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Article

Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones

by
Domna Iordanidou
1,2,
Michael G. Kallitsakis
1,
Marina A. Tzani
1,
Dimitris I. Ioannou
1,
Tryfon Zarganes-Tzitzikas
3,
Constantinos G. Neochoritis
4,
Alexander Dömling
5,
Michael A. Terzidis
2,* and
Ioannis N. Lykakis
1,*
1
Department of Chemistry, Aristotle University of Thessaloniki, University Campus, 54124 Thessaloniki, Greece
2
Department of Nutritional Sciences and Dietetics, International Hellenic University, Sindos Campus, 57400 Thessaloniki, Greece
3
Alzheimer’s Research UK Oxford Drug Discovery Institute, University of Oxford, Oxford OX3 7FZ, UK
4
Department of Chemistry, University of Crete, Voutes Heraklion, 70013 Heraklion, Greece
5
Department of Pharmacy, University of Groningen, A. Deusinglaan 1, 9700 AV Groningen, The Netherlands
*
Authors to whom correspondence should be addressed.
Molecules 2022, 27(14), 4395; https://doi.org/10.3390/molecules27144395
Submission received: 9 June 2022 / Revised: 5 July 2022 / Accepted: 6 July 2022 / Published: 8 July 2022
(This article belongs to the Section Bioorganic Chemistry)
Browse Figures
Versions Notes

Abstract

:
The synthesis of 3,4-dihydroquinoxalin-2-ones via the selective reduction of aromatic, multifunctional nitro precursors catalyzed by supported gold nanoparticles is reported. The reaction proceeds through the in situ formation of the corresponding amines under heterogeneous transfer hydrogenation of the initial nitro compounds catalyzed by the commercially available Au/TiO2-Et3SiH catalytic system, followed by an intramolecular C-N transamidation upon treatment with silica acting as a mild acid. Under the present conditions, the Au/TiO2-TMDS system was also found to catalyze efficiently the present selective reduction process. Both transfer hydrogenation processes showed very good functional-group tolerance and were successfully applied to access more structurally demanding products bearing other reducible moieties such as chloro, aldehyde or methyl ketone. An easily scalable (up to 1 mmol), low catalyst loading (0.6 mol%) synthetic protocol was realized, providing access to this important scaffold. Under these mild catalytic conditions, the desired products were isolated in good to high yields and with a TON of 130. A library analysis was also performed to demonstrate the usefulness of our synthetic strategy and the physicochemical profile of the derivatives.

Graphical Abstract

1. Introduction

The pharmaceutical, fine chemical and agrochemical industries utilize a wide range of amines and their derivatives that result from the reduction of the nitro group [1]. These fundamental organic chemistry transformations usually rely on transition metal-catalyzed hydrogenation [2]. However, its low chemoselectivity remains a continuous and persisting problem when other easily reducible groups are present. The role of noble metal nanoparticles such as gold (AuNPs) [3,4,5,6,7,8,9] and silver (AgNPs) [10,11,12,13,14], cobalt, iron, palladium, nickel and manganese-based compounds or oxides in such transformations have been extensively explored [15,16,17,18,19,20,21,22,23,24]. Hydrogenation as well as transfer hydrogenation processes have been used for the selective reduction of nitro compounds into the corresponding amines, but in most cases with significant drawbacks. The hydrogenation process requires high H2 pressure and temperature, with a very good applicability in monosubstituted aromatic nitro compounds. However, transfer hydrogenation is considered as a more chemoselective process, requiring milder conditions (e.g., ambient temperature and pressure) and works efficiently in the presence of several reducing agents, such as borohydrides, hydrosilanes, hydrazines, CO/H2O and HCOONH4 [7,8,9]. Thus, new catalytic and synthetic strategies are focused on the development of more efficient transfer hydrogenation processes that allow the selective reduction of aromatic amines in the presence of diverse functional moieties or protecting groups [25,26].
New synthetic methodologies for the synthesis of anilines and/or N-aryl hydroxylamines (N-AHA) using catalytic systems based on supported AuNPs and AgNPs on mesoporous titania, silica or alumina (Au/TiO2, Ag/TiO2, Ag/HMS and Au/Al2O3) under mild conditions were already reported by our research groups [27,28,29,30,31,32,33,34]. The application of mild conditions along with simple reducing agents, such as borohydrides, boranes, hydrosilanes and hydrazines, allowed the clean and rapid synthesis of the target compounds in high yields and with high chemoselectivity (Scheme 1). In this study, we explored the efficiency of the Au/TiO2-hydrosilane catalytic system in the highly diverse and demanding environment of multicomponent reactions (MCRs) in the absence of protecting groups [17,18]. The described protocol was then applied to the synthesis of aromatic amines that could be used for the one-pot mild synthesis of N-substituted 3,4-dihydroquinoxalin-2-one derivatives. Τhe discovery of post-modifications on the original MCR “core structure” is of great importance, as they can significantly enhance the diversity and complexity of the resulting compounds [35,36,37,38,39,40,41].
Dihydroquinoxalinones are bioactive compounds of high interest, due to their anticancer [42,43,44] and anti-inflammatory [45] properties, as well as their activity against neurological diseases [46] (Scheme 2). Dihydroquinaxolinone derivatives have been mainly synthesized via coupling of o-nitroaryl- or o-aminoaryl halides with amino acids [43,45,47,48,49,50,51,52,53,54], or transition metal-catalyzed asymmetric hydrogenation of the corresponding quinoxaline derivatives (Scheme 2) [55,56,57,58,59,60,61,62,63]. However, these methods required air-sensitive catalysts, toxic organic solvents, and several ligands. Few studies have also reported the nucleophilic substitution/cyclization of o-phenylendiamines with α-bromo-α-phenyl ester, α-sulfonyl epoxides or substituted trichloromethylcarbinols (Scheme 2) [42,64,65,66,67,68,69,70]. Recently, the hetero-Diels–Alder reaction of ketene enolates with ortho-benzoquinone diimides [68,69] and a photo-organocatalytic approach have been reported for the synthesis of substituted dihydroquinoxalinones [70] (Scheme 2). Nevertheless, several sequential steps involving protecting groups and specific pre-synthesized starting materials were required.
Herein, we report a two-step protocol for the mild synthesis of N-substituted 3,4-dihydroquinoxalin-2-ones. Initially, the Au-catalyzed heterogeneous selective reduction of the multifunctional nitro compounds into the corresponding amines was achieved. The presence of other easily reducible groups, such as carbonyl, amide, ester and halogen moieties, did not affect the chemoselectivity. Subsequent treatment with silica, as an acidic medium, led to the in situ intramolecular transesterification of the initially formed amine (Scheme 1). To the best of our knowledge, a limited number of studies have reported on the success of MCR products transformed into quinoxaline derivatives in the presence of Pd/C (10 mol%) as a catalyst (a) under hydrogenation and acidic conditions using p-toluenesulfonic acid (Scheme 2, (i)) [71], and (b) through transfer hydrogenation with an excess of cyclohexene under refluxed conditions in ethanol (catalyst/substrate ratio = 1/2) (Scheme 2, (ii)) [72]. However, prolonged reaction times and multistep workup protocols were proposed for the final product isolation. Recently, our research group reported the selective reduction of aromatic nitro compounds into amines and, subsequently, into substituted dihydroquinoxalinones using AgNPs supported on mesoporous silica and NaBH4 as the reducing agent (Scheme 2, (iii)) [34]. The present approach is an ideal venue for the use of the commercially available Au/TiO2-Et3SiH and Au/TiO2-TMDS catalytic systems towards the mild and efficient selective transfer hydrogenation of a series of multifunctional, aromatic nitro precursors into amines and the synthesis of N-substituted 3,4-dihydroquinoxalin-2-ones (Scheme 2, (iii)) [34].

