Synthesis of Antifungal Heterocycle-Containing Mannich Bases: A Comprehensive Review

: Mannich bases are a class of organic compounds usually obtained by the condensation reaction between an amine, a compound with active hydrogens, and an aldehyde. They are versatile intermediates in organic synthesis, and those compounds containing this motif ﬁnd applications in pharmaceutical, agrochemical, and even material ﬁelds since they are widely known for their wide range of biological activities, including antimicrobial properties. Thus, as part of our interest in antifungal agents, this narrative review aimed to gather information from the literature on the synthesis of various representative Mannich-base-containing compounds, particularly centered on those exhibiting antifungal properties. In this context, the compilation indicated that Mannich bases could be considered as a relevant toxophore/pharmacophore by incorporating heterocyclic moieties to be implemented for the design of new antifungal agents, given its proven efﬁcacy against phytopathogens, other opportunistic human pathogens, and some dermatophytic fungal species, which can be further exploited as agrochemical agents or in medicinal applications to treat fungal infections. The antifungal effect exhibited by Mannich bases conjugated with oxa and/or aza-heterocycles suggests that compounds that have a heterocyclic system attached to the β -amino core are attractive alternatives oriented to the synthesis of novel and helpful antifungal agents.


Introduction
Mannich bases are structurally defined as 2-amino-ketones, compounds that contain the NCH 2 Y fragment with a central electrophilic carbon atom in the presence of two geminal heteroatoms, one of which is nitrogen.Mannich bases have been explored for their potential biological properties in drug design, especially O-Mannich bases (>NCH 2 OR) or N-Mannich bases (>NCH 2 NR 1 R 2 ) [1,2].They are usually formed from the condensation of an amine, a non-enolizable aldehyde (e.g., formaldehyde (HCOH)), and a hydrogenactive compound (Scheme 1).This reaction, consisting of the nucleophilic addition of the non-enolizable aldehyde and any primary or secondary amine to form a resonancestabilized imine intermediate (iminium ion or imine salt), is known as the Mannich reaction.A carbanion of an acid compound with active hydrogens (e.g., any enolizable carbonyl compound, amide, carbamate, hydantoin, or urea) favors an attack on the imine, giving rise to the formation of the Mannich base.The Mannich reaction has been proposed in several alkaloid biosynthetic pathways.Furthermore, it is one of organic synthesis's most versatile carbon-carbon bond formation methodologies [3][4][5].

Introduction
Mannich bases are structurally defined as 2-amino-ketones, compounds that contain the NCH2Y fragment with a central electrophilic carbon atom in the presence of two geminal heteroatoms, one of which is nitrogen.Mannich bases have been explored for their potential biological properties in drug design, especially O-Mannich bases (>NCH2OR) or N-Mannich bases (>NCH2NR 1 R 2 ) [1,2].They are usually formed from the condensation of an amine, a non-enolizable aldehyde (e.g., formaldehyde (HCOH)), and a hydrogen-active compound (Scheme 1).This reaction, consisting of the nucleophilic addition of the non-enolizable aldehyde and any primary or secondary amine to form a resonance-stabilized imine intermediate (iminium ion or imine salt), is known as the Mannich reaction.A carbanion of an acid compound with active hydrogens (e.g., any enolizable carbonyl compound, amide, carbamate, hydantoin, or urea) favors an attack on the imine, giving rise to the formation of the Mannich base.The Mannich reaction has been proposed in several alkaloid biosynthetic pathways.Furthermore, it is one of organic synthesis's most versatile carbon-carbon bond formation methodologies [3][4][5].
Mannich bases are well recognized as pivotal pharmacophores and bioactive scaffolds, often utilized in the synthesis of potential medicinal agents featuring aminoalkyl chains [14].These Mannich bases exhibit a wide array of promising properties, encompassing anti-inflammatory, anticancer, antifilarial, antibacterial, antifungal, anticonvulsant, anthelmintic, antituberculous, analgesic, anti-HIV, antimalarial, antipsychotic, and antiviral effects, among others.Beyond their biological roles, Mannich bases are valued for their incorporation into detergents, resins, polymers, and surfactants.Noteworthy instances of clinically relevant Mannich bases containing aminoalkyl chains encompass fluoxetine, atropine, ethacrynic acid, trihexyphenidyl, procyclidine, ranitidine, and biperiden-illustrating their pivotal contributions to pharmaceutical chemistry, both as bioactive compounds and as building blocks in synthesis [15].
Given the relevance involved in controlling fungal infections, particularly opportunistic human and animal pathogens and even plant pathogens that affect crops of economic importance in agriculture, several reports have demonstrated the use of Mannich bases and their potential as antifungal agents, some obtained from natural products [16][17][18][19][20].In this regard, thymol, a natural monoterpene phenol derived from cymene, used to treat the respiratory, nervous, and cardiovascular systems [21] and protect food from phytopathogens, has been recently used to produce a series of derivatives, including some Schiff and Mannich bases, and assessed against insects [22].These derivatives were also analyzed under in vitro conditions, identifying their potential as antifungals against three pathogenic fungi of maize, Fusarium moniliforme, Rhizoctonia solani, and Dreschlera maydis, showing promising results for controlling D. maydis.Studies under greenhouse conditions showed that thymol significantly controlled the leaf blight disease of corn, so it can be considered an alternative to synthetic fungicides and pesticides in cereal crops [23].Recently, Legesse et al. used knipholone (a compound of natural origin isolated from Kniphofia foliosa hochst, which possesses a structure based on anthraquinone [24]) as the precursor of a series of Mannich bases, which showed high solubility and potential antimicrobial activity against eight pathogenic bacterial and fungal strains.The potential MIC values of the fungus Trichophyton mentagrophytes were around 78.2 µg/mL, evidencing the potential biological activities of these aminoalkyl derivatives of knipholone [25].Thus, several studies have demonstrated the influence of the chemical structure of Mannich bases and their potential use in the chemical control of opportunistic fungal pathogens.
With these considerations in mind, the current review was constructed based on three significant motivations centered around identified gaps: (1) compiling information particularly centered on those Mannich bases that have antifungal activity against different fungal microorganisms with relevance in the agricultural and medicinal sectors since there is no review dedicated to this topic, (2) providing a valuable perspective by gathering those antifungal Mannich bases that are conjugated with different heterocyclic moieties since there is a lack of such a perspective in the existing literature, and (3) summarizing the main contributions in synthesizing antifungal heterocycle-containing Mannich as a helpful survey on the different synthetic strategies to produce this kind of bioactive agents.Based on these motivations, this review encompasses the period from 2000 to 2023, and it emerges from a comprehensive, non-systematic search across various databases (Scopus, Web of Science, PubMed consulted in Cajicá, Colombia) to aggregate the relevant sources.A meticulous analysis of the compiled information narrows the focus to heterocyclicbased Mannich bases, categorized into three subsections: oxygen-containing heterocycles, nitrogen-containing heterocycles, and heterocyclic systems with mixed heteroatoms.and it emerges from a comprehensive, non-systematic search across various databases (Scopus, Web of Science, PubMed consulted in Cajicá, Colombia) to aggregate the relevant sources.A meticulous analysis of the compiled information narrows the focus to heterocyclic-based Mannich bases, categorized into three subsections: oxygen-containing heterocycles, nitrogen-containing heterocycles, and heterocyclic systems with mixed heteroatoms.).The minimum inhibitory concentrations (MICs) of these compounds were performed through the serial plate dilution method using ofloxacin and ketoconazole as standard drugs.Some test products exhibited weaker antifungal activity than ketoconazole, with higher MIC values.Others failed to match the ketoconazole inhibitory activity even at higher concentrations.Structure-activity relationship considerations identified that the presence of chlorine at position 2 of the aromatic ring, coupled with a chlorobromine-substituted coumarin moiety, was pivotal for activity against certain fungi.Remarkably, these compounds demonstrated more potent antifungal activity than ketoconazole against P. citrinum [28].).The minimum inhibitory concentrations (MICs) of these compounds were performed through the serial plate dilution method using ofloxacin and ketoconazole as standard drugs.Some test products exhibited weaker antifungal activity than ketoconazole, with higher MIC values.Others failed to match the ketoconazole inhibitory activity even at higher concentrations.Structure-activity relationship considerations identified that the presence of chlorine at position 2 of the aromatic ring, coupled with a chlorobromine-substituted coumarin moiety, was pivotal for activity against certain fungi.Remarkably, these compounds demonstrated more potent antifungal activity than ketoconazole against P. citrinum [28].Continuing their studies, Yang et al. obtained sixteen novel derivatives via a cyclization methodology.They treated 7 with nitric acid and then reacted it with aromatic 1,2diamine (Scheme 5).These derivatives were also evaluated for antifungal activity against phytopathogenic fungi.Interestingly, most compounds exhibited reduced antifungal activity compared to the precursor 7, contrary to prior findings for Mannich bases.While none displayed antifungal activity against Alternaria solani, certain compounds showed better inhibitory activity against Fusarium solani.Specifically, compounds 12 and 13 demonstrated the highest inhibitory activity against F. solani.These findings suggested that introducing a monosubstituted benzene ring with electron-withdrawing groups (EWG) might lead to potential antifungal compounds [32].

