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Review

Advances in the Synthesis of Heteroaromatic Hybrid Chalcones

by
Ajay Mallia
* and
Joseph Sloop
Department of Chemistry, School of Science & Technology, Georgia Gwinnett College, 1000 University Center Lane, Lawrenceville, GA 30043, USA
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(7), 3201; https://doi.org/10.3390/molecules28073201
Submission received: 12 February 2023 / Revised: 18 March 2023 / Accepted: 21 March 2023 / Published: 4 April 2023
(This article belongs to the Special Issue Synthesis of Heteroaromatic Compounds)
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Abstract

:
Chalcones continue to occupy a venerated status as scaffolds for the construction of a variety of heterocyclic molecules with medicinal and industrial properties. Syntheses of hybrid chalcones featuring heteroaromatic components, especially those methods utilizing green chemistry principles, are important additions to the preparative methodologies for this valuable class of molecules. This review outlines the advances made in the last few decades toward the incorporation of heteroaromatic components in the construction of hybrid chalcones and highlights examples of environmentally responsible processes employed in their preparation.

1. Introduction

The chalcone class of enones has been a privileged scaffold in organic synthesis for more than a century. Kostanecki and Tambor are credited with the first reported preparation of E-1,3-diphenylprop-2-en-1-one and coined the term “chalcone” in 1899 [1]. Figure 1 shows the structure of E-chalcone, the most energetically favorable stereoisomer, as well as the sterically encumbered and less common Z-chalcone, both of which contain benzene rings at C1 and C3 joined by a three-carbon α,β-unsaturated ketone unit. The absolute configuration of solid chalcone stereochemistry obtained during synthesis can often be determined with X-ray crystallography [2,3].
By convention, the aromatic ring attached to C1 is designated as ring A while the aromatic ring attached to C3 is designated as ring B. For the purposes of this review, we will adhere to the conventional ring designations in describing preparations of heteroaromatic hybrid chalcones.
The utility of chalcones both as a pharmacophore and as a scaffold in the synthesis of a wide variety of heterocycles ranging from pyrazoles, isoxazoles, triazoles, barbituric acid derivatives, etc. has been investigated thoroughly over the years, with numerous research articles as well as several reviews appearing in the last decade describing the current chalcone synthetic strategies, the heterocycles derived from them, and the bioactivity and pharmaceutical uses of these compounds [4,5,6,7,8,9,10,11,12,13]. Within that context, the preparation of more highly functionalized chalcones that contain heteroaromatic components has been an area of intense research over the last decade [10,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30].
Research has established that heteroaromatic hybrid chalcones themselves possess broad medicinal value as anticancer [16,19,23], antimicrobial [11,20,23,28], antifungal [16], anti-tuberculosis [25] and anti-inflammatory agents [22] as well as having other important pharmacological functions [9,10], agrochemical utility as photosynthesis inhibitors [18] and industrial use as photoinitiators in 3D printing [17]. Figure 2 shows a representative selection of heteroaromatic hybrid chalcone pharmacophores and industrially important compounds.
Synthetic methodologies to prepare hybrid chalcones have developed rapidly over the last two decades. To the best of our knowledge, no reviews have been found that focus on heteroaromatic chalcone synthesis and the green synthesis methods employed to prepare them. This review will focus on the construction of heteroaromatic hybrid chalcones with the Claisen–Schmidt condensation, 1,3-dipolar additions, ring-opening reactions, 3+2 annulations and Wittig reactions. The review will discuss four different heteroaromatic hybrid chalcone types: A-ring and B-ring-substituted mono-heteroaromatic hybrid chalcones, hybrid chalcones possessing heteroaromatic moieties on both the A and B rings, and the synthesis strategies used to prepare heteroaromatic bis chalcone hybrids. Herein, we also detail the green methods that have been employed to prepare these hybrid chalcones including microwave irradiation, sonication, ball milling, continuous flow reactions, the use of benign solvents, solvent-free/solid-state processes and nanocatalysis. See Figure 3.

2. A-Ring Heteroaromatic Hybrid Chalcone Synthesis

This section catalogues several representative conventional and green processes by which hybrid chalcones bearing a heteroaromatic species at ring A may be prepared. Heteroaromatic components of the chalcone products include a variety of single-ring (furan, pyrrole, thiazole, thiophene, pyridine, pyrimidine) and fused-ring (indole, benzimidazole, benzothiazole, benzofuran, pyrazolopyridine, quinoline) systems.

2.1. Claisen–Schmidt Condensations

The Claisen–Schmidt (C-S) condensation has been widely used to prepare chalcones for many years. This reaction, which can be catalyzed by acids or bases, offers mild conditions that tolerate a wide scope of functionality in both the ketone donors and aldehyde acceptors.