2. Results and Discussion

2.1. Catalytic Conditions Evaluation

The synthesis of the multifunctional, aromatic nitro compounds 1–21 (Scheme 2) was performed based on the reported isocyanide-based MCRs [35,36,40,41,73,74]. Briefly, an equimolar mixture of the corresponding isocyanide and phenols (1–6, 16–21), isocyanide and carboxylic acids (7–9), or isocyanide and TMSN3 (10–15) were added into the solution of an amine (5 mmol) and a carbonyl compound in methanol at ambient conditions (for details, see Materials and Methods) [75,76,77,78,79,80,81,82,83,84]. After stirring for the appropriate time, yellow or light-yellow products were isolated by silica gel column chromatography in good to high yields (Scheme 3). All nitro compounds were characterized by NMR and HRMS spectroscopy (see SI).
To identify the optimum conditions of the present catalytic reaction, we first investigated the selective reduction of nitro derivative 1 into the corresponding amine 1a (Table 1). The supported AuNP catalysts, i.e., Au/TiO2, Au/Al2O3 and Au/ZnO, as well as the complex Ph3PAuNTf2 and the salts HAuCl4 and AuCl, were used without further purification. All commercial heterogeneous catalysts feature a ca. 1 wt% Au loading and exhibit an average AuNP size of about 2–3 nm. In all cases, MeOH or an equimolar mixture of THF/MeOH were used as the reaction medium. In blank experiments, common reducing agents, including NaBH4, NH3BH3, LiBH4, LiAlH4, NH3NH3.H2O and NaH were found to be inactive in the absence of a catalyst (Table 1, entries 1–4). However, several degradation products, such as the cleavage of the tert-amide of the anisole group, were observed with 1H NMR of the crude mixtures in the case of LiAlH4 and NaH. In contrast, an efficient reduction was observed, based on TLC analysis, in the presence of Au/TiO2, when NaBH4, NH3BH3 and LiBH4 were used as reducing agents within THF/MeOH (1/1) (Table 1, entries 5–7). In addition, NaBH4 was found to be active within THF or MeOH (Table 1, entries 8 and 9), as well as in their mixtures of different ratios (results not shown); however, in the lower amount of 1 equiv. (based on the amount of 1), a lower conversion was observed even at a prolonged reaction time of 18 h (Table 1, entry 10). Although the reactions showed high selectivity (>99%) based on the 1H NMR spectra of the crude mixtures, amine 1a was isolated in low yields ranging between 48 and 84% (Table 1, entries 5–10), probably due to the difficult separation of 1a by column chromatography.
Based on these results and our previous mechanistic studies on AuNP-catalyzed selective reduction of nitroarenes into anilines in the presence of 1,1,3,3-tetramethyldisiloxane (TMDS) [29], we subsequently used a series of different hydrosilanes as hydrogen donor molecules. To improve the solubility of the starting material, the following screening tests were conducted in an equimolar mixture of THF/MeOH. Among the examined hydrosilanes (Table 1, entries 11–19), TMDS, dimethylphenylsilane (DMPS), diphenylsilane (DPS) and triethylsilane (Et3SiH) favored the completion of the transfer hydrogenation process in a fast and clean manner (Table 1, entries 12–18). In all cases, the desired amine (1a) was obtained, along with the corresponding silanols and/or silylethers as by-products as determined by TLC and 1H NMR analysis of the crude mixture [85], and was isolated in high yield after chromatographic purification. Especially when TMDS and Et3SiH were used as reducing agents, 1a was observed in high yields within a short reaction time (Table 1, entries 12 and 18).
Hence, TMDS and Et3SiH were further used to evaluate the catalytic activity of Au catalysts. No reaction occurred in the presence of the gold salts AuCl3, AuCl and Ph3PAuNTf2, even after a prolonged reaction time (Table 1, entries 20–25). In contrast, AuNPs supported on alumina, Au/Al2O3, showed good activity towards the reduction of 1, leading to 75% and 77% isolated yields of 1a using Et3SiH and TMDS, respectively (Table 1, entries 26 and 27), whereas Au/ZnO was found to be inactive as a catalyst (Table 1, entries 28 and 29) under the present conditions.
In addition, the homogeneous (AuCl3, AuCl) and heterogeneous (Au/TiO2) reactions in the presence of Et3SiH were performed upon irradiation for 3 h with a 300 W Xenon Arc Lamp (λ > 320 nm) as the light source. During irradiation, the reaction mixtures were thermostated with a water bath (ca. 28 °C). In all cases, no significant changes were observed in the reaction conversion and selectivity. However, in the latter case (Au/TiO2/Et3SiH/hv), a mixture of the desired amine with unidentified degradation products was observed with the 1H NMR spectrum of the crude mixtures (results not shown).

2.2. Catalytic Application for the Sythesis of Several Multifunctional Amines

To explore the substrate broadness of the described catalytic reduction process, the synthesized multifunctional nitro compounds 1–15 were screened under the optimal catalytic conditions, using Au/TiO2-Et3SiH (4 eq.) (Scheme 4). To our delight, the corresponding amine derivatives 1a–15a were selectively formed in high conversions and isolated yields (84–94%) in a relatively short reaction time (1–3 h), as shown in Scheme 4. Interestingly, easily reducible moieties, such as chloro, carbonyl and carboxyl groups, were well tolerated under the present conditions. Under the present mild conditions, the measured diastereoselectivity (d.r. = 99/1) of the amine 15a corresponds to the initial ratio of the corresponding starting nitro compound 15, as concluded by 1H NMR (SI). For comparison, TMDS (2 eq.) was also used in the reduction of 1–3, 8 and 10–12 in the presence of Au/TiO2 and at ambient conditions. In all cases, high isolated yields (85–93%) for the amines 1a–3a, 8a and 10a–12a were measured (second value in parentheses, Scheme 4) within a short reaction time of 1 h. These results confirm the high catalytic activity of Au/TiO2-Et3SiH or Au/TiO2-TMDS for the chemoselective reduction of such multifunctional, aromatic nitro compounds into the corresponding amines, and suggest that this approach can be used as a facile and useful strategy for multigram scale synthesis. To that end, 1 mmol of 1 and 14 were reduced by 5 mmol of Et3SiH (or 2.5 mmol of TMDS) in 8 mL of MeOH/THF (1/1), in the presence of 0.6 mol% of Au/TiO2 (1% wt) at rt. After reaction completion (3 h, according to the TLC), the reaction mixture was centrifuged to separate the solid catalyst, and the residue was purified by silica gel column chromatography, affording the desired amines 1a (81% using Et3SiH and 83% using TMDS) and 14a (82% using Et3SiH and 80% using TMDS).