Allylphenol Derivatives
Obovatol, 7, a natural dimeric allylphenol isolated from various sources, possesses antioxidant, antiplatelet, antifungal, and anti-inflammatory properties.Recent investigations have examined Mannich base derivatives of 7 as plausible fungicides (Scheme 4).These derivatives, obtained through C-4-amino methylation of 7, were evaluated for inhibitory effects on spore germination and mycelial growth against phytopathogenic fungi.Notably, compounds 8 and 9 significantly inhibited Botrytis cinerea spore germination, while compounds 10, 11, and 9 exhibited a potent inhibition of B. cinerea mycelial growth.The structure-activity relationship analysis indicated that certain substituents at the C-4 position of 7 led to more potent antifungal derivatives.Chlorine substitution and chlorobrominesubstituted coumarin residues were particularly effective [29][30][31].Continuing their studies, Yang et al. obtained sixteen novel derivatives via a cy tion methodology.They treated 7 with nitric acid and then reacted it with aromat diamine (Scheme 5).These derivatives were also evaluated for antifungal activity a phytopathogenic fungi.Interestingly, most compounds exhibited reduced antifung tivity compared to the precursor 7, contrary to prior findings for Mannich bases.none displayed antifungal activity against Alternaria solani, certain compounds sh better inhibitory activity against Fusarium solani.Specifically, compounds 12 an demonstrated the highest inhibitory activity against F. solani.These findings sugg that introducing a monosubstituted benzene ring with electron-withdrawing g (EWG) might lead to potential antifungal compounds [32].Continuing their studies, Yang et al. obtained sixteen novel derivatives via a cyclization methodology.They treated 7 with nitric acid and then reacted it with aromatic 1,2-diamine (Scheme 5).These derivatives were also evaluated for antifungal activity against phytopathogenic fungi.Interestingly, most compounds exhibited reduced antifungal activity compared to the precursor 7, contrary to prior findings for Mannich bases.While none displayed antifungal activity against Alternaria solani, certain compounds showed better inhibitory activity against Fusarium solani.Specifically, compounds 12 and 13 demonstrated the highest inhibitory activity against F. solani.These findings suggested that introducing a monosubstituted benzene ring with electron-withdrawing groups (EWG) might lead to potential antifungal compounds [32].Continuing their studies, Yang et al. obtained sixteen novel derivatives via a cy tion methodology.They treated 7 with nitric acid and then reacted it with aromat diamine (Scheme 5).These derivatives were also evaluated for antifungal activity ag phytopathogenic fungi.Interestingly, most compounds exhibited reduced antifung tivity compared to the precursor 7, contrary to prior findings for Mannich bases.none displayed antifungal activity against Alternaria solani, certain compounds sh better inhibitory activity against Fusarium solani.Specifically, compounds 12 an demonstrated the highest inhibitory activity against F. solani.These findings sugg that introducing a monosubstituted benzene ring with electron-withdrawing g (EWG) might lead to potential antifungal compounds [32].).These oxazine flavonoids exhibited broad-spectrum fungicidal activities against several plant pathogenic fungi.Some compounds displayed excellent bioactivities against specific fungal phytopathogens, so introducing the oxazine motif in these adducts provided better activity.In addition, the position of the substituents on the benzene ring influenced fungicidal activity.In this regard, the EWG substituents on the benzene ring generally enhanced inhibitory activity [33][34][35].
Organics 2023, 4, FOR PEER REVIEW 2.1.3.Flavonoid Derivatives Flavonoids, a class of polyhydroxyphenolic natural products, are characterized the flavan nucleus (2-aryl-2H-chromene).They are abundant in fruits, vegetables, plant-based beverages and are known for their various antioxidant, antibacterial, and a inflammatory properties.Flavonoids have shown promise in synergistic combina therapy with conventional drugs against fungal pathogens, addressing the rising d resistance in fungal infections.A series of oxazine flavonoids were synthesized by M al. through a double Mannich reaction cyclization (Scheme 6).These oxazine flavon exhibited broad-spectrum fungicidal activities against several plant pathogenic fu Some compounds displayed excellent bioactivities against specific fungal phytopa gens, so introducing the oxazine motif in these adducts provided better activity.In a tion, the position of the substituents on the benzene ring influenced fungicidal activit this regard, the EWG substituents on the benzene ring generally enhanced inhibitory tivity [33][34][35].Kojic acid, 21, is a heterocyclic compound of natural origin having a 4H-pyran-4 moiety, which can be obtained from several fungal fermentations.It is usually used depigmentation product, mainly attributed to tyrosinase inhibition.Antioxidant, anti terial, and anti-inflammatory activities have also been reported [36].Aytemir et al. thesized a series of compounds related to 22 from 21 (Scheme 7).The antifungal acti of these derivatives against dermatophyte fungi such as Microsporum gypseum, chophyton mentagrophytes varerinacei, and Epidermophyton floccosum was evaluated, sh ing that some derivatives showed high activity against E. floccosum (MIC: 4 µg/mL).current activity of the starting material chlorokojic acid (MIC: 8 µg/mL) was increase these Mannich bases.According to the cytotoxicity assessment, Mannich bases were found to be active as chlorokojic acid but safer (MNTC: ≥512 µg/mL and ≥256 µg/mL).activity against E. floccosum was found to range between 4 and 8 µg/mL, showing action compared with the chlorinated precursor (MIC: 8-16 µg/mL).Regarding the a dermatophytic activity against M. gypseum, the MIC values were around 4 µg/mL.T results confirmed the enhancing effect of Mannich bases on biologically active heterocy natural compounds [37].

