The Scientific World Journal

Volume 2014 (2014), Article ID 649197, 15 pages

http://dx.doi.org/10.1155/2014/649197

Research Article

Facile and Promising Method for Michael Addition of Indole and Pyrrole to Electron-Deficient trans-β-Nitroolefins Catalyzed by a Hydrogen Bond Donor Catalyst Feist’s Acid and Preliminary Study of Antimicrobial Activity

Abdullah M. A. Al Majid,¹ Mohammad Shahidul Islam,¹ Assem Barakat,1,2 Mohamed H. M. Al-Agamy,³ and Mu. Naushad¹

¹Department of Chemistry, Faculty of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

²Department of Chemistry, Faculty of Science, Alexandria University, P.O. Box 426, Ibrahimia, Alexandria 21321, Egypt

³Division of Microbiology, Pharmaceutics Department, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia

Received 8 October 2013; Accepted 4 November 2013; Published 16 January 2014

Academic Editors: R. P. Herrera, N. T. Patil, Z. Shao, and L.-W. Xu

Copyright © 2014 Abdullah M. A. Al Majid et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The importance of cooperative hydrogen-bonding effects has been demonstrated using novel 3-methylenecyclopropane-1,2-dicarboxylic acid (Feist’s acid (FA)) as hydrogen bond donor catalysts for the addition of indole and pyrrole to trans-β-nitrostyrene derivatives. Because of the hydrogen bond donor (HBD) ability, Feist’s acid (FA) has been introduced as a new class of hydrogen bond donor catalysts for the activation of nitroolefin towards nucleophilic substitution reaction. It has effectively catalyzed the Michael addition of indoles and pyrrole to β-nitroolefins under optimum reaction condition to furnish the corresponding Michael adducts in good to excellent yields (up to 98%). The method is general, atom-economical, convenient, and eco-friendly and could provide excellent yields and regioselectivities. Some newly synthesized compounds were for examined in vitro antimicrobial activity and their preliminary results are reported.

1. Introduction

In the field of advanced organic synthesis, Michael addition reaction is one of the most powerful tools for carbon-carbon bond construction reactions [1–6]. Nitroolefins are very attractive among the many Michael acceptors because of their strong electron-withdrawing nitro group which could be easily transformed into a wide variety of different functionalities [7–9] that may lead to synthesizing important biologically active building blocks and products [10]. Until now a numerous number of catalysts have been reported in the literature, mainly for the Michael addition reactions of heteroarenes to carbonyls [11, 12]. Moreover a remarkable number of catalysts have been used to catalyze the Michael addition [13–21] reaction of indoles and pyrrole to trans-β-nitroolefins; however, most of them were Lewis acids [22–25]. Recently some small organic molecules with anion recognition abilities have provided a great deal of inspiration for the development of hydrogen-bonding catalysis [26–28]; in this context, hydrogen bond donor (HBD) catalysis has received some achievement in exploiting the anion recognition abilities offered by urea, thiourea, and guanidinium functionalities [29–31], silanediols [32, 33], silica gel [34], 2-aminopyridinium ions [35–38], sulfamic acid (SA) [9], dipicolinic acid [26], which were found to be highly potent in catalyzing the Michael addition reaction through hydrogen bonding catalysis [26, 39–47]. Yet such small organic molecules with hydrogen bond donor (HBD) ability received little attention in the context of noncovalent catalysis [48]. Excited by the potential of such hydrogen bond donor small molecule, we have initiated a program in our laboratory dedicated toward pioneering the development of Feist’s acid (FA) [49, 50] as a new class of catalysts that operate through hydrogen bonding interactions.

Indole and its analogs constitute the active class of compounds possessing wide spectrum of biological activities. A variety of indole derivatives have emerged that possess a range of bioactivities including potent anticancer, antiviral, anti-inflammatory, anti-hypertensive, anti-asthmatic and anti-tubercular properties. Some of these compounds are also known to possess anti-inflammatory and analgesic properties [51–53]. Pyrrole heterocyclic derivatives were reported as having important synthetic and biological activities such as COX-1/COX-2 inhibitors and cytotoxic activity against a variety of marine and human tumor models [54–59].

In this communication, we report initial successes with FA catalysis and its application toward the activation of nitroolefin via hydrogen-bonding mechanistic pathway, which effectively catalyze Michael addition of indoles and pyrrole to nitroolefins under optimum reaction condition to afford the corresponding Michael adducts in good to excellent yields. Some newly synthesized compounds were subjected to in vitro antimicrobial activity.

2. Experimental

2.1. General Information

Glassware was oven-dried overnight at 120°C before use. Reactions were performed under an inert atmosphere using an argon filled glove box and standard Schlenk-line techniques. All the reactions were monitored by TLC analysis using Merck Silica Gel 60 F-254 thin layer plates. Column chromatography was performed on silica gel 100–200 mesh.

2.1.1. Materials

Petroleum ether (PE), hexane, and ethyl acetate for column chromatography were distilled prior to use. CH₂Cl₂ and EtOH were distilled from P₂O₅ and Mg, respectively, and stored on 4 Å molecular sieves. Tetrahydrofuran, benzene, and toluene were distilled from sodium benzophenone ketyl. Acetonitrile and dimethylformamide were dried by distillation over calcium hydride. Nitroolefins 2(a–i) were prepared according to procedures reported in literature [60].

2.1.2. Instrumentation

NMR spectra were recorded with a Jeol spectrometer at 400 MHz (¹H-NMR) and 100 MHz (¹³C-NMR.). The chemical shifts (δ in ppm) were reported down field from tetramethylsilane (TMS, δ scale) with the deuterated solvent resonance referenced as internal standard. Elemental analyses were performed on a Perkin Elmer 2400 Elemental Analyzer. IR spectra were obtained using FTIR-800 Model. Mass spectrometric analysis was conducted by using ESI mode on AGILENT Technologies 6410-triple quad LC/MS instrument.

2.2. General Procedure for the Michael Addition Reaction of Indole with β-Nitroolefins Catalyzed by Feist’s Acid (GP1)

Indole 4 (50 mg, 0.425 mmol), β-nitroolefins 2(a–i) (0.425 mmol), and a catalytic amount of Feist’s acid (1) (6 mg, 0.084 mmol, 10 mol%) in dry ethanol (3 mL) were charged into a Schlenk tube under an argon atmosphere. The reaction was then stirred at 50°C for 48–72 hours. The reaction mixture was monitored by TLC until starting material was completely consumed. Then the solvent was removed under vacuum. The crude products were isolated by column chromatography to afford pure Michael adducts (7a–i). The analytical data of the known compounds were in accordance with reported literature [58].

