–Miyaura coupling reaction. This methodology provides the desired products in high yields for a wide range of substrates.

2. Results and Discussion

Initially, phenylboronic acid (1a) and 4-bromopyrrole (2a) were chosen as the model substrates for the Suzuki–Miyaura coupling reaction. In the presence of Pd(PPh3)4 (0.1 equiv.) and Na2CO3 (2 equiv.), the reaction between 1a and 2a in dioxane/H2O (4:1) at 90 °C afforded the desired coupling product (3a) in 61% yield (Table 1, entry 1). However, the use of Pd(II) salts, such as Pd(PPh3)2Cl2, Pd(AcO)2, and Pd(dppf)Cl2 ­as the catalysts reduced the yield of the product (Table 1, entries 2–4). Although the temperature was increased to 110 °C, almost no desired product was gained in DMF (N,N-dimethyl formamide) (Table 1, entry 5). We observed that the main by-product of the reaction was the homocoupling of the arylboronic acid. Therefore, we increased the amount of 1a to two equivalents; however, the product 3a was obtained in almost the same yield (Table 1, entry 6 versus entry 1). Moreover, increasing the amount of Na2CO3 (6 equiv.) did not lead to a discernible effect on the yield (Table 1, entry 7 versus entry 1). We further optimized the reaction conditions by reducing the amount of H2O, but the product was obtained in only 5% yield (Table 1, entry 8). For further improvement of the reaction, other bases such as K2CO3, KF, and Cs2CO3 were also examined (Table 1, entries 9–11). To our delight, the product was obtained in 85% yield with Cs2CO3 as the base. Furthermore, we observed that an increase or reduction of the reaction temperature were both unfavorable for the transformation (Table 1, entries 12 and 13). When the amount of Pd(PPh3)4 was reduced to 5 mol%, the product 3a was obtained in a slightly lower yield (Table 1, entry 14). From the above-mentioned results, it was concluded that the optimized conditions for this Suzuki–Miyaura coupling reaction protocol were 10 mol% Pd(PPh3)4, Cs2CO3 (2 equiv.) in dioxane/H2O (4:1) at 90 °C (Table 1, entry 11); especially, we have observed no dehalogenation in the reaction. To assess the effect of SEM-protected and BOC-protected pyrroles, BOC-protected pyrrole (2a’) was selected as the substrate. The reaction gave the product 3a in good yield, but the deprotected by-product (4a) was obtained in 5% yield (Table 1, entry 15). The result was confirmed with the assay conducted using Na2CO3 as the base, which led to 4a in 11% yield (Table 1, entry 16). In conclusion, the SEM-protecting group was stable under the optimal reaction conditions compared to the BOC protecting group, and a cross-coupling product was obtained in very good yield.

Table 1

Screening reaction conditions of Suzuki coupling a.

Entry	R	Catalyst	T(°C)	Base(equiv.)	Solvent	Time(h)	Yield (%) b
							3a (3a′)	4a
1	SEM	Pd(PPh3)4	90	Na2CO3 (2)	Dioxane/H2O (4:1)	1	61	0
2	SEM	Pd(PPh3)2Cl2	90	Na2CO3 (2)	Dioxane/H2O (4:1)	1	45	0
3	SEM	Pd(AcO)2	90	Na2CO3 (2)	Dioxane/H2O (4:1)	6	13	0
4	SEM	Pd(dppf)Cl2	90	Na2CO3 (2)	Dioxane/H2O (4:1)	6	28	0
5	SEM	Pd(PPh3)4	110	Na2CO3 (2)	DMF	6	trace	0
6 c	SEM	Pd(PPh3)4	90	Na2CO3 (2)	Dioxane/H2O (4:1)	1	57	0
7 c	SEM	Pd(PPh3)4	90	Na2CO3 (6)	Dioxane/H2O (4:1)	1	57	0
8	SEM	Pd(PPh3)4	90	Na2CO3 (2)	Dioxane/H2O (4:0.1)	6	5	0
9	SEM	Pd(PPh3)4	90	K2CO3 (2)	Dioxane/H2O (4:1)	5	45	0
10	SEM	Pd(PPh3)4	90	KF (2)	Dioxane/H2O (4:1)	6	32	0
11	SEM	Pd(PPh3)4	90	Cs2CO3 (2)	Dioxane/H2O (4:1)	5	85	0
12	SEM	Pd(PPh3)4	110	Cs2CO3 (2)	Dioxane/H2O (4:1)	3	75	0
13	SEM	Pd(PPh3)4	60	Cs2CO3 (2)	Dioxane/H2O (4:1)	5	53	0
14 d	SEM	Pd(PPh3)4	90	Cs2CO3 (2)	Dioxane/H2O (4:1)	2	78	0
15	BOC	Pd(PPh3)4	90	Cs2CO3 (2)	Dioxane/H2O (4:1)	2	76	5
16	BOC	Pd(PPh3)4	90	Na2CO3 (2)	Dioxane/H2O (4:1)	2	64	11