2.1.1. Base-Catalyzed C-S Condensations

The hydroxide bases KOH, NaOH and to a lesser extent Ba(OH)2 are the bases used to promote the condensations depicted below in Scheme 1, Scheme 2, Scheme 3, Scheme 4, Scheme 5, Scheme 6, Scheme 7, Scheme 8, Scheme 9, Scheme 10, Scheme 11 and Scheme 12. These bases may be introduced to the reaction medium as dilute or concentrated aqueous solutions or as solids. Ethanol or methanol are the solvents of choice in most reactions depicted herein. The reaction temperatures vary from 0 °C to those obtained by refluxing the alcoholic solvents. The reaction times range from less than a minute in the case of selected microwave-mediated reactions and can extend to 72 h for the conventional condensations.
In our first entry, three room-temperature C-S preparations of pyrrolyl chalcone 3 are presented that have differing reaction times and different base concentrations. Sweeting et al. (Scheme 1a) used strongly basic conditions (60% aqueous KOH) and centrifugation mixing to prepare the pyrrolyl chalcone 3 in a modest yield. The low yield is likely attributed to the short reaction time. Ref. [31] Robinson et al. reported that increasing the reaction time ([32], Scheme 1b) using NaOH (aq) in ethanol increased the yield of the pyrrolyl chalcone. Using 20 mol % NaOH (aq) in ethanol, Song et al. obtained a 91% yield in the preparation of the chalcone (Scheme 1c). Ref. [33] Lokeshwari’s team (Scheme 2a) and Liu’s group prepared furyl chalone 5 in an 87% yield using 0.1 mol % KOH (aq) in 4 h, while Liu’s group (Scheme 2b) obtained equally high yields with 20 mol% NaOH (aq) in 6 h [34,35]. Robinson et al. (Scheme 3) condensed 2-acetylfuran and 2-acetyl-5-methylfuran with assorted benzaldehydes at room temperature en route to the twelve furyl chalcones 8 in modest to medium yields [36].
Parveen et al. reported a nearly quantitative conversion for the room-temperature C-S condensation of 2-acetylthiophene and benzaldehyde using aqueous KOH (Scheme 4) in ethanol to the thienyl chalcone 10 [37].
Sunduru et al. reported the preparation of pyridyl chalcone derivatives 13 by condensing 4-acetylpyridine with the respective aromatic aldehyde (Scheme 5) [38]. In this reaction, one equivalent of 4-acetylpyridine was added dropwise to a cooled methanolic solution containing 10% aqueous NaOH. Then, one equivalent of aldehyde was added slowly at 0 °C. After workup and recrystallization, the pyridyl chalcones were obtained in yields ranging from 67 to 76% (Scheme 5).
Sinha and coworkers (Scheme 6) used similar conditions to synthesize eighteen 1,3-thiazolylchalcones 16 in very good overall yields [39].
Zhao et al. (Scheme 7) used reflux conditions to achieve yields in excess of 60% for the small series of fused-ring indolyl chalcones 18 [40]. In two separate publications, Hsieh and coworkers used base-catalyzed C-S condensations to prepare indolyl (Scheme 8, [41]), thiazolyl and benzothiazolyl hybrid chalcones (Scheme 9, [42]).
Saito’s team used 5% KOH in ethanol at room temperature to prepare a series of functionalized benzofuran hybrid chalcones in yields as high as 97% (Scheme 10) [43].
Grigoropoulou’s team found barium hydroxide octahydrate effective in promoting the condensation of both single- and fused-ring heteroaromatic ketones with dehydroabietic acid methyl ester en route to sixteen hybrid chalcones in good overall yields (Scheme 11) [44].
Base-catalyzed C-S condensations have also been demonstrated using green principles. These processes include the use of benign solvents including water and microwave irradiation. Mubofu and Engberts reported a C-S condensation reaction of 2-acetylpyridine and benzaldehyde using 10% NaOH (Scheme 12) [45]. The reagents were finely dispersed in water at 4 °C and after workup the pyridyl chalcone 31 was obtained in a good yield (Scheme 12).
Jianga et al. showed that the condensation of 2-acetylfuran or 2-acetylthiophene and benzaldehyde using 2 mol% NaOH (aq) gave (E)-1-(Furan-2-yl)-3-phenylprop-2-en-1-one or (E)-1-(thiophen-2-yl)-3-phenylprop-2-en-1-one at room temperature in nearly quantitative yields (Scheme 13) [46].
Ritter et al. (Scheme 14) used 2-acetylthiophene 9 and assorted benzaldehydes in glycerin solvent to prepare seven 2-thienochalcones 10 and 32a–f in very good yields [47].
Khan and Asiri (Scheme 15) showed that 3-acetylthiophene 33 underwent a microwave-mediated C-S condensation with several benzaldehydes in less than a minute to give thienyl chalcones 34a–f in yields exceeding 82% [48].
Sarveswari and Vijayakumar (Scheme 16) conducted a comparative study of conventional and microwave processes in which four examples of highly substituted quinolinyl hybrid chalcones 36a–d were prepared [49]. Both processes gave the desired chalcones in yields greater than 75%. Particularly noteworthy is the fact that the microwave reaction time is 1/144 of the conventional reaction time.
Polo et al. demonstrated that sonochemical mediation was very effective in preparing a series of pyrazolopyridyl hybrid chalcones 38a–e (Scheme 17) in high yields that compare favorably with conventional base-catalyzed C-S condensations [50].

2.1.2. Acid-Catalyzed C-S Condensations

In the recent literature, Adnan et al. showed that p-toluenesulfonic acid (PTSA) effectively catalyzed the condensation of 2-acetylthiophene (9) and p-tolualdehyde (2) in a green solventless process in which the reactants were ground in a warm mortar and pestle for 4 min to give the thienyl chalcone 32e in a very good yield [13]. See Scheme 18.
Shaik et al. reported an acid-catalyzed condensation reaction of 2,4-dimethyl-5-acetylthiazole with 2,4-difluorobenzaldehyde to prepare (E)-1-(2′,4′-dimethyl)-(5-acetylthiazole)-(2,4″-difluorophenyl)-prop-2-en-1-one (Scheme 19) [23].