2.2.1. 3-(2-Nitro-1-phenylethyl)-1H-indole (Table 2, Entry 1, 7a)

Indole 4 (50 mg, 0.43 mmol) and β-nitrostyrene 2a (64 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (6 mg, 0.084 mmol, 10 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7a as yellow oil [58] (111 mg, 0.42 mmol, 97%). IR (KBr): 3417, 15461375, 742, 700, 587 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.89–4.99 (m, 1H, CHCH 2(a)), 5.02–5.12 (m, 1H, CHCH 2(b)), 5.15–5.23 (m, 1H, CHCH₂), 7.01–7.11 (m, 2H, ArH), 7.17–7.24 (m, 1H, ArH), 7.25 (s, 1H, NHCH), 7.26–7.36 (m, 5H, ArH), 7.44 (d,  Hz, 1H. ArH), 8.09 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃, 100 MHz): δ 41.6, 79.9, 111.4, 114.5, 119.0, 120.0, 121.7, 122.8, 126.7, 127.7, 127.8, 129.0, 136.6, 139.2; [Anal. Calcd. for C₁₆H₁₄N₂O₂: C, 72.16; H, 5.30; N, 10.52; found: C, 72.37; H, 5.23; N, 10.41]; LC/MS (ESI): M⁺, found 266.08, C₁₆H₁₄N₂O₂ requires 266.11.

2.2.2. 3-[1-(4-Methylphenyl)-2-nitroethyl]-1H-indole (Table 2, Entry 2, 7b)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2b (70 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (6 mg, 0.084 mmol, 10 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7b as yellow oil [58] (117 mg, 0.42 mmol, 97.2%). IR (KBr): 3418, 1547, 1377, 739 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 2.31 (s, 1H, CH ₃), 4.86–4.98 (m, 1H, CHCH 2(a)), 5.01–5.10 (m, 1H, CHCH 2(b)), 5.10–5.20 (m, 1H, CHCH₂), 6.98–7.02 (m, 2H, ArH), 7.06–7.25 (m, 5H, ArH), 7.34 (d,  Hz, 1H, ArH), 7.46 (d,  Hz, 1H. ArH), 8.06 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃,, 100 MHz): δ 21.1, 41.3, 80.0, 111.4, 114.7, 119.0, 120.0, 121.6, 122.7, 126.2, 127.7, 129.7, 136.2, 136.6, 137.3; [Anal. Calcd. for C₁₇H₁₆N₂O₂: C, 72.84; H, 5.75; N, 9.99; found: C, 73.03; H, 5.66; N, 10.11]; LC/MS (ESI): M⁺, found 280.16, C₁₇H₁₆N₂O₂ requires 280.12.

2.2.3. 3-(1-(4-Methoxyphenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 3, 7c)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2c (77 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (6 mg, 0.084 mmol, 10 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7c as white solid (107 mg, 0.36 mmol, 84%). m.p. 149−151°C [Lit [58] m.p. 148–150°C]; IR (KBr): 3373, 1545, 1509, 1458, 1420, 1374, 1241, 1179, 1027, 742, 608, 548, 525 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 3.76 (s, 1H, OCH ₃), 4.84–4.93 (m, 1H, CHCH 2(a)), 5.00–5.08 (CHCH₂m, 1H, CHCH 2(b)), 5.08–5.17 (m, 1H,), 6.84 (d,  Hz, 2H. ArH), 7.01 (s, 1H, NHCH), 7.02–7.10 (m, 1H, ArH), 7.19–7.28 (m, 3H, ArH), 7.36 (d,  Hz, 1H. ArH), 7.44 (d,  Hz, 2H. ArH), 8.07 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃, 100 MHz): δ 40.9, 55.3, 80.0, 111.4, 114.3, 119.1, 120.0, 121.5, 122.8, 126.1, 128.9, 131.2, 136.6, 139.3, 158.9; [Anal. Calcd. for C₁₇H₁₆N₂O₃: C, 68.91; H, 5.44; N, 9.45; found: C, 79.09; H, 5.53; N, 9.36]; LC/MS (ESI): M⁺, found 296.18, C₁₇H₁₆N₂O₂ requires 296.12.

2.2.4. 3-(1-(4-Chlorophenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 4, 7d)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2d (79 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (6 mg, 0.084 mmol, 10 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7d as oily liquid (124 mg, 0.42 mmol, 97.4%). IR (KBr): 3417, 1548, 1376, 1091, 736, 423 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.83–4.96 (m, 1H, CHCH 2(a)), 5.02–5.10 (m, 1H, CHCH 2(b)), 5.10–5.22 (m, 1H, CHCH₂), 6.96–7.03 (m, 1H. ArH), 7.04–7.12 (m, 1H, ArH), 7.15–7.34 (m, 4H, ArH), 7.34–7.46 (m, 3H, ArH), 8.12 (s, 1H, NH of Indole); ¹³C-NMR (CDCl3, 100 MHz): δ 41.0, 79.4, 111.6, 114.0, 118.1, 118.9, 120.2, 121.6, 123.0, 126.0, 129.2, 133.5, 136.6, 137.8; [Anal. Calcd. for C₁₆H₁₃ClN₂O₂: C, 63.90; H, 4.36; N, 9.31; found: C, 64.11; H, 4.05; N, 9.57]; LC/MS (ESI): M⁺ & [M+2]⁺, found 300.01 & 302.05, C₁₆H₁₃ClN₂O₂ requires 300.07.

2.2.5. 3-(1-(4-Bromophenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 6, 7e)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2e (98 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 20 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7e as yellow oil (130 mg, 0.38 mmol, 88%). IR (KBr): 3405, 1539, 1380, 1006, 743, 594, 533, 424 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.86–4.98 (m, 1H, CHCH 2(a)), 4.99–5.10 (m, 1H, CHCH 2(b)), 5.10–5.18 (m, 1H, CHCH₂), 6.95–7.02 (m, 1H. ArH), 7.02–7.14 (m, 1H, ArH), 7.15–7.27 (m, 4H, ArH), 7.29–7.48 (m, 3H, ArH), 8.11 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃, 100 MHz): δ 41.1, 79.3, 111.8, 113.9, 118.9, 120.2, 121.6, 123.0, 126.0, 129.6, 132.2, 136.6, 138.3, 140.0; [Anal. Calcd. for C₁₆H₁₃BrN₂O₂: C, 55.67; H, 3.80; N, 8.12; found: C, 55.27; H, 3.73; N, 7.98]; LC/MS (ESI): M⁺ & [M+2]⁺, found 344.10 & 346.13, C₁₆H₁₃BrN₂O₂ requires 344.02.