2.3. Synthetic Application towards the One-Pot Synthesis of 3,4-Dihydroquinoxalin-2-Ones

The reduction of ortho-phenyl-substituted nitro compound 18 formed the corresponding amine 18a in a 90% relative yield along with a small amount of the 3,4-dihydroquinoxalin-2-one 18b (~10%), according to 1H NMR analysis of the crude reaction mixture. After chromatographic purification (with silica gel), the initial ratio of 18a/18b changed from 90/10 to 5/95 (Figure S1), indicating that the heterocycle 18b was undoubtedly formed from 18a via a silica-acid-catalyzed one-pot ring-closing pathway involving an intramolecular C-N cyclization process. This pathway was observed when the starting material contains a methyl carbamate group (such as in substrate 18); however, no cyclization products were formed when simple alkyl, cycloalkyl or benzyl moieties were present (i.e., substrates 3a–5a) (Scheme 5 and Figure S1). This intramolecular transamidation probably occurred due to the rapid elimination of the glycine methyl ester as a good living group under the intramolecular nucleophilic pathway.
The reaction profile of amine 18a was studied in deuterated solvent (CDCl3) and monitored directly by 1H NMR after the addition of a small amount of silica gel. After 8 h, a mixture of the amine 18a, the 3,4-dihydroquinoxalin-2-one 18b and the glycine methyl ester C was observed (Figure S2). This observation prompted us to further investigate the plausible one-pot, two-step facile synthesis of a series of 3,4-dihydroquinoxalin-2-ones 16b–21b, as shown in Scheme 6. Specifically, the corresponding nitro compounds 16–21 were selectively reduced under the present heterogeneous transfer hydrogenation process (Au/TiO2-Et3SiH), on a 0.2 mmol reaction scale. After the reduction completion (3 h, based on TLC analysis), a small amount of SiO2 (ca. 20 mg) was added and the mixture stirred for an additional 18 h (TLC monitoring). In all cases, good to high isolated yields (71–85%, first value in parentheses) were measured for the final desired cyclic products 21b–27b, based on the amount of the initial nitro compound (Scheme 6). The corresponding amines 16a–21a could also be isolated in high yields (89–96%) immediately after reduction completion (ca 3 h, results not shown), using neutralized silica for the purification procedure (see Materials and Methods). Furthermore, the Au/TiO2-TMDS was also used for the reduction of 16, 17 and 19. In these reductive/cyclization processes, good to high isolated yields were measured for the corresponding 3,4-dihydriquinoxalin-2-ones 16b, 17b and 19b with the values of 81%, 84% and 74%, respectively. These results support the clean and mild efficacy of the present heterogeneous AuNP catalytic process. To the best of our knowledge, this is the first study based on the gold nanoparticle heterogeneous catalysis of the reductive/cyclization transformation of several MCR, multifunctional nitro compounds into 3,4-dihydroquinoxalin-2-ones.
Based on these encouraging results, the Au/TiO2-Et3SiH and Au/TiO2-TMDS catalytic systems towards dihydroquinoxalino-2-ones were further tested at a lab-scale. Thus, 1 mmol of the nitro derivative 17 was reduced in the presence of Au/TiO2 1% wt (120 mg, 0.006 mmol) with 5 mmol of Et3SiH or 2.5 mmol of TMDS in 10 mL THF/MeOH (1/1). After the reduction was completed (3 h, based on TLC), 50 mg of silica gel was added in each reaction mixture and stirred for 18 h (monitored by TLC). The corresponding 3,4-dihydroquinoxalin-2-one 17b was isolated after chromatographic purification (see Materials and Methods), in 74% and 78% yields (TON = 123 and 130, Scheme 7). When a lower catalyst amount (0.4 mmol) was used, no reaction completion was observed by TLC analysis.

2.4. Library Analysis of the Dihydroquinoxalin-2-Ones

Dihydroquinoxaline belongs to the so-called privileged structures. We created a random >200-member virtual library based on this scaffold by using the DataWarrior software (see SI) [86]. Next, we calculated certain physicochemical parameters of this library such as molecular weight (MW), lipophilicity (clogP), polar surface area (PSA), number of hydrogen bonds acceptors and donors (HBA, HBD), drug-likeness and shape index (Figure 1). clogP, MW and PSA are key parameters determining important drug properties such as oral bioavailability and metabolism. Our analysis showed that 60% of our virtual library obeyed the rule of five (Ro5). Moreover, there is a strong drug-like profile (positive values, Figure 1B) as 80% of our library fell into these constraints. Regarding the shape index, using the parameters of spherical <0.5 and linear >0.5, a more spherical type of shape was observed overall.

3. Conclusions

In conclusion, we showed that titania-supported gold nanoparticles can be applied to more complicated organic compounds and catalyze the reduction of a series of multifunctional, aromatic nitro compounds into the corresponding amine derivatives using Et3SiH or TMDS as reducing agents. The Au/TiO2-Et3SiH and Au/TiO2-TMDS catalytic systems were also found to be highly chemoselective, even for more complex molecules such as tetrazole and amino acid-substituted derivatives, serving as a rapid approach towards N-substituted 3,4-dihydroquinoxalin-2-ones. The proposed one-pot, two-step, acid-promoted ring-closing reaction pathway afforded the desired products in good to high isolated yields, even at the lab-scale. The key parameters clogP, MW and PSA were also calculated; thus, important related drug properties, such as oral bioavailability and metabolism, were also reported.

4. Materials and Methods

4.1. General and Aparatus

All the reagents and solvents were purchased from Sigma-Aldrich, AK Scientific, Fluorochem, Abcr GmbH, Acros, and were used without further purification. Thin-layer chromatography was performed on Millipore precoated silica gel plates (0.20 mm thick, particle size 25 μm). Nuclear magnetic resonance spectra were recorded on a Bruker Avance 500 or 600 spectrometer and on Agilent 500 {1H NMR (500 MHz; 600 MHz), 13C{H} NMR (125 MHz; 150 MHz)}. Chemical shifts for 1H NMR were reported as δ values and coupling constants were in hertz (Hz). The following abbreviations were used for spin multiplicity: s = singlet, br s = broad singlet, d = doublet, t = triplet, q = quartet, quin = quintet, dd = double of doublets, ddd = double doublet of doublets, m = multiplet. Chemical shifts for 13C{H} NMR were reported in ppm relative to the solvent peak. Light Source: The reaction mixtures were irradiated for an appropriate time with a variac Cermax® 300W Xenon Arc Lamp (λ > 320 nm) as the light source (PE300BF CERMAX® XENON ARC LAMPS, 300W, Cat No: CE-303/540). Please refer to the homepage of PerkinElmer Optoelectronics (https://www.perkinelmer.com/, accessed on 8 June 2022) for further details. Flash chromatography was performed on a Reveleris® X2 Flash Chromatography System, using Grace® Reveleris Silica Flash Cartridges (12 g). Mass spectra were measured on a Waters Investigator Supercritical Fluid Chromatography System with a 3100 MS Detector (ESI) using a solvent system of methanol and CO2 on a Viridis silica gel column (4.6 × 250 mm, 5 µm particle size) or Viridis 2-ethylpyridine column (4.6 × 250 mm, 5 µm particle size). Mass spectra (HRMS) were determined through electrospray ionization mass spectrometry (ESI-MS) by using a Thermo Fisher Scientific (Bremen, Germany) model, the LTQ Orbitrap Discovery MS, at a flow rate of 10 μL/min using a syringe pump. The infusion experiments were run using a standard ESI source operating in a positive ionization mode. Source operating conditions were a 3.7 kV spray voltage and a 300 °C heated capillary temperature.

4.2. Synthesis of Nitro Compounds via the Ugi-Smiles MCR

A solution of the corresponding aldehyde (5.0 mmol), nitro-substituted phenol (5.0 mmol) and amine (5.0 mmol) in methanol (5 mL) was stirred at room temperature for 15 min. Subsequently, isocyanide (5.0 mmol) was added and the reaction was stirred at room temperature for approximately 20 h. After reaction completion, monitored by TLC, the reaction mixture was concentrated in vacuo and the residue was purified by column chromatography using silica and an eluent solvent mixture of hexane/ethyl acetate in a ratio from 5:1 to 1:3, affording the desired nitro compounds 1–6 and 16–21 in good to high yields [73,87].

4.3. Synthesis of Nitro Compounds via the Ugi-Tetrazole MCR

A solution of the corresponding aldehyde or ketone (5.0 mmol) and amine or amino acid methylester (5.0 mmol) in methanol (5 mL) was stirred at room temperature for 15 min. Subsequently, isocyanide (5.0 mmol) and TMSN3 (5.0 mmol, 665 μL) were added and the reaction mixture was stirred at room temperature for approximately 20 h. After reaction completion, monitored by TLC, the reaction mixture was concentrated in vacuo and the residue was purified by column chromatography using silica and an eluent solvent mixture of hexane/ethyl acetate in a ratio from 5:1 to 1:5, affording the desired compounds 10–15 in high yields [87].

4.4. Synthesis of Nitro Compounds via the Ugi-Four MCR

A solution of the corresponding aldehyde (5.0 mmol), carboxylic acid (5.0 mmol) and amine (5.0 mmol) in methanol (5 mL) was stirred at room temperature for 15 min. Subsequently, isocyanide (5.0 mmol) was added and the reaction was stirred at room temperature for approximately 20 h. After reaction completion, monitored by TLC, the reaction mixture was concentrated in vacuo and the residue was purified by column chromatography using silica and an eluent solvent mixture of hexane/ethyl acetate in a ratio from 5:1 to 1:2, affording the desired compounds 7–9 in good to high yields [87].