a General conditions: 1a (1.5 mmol), 2a (1 mmol), catalyst (10 mol %), and base in 10 mL of the indicated solvent under Ar2 atmosphere. b Isolated yield. c The equivalent ratio of 1a:2a = 2:1. d 5 mol% Pd(PPh3)4.

With these conditions in hand, we next evaluated the substrate scope of the reaction (Scheme 1). Overall, it was found that all the attempted phenylboronic acid analogues produced the desired aryl-substituted pyrroles in moderate to excellent yields. To evaluate the effect of boronic acid substituents, we first studied the reaction of the substrate bearing the electron-withdrawing groups such as Cl, F, NO2, and CF3 (3b−i). When phenylboronic acid with Cl and F substituents were used in the ortho position, the target compounds (3c and 3f) were isolated in 93% and 77% yield, respectively. In contrast, para substitution resulted in a decreased yield (3b and 3e). The same behavior was observed with the 2,4-dichloro or 2,4-difluro phenylboronic acid (3d and 3g). The presence of the strong electron-withdrawing NO2 and CF3 groups on the phenylboronic acid did not drastically affect the efficiency of the reaction (3h and 3i).

Scheme 1

Scope of the Suzuki coupling reaction. Yields refer to the isolated yields.

Then, we focused our attention on the reactivity of the phenylboronic acid with the electron-donating groups. When the phenylboronic acid was substituted with an OMe group at the C-4 position, the reaction gave the product 3j in 77% yield, while the OMe in the ortho position afforded the desired product in 87% yield (3k). The results displayed that this reaction followed the same behavior as the cross-coupling reaction compared to 2-fluorophenylboronic acid and 2-chlorophenylboronic acid as the substrate. Nevertheless, the Me group in the ortho position of phenylboronic acid lowered the efficiency of the reaction (3l versus 3m). The reaction with the fused aromatic compounds gave the corresponding products in good yields as well (3n and 3o). Notably, the reaction can also be carried out successfully with the heterocyclic substrates to furnish the desired products (3p and 3q). Finally, 5-bromopyrrole and 3-bromopyrrole (2b and 2c) were chosen as the substrates to document the potential of the method. The reactions worked very smoothly, giving the corresponding products in excellent yields (3r and 3s).

To further explore this synthetic potential, several common transformations of the product 3a were conducted (Scheme 2). First, the SEM-protecting group was removed smoothly in the presence of TBAF (tetrabutyl ammonium fluoride) to provide the N-H-4-phenyl pyrrole 4a in 83% yield. Hydrolysis and reduction reactions readily occurred, leading to the fascinating pyrrole-2-carboxylic acid 4b and 2-hydroxymethyl substituted pyrrole compound 4c in good yields, respectively. No SEM deprotection of pyrrole was observed in the aforementioned hydrolysis and reduction reactions as anticipated.

Scheme 2

The application of SEM-protected pyrroles. Yields refer to the isolated yields.