2.2.6. 3-(1-(4-Nitrophenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 8, 7f)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2f (83 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 20 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7f as yellow oil (94 mg, 0.30 mmol, 70%). IR (KBr): 3418, 1549, 1520, 1341, 713, 424 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 5.00–5.19 (m, 2H, CHCH ₂), 5.79–5.96 (m, 1H, CHCH₂), 6.96–7.08 (m, 1H. ArH), 7.08–7.61 (m, 7H. ArH), 7.90 (d,  Hz, 1H. ArH), 8.16 (s, 1H, NH of Indole); ¹³C-NMR (CDCl3, 100 MHz): δ 36.5, 80.1, 111.5, 112.9, 118.6, 120.4, 122.1, 123.1, 125.2, 126.0, 128.7, 130.0, 133.3, 136.4; [Anal. Calcd. for C₁₆H₁₃N₃O₄: C, 61.73; H, 4.21; N, 13.50; found: C, 68.05; H, 4.42; N, 13.69]; LC/MS (ESI): M⁺, found 344.08, C₁₆H₁₃N₃O₄ requires 311.09.

2.2.7. 3-(1-(2,4-Dichlorophenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 10, 7g)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2g (93 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 20 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7g as yellow oil (140 mg, 0.42 mmol, 97.5%). IR (KBr): 3417, 1549, 1464, 1376, 1101, 820, 738 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.88–5.01 (m, 2H, CHCH ₂), 5.62–5.75 (m, 1H, CHCH ₂), 7.03–7.16 (m, 4H. ArH), 7.18–7.27 (m, 1H, ArH), 7.32–7.42 (m, 2H, ArH), 7.45 (s, 1H, ArH), 8.16 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃, 100 MHz): δ 37.7, 80.0, 111.5, 112.9, 118.9, 120.3, 122.0, 123.1, 126.0, 127.7, 129.9, 132.2, 134.0, 134.8, 135.3, 136.6; [Anal. Calcd. for C₁₆H₁₂Cl₂N₂O₂: C, 57.33; H, 3.61; N, 8.36; found: C, 57.08; H, 3.43; N, 8.19]; LC/MS (ESI): M⁺ & [M+2]⁺, found 334.12 & 336.09, C₁₆H₁₂Cl₂N₂O₂ requires 334.03.

2.2.8. 3-(1-(2,6-Dichlorophenyl)-2-nitroethyl)-1H-indole (Table 2, Entry 12, 7h)

Indole 4 (50 mg, 0.43 mmol) and β-nitroolefin 2h (93 mg, 0.43 mmol) in dry ethanol (3 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 20 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7h yellow oily (108 mg, 0.32 mmol, 75.2%). IR (KBr): 3417, 1549, 1464, 1376, 1101, 820, 738 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 5.28–5.52 (m, 2H, CHCH ₂), 6.12–6.34 (m, 1H, CHCH₂), 6.95–7.10 (m, 1H. ArH), 7.10–7.24 (m, 3H. ArH), 7.24–7.65 (m, 4H. ArH), 8.14 (s, 1H, NH of Indole); ¹³C-NMR (CDCl₃, 100 MHz): δ 38.0, 78.9, 111.4, 114.0, 115.1, 117.8, 119.0, 120.1, 121.6, 122.5, 126.4, 129.4, 134.2, 136.1; [Anal. Calcd. for C₁₆H₁₂Cl₂N₂O₂: C, 57.33; H, 3.61; N, 8.36; found: C, 57.08; H, 3.43; N, 8.19]; LC/MS (ESI): M⁺ & [M+2]⁺; found 334.09 & 336.07, C₁₆H₁₂Cl₂N₂O₂ requires 334.03.

2.2.9. 3-(1-Ferrocenyl)-2-nitroethyl)-1H-indole (Table 1, Entry 12, 7i)

Table 1: Condition optimization of Feist’s acid catalysis in the addition of indolea (4) to β-nitro-styrene (2a).

Entry
Solvent
(°C)
Time (h)
Cat. mol%
Yieldb (%)

1
ACN
60
60
10
49

2
CH₂Cl₂
40
16
10
—

3
THF
50
72
10
—

4
MeOH
60
72
10
62

5
DMF
60
24
10
96

6
PrOH
60
42
10
98

7
AcOH
60
18
10
91

8
Xylene
60
42
10
88

9
Tolene
60
42
10
89

10
Benzene
60
42
10
86

11
EtOH
rt
120
0
—

12
EtOH
60
72
0
—

13
EtOH
40
60
5
59

14
EtOH
50
42
10
95

15
EtOH
50
42
15
98

16
EtOH
50
42
20
98

The reactions were performed on an 0.425 mmol scale; bthe isolated yield after column purification.

Table 2: Michael addition of indole (4) to nitroolefins 2(a–i) catalyzed by Feist’s acid.

No.
Nitroolefins (2a–i)
R = (a–i)
Products
Cat. mol%
Prod. ID
Time (h)
Yielda(%)

1

Ph

10
7a
42
97

2

4-MePh

10
7b
42
97

3

4-MeOPh

10
7c
42
84

4

4-ClPh

10
7d
42
97

5

4-BrPh

10
7e
42
49

6c

4-BrPh

20
7e
72
88

7

4-NitroPh

10
7f
42
55

8c

4-NitroPh

20
7f
72
70

9

2,4-diClPh

10
7g
42
63

10c

2,4-diClPh

20
7g
72
97

11

2,6-diClPh

10
7h
42
62

12c

2,6-diClPh

20
7h
72
75

13c

2-Ferrocene

20
7i
72
46

The reactions were performed on 0.425 mmol scale; bthe isolated yield after column purification; c20 mol% catalyst was used and reactions were run for 72 hours.

Indole 4 (50 mg, 0.43 mmol) and β-nitro styrene 2i (118 mg, 0.43 mmol) in dry ethanol (5 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 20 mol%) according to GP1. The product was purified by column chromatography on silica (EtOAc/hexane 1 : 9) yielded 7i as oily liquid (78 mg, 0.20 mmol, 46.4%). IR (KBr): 3417, 1549, 1464, 1376, 1101, 820, 738 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.09 (s, 5H, protons of Cp), 4.11–4.25 (m, 4H, protons of Cp), 4.83–5.89 (m, 1H, CpCHCH₂), 4.93–5.65 (m, 2H, CpCHCH ₂), 7.01 (s, 1H. ArH), 7.11 (t,  Hz, 1H. ArH), 7.18 (t,  Hz, 1H. ArH), 7.34 (d,  Hz, 1H. ArH), 7.57 (d,  Hz, 1H. ArH), 8.06 (s, 1H, NH of Indole); ¹³C-NMR (CDCL₃, 100 MHz): δ 36.7, 66.8, 67.7, 68.2, 69.0, 80.6, 111.5, 113.9, 119.1, 119.9, 121.8, 122.5, 126, 129.3; [Anal. Calcd. for C₂₀H₁₈FeN₂O₂: C, 64.19; H, 4.84; N, 7.48; found: C, 63.97; H, 4.71; N, 7.59]; LC/MS (ESI): M⁺, found 374.22, C₂₀H₁₈FeN₂O₂ requires 374.19.