4.5. Catalytic Reduction for Synthesis of the Corresponding Amines 1a–21a

To a sealed tube containing the corresponding nitro-substituted compounds (0.2 mmol) in 1 mL THF/MeOH/ (1/1), Et3SiH (0.8 mmol) or TMDS (0.4 mmol) and Au/TiO2, 1 % wt (0.8 mol%, 30 mg) was added. The reaction mixture was stirred at room temperature for the appropriate time. After reaction completion (monitored by TLC), the reaction mixture was centrifuged to separate the solid catalyst, and the cake was spray-washed with MeOH (~10 mL). The solvents were removed under vacuum and the residue was chromatographed on neutralized silica gel by using hexane/EtOAc mixtures from 10:1 to 1:1 as eluent, to give the corresponding amines 1a–21a in pure form. It is worth noting that the amines in most cases were unstable during the chromatographic purification procedure; for this reason, neutralized silica (with the addition of a few drops of triethylamine in the eluent solvent mixture) was used for the column chromatography, and pre-treated CDCl3 with anhydrous K2CO3 was used as the NMR solvent.

4.6. Lab-Scale Reduction for Synthesis of 1a and 14a

To a sealed tube containing the corresponding nitro-substituted compounds 1 or 14 (1 mmol) in 8 mL THF/MeOH (1/1), Et3SiH (5 mmol) or TMDS (2.5 mmol) and Au/TiO2, 1 % wt (0.6 mol%, 120 mg) was added. The reaction mixture was stirred at room temperature for the appropriate time (3 h). After reaction completion (monitored by TLC), the slurry was centrifuged to separate the catalyst, and the solid residue was washed with MeOH (~10 mL). The solvent was then removed under vacuum and the residue was purified by column chromatography on neutralized silica (with the addition of a few drops of triethylamine in the eluent solvent mixture) by using hexane/EtOAc mixtures from 5:1 to 1:5 as eluent, affording the corresponding amines 1a and 14a in pure forms, at 365 mg (81% yield) and 272 mg (82% yield), respectively.

4.7. One-Pot Process for Synthesis of the 3,4-Dihydroquinoxalin-2-Ones 16b–21b

To a sealed tube containing the corresponding nitro compounds (0.2 mmol) in 1 mL THF/MeOH (1/1), Et3SiH (0.8 mmol) or TMDS (0.4 mmol) and Au/TiO2, 1 % wt (0.8 mol%, 30 mg) was added. The reaction mixture was stirred at room temperature for the appropriate time and was monitored by TLC. After completion of the reduction, silica gel (20 mg) was added in the mixture, forming the corresponding cyclized adducts (18 h). After that, the slurry was filtered to remove the catalyst and the filter cake was washed with MeOH (~5 mL). The solvents of the filtrate were evaporated under vacuum and the resulting residues lead to the corresponding 3,4-dihydroquinoxalin-2-one derivatives 16b–21b in pure forms, after chromatographic purification with hexane/ethyl acetate from 30:1 to 2:1 as eluent.

4.8. Lab-Scale Synthesis of Dihydroquinoxalin-2-One 17b

To a sealed tube containing the corresponding nitro compound 17 (1 mmol) in 10 mL THF/MeOH (1/1), Et3SiH (5 mmol) or TMDS (2.5 mmol) and Au/TiO2, 1 % wt (0.6 mol%, or 0.006 mmol, 120 mg) was added. The reaction mixture was stirred at room temperature for the appropriate time and was monitored by TLC (ca. 3 h). After completion of the reduction, silica gel (50 mg) was added in the mixture, forming the corresponding cyclized adduct (18 h). After that, the slurry was filtered to remove the catalyst and the silica, and the filter cake was washed with MeOH (~10 mL). The solvents of the filtrate were evaporated under vacuum and the resulting residue lead to the corresponding 3,4-dihydroquinoxalin-2-one 17b in pure forms (Et3SiH: 74% yield, 198 mg and TMDS: 78% yield, 205 mg), after chromatographic purification as described above with hexane/ethyl acetate from 20:1 to 2:1 as eluent.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27144395/s1, Figures S1–S3: NMR data and spectra of nitro compounds, amines and 3,4-dihydroquinoxalin-2-ones.

Author Contributions

D.I. conducted the experiments, proceeded with the NMR studies and analyzed the data. M.G.K., M.A.T. (Marina A. Tzani) and D.I.I. collected the literature and assisted with the synthesis of amines and photochemical experiments. C.G.N., T.Z.-T. and A.D. assisted with the synthesis of nitro compounds and the library analysis data collection. M.A.T. (Michael A. Terzidis) analyzed the photochemical experiments and helped with manuscript corrections. I.N.L. and M.A.T. (Michael A. Terzidis) supervised the study. I.N.L. conducted the idea and wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The project has received funding from the Hellenic Foundation for Research and Innovation (HFRI) and the General Secretariat for Research and Innovation (GSRI) under grant agreement No [776].

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors kindly acknowledge financial support from the Hellenic Foundation for Research and Innovation (HFRI) and the General Secretariat for Research and Innovation (GSRI) under grant agreement no [776], “PhotoDaLu” (KA97507).

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not available.