3. Materials and Methods

3.1. General Methods

All the starting materials were obtained from commercial suppliers and were used without further purification unless stated otherwise. Reactions were monitored by Thin Layer Chromatography (silica gel GF254). Products were purified by column chromatography on silica gel (300–400 mesh). 1H and 13C spectra were recorded on a Varian (Palo Alto, CA, USA) 400 NMR or 500 NMR spectrometer using DMSO-d6 as a solvent and tetramethylsilane (TMS) as an internal standard. Chemical shifts (δ) are reported in parts per million (ppm), and coupling constants (J) are reported in Hertz (Hz). Data are represented as follows: chemical shift, multiplicity (br = broad, s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet), coupling constants in Hertz (Hz), and integration. All the melting points were measured with a microscope melting point apparatus (MP-J3, Yanaco, Kyoto, Japan) and were uncorrected. High-resolution mass spectra were determined on ThermoExactive Orbitrap plus mass spectrometer (Waltham, MA, USA). 1H-NMR and HRMS spectra are available in Supplementary Materials.

3.2. Typical Procedure to Synthesize Compounds

First, t-BuOK (330 mg, 2.94 mmol) was added to a solution of bromopyrroles (500 mg, 2.45 mmol) in anhydrous DMF (5 mL) in an ice-bath, and the mixture was stirred for 0.5 h. SEM-Cl (449 mg, 2.7 mmol) was added to the resulting mixture. The reaction mixture was stirred at rt for 2 h, and then quenched with H2O. The mixture was extracted with EtOAc (15 mL × 3), and the combined organic layer was washed with sat. NaHCO3 and brine, dried with Na2SO4, and concentrated. The product was obtained by flash chromatography (EtOAc in PE = 3%).

Methyl 4-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (2a). Colorless oil, 71% yield. 1H-NMR (400 MHz, DMSO-d) δ: 7.50 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 6.94 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 5.58 (s, 2H, NCH2O), 3.74 (s, 3H, CH3), 3.46 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.79 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). HRMS (ESI): m/z [M + H]+ calcd for C12H21BrNO3Si: 334.0469; found: 334.0448.

Methyl 5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (2b). Colorless oil, 96% yield. 1H-NMR (400 MHz, DMSO-d) δ: 6.99 (d, J = 4.0 Hz, 1H, Pyrrole-3H), 6.40 (d, J = 4.0 Hz, 1H, Pyrrole-4H), 5.71 (s, 2H, NCH2O), 3.75 (s, 3H, CH3), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.80 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). HRMS (ESI): m/z [M + H]+ calcd for C12H21BrNO3Si: 334.0469; found: 334.0463.

Methyl 3-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (2c). Colorless oil, 81% yield. 1H-NMR (500 MHz, DMSO-d) δ: 7.33 (d, J = 2.5 Hz, 1H, Pyrrole-5H), 6.35 (d, J = 2.5 Hz, 1H, Pyrrole-4H), 5.57 (s, 2H, NCH2O), 3.78 (s, 3H, CH3), 3.41 (t, J = 7.5 Hz, 2H, OCHCH2Si), 0.78 (t, J = 7.5 Hz, 2H, OCH2CHSi), −0.08 (s, 9H, Si(CH3)3). HRMS (ESI): m/z [M + H]+ calcd for C12H21BrNO3Si: 334.0469; found: 334.0460.

3.3. Typical Procedure to Synthesize Products

Dioxane (8 mL) and H2O (2 mL) were added to the mixture of 1a–q (1.5 mmol), 2a–c (1 mmol), Cs2CO3 (652 mg, 2 mmol), and Pd(PPh3)4 (116 mg, 0.1 mmol) under Ar2 atmosphere. The reaction mixture was stirred at 90 °C for about 5 h (monitored by Thin Layer Chromatography) and cooled to rt. Then, the mixture was filtered to remove the solids, and the filtrate was concentrated. Purification by flash chromatography (EtOAc in PE = 3%) gave the desired product.

Methyl 4-phenyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3a). Colorless oil, 85% yield. 1H-NMR (400 MHz, DMSO-d) δ: 7.80 (d, J = 1.2 Hz, 1H, Pyrrole-5H), 7.61 (d, J = 8.0 Hz, 2H, Ar-2,6H), 7.36–7.32 (m, 3H, Ar-3,5H, Pyrrole-3H), 7.19 (t, J = 8.0 Hz, 1H, Ar-4H), 5.64 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.50 (t, J = 7.6 Hz, 2H, OCHCH2Si), 0.82 (t, J = 7.6 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 161.0, 134.2, 129.2, 127.4, 126.6, 125.2, 123.9, 122.7, 116.1, 76.9, 65.6, 51.6, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H26NO3Si: 332.1677; found: 332.1662.