2.2. Non C-S Condensations

Our final installment of A-ring hybrid chalcone synthesis is an interesting green coupling reaction between a series of arylacetylene derivatives (42a–j) and various pyridine and benzopyridine carboxaldehydes (Scheme 20). Yadav’s group showed that a copper-based silica-coated magnetic nanocatalyst (Cu@DBM@ASMNPs) used in conjunction with a piperidine base was very effective in preparing ten hybrid chalcones in yields ranging from 49 to 94% [51]. A noteworthy feature of this reaction was the ability to recover the catalyst via a magnet. The catalyst was reported to be efficient for up to seven reaction cycles.

3. B-Ring Heteroaromatic Hybrid Chalcone Synthesis

This section catalogues selected conventional and green processes by which hybrid chalcones containing a heteroaromatic component at ring B may be prepared. In addition, examples of tandem ring-opening dipolar additions to obtain ring B heteroaromatic substituted chalcones are presented. The heteroaromatic components of the chalcone products highlighted in this section include a variety of single-ring (furan, pyrrole, pyrazole, thiazole, thiophene, pyridine) and fused-ring (indole, benzimidazole, benzothiazole, benzofuran, quinoline, imidazo [1,2-a]pyrimidine or imidazo [1,2-a]pyridine, quinoxaline, carbazole) systems.

3.1. Claisen–Schmidt Condensations

As in the preceding section, Claisen–Schmidt (C-S) condensation has been widely used to prepare B-ring heteroaromatic chalcones. This reaction, which can be catalyzed by bases or acids, offers mild conditions that tolerate a wide scope of functionality in both the ketone donors and aldehyde acceptors.

Base-Catalyzed C-S Condensations

In the preparations shown below, NaOH and KOH are the bases of choice. Shown in Scheme 21, Li et al. used dilute aqueous KOH to prepare pyrrolyl chalcone (46) in a very good yield. Using mild conditions, Robinson et al. (Scheme 22) condensed acetophenones 47 and furfural derivatives 48 to prepare five furyl chalcones (49a–e) that show promise as monoamine oxidase inhibitors in low to medium yields [36].
In Scheme 23, Fu and coworkers reacted 1,2,3-triazole-substituted acetophenones 50 with furfural 48 and thiophene-2-carbaldehyde 51 in ethanolic KOH for 3 h to prepare hybrid chalcones 52a and 52b in satisfactory yields. Condensation of 50 and pyridine carbaldehydes 53a–b under the same conditions provided eight additional pyridyl hybrid chalcone examples 54a–h in yields ranging from 50 to 79% [52].
Gadhave and Uphade demonstrated the satisfactory condensation of 4-morpholinoacetophenone 55 with 4-pyrazolocarbaldehydes 56 conducted at room temperature, which provided five examples of 4-pyrazolylchalcones 57 [53]. See Scheme 24.
An interesting study conducted by Mallik and associates involves the preparation of pyrrole-substituted hybrid chalcones from the C-S condensation of several acetophenones 58 and 2-formylpyrrole 44 under different molar ratios of 58:44 [54]. As Scheme 25 shows, the desired product 59 predominated when the reactant molar ratios were 1:1, but when the ratio was lowered to 1:2, a nearly equal proportion of the product mixture was found to be the heteroaromatic ketone 60. Upon increasing the molar proportion of 58 to four times that of 44, ketone 60 was the major product. The authors propose an interesting mechanism by which 60 is formed—a twin aldol addition—intramolecular cyclization-dehydration.
Fused-ring heteroaromatic aldehydes have also been successfully condensed with various acetophenones to prepare B-ring hybrid chalcones under typical C-S reaction conditions. Zhao et al. prepared indole hybrid chalcones 63a–e (Scheme 26) from assorted acetophenones and N-methylindolycarbaldehydes 62 in yields ranging from 60 to 90% [40].
Bandgar and coworkers (Scheme 27) synthesized a diverse library of carbazole hybrid chalcones 66 [30], while Bindu’s team condensed acetophenone derivatives with quinoline carboxaldehdes 68 under mild C-S conditions (Scheme 28) to prepare eight examples of B-ring-substituted quinolinoid hybrid chalcones 68a–h [55]. Abonia et al. prepared the chromen-4-one—quinoline hybrid chalcone 71 under similar conditions [56]. See Scheme 29.
Desai and coworkers used mild C-S reaction conditions to prepare a series of thirteen quinoxalinyl hybrid chalcones 73a–m in yields ranging from 60 to 95%, as shown in Scheme 29 [24].
In a study of microtubule polymerization inhibition, Sun et al. synthesized a library of fused-ring heteroaromatic chalcones featuring indoles, benzofurans, dibenzofurans, benzothiophenes, dibenzothiophenes, and benzimidazoles [57]. See Figure 4. Of particular note were the numerous methods used in the preparation of these hybrid chalcones, which included both base-promoted processes (piperidine, NaOH, KOH, NaOMe, Cs2CO3 and NaH) in methanolic and ethanolic solvents, Lewis acid catalysis (BF3•etherate) in dioxane solvent and Brønsted (glacial acetic acid) acid catalysis in toluene. Scheme 30 depicts the scope of this work.
Base-catalyzed C-S condensations that employ green chemistry principles to produce B-ring-substituted hybrid chalcones have also been successfully conducted. See Scheme 31. These processes include the use of benign solvents, solvent-free reactions, microwave irradiation, ultrasound and ball milling. For example, Ashok’s group compared a typical base-catalyzed C-S condensation of 83 and 84 with a solvent-free, microwave-mediated process to prepare a series of carbazolyl hybrid chalcones 85 [58]. The yields for the short-duration microwave-mediated reactions exceeded those of the lengthy conventional C-S reactions in every case. Bhatt et al. prepared the furyl chalcone 87 using both conventional C-S and ultrasound processes to condense furfural 48 and 2,4-dihydroxyacetophenone 86 [59]. The effectiveness of sonication is evident—a 10% increase in yield in 1/20 the reaction time. Jadhava’s team used PEG-400 as a benign solvent to mediate the condensation of 4-fluoroacetophenone 84 and a series of pyrazole carbaldehydes 85 en route to eight fluorinated pyrazolyl hybrid chalcones 86 [60]. Kudlickova and coworkers employed a mechanochemical ball-milling process to prepare a series of indoylchalcones 92 in yields ranging from 28 to 79% in only 30 min [61]. Nimmala’s group used a solventless process to condense various acetophenones and imidazo [1,2-a]pyrimidine 93 or imidazo [1,2-a]pyridine 95 en route to hybrid chalcones 94a–f and 96a–f, respectively, in very good yields [62]. Joshi and Saglani employed ultrasound to assist in the condensation of the fused-ring ketone 97 and a series of quinoline carbaldehydes 98 to prepare the quinolinyl hybrid chalcones 99 [63].