References

  1. Orlandi, M.; Brenna, D.; Harms, R.; Jost, S.; Benaglia, M. Recent Developments in the Reduction of Aromatic and Aliphatic Nitro Compounds to Amines. Org. Process Res. Dev. 2018, 22, 430–445. [Google Scholar] [CrossRef]
  2. Blaser, H.-U.; Steiner, H.; Studer, M. Selective Catalytic Hydrogenation of Functionalized Nitroarenes: An Update. ChemCatChem 2009, 1, 210–221. [Google Scholar] [CrossRef]
  3. Takale, B.S.; Bao, M.; Yamamoto, Y. Gold nanoparticle (AuNPs) and gold nanopore (AuNPore) catalysts in organic synthesis. Org. Biomol. Chem. 2014, 12, 2005–2027. [Google Scholar] [CrossRef]
  4. Liu, X.; He, L.; Liu, Y.-M.; Cao, Y. Supported Gold Catalysis: From Small Molecule Activation to Green Chemical Synthesis. Acc. Chem. Res. 2014, 47, 793–804. [Google Scholar] [CrossRef] [PubMed]
  5. Mikami, Y.; Dhakshinamoorthy, A.; Alvaro, M.; García, H. Catalytic activity of unsupported gold nanoparticles. Catal. Sci. Technol. 2012, 3, 58–69. [Google Scholar] [CrossRef]
  6. Corma, A.; Garcia, H. Supported gold nanoparticles as catalysts for organic reactions. Chem. Soc. Rev. 2008, 37, 2096–2126. [Google Scholar] [CrossRef] [PubMed]
  7. Mitsudome, T.; Kaneda, K. Gold nanoparticle catalysts for selective hydrogenations. Green Chem. 2013, 15, 2636–2654. [Google Scholar] [CrossRef]
  8. Stratakis, M.; Garcia, H. Catalysis by Supported Gold Nanoparticles: Beyond Aerobic Oxidative Processes. TL—112. Chem. Rev. 2012, 112, 4469–4506. [Google Scholar] [CrossRef]
  9. Zhang, Y.; Cui, X.; Shi, F.; Deng, Y. Nano-Gold Catalysis in Fine Chemical Synthesis. Chem. Rev. 2012, 112, 2467–2505. [Google Scholar] [CrossRef]
  10. Abbiati, G.; Rossi, E. Silver and gold-catalyzed multicomponent reactions. Beilstein J. Org. Chem. 2014, 10, 481–513. [Google Scholar] [CrossRef] [Green Version]
  11. Dong, X.-Y.; Gao, Z.-W.; Yang, K.-F.; Zhang, W.-Q.; Xu, L.-W. Nanosilver as a new generation of silver catalysts in organic transformations for efficient synthesis of fine chemicals. Catal. Sci. Technol. 2015, 5, 2554–2574. [Google Scholar] [CrossRef]
  12. Bhosale, M.A.; Bhanage, B.M. Silver Nanoparticles: Synthesis, Characterization and their Application as a Sustainable Catalyst for Organic Transformations. Curr. Org. Chem. 2015, 19, 708–727. [Google Scholar] [CrossRef]
  13. Abou El-Nour, K.M.M.; Eftaiha, A.; Al-Warthan, A.; Ammar, R.A.A. Synthesis and Applications of Silver Nanoparticles. Arab. J. Chem. 2010, 3, 135–140. [Google Scholar] [CrossRef] [Green Version]
  14. Díez-González, S.; Nolan, S.P. Copper, Silver, and Gold Complexes in Hydrosilylation Reactions. Acc. Chem. Res. 2008, 41, 349–358. [Google Scholar] [CrossRef]
  15. Jagadeesh, R.V.; Wienhöfer, G.; Westerhaus, F.A.; Surkus, A.E.; Pohl, M.M.; Junge, H.; Junge, K.; Beller, M. Efficient and Highly Selective Iron-Catalyzed Reduction of Nitroarenes. Chem. Commun. 2011, 47, 10972–10974. [Google Scholar] [CrossRef]
  16. Jagadeesh, R.V.; Surkus, A.E.; Junge, H.; Pohl, M.M.; Radnik, J.; Rabeah, J.; Huan, H.; Schünemann, V.; Brückner, A.; Beller, M. Nanoscale Fe2O3-Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines. Science 2013, 342, 1073–1076. [Google Scholar] [CrossRef]
  17. Jagadeesh, R.V.; Stemmler, T.; Surkus, A.E.; Junge, H.; Junge, K.; Beller, M. Hydrogenation Using Iron Oxide–Based Nanocatalysts for the Synthesis of Amines. Nat. Protoc. 2015, 10, 548–557. [Google Scholar] [CrossRef]
  18. Junge, K.; Wendt, B.; Shaikh, N.; Beller, M. Iron-Catalyzed Selective Reduction of Nitroarenes to Anilines Using Organosilanes. Chem. Commun. 2010, 46, 1769–1771. [Google Scholar] [CrossRef]
  19. Wienhöfer, G.; Baseda-Krüger, M.; Ziebart, C.; Westerhaus, F.A.; Baumann, W.; Jackstell, R.; Junge, K.; Beller, M. Hydrogenation of Nitroarenes Using Defined Iron–Phosphine Catalysts. Chem. Commun. 2013, 49, 9089–9091. [Google Scholar] [CrossRef]
  20. Jagadeesh, R.V.; Junge, H.; Beller, M. Green Synthesis of Nitriles Using Non-Noble Metal Oxides-Based Nanocatalysts. Nat. Commun. 2014, 51, 4123. [Google Scholar] [CrossRef] [Green Version]
  21. Westerhaus, F.A.; Jagadeesh, R.V.; Wienhöfer, G.; Pohl, M.M.; Radnik, J.; Surkus, A.E.; Rabeah, J.; Junge, K.; Junge, H.; Nielsen, M.; et al. Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes. Nat. Chem. 2013, 5, 537–543. [Google Scholar] [CrossRef] [PubMed]
  22. Renaud, J.L.; Gaillard, S. Recent Advances in Iron- and Cobalt-Complex-Catalyzed Tandem/Consecutive Processes Involving Hydrogenation. Synthesis 2016, 48, 3659–3683. [Google Scholar] [CrossRef]
  23. Pellissier, H.; Clavier, H. Enantioselective Cobalt-Catalyzed Transformations. Chem. Rev. 2014, 114, 2775–2823. [Google Scholar] [CrossRef] [PubMed]
  24. Filonenko, G.A.; Van Putten, R.; Hensen, E.J.M.; Pidko, E.A. Catalytic (de)Hydrogenation Promoted by Non-Precious Metals—Co, Fe and Mn: Recent Advances in an Emerging Field. Chem. Soc. Rev. 2018, 47, 1459–1483. [Google Scholar] [CrossRef] [Green Version]
  25. Trost, B.M. The Atom Economy—A Search for Synthetic Efficiency. Science 1991, 254, 1471–1477. [Google Scholar] [CrossRef]
  26. Kolesnikov, P.N.; Yagafarov, N.Z.; Usanov, D.L.; Maleev, V.I.; Chusov, D. Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source. Org. Lett. 2015, 17, 173–175. [Google Scholar] [CrossRef]
  27. Gkizis, P.L.; Stratakis, M.; Lykakis, I.N. Catalytic Activation of Hydrazine Hydrate by Gold Nanoparticles: Chemoselective Reduction of Nitro Compounds into Amines. Catal. Commun. 2013, 36, 48–51. [Google Scholar] [CrossRef]
  28. Vasilikogiannaki, E.; Gryparis, C.; Kotzabasaki, V.; Lykakis, I.N.; Stratakis, M. Facile Reduction of Nitroarenes into Anilines and Nitroalkanes into Hydroxylamines via the Rapid Activation of Ammonia⋅ Borane Complex by Supported Gold Nanoparticles. Adv. Synth. Catal. 2013, 355, 907–911. [Google Scholar] [CrossRef]
  29. Fountoulaki, S.; Daikopoulou, V.; Gkizis, P.L.; Tamiolakis, I.; Armatas, G.S.; Lykakis, I.N. Mechanistic Studies of the Reduction of Nitroarenes by NaBH4 or Hydrosilanes Catalyzed by Supported Gold Nanoparticles. ACS Catal. 2014, 4, 3504–3511. [Google Scholar] [CrossRef]
  30. Tzani, M.A.; Kallitsakis, M.G.; Symeonidis, T.S.; Lykakis, I.N. Alumina-Supported Gold Nanoparticles as a Bifunctional Catalyst for the Synthesis of 2-Amino-3-Arylimidazo[1,2-a]Pyridines. ACS Omega 2018, 3, 17947–17956. [Google Scholar] [CrossRef] [Green Version]