Methyl 4-(4-chlorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3b). Colorless oil, 66% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.84 (s, 1H, Pyrrole-5H), 7.65 (d, J = 8.5 Hz, 2H, Ar-2,6H), 7.39 (d, J = 8.5 Hz, 2H, Ar-3,5H), 7.35 (s, 1H, Pyrrole-3H), 5.64 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.50 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.82 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 160.9, 133.2, 130.9, 129.2, 127.7, 126.9, 122.9, 122.6, 116.2, 76.9, 65.6, 51.7, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H25ClNO3Si: 366.1287; found: 366.1271.

Methyl 4-(2-chlorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3c). Colorless oil, 93% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.75 (s, 1H, Pyrrole-5H), 7.56 (d, J = 7.5 Hz, 1H, Ar-3H), 7.50 (d, J = 7.5 Hz, 1H, Ar-6H), 7.36 (t, J = 7.0 Hz, 1H, Ar-5H), 7.29–7.27 (m, 2H, Ar-4H, Pyrrole-3H), 5.68 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.52 (t, J = 7.5 Hz, 2H, OCHCH2Si), 0.82 (t, J = 7.5 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 160.9, 133.0, 131.1, 130.7, 130.0, 128.5, 128.0, 121.9, 120.8, 119.1, 77.0, 65.6, 51.7, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H25ClNO3Si: 366.1287; found: 366.1274.

Methyl 4-(2,4-dichlorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3d). Colorless oil, 67% yield. 1H-NMR (500 MHz, DMSO-d6) δ 7.78 (d, J = 1.5 Hz, 1H, Pyrrole-5H), 7.65 (d, J = 1.5 Hz, 1H, Ar-3H), 7.60 (d, J = 8.5 Hz, 1H, Ar-6H), 7.43 (dd, J = 8.0, 1.5 Hz, 1H, Ar-5H), 7.28 (d, J = 1.5 Hz, 1H, Pyrrole-3H), 5.68 (s, 2H, NCH2O), 3.78 (s, 3H, CH3), 3.52 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.82 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 160.8, 132.0, 131.9, 131.8, 130.1, 130.0, 128.1, 122.0, 119.7, 119.0, 77.0, 65.6, 51.7, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H24Cl2NO3Si: 400.0897; found: 400.0892.

Methyl 4-(4-fluorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3e). Colorless oil, 70% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 7.77 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.66–7.63 (m, 2H, Ar-2,6H), 7.31 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 7.17 (t, J = 8.8 Hz, 2H, Ar-3,5H), 5.63 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.50 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.81 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.08 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 161.2 (d, J = 241.1 Hz), 160.9, 130.8 (d, J = 2.9 Hz), 127.3, 127.1 (d, J = 7.8 Hz), 122.8 (d, J = 23.6 Hz), 116.1, 116.0, 115.9, 76.9, 65.6, 51.6, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H25FNO3Si: 350.1582; found: 350.1565.

Methyl 4-(2-fluorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3f). Colorless oil, 77% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.76–7.72 (m, 2H, Pyrrole-5H, Ar-6H), 7.36 (s, 1H, Pyrrole-3H), 7.26–7.21 (m, 3H, Ar-3,4,5H), 5.68 (s, 2H, NCH2O), 3.78 (s, 3H, CH3), 3.51 (t, J = 7.5 Hz, 2H, OCHCH2Si), 0.81 (t, J = 7.5 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 160.9, 159.3 (d, J = 244.4 Hz), 129.3 (d, J = 8.6 Hz), 128.3 (d, J = 4.2 Hz), 128.2 (d, J = 8.4 Hz), 125.2 (d, J = 3.1 Hz), 122.4, 121.8 (d, J = 12.8 Hz), 117.5, 117.4, 116.5 (d, J = 22.1 Hz), 76.9, 65.6, 51.7, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H25FNO3Si: 350.1582; found: 350.1572.