4H-Pyran-4-one Derivatives
Kojic acid, 21, is a heterocyclic compound of natural origin having a 4H-pyran-4-one moiety, which can be obtained from several fungal fermentations.It is usually used as a depigmentation product, mainly attributed to tyrosinase inhibition.Antioxidant, antibacterial, and anti-inflammatory activities have also been reported [36].Aytemir et al. synthesized a series of compounds related to 22 from 21 (Scheme 7).The antifungal activity of these derivatives against dermatophyte fungi such as Microsporum gypseum, Trichophyton mentagrophytes varerinacei, and Epidermophyton floccosum was evaluated, showing that some derivatives showed high activity against E. floccosum (MIC: 4 µg/mL).The current activity of the starting material chlorokojic acid (MIC: 8 µg/mL) was increased by these Mannich bases.According to the cytotoxicity assessment, Mannich bases were also found to be active as chlorokojic acid but safer (MNTC: ≥512 µg/mL and ≥256 µg/mL).The activity against E. floccosum was found to range between 4 and 8 µg/mL, showing high action compared with the chlorinated precursor (MIC: 8-16 µg/mL).Regarding the antidermatophytic activity against M. gypseum, the MIC values were around 4 µg/mL.These results confirmed the enhancing effect of Mannich bases on biologically active heterocyclic natural compounds [37].Within small heterocyclic systems, the 2-azetidinone structural core is exceptionally versatile and helpful and has appeared in many widely used biologically active chemical compounds [38].Some 2-azetidinone derivatives have shown potent ability as cephalosporinase and ezetimibe inhibitors, cholesterol absorption inhibitors, mechanism-based inhibitors of various enzymes such as human tryptase, chymase, thrombin, leukocyte elastase, protease of the human cytomegalovirus, and the enzyme serine protease.In addition, its antituberculous, anti-inflammatory, antitumor, anti-HIV, antiparkinsonian, antidiabetic, antimicrobial, and antifungal activities have been described [39].Mannich bases derived containing the 2-azetidinone motif ( 23) have recently been synthesized (Scheme 8), and their antimicrobial activity was also evaluated, whose outcome involved significant bioactivity.In particular, the activity of 23a, 23b, 23c, and 23d was comparable to that of the standard antibiotics commonly employed.Compound 23d with the N-methylpiperazine substituent showed a satisfactory result, allowing them to infer that the presence of the halogen and methoxy groups in position 4 and also that the presence of the N-CH3 group in the piperazine ring improved the tested biological activities [40].

Azole Derivatives
Heterocyclic compounds such as imidazoles and benzimidazoles have distinctive roles in the scope of chemistry and pharmacology due to their versatile properties.They exhibit a wide array of bioactivities, encompassing antibacterial, anticancer, antituberculosis, analgesic, anti-HIV, and antifungal effects [41,42].This class of derivatives has demonstrated potential in inhibiting various agriculturally relevant fungi, including Fusarium oxysporum, Rhizoctonia solani, Botrytis cinerea Pers, Gibberella zeae, Dothiorella gregaria, and Colletotrichum gossypii [43].In a notable study by Roman et al., a series of βaminoketone Mannich bases were synthesized through the N-alkylation of imidazole with 3-dimethylamino-1-aryl-1-propanone hydrochloride, 24 (Scheme 9).The antifungal potency of these compounds was assessed against sixteen Candida strains.Particularly, 3-

Nitrogen-Heterocycle Derivatives 2.2.1. 2-Azetidinone Derivatives
Within small heterocyclic systems, the 2-azetidinone structural core is exceptionally versatile and helpful and has appeared in many widely used biologically active chemical compounds [38].Some 2-azetidinone derivatives have shown potent ability as cephalosporinase and ezetimibe inhibitors, cholesterol absorption inhibitors, mechanismbased inhibitors of various enzymes such as human tryptase, chymase, thrombin, leukocyte elastase, protease of the human cytomegalovirus, and the enzyme serine protease.In addition, its antituberculous, anti-inflammatory, antitumor, anti-HIV, antiparkinsonian, antidiabetic, antimicrobial, and antifungal activities have been described [39].Mannich bases derived containing the 2-azetidinone motif ( 23) have recently been synthesized (Scheme 8), and their antimicrobial activity was also evaluated, whose outcome involved significant bioactivity.In particular, the activity of 23a, 23b, 23c, and 23d was comparable to that of the standard antibiotics commonly employed.Compound 23d with the N-methylpiperazine substituent showed a satisfactory result, allowing them to infer that the presence of the halogen and methoxy groups in position 4 and also that the presence of the N-CH 3 group in the piperazine ring improved the tested biological activities [40].Within small heterocyclic systems, the 2-azetidinone structural core is exceptionally versatile and helpful and has appeared in many widely used biologically active chemical compounds [38].Some 2-azetidinone derivatives have shown potent ability as cephalosporinase and ezetimibe inhibitors, cholesterol absorption inhibitors, mechanism-based inhibitors of various enzymes such as human tryptase, chymase, thrombin, leukocyte elastase, protease of the human cytomegalovirus, and the enzyme serine protease.In addition, its antituberculous, anti-inflammatory, antitumor, anti-HIV, antiparkinsonian, antidiabetic, antimicrobial, and antifungal activities have been described [39].Mannich bases derived containing the 2-azetidinone motif (23) have recently been synthesized (Scheme 8), and their antimicrobial activity was also evaluated, whose outcome involved significant bioactivity.In particular, the activity of 23a, 23b, 23c, and 23d was comparable to that of the standard antibiotics commonly employed.Compound 23d with the N-methylpiperazine substituent showed a satisfactory result, allowing them to infer that the presence of the halogen and methoxy groups in position 4 and also that the presence of the N-CH3 group in the piperazine ring improved the tested biological activities [40].