2.3. General Procedure for the Michael Addition Reaction of Indole with Pyrrole Catalyzed by Feist’s Acid (GP2)

Pyrrole 5 (100 mg, 0.86 mmol), β-nitrostyrene 2(a–i) (0.86 mmol), and a catalytic amount of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) in dry isopropanol (7 mL) were charged into a Schlenk tube under an argon atmosphere. The reaction was then stirred at 50°C for 24–48 hours. The reaction mixture was monitored by TLC until starting material was completely consumed. Then the solvent was removed under vacuum. The crude products were isolated by column chromatography to afford pure Michael adducts 8(a–i) as major region-isomer, 9(a–d) and 9h as minor region-isomer.

2.3.1. 2-(2-Nitro-1-phenylethyl)-1H-pyrrole (Table 3, Entry 1, 8a) and 2,5-Bis(2-nitro-1-phenylethyl)-1H-pyrrole (Table 3, Entry 1, 9a)

Table 3: Feist’s acid catalysis substrate scopea, pyrrole 5.

No.
Nitroolefin (2a–i)
Time (h)
Products
Product ID
Yieldb (%)

1

50

8a
81

9a
13

2

24

8b
51

9b
21

3

44

8c
84

9c
14

4

20

8d
65

9d
11

5

20

8e
48

6

20

8f
99

7

20

8g
99

8

44

8h
90

9h
09

9

44

8i
18

The reactions were performed on 0.86 mmol scale; bthe isolated yield after column purification.

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitrostyrene 2a (128 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The products were isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded as yellow solid 8a (major region-isomer) (165 mg, 0.74 mmol, 86.0%) and 9a (minor region-isomer) as yellow oil (40 mg, 0.11 mmol, 12.7%). (Major region-isomer 8a): IR (KBr): 3423, 1548, 1376, 723, 703, 524 (cm⁻¹); ¹H-NMR (CDCl₃, 400 MHz) δ 4.69–4.85 (m, 1H, CHCH 2(a)), 4.85–4.93 (m, 1H, CHCH 2(b)), 4.93–5.02 (m, 1H, CHCH₂), 6.03–6.10 (m, 1H, ArH), 6.14–6.17 (m, 1H, ArH), 6.64–6.72 (m, 1H. ArH), 7.17–7.26 (m, 2H, ArH), 7.26–7.40 (m, 3H, ArH), 7.84 (s, 1H,NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 43.0 (CHCH₂), 79.6 (CHCH₂), 105.9 (PyC ₂), 108.8 (PyC ₃), 118.3 (PyC ₄), 128.0 (2C, PhC ₂), 128.24 (PhC ₄), 129.0 (PyC ₁), 129.3 (2C, PhC ₃), 138.0 (PhC ₁); [Anal. Calcd. for C₁₂H₁₂N₂O₂: C, 66.65; H, 5.59; N, 12.96; found: C, 66.45; H, 5.51; N, 13.11]; LC/MS (ESI): M⁺, found 216.11, C₁₂H₁₂N₂O₂ requires 216.09; (minor region-isomer 9a): IR (KBr): 3407, 1548, 1376, 703, 524 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.68–4.86 (m, 4H, CHCH ₂), 4.86–4.98 (m, 2H, CHCH₂), 5.98 (d,  Hz, 2H, pyrrole), 7.05–7.18 (m, 4H, ArH), 7.18–7.39 (m, 6H, ArH), 7.54 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl3, 100 MHz): δ 42.9 (CHCH₂), 79.2 (CHCH₂), 106.2 (PyC ₂), 106.6 (PyC ₂), 127.85 (PhC ₂), 127.92 (PhC ₄), 128.24 (PhC ₃), 129.30 (PyC ₁), 138.1 (PhC ₁); [Anal. Calcd. for C₂₀H₁₉N₃O₄: C, 65.74; H, 5.24; N, 11.50; found: C, 66.03; H, 5.37; N, 11.69]; LC/MS (ESI): M⁺, found 365.13, C₁₂H₁₂N₂O₂ requires 365.14.

2.3.2. 2-(2-Nitro-1-(p-tolyl)ethyl)-1H-pyrrole (Table 3, Entry 2, 8b) and 2,5-Bis(2-nitro-1-(p-tolyl)ethyl)-1H-pyrrole (Table 3, Entry 2, 9b)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2b (140 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The products were isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded as oily liquid 8b (major region-isomer) (100 mg, 0.43 mmol, 51%) and 9b (minor region-isomer) as yellow oil (70 mg, 0.18 mmol, 21%). (Minor region-isomer 8b): IR (KBr): 3388, 1542, 1378, 716, 584 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 2.25 (s, 1H, CH ₃), 4.67–4.73 (m, 1H, CHCH 2(a)), 4.73–4.81 (m, 1H, CHCH 2(b)), 4.82–4.93 (m, 1H, CHCH₂), 5.99 (s, 1H, ArH), 6.07–6.13 (m, 1H, ArH), 6.58–6.59 (m, 1H. ArH), 7.02–7.05 (m, 2H, ArH), 7.05–7.08 (m, 2H, ArH), 7.73 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl3, 100 MHz): δ 21.2 (CH₃), 42.7 (CHCH₂), 79.4 (CHCH₂), 105.7 (PyC ₂), 108.7 (PyC ₃), 118.2 (PyC ₄), 127.9 (2C, PhC ₂), 129.2 (PyC ₁), 130 (2C, PhC ₃), 134.9 (PhC ₄), 138.0 (PhC ₁); [Anal. Calcd. for C₁₃H₁₄N₂O₂: C, 67.81; H, 6.13; N, 12.17; found: C, 68.07; H, 5.95; N, 11.91]; LC/MS (ESI): M⁺, found 230.06, C₁₃H₁₄N₂O₂ requires 230.11; (minor region-isomer 9b): IR (KBr): 3388, 1514, 1377, 717, 519 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 2.25 (s, 1H, CH ₃), 4.54–4.79 (m, 4H, CHCH ₂), 4.79–4.82 (m, 2H, CHCH₂), 5.86–5.94 (m, 2H, ArH), 6.89–6.98 (m, 4H, ArH), 6.98–7.09 (m, 4H, ArH), 7.45 (s, 1H,NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 21.1 (CH₃), 42.6 (CHCH₂), 79.3 (CHCH₂), 106.0 (PyC ₂), 106.4 (PyC ₂), 127.7 (PhC ₂), 129.9 (PyC ₁), 129.9 (PhC ₃), 134.7 (PhC ₄), 137.9 (PhC ₁); [Anal. Calcd. for C₂₂H₂₃N₃O₄: C, 67.16; H, 5.89; N, 10.68; found: C, 66.86; H, 6.13; N, 10.94]; LC/MS (ESI): M⁺, found 393.19, C₂₂H₂₃N₃O₄ requires 393.17.