Methyl 4-(2,4-difluorophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3g). Colorless oil, 70% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.78 (dd, J = 16.0, 9.0 Hz, 1H, Ar-3H), 7.74 (s, 1H, Pyrrole-5H), 7.34 (s, 1H, Pyrrole-3H), 7.28 (t, J = 9.5 Hz, 1H, Ar-6H), 7.10 (t, J = 8.5 Hz, 1H, Ar-5H), 5.68 (s, 2H, NCH2O), 3.79 (s, 3H, CH3), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.82 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 161.1 (dd, J = 244.0, 12.2 Hz), 160.8, 159.3 (dd, J = 247.3, 11.9 Hz), 129.4 (dd, J = 9.3, 5.9 Hz), 129.0 (d, J = 8.5 Hz), 122.4, 118.5 (dd, J = 13.0, 3.6 Hz), 117.3 (d, J = 3.5 Hz), 116.8, 112.3 (dd, J = 21.0, 3.2 Hz), 104.8 (t, J = 26.1 Hz), 76.9, 65.6, 51.6, 17.5, −1.1. HRMS (ESI): m/z [M + H]+ calcd for C18H24F2NO3Si: 368.1488; found: 368.1480.

Methyl 4-(4-nitrophenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3h). Yellow solid, 62% yield. M.p. 82–83 °C. 1H-NMR (400 MHz, DMSO-d6) δ: 8.20 (d, J = 8.4 Hz, 2H, Ar-3,5H), 8.08 (d, J = 1.6 Hz, 1H, Pyrrole-5H), 7.91 (d, J = 8.4 Hz, 2H, Ar-2,6H), 7.51 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 5.66 (s, 2H, NCH2O), 3.79 (s, 3H, CH3), 3.52 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.83 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 160.8, 145.7, 141.3, 129.4, 125.8, 124.7, 123.5, 121.8, 116.8, 77.2, 65.8, 51.8, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H25N2O5Si: 377.1527; found: 377.1545.

Methyl 4-(4-(trifluoromethyl)phenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3i). Colorless oil, 68% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.95 (s, 1H, Pyrrole-5H), 7.83 (d, J = 5.0 Hz, 2H, Ar-3,5H), 7.67 (brs, 2H, Ar-2, 6H), 7.43 (s, 1H, Pyrrole-3H), 5.65 (s, 2H, NCH2O), 3.78 (s, 3H, CH3), 3.51 (t, J = 7.5 Hz, 2H, OCHCH2Si), 0.82 (t, J = 7.5 Hz, 2H, OCH2CHSi), −0.08 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 160.9, 138.4, 128.5, 126.9, 126.1 (q, J = 3.7 Hz), 125.6, 125.1 (q, J = 236.0 Hz), 123.2, 122.3, 116.5, 77.1, 65.7, 51.7, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C19H25F3NO3Si: 400.1550; found: 400.1567.

Methyl 4-(4-methoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3j). Colorless oil, 77% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 7.68 (d, J = 1.6 Hz, 1H, Pyrrole-5H), 7.53 (d, J = 8.8 Hz, 2H, Ar-2,6H), 7.25 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 6.92 (d, J = 8.8 Hz, 2H, Ar-3,5H), 5.63 (s, 2H, NCH2O), 3.76 (s, 3H, CH3), 3.75 (s, 3H, CH3), 3.50 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.81 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 161.0, 158.3, 126.8, 126.6, 126.4, 123.8, 122.5, 115.8, 114.6, 76.8, 65.5, 55.5, 51.5, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C19H28NO4Si: 362.1782; found: 362.1792.

Methyl 4-(2-methoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3k). Colorless oil, 87% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 7.76 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.59 (dd, J = 8.0, 2.0 Hz, 1H, Ar-6H), 7.37 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 7.20 (td, J = 7.6, 1.6 Hz, 1H, Ar-4H), 7.05 (d, J = 7.6 Hz, 1H, Ar-3H), 6.95 (td, J = 7.6, 1.2 Hz, 1H, Ar-5H), 5.67 (s, 2H, NCH2O), 3.86 (s, 3H, CH3), 3.77 (s, 3H, CH3), 3.51 (t, J = 7.6 Hz, 2H, OCHCH2Si), 0.82 (t, J = 7.6 Hz, 2H, OCH2CHSi), −0.06 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 161.1, 156.3, 129.9, 127.7, 122.6, 121.6, 121.2, 120.0, 118.0, 112.1, 76.7, 65.4, 55.8, 51.5, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C19H28NO4Si: 362.1782; found: 362.1784.