3.2. Non C-S Condensations

The final entries describing ring-B-substituted heteroaromatic hybrid chalcones feature unique tandem reactions involving pyrylium tetrafluoroborate derivatives. Devi and colleagues conducted a very interesting examination of a single-pot, base-mediated, tandem-ring-opening, 1,3-dipolar addition reaction between several electron withdrawing group (EWG)-substituted diazo compounds 101 with tri-substituted pyrylium salts 100, producing an extensive array of pyrazole hybrid chalcones 102 in moderate to high yields, as shown in Scheme 32 [64].
Tan and Wang leveraged a similar pyrilium ring-opening strategy in a single-pot 3+2 reductive annulation with benzil derivatives 103 to prepare a comprehensive library of tetra-substituted Furano chalcones 105a–ii in yields as high as 70% [65]. See Scheme 33. A noteworthy observation in both works was the finding that Z-chalcone derivatives were the major or sole product in all instances.

4. A–B Ring Dual Heteroaromatic Hybrid Chalcone Synthesis

This section catalogues selected processes by which hybrid chalcones bearing a heteroaromatic species at both rings A and B may be prepared. Of particular note is the incredibly diverse array of chalcones produced that feature 21 different heteroaromatic A–B ring-substituted groups on the hybrid chalcones shown in Scheme 34, Scheme 35, Scheme 36, Scheme 37, Scheme 38, Scheme 39, Scheme 40, Scheme 41, Scheme 42, Scheme 43, Scheme 44, Scheme 45 and Scheme 46.

4.1. Claisen–Schmidt Condensations

As noted in the preceding sections, the Claisen–Schmidt (C-S) condensation is the most common method used to prepare A–B ring heteroaromatic chalcones. This reaction, which can be catalyzed by bases or acids, offers mild conditions that tolerate a wide scope of functionality in both the ketone donors and aldehyde acceptors.

4.1.1. Base-Catalyzed C-S Condensations

In most instances, NaOH and KOH are the most widely used bases. Sweeting’s group synthesized and obtained an X-ray crystal structure for the pyrrolyl–thienyl hybrid chalcone 106 as part of a chalcone solubility and stability study [30]. See Scheme 34. While the use of centrifuging to mix the reagents is of interest, the low yield is likely attributable to the limited reaction time of 30 min. Sinha and coworkers prepared two thiazolyl–furyl hybrid chalcones in high yields (Scheme 35) while investigating potential ant-lipoxygenase agents [37].
Fused-ring A–B hybrid chalcone examples have also been successfully prepared under very mild, base-catalyzed C-S conditions. Bandgar’s team prepared the pyridyl and thienyl–carbazolyl heteroaromatic hybrid chalcones 108–109 in very good yields (Scheme 36) [29]. While investigating ACP reductase inhibition, Desai’s group prepared the pyridyl/quinoxazolyl chalcone 110 in a good yield as shown in Scheme 37 [23]. Mallik et al. found that when one equivalent of acetone and four equivalents of 2-pyrrole carbaldehyde were condensed in 20% KOH, the unusual pyrrolizinyl–pyrrolyl chalcone 112 was formed in modest yield (32%), accompanied by the acetylpyrrolizine 113 (17%) [53]. See Scheme 38. This finding is complementary to the work shown in Scheme 25 in which similar pyrrolizine products were formed. In an examination of chalcones with potential anticancer properties, Bukhari prepared a diverse set of furyl-, thienyl-, benzofuryl, and benzothienyl-1,4-pyrazinyl chalcones 116 in yields ranging from 42 to 75%. Extending that work to include condensations of 4-heteroaromatic acetophenones 117 with pyrazine carbaldehyde 115 gave rise to an array of hybrid chalcones 118 in moderate yields [18]. See Scheme 39.