2.3.3. 2-(1-(4-Methoxyphenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 3, 8c) and 2,5-Bis(1-(4-methoxy-phenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 3, 9c)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2c (154 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The products were isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded as oily liquid 8c (major region-isomer) (177 mg, 0.72 mmol, 84%) and 9c (minor region-isomer) as yellow oil (50 mg, 0.12 mmol, 14%). Major region-isomer 8c: IR (KBr): 3388, 1542, 1378, 716, 584 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 3.78 (s, 1H, OCH ₃), 4.69–4.80 (m, 1H, CHCH 2(a)), 4.80–4.89 (m, 1H, CHCH 2(b)), 4.90–5.01 (m, 1H, CHCH₂), 6.06 (s, 1H, ArH), 6.15–6.22 (m, 1H, ArH), 6.67 (s, 1H. ArH), 6.86 (d, 2H,  Hz, ArH), 7.13 (d, 2H,  Hz, ArH), 7.87 (s, 1H,NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 42.3 (CHCH₂), 55.4 (OCH₃), 79.5 (CHCH₂), 105.6 (PyC ₂), 108.7 (PyC ₃), 114.6 (2C, PhC ₃), 118.2 (PyC ₄), 129.1 (2C, PhC ₂), 129.4 (PyC ₁), 130 (PhC ₄), 159.4 (PhC ₁); [Anal. Calcd. for C₁₃H₁₄N₂O₃: C, 63.40; H, 5.73; N, 11.38; found: C, 63.62; H, 5.58; N, 11.19]; LC/MS (ESI): M⁺, found 246.14, C₁₃H₁₄N₂O₃ requires 246.10; minor region-isomer 9c: IR (KBr): 3388, 1514, 1377, 717, 519 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 3.76 (s, 1H, CH ₃), 4.60–4.78 (m, 4H, CHCH ₂), 4.78–4.93 (m, 2H, CHCH₂), 5.92–6.01 (m, 2H, ArH), 6.80–6.84 (m, 4H, ArH), 6.01–7.12 (m, 4H, ArH), 7.54 (s, 1H,NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 41.2 (CHCH₂), 55.4 (CH₃), 79.4 (CHCH₂), 105.9 (PyC ₂), 106.3 (PyC ₂), 114.6 (PhC ₃), 128.96 (PhC ₂), 129.02 (PyC ₁), 129.8 (PhC ₁), 159.4 (PhC ₄); [Anal. Calcd. for C₂₂H₂₃N₃O₆: C, 62.11; H, 5.45; N, 9.88; found: C, 62.27; H, 5.39; N, 10.13]; LC/MS (ESI): M⁺, found 425.13, C₂₂H₂₃N₃O₆ requires 425.16.

2.3.4. 2-(1-(4-Chlorophenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 4, 8d) and 2,5-Bis(1-(4-chlorophenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 4, 9d)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2d (157 mg, 0.86 mmol) in dry ethanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The products were isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded white solid 8d (major region-isomer) (140 mg, 0.56 mmol, 65%) and 9d (minor region-isomer) as yellow oil (40 mg, 0.09 mmol, 11%). Major region-isomer 8d: IR (KBr): 3379, 1740, 1545, 1377, 1092, 725, 512, 452 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.66–4.83 (m, 2H, CHCH 2(a)), 4.83–4.91 (m, 2H, CHCH 2(b)), 4.91–5.06 (m, 1H, CHCH₂), 6.07 (s, 1H, ArH), 6.12–6.21 (m, 1H, ArH), 6.70 (s, 1H. ArH), 7.17 (d, 2H,  Hz, ArH), 7.33 (d, 2H, , Hz, ArH), 7.84 (s, 1H,NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 42.4 (CHCH₂), 79.0 (CHCH₂), 106.1 (PyC ₂), 108.9 (PyC ₃), 118.6 (PyC ₄), 128.4 (PhC ₄), 129.4 (2C, PhC ₂), 129.5 (2C, PhC ₃), 134.2 (PyC ₁), 136.6 (PhC ₁); [Anal. Calcd. for C₁₂H₁₁ClN₂O₂: C, 57.49; H, 4.42; N, 11.17; found: C, 57.36; H, 4.53; N, 11.01]; LC/MS (ESI): M⁺ & [M+2]⁺, found 250.08 & 252.03, C₁₂H₁₁ClN₂O₂ requires 250.05; minor region-isomer 9d: IR (KBr): 3413, 1549, 1490, 1375, 1091, 726, 512 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.61–4.82 (m, 4H, CHCH ₂), 4.82–5.03 (m, 2H, CHCH₂), 5.93–6.02 (m, 2H, ArH), 7.01–7.20 (m, 4H, ArH), 7.20–7.39 (m, 4H, ArH), 7.53 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 42.2 (CHCH₂), 78.9 (CHCH₂), 106.5 (PyC ₂), 106.9 (PyC ₂), 129.2 (PhC ₃), 129.3 (PhC ₂), 129.52 (PyC ₁), 134.3 (PhC ₄), 136.2 (PhC ₁); [Anal. Calcd. for C₂₀H₁₇Cl₂N₃O₄: C, 55.31; H, 3.95; N, 9.68; found: C, 55.19; H, 4.14; N, 9.43]; LC/MS (ESI): M⁺ & [M+2]⁺, found 433.11 & 435.15, C₂₀H₁₇Cl₂N₃O₄ requires 433.05.

2.3.5. 2-(1-(4-Bromophenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 5, 8e)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2e (195 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The product was isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded as white solid 8e (120 mg, 0.41 mmol, 47%). IR (KBr): 3376, 1543, 1377, 1007, 725, 510 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.71–4.81 (m, 1H, CHCH 2(a)), 4.81–4.90 (m, 1H, CHCH 2(b)), 4.90–5.02 (m, 2H, CHCH₂), 6.07 (s, 1H, ArH), 6.12–6.22 (m, 1H, ArH), 6.70 (s, 1H. ArH), 7.11 (d, 2H,  Hz, ArH), 7.48 (d, 2H, , Hz, ArH), 7.86 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 42.5 (CHCH₂), 79.0 (CHCH₂), 106.1 (PyC ₂), 108.9 (PyC ₃), 118.6 (PyC ₄), 122.3 (PhC ₄), 128.3 (PyC ₁), 129.7 (2C, PhC ₂), 132.4 (PhC ₃), 137.1 (PhC ₁); [Anal. Calcd. for C₁₂H₁₁BrN₂O₂: C, 48.84; H, 3.76; N, 9.49; found: C, 49.07; H, 3.89; N, 9.35]; LC/MS (ESI): M⁺ & [M+2]⁺, found 294.01 & 296.05, C₁₂H₁₁BrN₂O₂ requires 294.0.