Methyl 4-(p-tolyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3l). Colorless oil, 73% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 7.74 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.49 (d, J = 8.0 Hz, 2H, Ar-2,6H), 7.28 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 7.16 (d, J = 8.0 Hz, 2H, Ar-3,5H), 5.63 (s, 2H, NCH2O), 3.76 (s, 3H, CH3), 3.50 (t, J = 8.0 Hz, 2H, OCHCH2Si), 2.29 (s, 3H, CH3), 0.81 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 161.0, 135.7, 131.4, 129.8, 127.1, 125.1, 123.9, 122.6, 116.0, 76.8, 65.5, 51.6, 21.1, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C19H28NO3Si: 346.1833; found: 346.1839.

Methyl 4-(o-tolyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3m). Colorless oil, 52% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 7.52 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.32 (dd, J = 7.6, 2.0 Hz, 1H, Ar-6H), 7.25–7.16 (m, 3H, Ar-3,4,5H), 7.09 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 5.66 (s, 2H, NCH2O), 3.76 (s, 3H, CH3), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 2.37 (s, 3H, CH3), 0.81 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 161.0, 135.1, 134.2, 131.1, 129.5, 129.2, 127.0, 126.5, 123.4, 121.8, 119.1, 76.9, 65.5, 51.6, 21.5, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C19H28NO3Si: 346.1833; found: 346.1843.

Methyl 4-(naphthalen-2-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3n). Colorless oil, 76% yield. 1H-NMR (400 MHz, DMSO-d6) δ: 8.16 (dd, J = 7.2, 2.4 Hz, 1H, Ar-5H), 7.98–7.95 (m, 1H, Ar-4H), 7.87 (d, J = 8.0 Hz, 1H, Ar-8H), 7.65 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.54–7.46 (m, 4H, Ar-1,3,6,7H), 7.18 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 5.73 (s, 2H, NCH2O), 3.79 (s, 3H, CH3), 3.57 (t, J = 7.6 Hz, 2H, OCHCH2Si), 0.84 (t, J = 7.6 Hz, 2H, OCH2CHSi), −0.05 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 161.0, 134.1, 132.8, 131.3, 129.9, 128.9, 127.5, 127.0, 126.7, 126.3, 126.2, 125.5, 122.4, 122.2, 119.7, 77.0, 65.6, 51.7, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C22H28NO3Si: 382.1833; found: 382.1839.

Methyl 4-(quinolin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3o). Colorless solid, 66% yield. M.p. 52–54 °C. 1H-NMR (400 MHz, DMSO-d6 ) δ: 9.21 (d, J = 2.0 Hz, 1H, Ar-2H), 8.53 (d, J = 2.0 Hz, 1H, Ar-4H), 8.06 (d, J = 2.0 Hz, 1H, Pyrrole-5H), 7.94 (d, J = 8.4 Hz, 1H, Ar-8H), 7.89 (d, J = 7.2 Hz, 1H, Ar-5H), 7.65 (td, J = 7.2, 1.6 Hz, 1H, Ar-6H), 7.57–7.53 (m, 2H, Ar-7H, Pyrrole-3H), 5.65 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.80 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.1 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 160.9, 149.0, 146.7, 130.1, 129.2, 129.1, 128.4, 128.3, 128.2, 127.5, 127.4, 123.2, 120.8, 116.5, 77.1, 65.7, 51.8, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C21H27N2O3Si: 383.1786; found: 383.1783.