Azole Derivatives
Heterocyclic compounds such as imidazoles and benzimidazoles have distinctive roles in the scope of chemistry and pharmacology due to their versatile properties.They exhibit a wide array of bioactivities, encompassing antibacterial, anticancer, antituberculosis, analgesic, anti-HIV, and antifungal effects [41,42].This class of derivatives has demonstrated potential in inhibiting various agriculturally relevant fungi, including Fusarium oxysporum, Rhizoctonia solani, Botrytis cinerea Pers, Gibberella zeae, Dothiorella gregaria, and Colletotrichum gossypii [43].In a notable study by Roman et al., a series of βaminoketone Mannich bases were synthesized through the N-alkylation of imidazole with 3-dimethylamino-1-aryl-1-propanone hydrochloride, 24 (Scheme 9).The antifungal potency of these compounds was assessed against sixteen Candida strains.Particularly, 3-

Azole Derivatives
Heterocyclic compounds such as imidazoles and benzimidazoles have distinctive roles in the scope of chemistry and pharmacology due to their versatile properties.They exhibit a wide array of bioactivities, encompassing antibacterial, anticancer, antituberculosis, analgesic, anti-HIV, and antifungal effects [41,42].This class of derivatives has demonstrated potential in inhibiting various agriculturally relevant fungi, including Fusarium oxysporum, Rhizoctonia solani, Botrytis cinerea Pers, Gibberella zeae, Dothiorella gregaria, and Colletotrichum gossypii [43].

Quinoline Derivatives
Quinoline is a bicyclic heteroaromatic compound consisting of a six-membered benzene ring fused with pyridine, reported as an essential component in chemistry and medicine.Their quaternary ammonium salt can be used to synthesize multiple derivatives [57].They have been demonstrated to have high biological potential due to their anticancer, antimycobacterial, antimicrobial, anticonvulsant, anti-inflammatory, cardiovascular, antibacterial, antifungal, and antiviral activities, among others reported [58,59].Patel reported the multicomponent synthesis of several Mannich bases, 35, with a quinoline moiety in good yield using a methodology under solvent-free conditions (Scheme 15).Thus, 2,4-dihydroxybenzophenone, a chlorinated derivative from quinoline-3-carboxaldehyde, various amines, and ethylammonium nitrate (EAN) were mixed at 80 °C.The products were in vitro explored against Gram-positive and Gram-negative bacteria and fungi, demonstrating that all compounds showed excellent antifungal activity against C. albicans and A. niger, even though some were more potent than nystatin and griseofulvin [60].Scheme 14. Synthesis of pipemidic acid derivatives.

Quinoline Derivatives
Quinoline is a bicyclic heteroaromatic compound consisting of a six-membered benzene ring fused with pyridine, reported as an essential component in chemistry and medicine.Their quaternary ammonium salt can be used to synthesize multiple derivatives [57].They have been demonstrated to have high biological potential due to their anticancer, antimycobacterial, antimicrobial, anticonvulsant, anti-inflammatory, cardiovascular, antibacterial, antifungal, and antiviral activities, among others reported [58,59].Patel reported the multicomponent synthesis of several Mannich bases, 35, with a quinoline moiety in good yield using a methodology under solvent-free conditions (Scheme 15).Thus, 2,4-dihydroxybenzophenone, a chlorinated derivative from quinoline-3-carboxaldehyde, various amines, and ethylammonium nitrate (EAN) were mixed at 80 • C. The products were in vitro explored against Gram-positive and Gram-negative bacteria and fungi, demonstrating that all compounds showed excellent antifungal activity against C. albicans and A. niger, even though some were more potent than nystatin and griseofulvin [60].For their part, Shehab et al. synthesized several Mannich bases derived from quinolinol, 36 (Scheme 16), which were evaluated using in vitro experiments against relevant microorganisms.The antimicrobial bioassay outcome suggested that most synthesized compounds showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli.However, most compounds showed suitable activities against the evaluated fungi.In such a case, the most active compounds against Aspergillus niger and Penicillium sp.exhibited MIC values ranging from 0.25 to 2.5 mg/mL [61].For their part, Shehab et al. synthesized several Mannich bases derived from quinolinol, 36 (Scheme 16), which were evaluated using in vitro experiments against relevant microorganisms.The antimicrobial bioassay outcome suggested that most synthesized compounds showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli.However, most compounds showed suitable activities against the evaluated fungi.In such a case, the most active compounds against Aspergillus niger and Penicillium sp.exhibited MIC values ranging from 0.25 to 2.5 mg/mL [61].
For their part, Shehab et al. synthesized several Mannich bases derived from quinolinol, 36 (Scheme 16), which were evaluated using in vitro experiments against relevant microorganisms.The antimicrobial bioassay outcome suggested that most synthesized compounds showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli.However, most compounds showed suitable activities against the evaluated fungi.In such a case, the most active compounds against Aspergillus niger and Penicillium sp.exhibited MIC values ranging from 0.25 to 2.5 mg/mL [61].
Scheme 16.Synthesis of Mannich bases derivated from 8-hydroxyquinoline 2.2.5.Pyrrole Derivatives Pterolactam, also recognized as 5-methoxypyrrolidin-2-one, represents a heterocyclic compound naturally occurring within the leaves of ferns, specifically Phyteuma japonicum [62].Dascalu et al. devised, synthesized, and evaluated the antifungal activities of a pterolactam-derived Mannich base series, namely 37 and 38, against nine fungal strains and three non-albicans Candida yeast species.These compounds were synthesized employing a solvent-free protocol at 80 °C by maintaining a mixture of pterolactam, CsF, and the nucleophile.Under these conditions, N,O-, N,S-acetals, and N,N′-aminals were produced with varying yields, ranging from moderate to excellent (Scheme 17).The inhibitory potential of these derivatives was assessed against a comprehensive spectrum of fungal and yeast strains.Based on structure-activity correlations, pterolactam N,N′-aminals demonstrated heightened antimicrobial potency compared to N,O--or N,S-acetals.Moreover, aromatic compounds featuring a nitro group showed significant promise, particularly against F. solani.This selection highlighted compound 38a, characterized by R 1 = H and R 2 = 5-NO2-3-OMePh, combining pyrrolidin-2-one and 3-methoxy-5-nitroaniline moieties, as a versatile antifungal agent boasting fungicide-like attributes and negligible cytotoxicity [63].