4.1.2. Green C-S Condensations

The recent literature reports a number of green, base-promoted C-S condensations used to prepare A–B ring heteroaromatic hybrid chalcones. While studying potential antimicrobial agents, Kumar et al. synthesized ten furyl-triazolyl chalcones 120a–j via a continuous-flow reactor [66]. Of note are the exceptional yields (84–90%) obtained in only 15 min. See Scheme 40. Moreover, in pursuit of suitable chalcones that have antimicrobial properties, Usta’s team prepared two pyrrole–pyridyl chalcones using both conventional and microwave processes [27]. The yields reported were as high as 90% after only 3 min of irradiation. See Scheme 41.
Several syntheses of A–B ring heteroaromatic chalcones having fused-ring systems have also been reported. Khan and Asiri prepared two hybrid chalcones and tested them for antibacterial activity, a thienyl–pyrazole chalcone as well as a thienyl–carbazolyl chalcone using a microwave oven [46]. See Scheme 42. The base-catalyzed process, completed in only 45 s, provided the chalcones in 89–90%. Quinolinyl chalcones, such as those prepared by Sarveswari and Vijayakumar in Scheme 43, have also shown promise as antibacterial and antifungal agents [47]. Again, yields for the short-duration, microwave-mediated process was on par with or exceeded those obtained by the conventional C-S reactions conducted in their comparative study.
Acetylated pyrazolo pyridines 37 and 128 were condensed with five heteroaryl aldehydes by Polo et al. under both ultrasonic and conventional conditions to prepare interesting A–B ring hybrid chalcones substituted with furyl, pyridyl, imidazolyl and quinolinyl groups [48]. See Scheme 44. Chalcone series 38 was part of a larger study discussed earlier in the review (Scheme 17). Yields for the short-duration ultrasound-assisted condensation met or exceeded those obtained by the conventional, base-promoted C-S condensations performed by the group.
In Scheme 45, Kumar et al. employed piperidine base to catalyze the microwave-mediated condensation of indoles 131 and 132 en route to a large array of highly differentially functionalized twin indolyl hybrid chalcones 133 [67]. The yields reported were excellent, ranging from 72 to 92%, especially given the reaction time of 5 min.
Our final entry in this section is a green, solid-state, acid-catalyzed condensation of 2-acetylthiophene 9 and the thienyl carboxaldehyde 51 conducted by Adnan and associates, which produced the twin thienyl chalcone 134 in an excellent yield [13]. See Scheme 46.

5. Heteroaromatic Bis Chalcone Hybrid Synthesis

This section catalogues several processes by which heteroaromatic bis chalcone hybrids bearing two or more heteroaromatic species have been prepared. The reactions feature both heteroaromatic donors and acceptors as the linker unit in the bis hybrid chalcone systems. Conventional and green condensations as well as a unique Wittig preparation are discussed.

5.1. Claisen–Schmidt Condensations

The Claisen–Schmidt (C-S) condensation is the most widely used method to prepare heteroaromatic bis chalcone hybrids. In this section, we present base-promoted condensations that tolerate a wide scope of functionality in both the bis-ketone donors and bis-aldehyde acceptors.

5.1.1. Base-Catalyzed C-S Condensations

As seen in the previous sections, NaOH and KOH are the most widely used bases. Methanol and ethanol are the solvents of choice in these condensations. In the first entry of bis hybrid chalcone preparation (Scheme 47), Alidmat et al. prepared three examples of mono- and dichlorinated bis-thienyl chalcones with potential as anticancer agents [68]. Of note is the one-pot preparation of the non-symmetric bis hybrid chalcone 138 from the condensation of 4-formylbenzaldehyde 135 (1 mole) and equimolar quantities of acetylthiophenes 136 and 137. In contrast, the condensation of 135 (1 mole) with two moles of 136 or 137 resulted in the symmetric bis hybrid chalcones 139 or 141, respectively.
While investigating photoinitiators with applications in 3D/4D printing, Chen’s group prepared several bis hybrid chalcones that show promise as light-sensitive photoinitiators. See Scheme 48. 4,4′-diacetylbiphenyl 142 was condensed with 2-formylthiophene under mild, base-promoted conditions to synthesize the bis thienyl biphenyl chalcone 143 in a good yield [17]. Under the same reaction conditions, 2,6-diacetylpyridine 144 was condensed with several substituted benzaldehydes 145 en route to three pyridyl bis aryl hybrid chalcones 146a–c in yields ranging from 58 to 86%.
While investigating lung cancer cell growth inhibitors, Zhao et al. prepared the indole bis phenyl chalcone 148 by condensing 1,2-diacetyl-3-methylindole 147 with benzaldehyde in 60% yield [54]. See Scheme 49.
Presented in Scheme 50 and Scheme 51 are green methods used to prepare bis heteroaromatic chalcones. Asir and coworkers used sonochemical mediation to prepare examples of bis thienyl and bis furyl hybrid chalcones 150a–b. The reaction time of 5 min was sufficient to give product yields in excess of 70%. [69] In a study of the anti-inflammatory activity of 3,4-bis-chalcone-N-arylpyrazoles, Abdel-Aziz et al. prepared eight examples of assorted aryl- and heteroaryl-substituted chalcone pyrazoles 152 using an aqueous KOH/EtOH medium at 60 °C and microwave irradiation [70]. The total reaction time reported was only four minutes to achieve yields ranging from 70 to 93%. Analogous conventional C-S condensations were also carried out over a 12 h period; the yields obtained were about 75–85% of those obtained with μwave mediation.