2.3.6. 2-(2-Nitro-1-(4-nitrophenyl) ethyl)-1H-pyrrole (Table 3, Entry 6, 8f)

Pyrrole 5 (100 mg, 0.8 mmol) and β-nitroolefin 2f (167 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The product was isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded as oily liquid 8f (224 mg, 0.86 mmol, 99.8%). IR (KBr): 3421, 1551, 1520, 1373, 1349, 784, 717 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.93–5.05 (m, 2H, CHCH ₂), 5.51–5.57 (m, 1H, CHCH₂), 6.12–6.19 (m, 2H, ArH), 6.73 (s, 1H. ArH), 7.31–7.48 (m, 2H, ArH), 7.48–7.61 (m, 1H, ArH), 7.81–7.93 (m, 1H, ArH), 8.45 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 36.9 (CHCH₂), 79.8 (CHCH₂), 105.6 (PyC ₂), 108.8 (PyC ₃), 118.9 (PyC ₄), 127.8 (PyC ₃), 128.8 (2C, PhC ₂), 129.4 (PyC ₁), 133.7 (PhC ₄), 149.6 (PhC ₁); [Anal. Calcd. for C₁₂H₁₁N₃O₄: C, 55.17; H, 4.24; N, 16.09; found: C, 55.36; H, 4.19; N, 15.93]; LC/MS (ESI): M⁺, found 261.15, C₁₂H₁₁N₃O₄ requires 261.07.

2.3.7. 2-(1-(2,4-Dichlorophenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 7, 8g)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2g (187 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The product was isolated by column chromatography on silica (EtOAc/hexane 1 : 9) yielded as oily liquid 8g (245 mg, 0.86 mmol, 99.9%). IR (KBr): 3417, 1550, 1469, 1376, 1099, 797, 726 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.71–4.98 (m, 2H, CHCH ₂), 5.32–5.49 (m, 1H, CHCH₂), 6.06–6.23 (m, 2H, ArH), 6.71 (s, 1H, ArH), 6.94–7.10 (m, 1H, ArH), 7.10–7.29 (m, 1H, ArH), 7.31–7.58 (m, 1H, ArH), 8.02 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 39.0 (CHCH₂), 79.9 (CHCH₂), 106.6 (PyC ₂), 108.9 (PyC ₃), 118.7 (PyC ₄), 127.4 (PyC ₁), 128.0 (PhC ₆), 130.0 (PhC ₅), 130.1 (PhC ₃), 134.3–134.6 (PhC ₁, PhC ₂ & PhC ₄); [Anal. Calcd. for C₁₂H₁₀Cl₂N₂O₂: C, 50.55; H, 3.54; N, 9.82; found: C, 50.33; H, 3.69; N, 10.07]; LC/MS (ESI): M⁺, found 284.05, C₁₂H₁₁N₃O₄ requires 284.01.

2.3.8. 2-(1-(2,6-Dichlorophenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 8, 8h) and 2,5-Bis(1-(2,6-dichloro-phenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 8, 9h)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitrostyrene 2h (187 mg, 0.86 mmol) in isopropanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The products were isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) yielded yellow oil 8h (major region-isomer) (220 mg, 0.77 mmol, 90%) and 9h (minor region-isomer) as yellow oil (40 mg, 0.09 mmol, 9%). Major region-isomer  8h: IR (KBr): 3439, 1550, 1430, 1374, 775, 720, 536 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 5.21–5.30 (m, 1H, CHCH 2(a)), 5.30–4.42 (m, 1H, CHCH 2(b)), 5.90–6.01 (m, 1H, CHCH₂), 6.09 (s, 1H, ArH), 6.12–6.28 (m, 1H, ArH), 6.66–6.75 (m, 1H. ArH), 7.12–7.24 (m, 1H, ArH), 7.28–7.48 (m, 2H, ArH), 8.06 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 39.0 (CHCH₂), 79.5 (CHCH₂), 106.8 (PyC ₂), 108.7 (PyC ₃), 118.1 (PyC ₄), 124.4 (2C, PhC ₃), 126.8 (PhC ₄), 129.8 (2C, PhC ₂), 133.8 (PyC ₁), 142.8 (PhC ₁); [Anal. Calcd. for C₁₂H₁₀Cl₂N₂O₂: C, 50.55; H, 3.54; N, 9.82; found: C, 50.45; H, 3.43; N, 9.74]; LC/MS (ESI): M⁺ & [M+2]⁺, found 284.05 & 286.11, C₁₂H₁₀Cl₂N₂O₂ requires 284.01; minor region-isomer  9h: IR (KBr): 3437, 1741, 1551, 1431, 1372, 1210, 773, 532 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 5.14–5.32 (m, 4H, CHCH ₂), 5.83 (t,  Hz, 2H, CHCH₂), 5.93–6.02 (m, 2H, ArH), 7.12–7.23 (m, 2 h, ArH), 7.26–7.42 (m, 4 h, ArH), 8.16 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃,100 MHz): δ 42.2 (CHCH₂), 78.9 (CHCH₂), 106.5 (PyC ₂), 106.9 (PyC ₂), 129.2 (PhC ₃), 129.3 (PhC ₂), 129.52 (PyC ₁), 134.3 (PhC ₄), 136.2 (PhC ₁); [Anal. Calcd. for C₂₀H₁₅Cl₄N₃O₄: C, 47.74; H, 3.0; N, 8.35; found: C, 48.09; H, 3.11; N, 8.51]; LC/MS (ESI): M⁺ & [M+2]⁺, found 501.03 and 503.06, C₂₀H₁₅Cl₄N₃O₄ requires 500.98.