Pyrrole Derivatives
Pterolactam, also recognized as 5-methoxypyrrolidin-2-one, represents a heterocyclic compound naturally occurring within the leaves of ferns, specifically Phyteuma japonicum [62].Dascalu et al. devised, synthesized, and evaluated the antifungal activities of a pterolactamderived Mannich base series, namely 37 and 38, against nine fungal strains and three non-albicans Candida yeast species.These compounds were synthesized employing a solvent-free protocol at 80 • C by maintaining a mixture of pterolactam, CsF, and the nucleophile.Under these conditions, N,O-, N,S-acetals, and N,N -aminals were produced with varying yields, ranging from moderate to excellent (Scheme 17).The inhibitory potential of these derivatives was assessed against a comprehensive spectrum of fungal and yeast strains.Based on structure-activity correlations, pterolactam N,N -aminals demonstrated heightened antimicrobial potency compared to N,Oor N,S-acetals.Moreover, aromatic compounds featuring a nitro group showed significant promise, particularly against F. solani.This selection highlighted compound 38a, characterized by R 1 = H and R 2 = 5-NO 2 -3-OMePh, combining pyrrolidin-2-one and 3-methoxy-5-nitroaniline moieties, as a versatile antifungal agent boasting fungicide-like attributes and negligible cytotoxicity [63].Isatin (39a) is a naturally occurring indole derivative (1H-indole-2,3-dione) renowned for its distinct structure and array of biological activities, manifesting both in natural settings and through laboratory synthesis, catering to diverse applications [64].With its adaptable structure, isatin is a valuable foundational material for generating an extensive spectrum of compounds with diverse functions.This quality has garnered significant attention in medicinal chemistry and organic synthesis as it is a pivotal building block for intricate molecular architectures [65].Serving as a precursor, it facilitates the creation of myriad biologically active compounds, pharmaceuticals, and dyes.Some of its derivatives stand out for their remarkable medicinal attributes, encompassing antiviral, antitumor, anti-inflammatory, and especially antimicrobial properties [66].In this sense, a set of nine N-Mannich bases was prepared from the corresponding Schiff bases of 4-(4′-chlorophenyl)-6-(4″-methylphenyl)-2-aminopyrimidine (40).The Schiff bases (41a-c) were formed by condensing 40 with isatin derivatives (39a-c), and, subsequently, the corresponding N-Mannich bases (42a-i) through the reaction of the isatin acidic imino moiety with symmetrical secondary amines (substituted with methyl, morpholine, or piperidine) and HCOH (Scheme 18).Conjugates were produced in moderate-to-good yields (47-91%) and subsequently evaluated against a panel of pathogenic bacteria and fungi (twentyeight and eight, respectively) [67].The target compounds displayed robust effectiveness against dermatophytes, including Microsporum gypseum, M. audouinii, and Trichophyton Scheme 17. Synthesis of pyrrolidin-2-one type compounds.