5.1.2. Non C-S Condensations

Our final installment for the bis hybrid chalcone section is an early example published by Saikachi and Muto in 1971 [71]. Their work, shown in Scheme 52, which focused on the preparation and utility of bisphosphoranes in oligimerization studies, exemplified how the bis-Wittig reagents 153, 155 and 157 could be successfully coupled with furan or thienylcarbaldehydes to provide a series of bis heteroaromatic chalcones 154, 156 and 158 in yields ranging from 45 to 99%. This work was unique in providing the bis hybrid chalcone system with benzene, biphenyl, diphenyl ether, diphenylmethylene, and diphenylethylene linker units.

6. Conclusions and Future Directions

This review of the preparation of heteroaromatic hybrid chalcones gives a robust accounting of more than 50 historic and current synthetic processes leading to more than 430 different hybrid chalcone examples that include single-ring and multi-ring heteroaromatic moieties. We have shown that the venerable Claisen–Schmidt reaction, by far the most common condensation method discussed herein, has been successfully used in either base-promoted or acid-catalyzed processes en route to heteroaromatic hybrid chalcones. We note that variations in the base or acid identity, solution concentration and physical state often make direct comparisons of the yields challenging. Also discussed has been the wide array of reaction conditions, such as the temperature and reaction time, which likewise impact the overall yield. Finally, the topology and electronic reactivity of the ketone donors and aldehyde acceptors likely modulate the product stereochemistry and yields as well.
Additionally, this review has provided the reader with an appreciation of alternative methods used to prepare these hybrid chalcones. Presented in our review are metal-catalyzed coupling reactions, cycloadditions, ring-opening processes and Wittig reactions that enable the formation of more than 75 hybrid chalcone examples.
A key thrust of this review has been to highlight the application of green chemistry methods in heteroaromatic hybrid chalcone synthesis. From the use of benign/renewable solvents and solvent-free and solid-state processes, researchers have demonstrated the ability to minimize waste streams. Through the use of sonochemical, mechanochemical, microwave irradiation, continuous-flow reactions and nanocatalytic methods, scientists minimize the reagent costs, reaction times and energy expenditure while optimizing the yields. Taken together, the important advances in green method uses noted herein portend well for future investigations of heteroaromatic chalcone synthesis.