  31. Kallitsakis, M.G.; Ioannou, D.I.; Terzidis, M.A.; Kostakis, G.E.; Lykakis, I.N. Selective Photoinduced Reduction of Nitroarenes to N-Arylhydroxylamines. Org. Lett. 2020, 22, 4339–4343. [Google Scholar] [CrossRef] [PubMed]
  32. Andreou, D.; Iordanidou, D.; Tamiolakis, I.; Armatas, G.S.; Lykakis, I.N. Reduction of Nitroarenes into Aryl Amines and N-Aryl Hydroxylamines via Activation of NaBH4 and Ammonia-Borane Complexes by Ag/TiO2 Catalyst. Nanomaterials 2016, 6, 54. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Charistoudi, E.; Kallitsakis, M.G.; Charisteidis, I.; Triantafyllidis, K.S.; Lykakis, I.N. Selective Reduction of Azines to Benzyl Hydrazones with Sodium Borohydride Catalyzed by Mesoporous Silica-Supported Silver Nanoparticles: A Catalytic Route towards Pyrazole Synthesis. Adv. Synth. Catal. 2017, 359, 2949–2960. [Google Scholar] [CrossRef]
  34. Iordanidou, D.; Zarganes-Tzitzikas, T.; Neochoritis, C.G.; Dömling, A.; Lykakis, I.N. Application of Silver Nanoparticles in the Multicomponent Reaction Domain: A Combined Catalytic Reduction Methodology to Efficiently Access Potential Hypertension or Inflammation Inhibitors. ACS Omega 2018, 3, 16005–16013. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Dömling, A.; Wang, W.; Wang, K. Chemistry and Biology of Multicomponent Reactions. Chem. Rev. 2012, 112, 3083–3135. [Google Scholar] [CrossRef] [Green Version]
  36. Dömling, A. Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry. Chem. Rev. 2006, 106, 17–89. [Google Scholar] [CrossRef]
  37. Slobbe, P.; Ruijter, E.; Orru, R.V.A. Recent Applications of Multicomponent Reactions in Medicinal Chemistry. MedChemComm 2012, 3, 1189–1218. [Google Scholar] [CrossRef]
  38. Zarganes-Tzitzikas, T.; Chandgude, A.L.; Dömling, A. Multicomponent Reactions, Union of MCRs and Beyond. Chem. Rec. 2015, 15, 981–996. [Google Scholar] [CrossRef]
  39. Cioc, R.C.; Ruijter, E.; Orru, R.V.A. Multicomponent Reactions: Advanced Tools for Sustainable Organic Synthesis. Green Chem. 2014, 16, 2958–2975. [Google Scholar] [CrossRef]
  40. Touré, B.B.; Hall, D.G. Natural Product Synthesis Using Multicomponent Reaction Strategies. Chem. Rev. 2009, 109, 4439–4486. [Google Scholar] [CrossRef]
  41. Dömling, A.; Ugi, I. Multicomponent Reactions with Isocyanides. Angew. Chem. Int. Ed. 2000, 39, 3168–3210. [Google Scholar] [CrossRef]
  42. Galal, S.A.; Abdelsamie, A.S.; Soliman, S.M.; Mortier, J.; Wolber, G.; Ali, M.M.; Tokuda, H.; Suzuki, N.; Lida, A.; Ramadan, R.A.; et al. Design, Synthesis and Structure–Activity Relationship of Novel Quinoxaline Derivatives as Cancer Chemopreventive Agent by Inhibition of Tyrosine Kinase Receptor. Eur. J. Med. Chem. 2013, 69, 115–124. [Google Scholar] [CrossRef] [PubMed]
  43. Tanimori, S.; Nishimura, T.; Kirihata, M. Synthesis of Novel Quinoxaline Derivatives and Its Cytotoxic Activities. Bioorg. Med. Chem. Lett. 2009, 19, 4119–4121. [Google Scholar] [CrossRef] [PubMed]
  44. Amano, Y.; Yamaguchi, T.; Tanabe, E. Structural Insights into Binding of Inhibitors to Soluble Epoxide Hydrolase Gained by Fragment Screening and X-Ray Crystallography. Bioorg. Med. Chem. 2014, 22, 2427–2434. [Google Scholar] [CrossRef]
  45. Yang, Y.; Zhao, L.; Xu, B.; Yang, L.Y.; Zhang, J.; Zhang, H.; Zhou, J. Design, Synthesis and Biological Evaluation of Dihydroquinoxalinone Derivatives as BRD4 Inhibitors. Bioorg. Chem. 2016, 68, 236–244. [Google Scholar] [CrossRef]
  46. Gitto, R.; Barreca, M.L.; De Luca, L.; Chimirri, A. New Trends in the Development of AMPA Receptor Antagonists. Expert Opin. Ther. Pat. 2004, 14, 1199–1213. [Google Scholar] [CrossRef]
  47. Wang, Y.; Wach, J.Y.; Sheehan, P.; Zhong, C.; Zhan, C.; Harris, R.; Almo, S.C.; Bishop, J.; Haggarty, S.J.; Ramek, A.; et al. Diversity-Oriented Synthesis as a Strategy for Fragment Evolution against GSK3β. ACS Med. Chem. Lett. 2016, 7, 852–856. [Google Scholar] [CrossRef] [Green Version]
  48. Kanyiva, K.S.; Horiuchi, M.; Shibata, T. Metal-Free N–H/C–H Coupling for Efficient Asymmetric Synthesis of Chiral Dihydroquinoxalinones from Readily Available α-Amino Acids. Eur. J. Org. Chem. 2018, 2018, 1067–1070. [Google Scholar] [CrossRef]
  49. Li, D.; Ollevier, T. Iron- or Zinc-Mediated Synthetic Approach to Enantiopure Dihydroquinoxalinones. Eur. J. Org. Chem. 2019, 2019, 1273–1280. [Google Scholar] [CrossRef]
  50. Jiang, Q.; Jiang, D.; Jiang, Y.; Fu, H.; Zhao, Y. A Mild and Efficient Method for Copper-Catalyzed Ullmann-Type N-Arylation of Aliphatic Amines and Amino Acids. Synlett 2007, 2007, 1836–1842. [Google Scholar] [CrossRef]
  51. Tanimori, S.; Kashiwagi, H.; Nishimura, T.; Kirihata, M. A General and Practical Access to Chiral Quinoxalinones with Low Copper-Catalyst Loading. Adv. Synth. Catal. 2010, 352, 2531–2537. [Google Scholar] [CrossRef]
  52. Neagoie, C.; Krchňák, V. Piperazine Amide Linker for Cyclative Cleavage from Solid Support: Traceless Synthesis of Dihydroquinoxalin-2-Ones. ACS Comb. Sci. 2012, 14, 399–402. [Google Scholar] [CrossRef] [PubMed]
  53. Carbain, B.; Schütznerová, E.; Přibylka, A.; Krchňák, V. Solid-Phase Synthesis of 3,4-Dihydroquinoxalin-2(1H)-Ones via the Cyclative Cleavage of N-Arylated Carboxamides. Adv. Synth. Catal. 2016, 358, 701–706. [Google Scholar] [CrossRef]
  54. Dalvi, P.B.; Lin, S.F.; Paike, V.; Sun, C.M. Microwave-Assisted Multicomponent Synthesis of Dihydroquinoxalinones on Soluble Polymer Support. ACS Comb. Sci. 2015, 17, 421–425. [Google Scholar] [CrossRef]
  55. Xue, Z.Y.; Jiang, Y.; Peng, X.Z.; Yuan, W.C.; Zhang, X.M. The First General, Highly Enantioselective Lewis Base Organo- Catalyzed Hydrosilylation of Benzoxazinones and Quinoxalinones. Adv. Synth. Catal. 2010, 352, 2132–2136. [Google Scholar] [CrossRef]
  56. Rueping, M.; Tato, F.; Schoepke, F.R. The First General, Efficient and Highly Enantioselective Reduction of Quinoxalines and Quinoxalinones. Chem. Eur. J. 2010, 16, 2688–2691. [Google Scholar] [CrossRef]
  57. Zhang, X.; Xu, B.; Xu, M.H. Rhodium-Catalyzed Asymmetric Arylation of N-and O-Containing Cyclic Aldimines: Facile and Efficient Access to Highly Optically Active 3,4-Dihydrobenzo[1,4]Oxazin-2-Ones and Dihydroquinoxalinones. Org. Chem. Front. 2016, 3, 944–948. [Google Scholar] [CrossRef]