2-Oxoindole Derivatives
Isatin (39a) is a naturally occurring indole derivative (1H-indole-2,3-dione) renowned for its distinct structure and array of biological activities, manifesting both in natural settings and through laboratory synthesis, catering to diverse applications [64].With its adaptable structure, isatin is a valuable foundational material for generating an extensive spectrum of compounds with diverse functions.This quality has garnered significant attention in medicinal chemistry and organic synthesis as it is a pivotal building block for intricate molecular architectures [65].Serving as a precursor, it facilitates the creation of myriad biologically active compounds, pharmaceuticals, and dyes.Some of its derivatives stand out for their remarkable medicinal attributes, encompassing antiviral, antitumor, anti-inflammatory, and especially antimicrobial properties [66].In this sense, a set of nine N-Mannich bases was prepared from the corresponding Schiff bases of 4-(4 -chlorophenyl)-6-(4 -methylphenyl)-2-aminopyrimidine (40).The Schiff bases (41a-c) were formed by condensing 40 with isatin derivatives (39a-c), and, subsequently, the corresponding N-Mannich bases (42a-i) through the reaction of the isatin acidic imino moiety with symmetrical secondary amines (substituted with methyl, morpholine, or piperidine) and HCOH (Scheme 18).Conjugates were produced in moderate-to-good yields (47-91%) and subsequently evaluated against a panel of pathogenic bacteria and fungi (twenty-eight and eight, respectively) [67].The target compounds displayed robust effectiveness against dermatophytes, including Microsporum gypseum, M. audouinii, and Trichophyton mentagrophytes, with a minimum inhibitory concentration (MIC) below 10 µg/mL.In fact, six compounds displayed an equivalent potency (4.88 µg/mL) to that of clotrimazole (the reference antifungal agent), while one compound (42e) demonstrated heightened activity against M. audouinii (MIC = 2.44 µg/mL).19).The Schiff bases were synthesized by reacting isatin with substituted anilines.The compounds yielded in the range of 43 to 78% and were also assessed against six bacteria and three fungi [68].Within the array of synthesized Mannich bases, 45b exhibited a moderate antibacterial effect on B. subtilis, while 45a-d displayed a moderate response against P. aeruginosa.Regarding antifungal properties, 45e (hydrazone-containing Schiff base) and 45f (Mannich base from unmodified isatin) exhibited moderate-to-good antifungal effects on P. notatum (MIC = 6.25 and 12.5 µg/mL, respectively), while 45a and 45e moderately inhibited A. niger (MIC = 12.5 µg/mL).C. albicans was not inhibited by the test compounds (MIC > 50 µg/mL).A similar strategy was employed to produce a set of six 2,3-dihydro-2-oxo-1,3-disubstituted indoles (45a-f) through condensation between isatin Schiff bases 43a-e and unmodified isatin, 2-[(2,6-dichlorophenyl)amino]phenylacetic acid (44) and HCOH (Scheme 19).The Schiff bases were synthesized by reacting isatin with substituted anilines.The compounds yielded in the range of 43 to 78% and were also assessed against six bacteria and three fungi [68].Within the array of synthesized Mannich bases, 45b exhibited a moderate antibacterial effect on B. subtilis, while 45a-d displayed a moderate response against P. aeruginosa.Regarding antifungal properties, 45e (hydrazone-containing Schiff base) and 45f (Mannich base from unmodified isatin) exhibited moderate-to-good antifungal effects on P. notatum (MIC = 6.25 and 12.5 µg/mL, respectively), while 45a and 45e moderately inhibited A. niger (MIC = 12.5 µg/mL).C. albicans was not inhibited by the test compounds (MIC > 50 µg/mL).and three fungi [68].Within the array of synthesized Mannich bases, 45b exhibited a moderate antibacterial effect on B. subtilis, while 45a-d displayed a moderate response against P. aeruginosa.Regarding antifungal properties, 45e (hydrazone-containing Schiff base) and 45f (Mannich base from unmodified isatin) exhibited moderate-to-good antifungal effects on P. notatum (MIC = 6.25 and 12.5 µg/mL, respectively), while 45a and 45e moderately inhibited A. niger (MIC = 12.5 µg/mL).C. albicans was not inhibited by the test compounds (MIC > 50 µg/mL).This process, carried out under moderate conditions, resulted in commendable yields, thereby underscoring its industrial potential (Scheme 20).The in vitro antifungal efficacy of Mannich bases 46 and 47 was gauged by their mycelial growth inhibitory impact on several test fungi, including F. oxysporum, Cercospora arachidicola, Phytophthora piricola, and R. cerealis.Notably, compounds 46a-c exhibited superior inhibition against F. oxysporum when compared to tridimefon, with compound 46a standing out by maintaining inhibitory rates surpassing those of the commercial controls, i.e., tridimefon and chlorothalonil.The presence of a 4-chlorophenyl group (R 1 = Cl) consistently correlated with enhanced antifungal activity against F. oxysporum, while compounds 46d and 46e, with R 1 = F, R 2 = phenyl, and dimethylpyrimidyl, demonstrated heightened efficacy against Cercospora arachidicola.Encouragingly, all the tested compounds displayed remarkable antifungal activity against Phytophthora piricola, with those containing trifluoromethyl (R 1 = CF 3 ) displaying a distinct advantage.For R. cerealis, most compounds maintained robust inhibition rates ranging from 80.2% to 97.5%.Additionally, all the compounds exhibited commendable antifungal properties against A. solani and G. sanbinetti.Applying a comparative molecular field analysis (CoMFA) based on antifungal activity data established a 3D-QSAR model, highlighting steric and electrostatic fields as pivotal contributors to compound bioactivity.This insight can potentially guide the optimization of novel structures to develop more potent agrochemicals [69].This process, carried out under moderate conditions, resulted in commendable yields, thereby underscoring its industrial potential (Scheme 20).The in vitro antifungal efficacy of Mannich bases 46 and 47 was gauged by their mycelial growth inhibitory impact on several test fungi, including F. oxysporum, Cercospora arachidicola, Phytophthora piricola, and R. cerealis.Notably, compounds 46a-c exhibited superior inhibition against F. oxysporum when compared to tridimefon, with compound 46a standing out by maintaining inhibitory rates surpassing those of the commercial controls, i.e., tridimefon and chlorothalonil.The presence of a 4chlorophenyl group (R 1 = Cl) consistently correlated with enhanced antifungal activity against F. oxysporum, while compounds 46d and 46e, with R 1 = F, R 2 = phenyl, and dimethylpyrimidyl, demonstrated heightened efficacy against Cercospora arachidicola.Encouragingly, all the tested compounds displayed remarkable antifungal activity against Phytophthora piricola, with those containing trifluoromethyl (R 1 = CF3) displaying a distinct advantage.For R. cerealis, most compounds maintained robust inhibition rates ranging from 80.2% to 97.5%.Additionally, all the compounds exhibited commendable antifungal properties against A. solani and G. sanbinetti.Applying a comparative molecular field analysis (CoMFA) based on antifungal activity data established a 3D-QSAR model, highlighting steric and electrostatic fields as pivotal contributors to compound bioactivity.This insight can potentially guide the optimization of novel structures to develop more potent agrochemicals [69].The condensation between 5-(1-adamantyl)-4-phenyl-1,2,4-triazoline-3-thione and HCOH and 1-substituted piperazines produced the respective N-Mannich bases, 48.Adamantane-1-carbohydrazide, 49, was obtained via the extended heating of methyl adamantane-1-carboxylate with hydrazine.The reaction of compound 49 with phenyl isothiocyanate produced intermediate 1-(1-adamantylcarbonyl)-4-phenylthiosemicarbazide, 50, which was cyclized to 5-(1-adamantyl)-4-phenyl-1,2,4-triazoline-3-thione, 51, by heating in 10% aqueous sodium hydroxide.Compound 51 was condensed with the corresponding 1-substituted piperazine and ethanol/HCOH solution to produce the corresponding N-Mannich bases, 48, in good yields (Scheme 21).The outcome of this reaction was found to be influenced by the substituent nature, reaction solvent, temperature, and the presence of a catalyst.Notably, polar protic solvents such as ethanol in the presence of strong alkaline agents favored the formation of S-alkyl derivatives as the main products, with N-alkyl derivatives having lower yields.The synthesized compounds underwent a comprehensive antimicrobial evaluation against a range of Gram-positive bacteria, Gram-negative bacteria, and C. albicans.The antimicrobial activity was found to be influenced by the nature of the 4-piperazine substituent and the lipophilicity.The substitution of aliphatic groups with aromatic, benzyl, or 2-pyridyl substituents increased activity against Gram-positive bacteria and imparted substantial-to-moderate activity against Gram-negative bacteria.Interestingly, the 2-pyridyl substituent demonstrated optimal bioactivity, exhibiting broadspectrum antibacterial activity and a notable effect against C. albicans, notwithstanding its lipophilic nature [70].
Organics 2023, 4, FOR PEER REVIEW 14 Gram-negative bacteria, and C. albicans.The antimicrobial activity was found to be influenced by the nature of the 4-piperazine substituent and the lipophilicity.The substitution of aliphatic groups with aromatic, benzyl, or 2-pyridyl substituents increased activity against Gram-positive bacteria and imparted substantial-to-moderate activity against Gram-negative bacteria.Interestingly, the 2-pyridyl substituent demonstrated optimal bioactivity, exhibiting broad-spectrum antibacterial activity and a notable effect against C. albicans, notwithstanding its lipophilic nature [70].
Scheme 21.Synthesis of 5-((3r,5r,7r Cebeci et al. embarked on the synthesis of novel Mannich bases and conazole derivatives, incorporating a 1,2,4-triazol-3-one nucleus derived from tryptamine via a microwave-assisted methodology.The synthesis entailed the transformation of tryptamine-derived carbox(thio)amides into 1,2,4-triazole derivatives, which were subsequently subjected to HCOH-mediated Mannich reactions with various heterocyclic secondary amines (Scheme 22).The MIC values indicated that the synthesized compounds exhibited antimicrobial activity against E. coli, Yersinia pseudotuberculosis, P. aeruginosa, S. aureus, Enterococcus faecalis, Bacillus cereus, Mycobacterium smegmatis, C. albicans, and Saccharomyces cerevisiae.The authors concluded that the amino alkylation of triazole derivatives 52 and 53 with fluoroquinolones such as ciprofloxacin and norfloxacin improved the bioactivity of Mannich bases, with MIC values between 0.24 and 3.9 µg/mL [71,72].The authors established that, in addition to the 1,2,4-triazole moiety, known for its biological properties, the presence of the N-methylpiperazine, morpholine, norfloxacin, and ciprofloxacin motifs is critical in aiding the net bioactivity of this kind of hybrid.Cebeci et al. embarked on the synthesis of novel Mannich bases and conazole derivatives, incorporating a 1,2,4-triazol-3-one nucleus derived from tryptamine via a microwaveassisted methodology.The synthesis entailed the transformation of tryptamine-derived carbox(thio)amides into 1,2,4-triazole derivatives, which were subsequently subjected to HCOH-mediated Mannich reactions with various heterocyclic secondary amines (Scheme 22).The MIC values indicated that the synthesized compounds exhibited antimicrobial activity against E. coli, Yersinia pseudotuberculosis, P. aeruginosa, S. aureus, Enterococcus faecalis, Bacillus cereus, Mycobacterium smegmatis, C. albicans, and Saccharomyces cerevisiae.The authors concluded that the amino alkylation of triazole derivatives 52 and 53 with fluoroquinolones such as ciprofloxacin and norfloxacin improved the bioactivity of Mannich bases, with MIC values between 0.24 and 3.9 µg/mL [71,72].The authors established that, in addition to the 1,2,4-triazole moiety, known for its biological properties, the presence of the N-methylpiperazine, morpholine, norfloxacin, and ciprofloxacin motifs is critical in aiding the net bioactivity of this kind of hybrid.Organics 2023, 4, FOR PEER REVIEW Scheme 22. Synthesis of Mannich bases derived from tryptamine