Methyl 4-(pyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3p). Colorless oil, 41% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 8.88 (s, 1H, Py-2H), 8.40 (d, J = 3.5 Hz, 1H, Py-6H), 8.01 (d, J = 7.5 Hz, 1H, Py-4H), 7.93 (s, 1H, Pyrrole-5H), 7.43 (s, 1H, Pyrrole-3H), 7.36 (dd, J = 7.5, 5.0 Hz, 1H, Py-5H), 5.65 (s, 2H, NCH2O), 3.78 (s, 3H, CH3), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.82 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 160.9, 147.6, 146.5, 132.3, 130.0, 127.9, 124.2, 123.1, 120.6, 116.2, 77.0, 65.7, 51.7, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C17H25N2O3Si: 333.1629; found: 333.1622.

Methyl 4-(furan-2-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3q). Colorless oil, 45% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.61 (s, 1H, Furan-5H), 7.58 (s, 1H, Pyrrole-5H), 7.16 (s, 1H, Furan-4H), 6.57 (d, J = 2.5 Hz, 1H, Furan-3H), 6.49 (s, 1H, Pyrrole-3H), 5.64 (s, 2H, NCH2O), 3.76 (s, 3H, CH3), 3.49 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.81 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.08 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d6) δ: 160.8, 149.6, 141.5, 126.1, 122.6, 115.6, 115.1, 111.9, 104.1, 76.9, 65.6, 51.7, 17.5, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C16H24NO4Si: 322.1469; found: 322.1483.

Methyl 5-phenyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3r). Colorless oil, 95% yield. 1H-NMR (500 MHz, DMSO-d6) δ: 7.55 (d, J = 7.5 Hz, 2H, Ar-2,6H), 7.49–7.44 (m, 3H, Ar-3,4,5H), 7.03 (d, J = 3.5 Hz, 1H, Pyrrole-3H), 6.33 (d, J = 4.0 Hz, 1H, Pyrrole-4H), 5.62 (s, 2H, NCH2O), 3.77 (s, 3H, CH3), 3.36 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.73 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.10 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 161.2, 142.5, 131.8, 129.5, 129.2, 128.8, 123.3, 119.3, 110.3, 73.4, 65.3, 51.6, 17.9, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H26NO3Si: 332.1677; found: 332.1661.

Methyl 3-phenyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylate (3s). Colorless solid, 99% yield. M.p. 87–88 °C. 1H-NMR (500 MHz, DMSO-d) δ: 7.35–7.30 (m, 6H, Ar-2,3,4,5,6H, Pyrrole-5H), 6.24 (d, J = 2.0 Hz, 1H, Pyrrole-4H), 5.60 (s, 2H, NCH2O), 3.58 (s, 3H, CH3), 3.46 (t, J = 7.5 Hz, 2H, OCHCH2Si), 0.81 (t, J = 7.5 Hz, 2H, OCH2CHSi), −0.06 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 161.8, 136.3, 134.2, 129.4, 129.2, 128.2, 127.1, 118.1, 110.6, 77.6, 65.5, 51.3, 17.6, −1.0. HRMS (ESI): m/z [M + H]+ calcd for C18H26NO3Si: 332.1677; found: 332.1663.

3.4. Procedure for the Preparation of Methyl 4-phenyl-1H-pyrrole-2-carboxylate ()

A mixture of 3a (500 mg, 1.5 mmol) and TBAF (3 mL, 1 mol/L THF) was stirred at 80 °C for 2 h and cooled to rt. Then, the reaction mixture was diluted with EtOAc and H2O. The aqueous phase was extracted with EtOAc, and the combined organic layer was washed with brine, dried with Na2SO4, and concentrated. Purification by flash chromatography (EtOAc in PE = 14%) gave 4a (251 mg, 83%) as a colorless solid. M.p. 198–200 °C. 1H-NMR (500 MHz, DMSO-d) δ: 12.07 (s, 1H, NH), 7.62 (d, J = 7.0 Hz, 2H, Ar-2,6H), 7.51 (s, 1H, Pyrrole-5H), 7.32 (t, J = 7.0 Hz, 2H, Ar-3,5H), 7.19–7.16 (m, 2H, Ar-4H, Pyrrole-3H), 3.79 (s, 3H, CH3). 1H-NMR data was in agreement with the literature [28]. 13C-NMR (100 MHz, DMSO-d) δ: 161.3, 135.0, 129.1, 126.2, 125.6, 125.2, 123.2, 121.7, 112.4, 51.6. HRMS (ESI): m/z [M + H]+ calcd for C12H12NO2: 202.0863; found: 202.0856.