2.3.9. 2-(1-Ferrocenyl)-2-nitroethyl)-1H-pyrrole (Table 3, Entry 9, 8i)

Pyrrole 5 (100 mg, 0.86 mmol) and β-nitroolefin 2g (167 mg, 0.86 mmol) in dry ethanol (7 mL) were reacted in the presence of Feist’s acid (1) (12 mg, 0.168 mmol, 10 mol%) according to GP2. The product was isolated by column chromatography on silica (EtOAc/hexane 0.5 : 9.5) dark red solid 8g (51 mg, 18%). IR (KBr): 3358, 1740, 1551, 1410, 1251, 1219, 1044, 728, 488 cm⁻¹; ¹H-NMR (CDCl₃, 400 MHz) δ 4.13 (s, 1H, protons of Cp), 4.23 (s, 5H, protons of Cp), 4.30–4.39 (m, 2H, protons of Cp), 4.64 (s, 2H, m, 2H, protons of Cp), 5.10–5.21 (m, 1H, CHCH₂), 5.21–5.40 (m, 2H, CHCH ₂), 6.26–6.36 (m, 1H, ArH), 6.81–6.90 (m, 1H, ArH), 7.18 (m, 1H, ArH), 7.79 (s, 1H, NH of pyrrole); ¹³C-NMR (CDCl₃, 100 MHz): δ 29.8, 69.1, 70.0, 70.6, 72.3, 84.0, 111.6, 123.0, 125.2, 126.6; [Anal. Calcd. for C₁₆H₁₆FeN₂O₂: C, 59.28; H, 4.98; N, 8.64; found: C, 59.17; H, 5.07; N, 8.49]; LC/MS (ESI): M⁺, found 324.12, C₁₆H₁₆FeN₂O₂ requires 324.16.

3. Result and Discussion

At the outset, synthetic strategies adopted in our work, for the preparation of Feist’s acid (FA) (1) as hydrogen bond donor catalyst, has been outlined in Scheme 1. Feist’s acid is commercially available but highly expensive therefore, it was prepared in our laboratory from a very cheap and readily available material ethyl acetoacetate with an overall yield of 19% in three steps, using the well-known method reported by Al-Majid et al. [50].

Scheme 1: Feist’s acid synthesis.

Initially, to evaluate the catalytic activity of Feist’s acid for the Michel addition reaction, indole 4 and β-nitrostyrene 2a have been chosen as model substrates. 5–20 mol% of FA (1) were used, aiming at screening the optimal conditions, and the results are summarized in Table 1.

By screening different solvents such as methanol, ethanol, isopropanol (iPrOH), toluene, benzene, xylene, acetonitrile, tetrahydrofuran (THF), and dichloromethane (CH₂Cl₂), using 10 mol% of Feist’s acid, we found that most of the solvents produced good to excellent yields (86–96%) for the Michael addition reaction of indole 4 to β-nitrostyrene 2a, affording the corresponding product 7a at 50–60°C temperature within 24–42 h, (Table 1, entries 5–10, 14), while in case of ACN and MeOH, moderate yields were observed (49% and 62%), respectively (Table 1, entries 1, 4). But in case of other solvents like CH₂Cl₂ and THF, no products were formed (Table 1, entries 2, 3). Without using Feist’s acid as catalyst, the reaction was carried out in ethanol at room temperature as well as at 60°C for 72 h; no product formation was observed at all (Table 1, entries 11, 12). But with the use 5 mol% catalyst in ethanol at 50°C for 60 h, 59% yield was observed (Table 1, entry 13). The yields of product were improved remarkably from 59% to 98% by increasing the loading of catalyst from 5 to 20 mol% in ethanol (Table 1, entries 13, 14). It is noteworthy to mention that solvents like DMF and AcOH with 10% catalyst produced very good results in 42 h and 18 h accordingly (Table 1, entries 5, 7). But due to the work-up problem these solvents cause they have been discarded from further reaction optimization. Xylene, toluene, and benzene also have been discarded for their high boiling point as compared to ethanol. The optimized procedure for Michael addition of indole to nitroolefin was found to be as follows: the mixture of indole 4 (0.43 mmol), β-nitrostyrene 2a (0.43 mmol), and FA (Feist’s acid, 10 mol%) was heated at 50°C in ethanol for 42 h according to general procedure GP1.

To illustrate the generality of this Michael addition reaction of indole 4, with various nitroolefins 2(a–i), sixteen examples were carried out catalyzed by Feist’s acid with 10 mol% and 20 mol% in ethanol at 50°C temperature and, the results are shown in Table 2.

The exclusive 3-substituted indole derivatives 7a–i were obtained in good to excellent yields (46–97%) with the use of 10 mol% of catalyst at 50°C temperature in 48 hours (Table 2, entries 1–13). The reaction of indole (4) with nitroolefins 2(e–h) bearing 4-bromophenyl, 2,4-dichlorophenyl, 2,6-dichlorophenyl, and 4-nitrophenyl produced the corresponding Michael adducts 7(e–h) with poor to moderate yield (49%, 55%, 63%, and 62%), respectively (Table 2, entries 5, 7, 9, and 11). The poor reactivity of these nitroolefins could be inferred due to their less solubility and bulkier environment. But the chemical yields were increased dramatically to 87%, 70%, 97%, and 75%, respectively, when the loading of catalyst were increased from10–20 mol% and the reactions were run for 72 hours (Table 2, entries , , , ). In contrast, the nitroolefin bearing phenyl, tolyl, and 4-chlorophenyl, afforded the corresponding Michael products in excellent yield (97%) (Table 2, entries 1, 2 and 4), while in the case of nitroolefin with 4-methoxyphenyl, the yield was slightly lower (84%) (Table 2, entry 3), which was probably attributed to the steric effect of the 4-methoxyphenyl group.

On the basis of the above results obtained for Michael addition reaction of indole with the derivatives of β-nitrostyrenes, the reaction was extended to pyrrole, and it was found that Feist’s acid (FA) can also efficiently catalyze the reaction of pyrrole with different β-nitroolefins in isopropanol, affording 2-substituted pyrrole and in some cases both 2-substituted and 2,4-disubstituted pyrrole derivatives in good to excellent yields; the results are summarized in Table 3.

The Michael addition of pyrrole 5 to nitroolefins 2(a–i) catalyzed by FA (10 mol%) in isopropanol at 50°C for 20–50 h afforded 2-substituted pyrrole 8(a–i) as major region-isomer (Table 3, entries 1–9), with some 2,4-disubstituted pyrrole derivatives 9(a–d) and 9h (Table 3, entries 1–4, 8), which also showed good regioselectivity of pyrrole at the 2-position. The reaction of pyrrole with nitroolefins bearing phenyl, tolyl, 4-methoxyphenyl, 4-chloroophenyl and, 24-dichlorophenyl 2(a–d) and 2h afforded major region-isomer 2-substituted pyrrole 8(a–d) and 8h (81%, 50%, 84%, 65%, and 90%) with some minor region-isomer 2,6-disubstituted pyrrole 9(a–d) and 9h (13%, 21%, 13%, 11%, and 9%) in 50 h, 24 h, 44 h, 20 h, and 44 h, respectively (Table 3, entries 1–4, 8). But 2-substituted Michael adducts 8(e–g) and 8i were formed exclusively with 48%, 99.8%, 99.9%, and 18%, when nitroolefins bearing 4-bromophenyl, 4-nitrophenyl, 2,4-dichlorophenyl, and ferrocene groups reacted with pyrrole in 20 h and 44 h, accordingly (Table 3, entries 5–7, 9). Obviously the best results were found in the case of nitroolefin 2f and 2g producing their corresponding adducts 8f and 8g with excellent yields 99.8 and 99.9%, respectively (Table 3, entries 6, 7). On the other hand, poor yields (8e and 8i with 48% and 18%) were observed corresponding to the nitroolefins 2e and 2i. The reason for this low yield could be attributed to the poor solubility of 2e and 2i.