Morpholine Derivatives
The 1,4-oxazines (morpholines) are heterocycles that can be present in num drugs and multiple molecules with potential biological activity, often used in med chemistry.Morpholine synthesis typically involves the transformation of vicinal a alcohols, oxiranes, and aziridines.Moreover, the morpholine ring serves as a va foundational component, facilitating its incorporation through standard amine reac Due to its favorable pharmacokinetic attributes, the morpholine nucleus has been r nized as a pharmacophore against specific enzyme inhibitors [73,74].Idhayadhulla documented the synthesis of a series of Mannich bases, characterized as 2-(phen (morpholine-4-yl)-N-phenylacetamide, 54, employing morpholine, acetanilide, an matic aldehydes (Scheme 23).The antibacterial and antifungal activities of these d tives were rigorously assessed against multiple strains, and several compounds exh noteworthy potential.Specifically, 3-(4-chlorophenyl)-3-(morpholine-4-yl)-N-phen panamide, 54a, displayed significant antibacterial activity against Streptococcus e midis, while compounds 54b and 54c exhibited equipotent activity against fungal s M. audouinii and C. albicans, respectively, comparable to the established standard mazole.These findings underscored the potency of these Mannich bases, further acc ating the advantageous effect of the morpholine moiety [75].

Some Heterocyclic Derivatives with Different Mixed Heteroatoms 2.3.1. Morpholine Derivatives
The 1,4-oxazines (morpholines) are heterocycles that can be present in numerous drugs and multiple molecules with potential biological activity, often used in medicinal chemistry.Morpholine synthesis typically involves the transformation of vicinal amino alcohols, oxiranes, and aziridines.Moreover, the morpholine ring serves as a valuable foundational component, facilitating its incorporation through standard amine reactions.Due to its favorable pharmacokinetic attributes, the morpholine nucleus has been recognized as a pharmacophore against specific enzyme inhibitors [73,74].Idhayadhulla et al. documented the synthesis of a series of Mannich bases, characterized as 2-(phenyl)-2-(morpholine-4yl)-N-phenylacetamide, 54, employing morpholine, acetanilide, and aromatic aldehydes (Scheme 23).The antibacterial and antifungal activities of these derivatives were rigorously assessed against multiple strains, and several compounds exhibited noteworthy potential.Specifically, 3-(4-chlorophenyl)-3-(morpholine-4-yl)-N-phenylpropanamide, 54a, displayed significant antibacterial activity against Streptococcus epidermidis, while compounds 54b and 54c exhibited equipotent activity against fungal strains M. audouinii and C. albicans, respectively, comparable to the established standard clotrimazole.These findings underscored the potency of these Mannich bases, further accentuating the advantageous effect of the morpholine moiety [75].The 1,4-oxazines (morpholines) are heterocycles that can be present in numerous drugs and multiple molecules with potential biological activity, often used in medicinal chemistry.Morpholine synthesis typically involves the transformation of vicinal amino alcohols, oxiranes, and aziridines.Moreover, the morpholine ring serves as a valuable foundational component, facilitating its incorporation through standard amine reactions.Due to its favorable pharmacokinetic attributes, the morpholine nucleus has been recognized as a pharmacophore against specific enzyme inhibitors [73,74].Idhayadhulla et al. documented the synthesis of a series of Mannich bases, characterized as 2-(phenyl)-2-(morpholine-4-yl)-N-phenylacetamide, 54, employing morpholine, acetanilide, and aromatic aldehydes (Scheme 23).The antibacterial and antifungal activities of these derivatives were rigorously assessed against multiple strains, and several compounds exhibited noteworthy potential.Specifically, 3-(4-chlorophenyl)-3-(morpholine-4-yl)-N-phenylpropanamide, 54a, displayed significant antibacterial activity against Streptococcus epidermidis, while compounds 54b and 54c exhibited equipotent activity against fungal strains M. audouinii and C. albicans, respectively, comparable to the established standard clotrimazole.These findings underscored the potency of these Mannich bases, further accentuating the advantageous effect of the morpholine moiety [75].
Scheme 23.Synthesis of 3-morpholino-N,3-diphenylpropanamides Thiomorpholines, saturated heterocycles comprising N and S atoms in 1,4 positions, parallel the nucleophilicity and N-alkylation(acylation) feasibility observed in secondary amines such as morpholine.These attributes render thiomorpholines valuable synthetic precursors [76].Demirci et al. prepared a group of thiomorpholine-containing compounds through condensation with 1,3,4-oxadiazole, arylidenehydrazide, and 1,2,4-triazole.In addition, Mannich bases were prepared from compounds 55-57 using piperidine, β-lactam, fluoroquinolone, piperazine, or morpholine core, affording compounds 58-62, respectively (Scheme 24).For this, three methods were used, including conventional and microwave (MW)-assisted synthesis and a catalyst.The MW irradiation offered a more Thiomorpholines, saturated heterocycles comprising N and S atoms in 1,4 positions, parallel the nucleophilicity and N-alkylation(acylation) feasibility observed in secondary amines such as morpholine.These attributes render thiomorpholines valuable synthetic precursors [76].Demirci et al. prepared a group of thiomorpholine-containing compounds through condensation with 1,3,4-oxadiazole, arylidenehydrazide, and 1,2,4-triazole.In addition, Mannich bases were prepared from compounds 55-57 using piperidine, β-lactam, fluoroquinolone, piperazine, or morpholine core, affording compounds 58-62, respectively (Scheme 24).For this, three methods were used, including conventional and microwave (MW)-assisted synthesis and a catalyst.The MW irradiation offered a more efficient and greener path for Mannich-type condensation with good to high yields compared to the long reflow time.The Mannich reaction in the presence of Lewis and Brønsted-Lowry acids demonstrated the latter's superiority, attributed to its facilitation of electrophilic iminium ion formation.The synthesized compounds were comprehensively evaluated for their antimicrobial, antiglucosidase, antilipase, antiurease, and antioxidant activities.Several compounds displayed favorable antibacterial and antifungal potential, with derivatives containing norfloxacin or ciprofloxacin backbone attached to a thiomorpholine core through an azole bond proving particularly potent.Importantly, most of these compounds exhibited MIC values surpassing those of established standard drugs such as ampicillin and fluconazole.These findings accentuate the therapeutic promise of these compounds and the synergistic role of the morpholine moiety in these Mannich bases [77].
Organics 2023, 4, FOR PEER REVIEW 16 efficient and greener path for Mannich-type condensation with good to high yields compared to the long reflow time.The Mannich reaction in the presence of Lewis and Brønsted-Lowry acids demonstrated the latter's superiority, attributed to its facilitation of electrophilic iminium ion formation.The synthesized compounds were comprehensively evaluated for their antimicrobial, antiglucosidase, antilipase, antiurease, and antioxidant activities.Several compounds displayed favorable antibacterial and antifungal potential, with derivatives containing norfloxacin or ciprofloxacin backbone attached to a thiomorpholine core through an azole bond proving particularly potent.Importantly, most of these compounds exhibited MIC values surpassing those of established standard drugs such as ampicillin and fluconazole.These findings accentuate the therapeutic promise of these compounds and the synergistic role of the morpholine moiety in these Mannich bases [77].