Author Contributions

Conceptualization, A.M. and J.S.; writing—original draft preparation, A.M. and J.S.; writing—review and editing, A.M. and J.S.; visualization, A.M. and J.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Molecules 28 03201 g001 550
Figure 1. Chalcone structure and stereochemistry.
Figure 1. Chalcone structure and stereochemistry.
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Molecules 28 03201 g002 550
Figure 2. Medicinally and industrially important heteroaromatic hybrid chalcones.
Figure 2. Medicinally and industrially important heteroaromatic hybrid chalcones.
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Molecules 28 03201 g003 550
Figure 3. Heteroaromatic hybrid chalcone construction.
Figure 3. Heteroaromatic hybrid chalcone construction.
Molecules 28 03201 g003
Molecules 28 03201 sch001 550
Scheme 1. Synthesis of pyrrolyl chalcone.
Scheme 1. Synthesis of pyrrolyl chalcone.
Molecules 28 03201 sch001
Molecules 28 03201 sch002 550
Scheme 2. Synthesis of furyl chalcone.
Scheme 2. Synthesis of furyl chalcone.
Molecules 28 03201 sch002
Molecules 28 03201 sch003 550
Scheme 3. Synthesis of furyl chalcone derivatives.
Scheme 3. Synthesis of furyl chalcone derivatives.
Molecules 28 03201 sch003
Molecules 28 03201 sch004 550
Scheme 4. Synthesis of thienyl chalcone.
Scheme 4. Synthesis of thienyl chalcone.
Molecules 28 03201 sch004
Molecules 28 03201 sch005 550
Scheme 5. Synthesis of pyridyl chalcone.
Scheme 5. Synthesis of pyridyl chalcone.
Molecules 28 03201 sch005
Molecules 28 03201 sch006 550
Scheme 6. Synthesis of thiazolyl chalcones.
Scheme 6. Synthesis of thiazolyl chalcones.
Molecules 28 03201 sch006
Molecules 28 03201 sch007 550
Scheme 7. Synthesis of indolyl chalcones.
Scheme 7. Synthesis of indolyl chalcones.
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Molecules 28 03201 sch008 550
Scheme 8. Synthesis of benzimidazolyl chalcones.
Scheme 8. Synthesis of benzimidazolyl chalcones.
Molecules 28 03201 sch008
Molecules 28 03201 sch009 550
Scheme 9. Synthesis of thiazolyl and benzothiazolyl chalcones.
Scheme 9. Synthesis of thiazolyl and benzothiazolyl chalcones.
Molecules 28 03201 sch009
Molecules 28 03201 sch010 550
Scheme 10. Synthesis of benzofuryl chalcones.
Scheme 10. Synthesis of benzofuryl chalcones.
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Molecules 28 03201 sch011 550
Scheme 11. Synthesis of heteroaromatic dehydroabietic acid-chalcone hybrids.
Scheme 11. Synthesis of heteroaromatic dehydroabietic acid-chalcone hybrids.
Molecules 28 03201 sch011
Molecules 28 03201 sch012 550
Scheme 12. Green synthesis of pyridyl chalcone.
Scheme 12. Green synthesis of pyridyl chalcone.
Molecules 28 03201 sch012
Molecules 28 03201 sch013 550
Scheme 13. Green synthesis of furyl and thienyl chalcones.
Scheme 13. Green synthesis of furyl and thienyl chalcones.
Molecules 28 03201 sch013
Molecules 28 03201 sch014 550
Scheme 14. Green synthesis of 2-thienyl chalcones.
Scheme 14. Green synthesis of 2-thienyl chalcones.
Molecules 28 03201 sch014
Molecules 28 03201 sch015 550
Scheme 15. Microwave synthesis of 3-thienyl chalcones.
Scheme 15. Microwave synthesis of 3-thienyl chalcones.
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Molecules 28 03201 sch016 550
Scheme 16. Synthesis of quinolinyl chalcones.
Scheme 16. Synthesis of quinolinyl chalcones.
Molecules 28 03201 sch016
Molecules 28 03201 sch017 550
Scheme 17. Sonochemical synthesis of pyrazolopyridyl chalcones.
Scheme 17. Sonochemical synthesis of pyrazolopyridyl chalcones.
Molecules 28 03201 sch017
Molecules 28 03201 sch018 550
Scheme 18. PTSA-catalyzed synthesis of thienyl chalcone.
Scheme 18. PTSA-catalyzed synthesis of thienyl chalcone.
Molecules 28 03201 sch018
Molecules 28 03201 sch019 550
Scheme 19. Acid-catalyzed synthesis of thiazolyl chalcone.
Scheme 19. Acid-catalyzed synthesis of thiazolyl chalcone.
Molecules 28 03201 sch019
Molecules 28 03201 sch020 550
Scheme 20. Cu-based nanocatalyzed A3 synthesis of pyridyl- and benzopyridyl chalcones.
Scheme 20. Cu-based nanocatalyzed A3 synthesis of pyridyl- and benzopyridyl chalcones.
Molecules 28 03201 sch020
Molecules 28 03201 sch021 550
Scheme 21. Pyrrolyl chalcone synthesis.
Scheme 21. Pyrrolyl chalcone synthesis.
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Molecules 28 03201 sch022 550
Scheme 22. Furyl chalcone synthesis.
Scheme 22. Furyl chalcone synthesis.
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Molecules 28 03201 sch023 550
Scheme 23. Furyl, thienyl and pyridyl chalcone synthesis.
Scheme 23. Furyl, thienyl and pyridyl chalcone synthesis.
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Molecules 28 03201 sch024 550
Scheme 24. Pyrazolyl chalcone synthesis.
Scheme 24. Pyrazolyl chalcone synthesis.
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Molecules 28 03201 sch025 550
Scheme 25. Pyrrolyl chalcone synthesis.
Scheme 25. Pyrrolyl chalcone synthesis.
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Molecules 28 03201 sch026 550
Scheme 26. Indolyl chalcone synthesis.
Scheme 26. Indolyl chalcone synthesis.
Molecules 28 03201 sch026
Molecules 28 03201 sch027 550
Scheme 27. Carbazolyl hybrid chalcone synthesis.
Scheme 27. Carbazolyl hybrid chalcone synthesis.
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Molecules 28 03201 sch028 550
Scheme 28. Quinolinyl hybrid chalcone synthesis.
Scheme 28. Quinolinyl hybrid chalcone synthesis.
Molecules 28 03201 sch028
Molecules 28 03201 sch029 550
Scheme 29. Quinoxalinyl hybrid chalcone synthesis.
Scheme 29. Quinoxalinyl hybrid chalcone synthesis.