We reasoned that, the catalytic cycle would begin with activation of an electrophile, such as β-nitrostyrenes (2a–i), with Feist’s acid (1) to afford intermediate 3 (Figure 1). Addition of nucleophiles (4 and 5), to the intermediate 3 give rise to another intermediate 6 followed by proton transfer and release of the catalyst (1), would complete the cycle and generate the desired products 7a–i, 8a–i, 9a–d and 9h corresponding to the substrate 4 and 5 (Tables 2 and 3). All the analytical data are available in the Supplementary Material available online at http//dox.doi.org/10.1155/2014/649197.

Figure 1: Activation of nitrostyrene via hydrogen bonding mechanism by Feist’s acid catalysis.

4. General Procedure for Antimicrobial Activity

Chemical compounds were individually tested against a panel of Gram-positive and Gram-negative bacterial pathogens. Antimicrobial tests were carried out by the agar well diffusion method using 100 mL of suspension containing 1 × 10⁸ CFU/mL of pathological tested bacteria, 1 × 10⁶ CFU/mL of yeast and 1 × 10⁴ spore/mL of fungi spread on nutrient agar (NA), Sabouraud dextrose agar (SDA), and potato dextrose agar (PDA) medium, respectively. After the media had cooled and solidified, wells (10 mm in diameter) were made in the solidified agar and loaded with 100 mL of tested compound solution prepared by dissolving 100 mg of the chemical compound in one mL of dimethyl sulfoxide (DMSO). The inculcated plates were then incubated for 24 h at 37°C for bacteria and 48 h at 28°C for fungi. Negative controls were prepared using DMSO employed for dissolving the tested compound. Ciprofloxacin (50 mg/mL) and Ketoconazole (50 mg/mL) were used as standard for antibacterial and antifungal activity, respectively. After incubation time, antimicrobial activity was evaluated by measuring the zone of inhibition against the test organisms and compared with that of the standard. The observed zone of inhibition is presented in Table 1. Antimicrobial activities were expressed as inhibition diameter zones in millimeters (mm) as follows: N.A. (no activity) ≤ 4 mm; + (weak) = 5–9 mm; ++ (moderate) = 10–15 mm; +++ (strong) = 16–20 mm, and ++++ (very strong) ≥ 21 mm. The experiment was carried out in triplicate and the average zone of inhibition was calculated.

4.1. Antimicrobial Activity

A sample of some synthesized compounds (7b, 7d, 7e, 7f and 8e, 8f, 8g) has been subjected to antimicrobial activity studies including Gram-positive bacteria (Bacillus subtilis and Staphylococcus aureus), Gram-negative bacteria (Pseudomonas Aeruginosa and Escherichia coli), and fungi (Candida albicans). Antimicrobial tests were carried out by the agar well diffusion method. When compared to the standard drug Ciprofloxacin, it was seen that compounds 7b, 7d, 7e, and 7f with frame structure of indole moiety showed an inhibition effect against Bacillus subtilis ATCC 10400 (Table 4). On the other hand, 8e, 8g with frame structure of pyrrole moiety showed effect against Bacillus subtilis ATCC 10400. Not worthy to mention that 8f showed potent inhibition against the same Gram-positive bacteria Bacillus subtilis ATCC 10400 compared with standard Ciprofloxacin (Table 4). Interestingly, 8e, 8g with frame structure of pyrrole moiety showed antifungal activity against Candida albicans ATTCC-10231, while 8f showed potent inhibition against the same fungi Candida albicans ATTCC-1023 compared to standard drug Ketoconazole. Nevertheless, 7b, 7d, 7e, 7f, 8e, 8f, and 8g were not active against S. aureus ATCC 29213, E. coli ATCC-35218, and P. aeruginosa ATCC 29336. The results obtained are summarized in Table 4 [59].

Table 4: Antimicrobial activity of the newly synthesized compounds against the pathological strains based on well diffusion assaya.

Comp. no.
Gram-positive bacteria
Gram-negative bacteria
Fungi

Staphylococcus aureus ATTCC-29213
Bacilils subtilis  ATTCC-10400
Escherichia coli ATTCC-35218
Pseudomonas aeruginosa ATTCC-29336
Candida albicans  ATTCC-10231

7b
N.A.
++
N.A.
N.A.
N.A.

7d
N.A.
++
N.A.
N.A.
N.A.

7e
N.A.
++
N.A.
N.A.
N.A.

7f
N.A.
++
N.A.
N.A.
N.A.

7g
N.A.
++
N.A.
N.A.
N.A.

8e
N.A.
++
N.A.
N.A.
+++

8f
N.A.
++++
N.A.
N.A.
++++

8g
N.A.
++
N.A.
N.A.
++

Ciprofloxacin
+++
++++
++++
++++
N.A.

Ketoconazole
N.A.
N.A.
N.A.
N.A.
++++

Antimicrobial activities were expressed as inhibition diameter zones in millimeters (mm) as follows: N.A. (no activity) ≤ 4 mm; + (weak) = 5–9 mm; ++ (moderate) = 10–15 mm; +++ (strong) = 16–20 mm; and ++++ (very strong) ≥ 21 mm. The experiment was carried out in triplicate and the average zone of inhibition was calculated.

5. Conclusion

In summary, Feist’s acid has been introduced as a new class of hydrogen bond donor catalysts for the activation of nitroalkene in conjugate addition reactions. This study includes the original report of Feist’s acid catalysis of Michel addition of indole and pyrrole to a variety of nitroolefins. All the synthesized indole and pyrrole derivatives have be screened for antimicrobial activity (MIC determination) in our laboratory and the results are reported here in. Investigations surrounding the potential associated with Feist’s acid catalysis, including the development of enantioselective variants, as a new tool for organic synthesis are under progress in our laboratory.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding the work through the research group Project no. RGP-VPP-044.

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