3.5. Procedure for the Preparation of 4-Phenyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carboxylic acid ()

A mixture of 3a (250 mg, 0.75 mmol) and NaOH (60 mg, 1.5 mmol) in ethanol (6 mL) and H2O (4 mL) was stirred at 100 °C for 6 h. Then, the reaction mixture was concentrated to remove ethanol, and the residue was adjusted to pH 7 with HCl (2M). The aqueous phase was extracted with EtOAc, and the combined organic layer was washed with brine, dried with Na2SO4, and concentrated to give 4b (200 mg, 84%) as a colorless solid. M.p. 83–85 °C. 1H-NMR (400 MHz, DMSO-d) δ: 12.44 (s, 1H, COOH), 7.72 (d, J = 1.6 Hz, 1H, Pyrrole-5H), 7.59 (d, J = 7.2 Hz, 2H, Ar-2,6H), 7.34 (t, J = 7.6 Hz, 2H, Ar-3,5H), 7.26 (d, J = 2.0 Hz, 1H, Pyrrole-3H), 7.18 (t, J = 7.6 Hz, 1H, Ar-4H), 5.66 (s, 2H, NCH2O), 3.51 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.82 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.07 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 162.2, 134.4, 129.2, 126.8, 126.5, 125.1, 123.9, 123.6, 115.9, 76.7, 65.5, 17.6, −0.9. HRMS (ESI): m/z [M + H]+ calcd for C17H24NO3Si: 318.1520; found: 318.1489.

3.6. Procedure for the Preparation of (4-Phenyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrol-2-yl)methanol ()

First, LiAlH4 (35 mg, 0.94 mmol) was added to a solution of 3a (155 mg, 0.47 mmol) in anhydrous THF (6 mL) at rt. After stirring overnight, the reaction mixture was quenched with 15% NaOH (0.11 mL) and extracted with EtOAc/H2O, and the organic layer was washed with brine, dried with Na2SO4, and concentrated. Purification by flash chromatography (EtOAc in PE = 14%) gave 4c (127 mg, 89%) as a yellow oil. 1H-NMR (500 MHz, DMSO-d) δ: 7.49 (d, J = 7.5 Hz, 2H, Ar-2,6H), 7.31–7.28 (m, 3H, Ar-3,5H, Pyrrole-5H), 7.11 (t, J = 7.5 Hz, 1H, Ar-4H), 6.41 (s, 1H, Pyrrole-3H), 5.29 (s, 2H, NCH2O), 4.98 (brs, 1H, OH), 4.47 (d, J = 4.0 Hz, 2H, CHOH), 3.50 (t, J = 8.0 Hz, 2H, OCHCH2Si), 0.84 (t, J = 8.0 Hz, 2H, OCH2CHSi), −0.04 (s, 9H, Si(CH3)3). 13C-NMR (100 MHz, DMSO-d) δ: 135.9, 134.7, 129.1, 125.5, 124.7, 122.6, 120.0, 107.1, 76.0, 65.2, 55.3, 17.6, −0.9. HRMS (ESI): m/z [M + H]+ calcd for C17H26NO2Si: 304.1727; found: 304.1708.

4. Conclusions

In summary, we have developed an efficient Suzuki–Miyaura coupling reaction of SEM-protected bromopyrroles and arylboronic acids under mild conditions leading to aryl-substituted pyrroles. This methodology is a practical and straightforward way to synthesize various pyrrole building blocks for delivering novel compounds with broad functional group compatibility. The protocol displays some advantages compared to the reported methods, such as commercially available materials, no debrominated by-products being formed, and the SEM-protecting group being more tolerant than the BOC-protecting group under the reaction conditions. Around the privileged SEM-protected aryl-substituted pyrroles, we demonstrate the versatility of the pyrrole ring framework in synthetic transformations for constructing new structures. This protocol will offer the opportunity to explore other metal-catalyzed cross-coupling reactions using SEM-protected pyrroles and generate new bioactive compounds containing polyfunctionalized pyrroles.