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Molecules 28 03201 g004 550
Figure 4. Hybrid chalcone heteroaromatic components prepared by Sun et al.
Figure 4. Hybrid chalcone heteroaromatic components prepared by Sun et al.
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Molecules 28 03201 sch030 550
Scheme 30. N, O, S Fused-ring heteroaromatic hybrid chalcone synthesis.
Scheme 30. N, O, S Fused-ring heteroaromatic hybrid chalcone synthesis.
Molecules 28 03201 sch030
Molecules 28 03201 sch031a 550Molecules 28 03201 sch031b 550
Scheme 31. Green syntheses of B-ring heteroaromatic hybrid chalcones.
Scheme 31. Green syntheses of B-ring heteroaromatic hybrid chalcones.
Molecules 28 03201 sch031aMolecules 28 03201 sch031b
Molecules 28 03201 sch032 550
Scheme 32. Synthesis of pyrazole hybrid Z-chalcones via a pyrilium.ring-opening dipolar addition.
Scheme 32. Synthesis of pyrazole hybrid Z-chalcones via a pyrilium.ring-opening dipolar addition.
Molecules 28 03201 sch032
Molecules 28 03201 sch033 550
Scheme 33. Synthesis of furanyl hybrid Z-chalcones via pyrilium ring-opening benzil-derivative reductive 3+2 annulation.
Scheme 33. Synthesis of furanyl hybrid Z-chalcones via pyrilium ring-opening benzil-derivative reductive 3+2 annulation.
Molecules 28 03201 sch033
Molecules 28 03201 sch034 550
Scheme 34. Synthesis of pyrrolyl–thienyl hybrid chalcones.
Scheme 34. Synthesis of pyrrolyl–thienyl hybrid chalcones.
Molecules 28 03201 sch034
Molecules 28 03201 sch035 550
Scheme 35. Synthesis of thiazolyl–furyl hybrid chalcones.
Scheme 35. Synthesis of thiazolyl–furyl hybrid chalcones.
Molecules 28 03201 sch035
Molecules 28 03201 sch036 550
Scheme 36. Synthesis of pyridyl– and thienyl–carbazole hybrid chalcones.
Scheme 36. Synthesis of pyridyl– and thienyl–carbazole hybrid chalcones.
Molecules 28 03201 sch036
Molecules 28 03201 sch037 550
Scheme 37. Synthesis of pyridyl–quinoxazolyl hybrid chalcone.
Scheme 37. Synthesis of pyridyl–quinoxazolyl hybrid chalcone.
Molecules 28 03201 sch037
Molecules 28 03201 sch038 550
Scheme 38. Synthesis of pyrrole–[(2-pyrrolyl)-3H-pyrrolizinyl] hybrid chalcone.
Scheme 38. Synthesis of pyrrole–[(2-pyrrolyl)-3H-pyrrolizinyl] hybrid chalcone.
Molecules 28 03201 sch038
Molecules 28 03201 sch039 550
Scheme 39. Synthesis of pyrazinyl hybrid chalcones.
Scheme 39. Synthesis of pyrazinyl hybrid chalcones.
Molecules 28 03201 sch039
Molecules 28 03201 sch040 550
Scheme 40. Synthesis of furyl–triazolyl hybrid chalcones.
Scheme 40. Synthesis of furyl–triazolyl hybrid chalcones.
Molecules 28 03201 sch040
Molecules 28 03201 sch041 550
Scheme 41. Synthesis of pyrrolyl–pyridyl hybrid chalcones.
Scheme 41. Synthesis of pyrrolyl–pyridyl hybrid chalcones.
Molecules 28 03201 sch041
Molecules 28 03201 sch042 550
Scheme 42. Synthesis of thienyl–pyrazolyl/carbazolyl hybrid chalcones.
Scheme 42. Synthesis of thienyl–pyrazolyl/carbazolyl hybrid chalcones.
Molecules 28 03201 sch042
Molecules 28 03201 sch043 550
Scheme 43. Synthesis of quinolinyl–pyridyl/thienyl hybrid chalcones.
Scheme 43. Synthesis of quinolinyl–pyridyl/thienyl hybrid chalcones.
Molecules 28 03201 sch043
Molecules 28 03201 sch044 550
Scheme 44. Synthesis of pyrazolopyridyl–heteroaryl hybrid chalcones.
Scheme 44. Synthesis of pyrazolopyridyl–heteroaryl hybrid chalcones.
Molecules 28 03201 sch044
Molecules 28 03201 sch045 550
Scheme 45. Synthesis of twin indolyl hybrid chalcones.
Scheme 45. Synthesis of twin indolyl hybrid chalcones.
Molecules 28 03201 sch045
Molecules 28 03201 sch046 550
Scheme 46. Synthesis of twin thienyl hybrid chalcone.
Scheme 46. Synthesis of twin thienyl hybrid chalcone.
Molecules 28 03201 sch046
Molecules 28 03201 sch047 550
Scheme 47. Synthesis of bis thienyl hybrid chalcones.
Scheme 47. Synthesis of bis thienyl hybrid chalcones.
Molecules 28 03201 sch047
Molecules 28 03201 sch048 550
Scheme 48. Synthesis of biphenyl bis thienyl and pyridyl bis aryl hybrid chalcones.
Scheme 48. Synthesis of biphenyl bis thienyl and pyridyl bis aryl hybrid chalcones.
Molecules 28 03201 sch048
Molecules 28 03201 sch049 550
Scheme 49. Synthesis of indolyl bis aryl hybrid chalcones.
Scheme 49. Synthesis of indolyl bis aryl hybrid chalcones.
Molecules 28 03201 sch049
Molecules 28 03201 sch050 550
Scheme 50. Sonochemical synthesis of bis thienyl and bis furyl hybrid chalcones.
Scheme 50. Sonochemical synthesis of bis thienyl and bis furyl hybrid chalcones.
Molecules 28 03201 sch050
Molecules 28 03201 sch051 550
Scheme 51. Microwave-mediated synthesis of bis aryl/heteroaryl chalcone pyrazoles.
Scheme 51. Microwave-mediated synthesis of bis aryl/heteroaryl chalcone pyrazoles.
Molecules 28 03201 sch051
Molecules 28 03201 sch052 550
Scheme 52. Wittig synthesis of bis thienyl and bis furyl hybrid chalcones.
Scheme 52. Wittig synthesis of bis thienyl and bis furyl hybrid chalcones.
Molecules 28 03201 sch052
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Mallia, A.; Sloop, J. Advances in the Synthesis of Heteroaromatic Hybrid Chalcones. Molecules 2023, 28, 3201. https://doi.org/10.3390/molecules28073201

AMA Style

Mallia A, Sloop J. Advances in the Synthesis of Heteroaromatic Hybrid Chalcones. Molecules. 2023; 28(7):3201. https://doi.org/10.3390/molecules28073201

Chicago/Turabian Style

Mallia, Ajay, and Joseph Sloop. 2023. "Advances in the Synthesis of Heteroaromatic Hybrid Chalcones" Molecules 28, no. 7: 3201. https://doi.org/10.3390/molecules28073201

APA Style

Mallia, A., & Sloop, J. (2023). Advances in the Synthesis of Heteroaromatic Hybrid Chalcones. Molecules, 28(7), 3201. https://doi.org/10.3390/molecules28073201

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