  58. Zhao, Z.B.; Li, X.; Chen, M.W.; Zhao, Z.K.; Zhou, Y.G. Biomimetic Asymmetric Reduction of Benzoxazinones and Quinoxalinones Using Ureas as Transfer Catalysts. Chem. Commun. 2020, 56, 7309–7312. [Google Scholar] [CrossRef]
  59. Núñez-Rico, J.L.; Vidal-Ferran, A. [Ir(P-OP)]-Catalyzed Asymmetric Hydrogenation of Diversely Substituted C=N-Containing Heterocycles. Org. Lett. 2013, 15, 2066–2069. [Google Scholar] [CrossRef]
  60. Pan, Y.; Chen, C.; Xu, X.; Zhao, H.; Han, J.; Li, H.; Xu, L.; Fan, Q.; Xiao, J. Metal-Free Tandem Cyclization/Hydrosilylation to Construct Tetrahydroquinoxalines. Green Chem. 2018, 20, 403–411. [Google Scholar] [CrossRef]
  61. Li, J.L.; Han, B.; Jiang, K.; Du, W.; Chen, Y.C. Organocatalytic Enantioselective Hetero-Diels–Alder Reaction of Aldehydes and o-Benzoquinone Diimide: Synthesis of Optically Active Hydroquinoxalines. Bioorg. Med. Chem. Lett. 2009, 19, 3952–3954. [Google Scholar] [CrossRef] [PubMed]
  62. Zhang, L.; Qiu, R.; Xue, X.; Pan, Y.; Xu, C.; Li, H.; Xu, L. Versatile (Pentamethylcyclopentadienyl)Rhodium-2,2′-Bipyridine (Cp*Rh-Bpy) Catalyst for Transfer Hydrogenation of N-Heterocycles in Water. Adv. Synth. Catal. 2015, 357, 3529–3537. [Google Scholar] [CrossRef]
  63. Chen, M.W.; Deng, Z.; Yang, Q.; Huang, J.; Peng, Y. Enantioselective Synthesis of Trifluoromethylated Dihydroquinoxalinones via Palladium-Catalyzed Hydrogenation. Org. Chem. Front. 2019, 6, 746–750. [Google Scholar] [CrossRef]
  64. Kamila, S.; Biehl, E.R. Synthetic Studies of Bioactive Quinoxalinones: A Facile Approach to Potent Euglycemic and Hypolipidemic Agents. Heterocycles 2006, 68, 1931–1939. [Google Scholar] [CrossRef]
  65. Lee, Y.M.; Park, Y.S. (S)-Mandelate-Mediated Dynamic Kinetic Resolution of α-Bromo Esters for Asymmetric Syntheses of Aminoflavones, Dihydroquinoxalinones and Dihydrobenzoxazinones. Heterocycles 2009, 78, 2233–2244. [Google Scholar] [CrossRef]
  66. Kim, Y.; Park, K.J.; Choi, Y.S.; Lee, M.S.; Park, Y.S. L-Lactate-Mediated Dynamic Kinetic Resolution of α-Bromo Esters for Asymmetric Syntheses of α-Amino Acid Derivatives. Bull. Korean Chem. Soc. 2013, 34, 2531–2534. [Google Scholar] [CrossRef] [Green Version]
  67. Volpe, C.; Meninno, S.; Crescenzi, C.; Mancinelli, M.; Mazzanti, A.; Lattanzi, A. Catalytic Enantioselective Access to Dihydroquinoxalinones via Formal α-Halo Acyl Halide Synthon in One Pot. Angew. Chem. Int. Ed. 2021, 60, 23819–23826. [Google Scholar] [CrossRef]
  68. Abraham, C.J.; Paull, D.H.; Scerba, M.T.; Grebinski, J.W.; Lectka, T. Catalytic, Enantioselective Bifunctional Inverse Electron Demand Hetero-Diels-Alder Reactions of Ketene Enolates and o-Benzoquinone Diimides. J. Am. Chem. Soc. 2006, 128, 13370–13371. [Google Scholar] [CrossRef]
  69. Huang, R.; Chen, X.; Mou, C.; Luo, G.; Li, Y.; Li, X.; Xue, W.; Jin, Z.; Chi, Y.R. Carbene-Catalyzed α-Carbon Amination of Chloroaldehydes for Enantioselective Access to Dihydroquinoxaline Derivatives. Org. Lett. 2019, 21, 4340–4344. [Google Scholar] [CrossRef]
  70. Rostoll-Berenguer, J.; Blay, G.; Muñoz, M.C.; Pedro, J.R.; Vila, C. A Combination of Visible-Light Organophotoredox Catalysis and Asymmetric Organocatalysis for the Enantioselective Mannich Reaction of Dihydroquinoxalinones with Ketones. Org. Lett. 2019, 21, 6011–6015. [Google Scholar] [CrossRef]
  71. Oble, J.; El Kaïm, L.; Gizzi, M.; Grimaud, L. Ugi-Smiles Access to Quinoxaline Derivatives. Heterocycles 2007, 73, 503–517. [Google Scholar] [CrossRef]
  72. Entwiste, I.D.; Johnstone, R.A.W.; Povall, T.J. Selective rapid transfer-hydrogenation of aromatic nitro-compounds. J. Chem. Soc. Perkin Trans. 1975, 1, 1300–1301. [Google Scholar] [CrossRef]
  73. Huang, Y.; Khoury, K.; Chanas, T.; Dömling, A. Multicomponent Synthesis of Diverse 1,4-Benzodiazepine Scaffolds. Org. Lett. 2012, 14, 5916–5919. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Hulme, C.; Peng, J.; Morton, G.; Salvino, J.M.; Herpin, T.; Labaudiniere, R. Novel Safety-Catch Linker and Its Application with a Ugi/De-BOC/Cyclization (UDC) Strategy to Access Carboxylic Acids, 1,4-Benzodiazepines, Diketopiperazines, Ketopiperazines and Dihydroquinoxalinones. Tetrahedron Lett. 1998, 39, 7227–7230. [Google Scholar] [CrossRef]
  75. El Kaïm, L.; Grimaud, L.; Oble, J. Phenol Ugi–Smiles Systems: Strategies for the Multicomponent N-Arylation of Primary Amines with Isocyanides, Aldehydes, and Phenols. Angew. Chem. Int. Ed. 2005, 117, 8175–8178. [Google Scholar] [CrossRef]
  76. El Kaim, L.; Grimaud, L. Beyond the Ugi Reaction: Less Conventional Interactions between Isocyanides and Iminium Species. Tetrahedron 2009, 65, 2153–2171. [Google Scholar] [CrossRef]
  77. Neochoritis, C.G.; Dömling, A. Towards a Facile and Convenient Synthesis of Highly Functionalized Indole Derivatives Based on Multi-Component Reactions. Org. Biomol. Chem. 2014, 12, 1649–1651. [Google Scholar] [CrossRef] [Green Version]
  78. Ugi, I. Neuere Methoden Der Präparativen Organischen Chemie IV Mit Sekundär-Reaktionen Gekoppelte α-Additionen von Immonium-Ionen Und Anionen an Isonitrile. Angew. Chem. 1962, 74, 9–22. [Google Scholar] [CrossRef]
  79. Gunawan, S.; Hulme, C. Bifunctional Building Blocks in the Ugi-Azide Condensation Reaction: A General Strategy toward Exploration of New Molecular Diversity. Org. Biomol. Chem. 2013, 11, 6036–6046. [Google Scholar] [CrossRef] [Green Version]
  80. Cárdenas-Galindo, L.E.; Islas-Jácome, A.; Alvarez-Rodríguez, N.V.; El Kaim, L.; Gámez-Montaño, R. Synthesis of 2-Tetrazolylmethyl-2,3,4,9-Tetrahydro-1H-β-Carbolines by a One-Pot Ugi-Azide/Pictet–Spengler Process. Synthesis 2014, 46, 49–56. [Google Scholar] [CrossRef]
  81. Zarganes-Tzitzikas, T.; Patil, P.; Khoury, K.; Herdtweck, E.; Dömling, A. Concise Synthesis of Tetrazole–Ketopiperazines by Two Consecutive Ugi Reactions. Eur. J. Org. Chem. 2015, 2015, 51–55. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  82. Patil, P.; Khoury, K.; Herdtweck, E.; Dömling, A. MCR Synthesis of a Tetracyclic Tetrazole Scaffold. Bioorg. Med. Chem. 2015, 23, 2699–2715. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Patil, P.; Zhang, J.; Kurpiewska, K.; Kalinowska-Tłuścik, J.; Dömling, A. Hydrazine in the Ugi Tetrazole Reaction. Synthesis 2016, 48, 1122–1130. [Google Scholar] [CrossRef] [Green Version]
  84. Wang, Y.; Patil, P.; Kurpiewska, K.; Kalinowska-Tluscik, J.; Dömling, A. Two Cycles with One Catch: Hydrazine in Ugi 4-CR and Its Postcyclizations. ACS Comb. Sci. 2017, 19, 193–198. [Google Scholar] [CrossRef] [PubMed]
  85. Kotzabasaki, V.; Lykakis, I.N.; Gryparis, C.; Psyllaki, A.; Vasilikogiannaki, E.; Stratakis, M. Gold-Catalyzed Dehydrogenative Cycloaddition of Tethered 1,n-Dihydrodisilanes to Alkynes. Organometallics 2013, 32, 665–672. [Google Scholar] [CrossRef]
  86. Sander, T.; Freyss, J.; Von Korff, M.; Rufener, C. DataWarrior: An Open-Source Program for Chemistry Aware Data Visualization and Analysis. J. Chem. Inf. Model. 2015, 55, 460–473. [Google Scholar] [CrossRef]
  87. Kroon, E.; Kurpiewska, K.; Kalinowska-Tłuścik, J.; Dömling, A. Cleavable β-Cyanoethyl Isocyanide in the Ugi Tetrazole Reaction. Org. Lett. 2016, 18, 4762–4765. [Google Scholar] [CrossRef]
Molecules 27 04395 sch001 550
Scheme 1. AuNP-catalyzed transfer hydrogenation processes towards the synthesis of N-substituted 3,4-dihydroquinoxalin-2-ones.
Scheme 1. AuNP-catalyzed transfer hydrogenation processes towards the synthesis of N-substituted 3,4-dihydroquinoxalin-2-ones.
Molecules 27 04395 sch001
Molecules 27 04395 sch002 550
Scheme 2. Synthetic approaches for the 3,4-dihydroquinoxalin-2-ones.
Scheme 2. Synthetic approaches for the 3,4-dihydroquinoxalin-2-ones.
Molecules 27 04395 sch002
Molecules 27 04395 sch003 550
Scheme 3. Synthetic procedures for multifunctional, aromatic nitro precursors 1–21.
Scheme 3. Synthetic procedures for multifunctional, aromatic nitro precursors 1–21.
Molecules 27 04395 sch003
Molecules 27 04395 sch004 550
Scheme 4. Au/TiO2-catalyzed chemoselective reduction of the multifunctional, aromatic nitro compounds 1–15 in the presence of Et3SiH or TMDS.
Scheme 4. Au/TiO2-catalyzed chemoselective reduction of the multifunctional, aromatic nitro compounds 1–15 in the presence of Et3SiH or TMDS.
Molecules 27 04395 sch004
Molecules 27 04395 sch005 550
Scheme 5. Reaction profile of the Au/TiO2-Et3SiH-catalyzed reduction of 18.
Scheme 5. Reaction profile of the Au/TiO2-Et3SiH-catalyzed reduction of 18.
Molecules 27 04395 sch005
Molecules 27 04395 sch006 550
Scheme 6. Synthesis of 3,4-dihydroquinoxalin-2-ones (16b–21b) in the presence of Au/TiO2-Et3SiH or Au/TiO2-TMDS.
Scheme 6. Synthesis of 3,4-dihydroquinoxalin-2-ones (16b–21b) in the presence of Au/TiO2-Et3SiH or Au/TiO2-TMDS.
Molecules 27 04395 sch006
Molecules 27 04395 sch007 550
Scheme 7. Au/TiO2-Et3SiH or Au/TiO2-TMDS catalytic system application to the lab-scale synthesis of 17b from 17.
Scheme 7. Au/TiO2-Et3SiH or Au/TiO2-TMDS catalytic system application to the lab-scale synthesis of 17b from 17.
Molecules 27 04395 sch007
Molecules 27 04395 g001 550
Figure 1. (A) Scatterplot of clogP vs. MW. The marker color is defined by the polar surface area values; (B) scatterplot of drug-likeness vs. MW; (C) scatterplot of shape index vs. MW; (D) scatterplot of HBA vs. MW.
Figure 1. (A) Scatterplot of clogP vs. MW. The marker color is defined by the polar surface area values; (B) scatterplot of drug-likeness vs. MW; (C) scatterplot of shape index vs. MW; (D) scatterplot of HBA vs. MW.
Molecules 27 04395 g001
Table
Table 1. Evaluation of Au catalysts, reducing agents and solvents in the catalytic reduction of 1 into 1a.
Table 1. Evaluation of Au catalysts, reducing agents and solvents in the catalytic reduction of 1 into 1a.
Molecules 27 04395 i001
EntryCatalyst [a]Solvent [a]Reducing Agent (eq.) [a]Time (h)1%/1a% [b]
1-THF/MeOHNaBH4 or LiBH4 (2)18100/0
2-THF/MeOHNH3BH3 (2)18100/0
3 [c]-THFLiAlH4 (2)1843/0
4 [c]-THFNaH (3)1847/0
5Au/TiO2THF/MeOHNH3BH3 (2)180/>99 (78)
6Au/TiO2THF/MeOHLiBH4 (2)10/>99 (62)
7Au/TiO2THF/MeOHNaBH4 (2)10/>99 (81)
8Au/TiO2THFNaBH4 (2)240/>99 (79)
9Au/TiO2MeOHNaBH4 (2)180/>99 (84)
10Au/TiO2THF/MeOHNaBH4 (1)1840/60 (48)
11-THF/MeOHTMDS (2)24100/0
12Au/TiO2THF/MeOHTMDS (2)10/>99 (89)
13Au/TiO2THF/MeOHTMDS (1)137/63 (55)
14Au/TiO2MeOHTMDS (2)240/>99 (85)
15Au/TiO2THF/MeOHDMPS (4)10/>99 (81)
16Au/TiO2THF/MeOHDPS (4)1.50/>99 (85)
17Au/TiO2THF/MeOH(EtO)3SiH (4)24100/0
18Au/TiO2THF/MeOHEt3SiH (4)10/>99 (92)
19Au/TiO2THF/MeOH(TMS)3SiH (4)227/73 (61)
20 [c,d]AuCl3THF/MeOHEt3SiH (4)374/0
21 [c,d]AuCl3THF/MeOHTMDS (2)171/0
22 [c,d]AuClTHF/MeOHEt3SiH (4)374/0
23 [c,d]AuClTHF/MeOHTMDS (2)179/0
24 [c,d]Ph3PAuNTf2THF/MeOHEt3SiH (4)378/0
25 [c,d]Ph3PAuNTf2THF/MeOHTMDS (2)182/0
26 [c]Au/Al2O3THF/MeOHEt3SiH (4)20/80 (75)
27 [c]Au/Al2O3THF/MeOHTMDS (2)20/83 (77)
28 [c]Au/ZnOTHF/MeOHEt3SiH (4)381/0
29Au/ZnOTHF/MeOHTMDS (2)397/3
[a] Conditions: 20 mg of Au/TiO2 (or Au/Al2O3 or Au/ZnO) 1 wt% (ca. 0.8 mol% based on 1), 0.1 mmol of 1, 1 mL of solvent (THF/MeOH = 1/1) and at rt. AuCl3, AuCl and Ph3PAuNTf2 were used in 20 mol% amount. [b] Relative yields of 1 and 1a at appropriate time measured by 1H NMR of the crude reduction mixture. Values in parentheses correspond to the isolated yields. [c] Unidentified products missing either the tert-amide or the anisole group from its structure as determined by 1H NMR in some cases. [d] All the salts were used in 20 mmol%.
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Iordanidou, D.; Kallitsakis, M.G.; Tzani, M.A.; Ioannou, D.I.; Zarganes-Tzitzikas, T.; Neochoritis, C.G.; Dömling, A.; Terzidis, M.A.; Lykakis, I.N. Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones. Molecules 2022, 27, 4395. https://doi.org/10.3390/molecules27144395

AMA Style

Iordanidou D, Kallitsakis MG, Tzani MA, Ioannou DI, Zarganes-Tzitzikas T, Neochoritis CG, Dömling A, Terzidis MA, Lykakis IN. Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones. Molecules. 2022; 27(14):4395. https://doi.org/10.3390/molecules27144395

Chicago/Turabian Style

Iordanidou, Domna, Michael G. Kallitsakis, Marina A. Tzani, Dimitris I. Ioannou, Tryfon Zarganes-Tzitzikas, Constantinos G. Neochoritis, Alexander Dömling, Michael A. Terzidis, and Ioannis N. Lykakis. 2022. "Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones" Molecules 27, no. 14: 4395. https://doi.org/10.3390/molecules27144395

APA Style

Iordanidou, D., Kallitsakis, M. G., Tzani, M. A., Ioannou, D. I., Zarganes-Tzitzikas, T., Neochoritis, C. G., Dömling, A., Terzidis, M. A., & Lykakis, I. N. (2022). Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones. Molecules, 27(14), 4395. https://doi.org/10.3390/molecules27144395

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