Oxadiazole Derivatives
Sydnone compounds, characterized by a 1,2,3-oxadiazole nucleus bearing a keto group at position 5, have exhibited compelling pharmacological and biological activities, rendering them relevant in plant growth regulation, fungicidal, herbicidal, and anti-algae applications [78].Arylsydnone serves as a precursor for Mannich bases through a sequence involving the transformation of 1,3,4-oxadiazole into 1,2,4-triazolones.The condensation of compound 63 with aromatic aldehydes followed by reduction yielded a secondary amine derivative (64), subsequently serving as the precursor for Mannich bases 65 Scheme 24.Schematic representation for the synthesis of some Mannich bases derived from piperidine, β-lactam, fluoroquinolone, piperazine, and morpholine.

Oxadiazole Derivatives
Sydnone compounds, characterized by a 1,2,3-oxadiazole nucleus bearing a keto group at position 5, have exhibited compelling pharmacological and biological activities, rendering them relevant in plant growth regulation, fungicidal, herbicidal, and anti-algae applications [78].Arylsydnone serves as a precursor for Mannich bases through a sequence involving the transformation of 1,3,4-oxadiazole into 1,2,4-triazolones.The condensation of compound 63 with aromatic aldehydes followed by reduction yielded a secondary amine derivative (64), subsequently serving as the precursor for Mannich bases 65 upon reaction with HCOH and secondary amines catalyzed by acid (Scheme 25).The synthesized compounds were rigorously evaluated for their antifungal activity against C. albicans, with certain compounds displaying notable promise.Remarkably, compound 65a exhibited superior activity compared to the standard fluconazole, and compound 65b displayed com-parable activity.While some derivatives exhibited sensitivity to higher drug concentrations, others demonstrated potential for further development [79].
Organics 2023, 4, FOR PEER REVIEW 17 upon reaction with HCOH and secondary amines catalyzed by acid (Scheme 25).The synthesized compounds were rigorously evaluated for their antifungal activity against C. albicans, with certain compounds displaying notable promise.Remarkably, compound 65a exhibited superior activity compared to the standard fluconazole, and compound 65b displayed comparable activity.While some derivatives exhibited sensitivity to higher drug concentrations, others demonstrated potential for further development [79].

Considerations and Future Outlook
Fungal infections significantly threaten human health and agriculture [80,81].As traditional antifungal agents face challenges of resistance and limited efficacy [82], the exploration of innovative solutions has led researchers to a promising avenue based on heterocycle-containing Mannich bases.As described, Mannich bases are structurally defined as 2-amino-ketones with central electrophilic carbon atoms and heteroatoms such as nitrogen or oxygen.They are formed through the Mannich reaction, an essential method of carbon-carbon bond formation in organic synthesis.Notably, the Mannich reaction with various oxa-and/or aza-heterocycles has garnered attention for its remarkable potential against opportunistic fungi [83].Indeed, the antifungal activity of Mannich bases stems from their unique molecular structure, which often combines a β-amino functionality with a carbonyl-containing moiety.This arrangement plausibly provides a platform for multifaceted interactions with fungal cells, disrupting vital cellular processes and ultimately inhibiting their growth and proliferation [84].In addition, one of the pivotal factors contributing to the potency of Mannich bases is the possibility of expanding their structural diversity.By tailoring the substituents and heterocyclic components, their physicochemical properties can be fine-tuned, influencing their interactions with fungal membranes and intracellular targets.This diversity allows for compounds that exhibit broad-spectrum and targeted antifungal effects to be developed [84].However, the mechanisms of action for diverse heterocycle-containing Mannich bases have not been extensively investigated.This gap in knowledge presents a valuable avenue for future research, particularly concerning compounds that display promising activity.As the field advances, incorporating computational techniques, structural biology, and high-throughput screening accelerates the discovery of potent Mannich-based antifungal candidates.Nevertheless, challenges remain in optimizing compound selectivity, pharmacokinetic properties, and formulation for clinical or practical applications [83].Furthermore, the emergence of resistance to existing antifungal agents underscores the urgency of finding new solutions [85].In this regard, heterocycle-containing Mannich bases, with their novel structures, offer a fresh approach to combating resistant fungal strains, and it would be even better if a multitarget action could be explored.
In this context, synthesizing antifungal heterocycle-containing Mannich bases represents a dynamic and promising field with substantial potential for scientific advancement and practical applications for managing diseases, particularly fungal infections [15].The fusion of heterocyclic moieties with Mannich bases has proven to be an effective strategy, endowing these compounds with enhanced biological properties and expanding their Scheme 25.Synthesis of 2,4-dihydro-3H-1,2,4-triazol-3-one type compounds.

Considerations and Future Outlook
Fungal infections significantly threaten human health and agriculture [80,81].As traditional antifungal agents face challenges of resistance and limited efficacy [82], the exploration of innovative solutions has led researchers to a promising avenue based on heterocycle-containing Mannich bases.As described, Mannich bases are structurally defined as 2-amino-ketones with central electrophilic carbon atoms and heteroatoms such as nitrogen or oxygen.They are formed through the Mannich reaction, an essential method of carbon-carbon bond formation in organic synthesis.Notably, the Mannich reaction with various oxa-and/or aza-heterocycles has garnered attention for its remarkable potential against opportunistic fungi [83].Indeed, the antifungal activity of Mannich bases stems from their unique molecular structure, which often combines a β-amino functionality with a carbonyl-containing moiety.This arrangement plausibly provides a platform for multifaceted interactions with fungal cells, disrupting vital cellular processes and ultimately inhibiting their growth and proliferation [84].In addition, one of the pivotal factors contributing to the potency of Mannich bases is the possibility of expanding their structural diversity.By tailoring the substituents and heterocyclic components, their physicochemical properties can be fine-tuned, influencing their interactions with fungal membranes and intracellular targets.This diversity allows for compounds that exhibit broad-spectrum and targeted antifungal effects to be developed [84].However, the mechanisms of action for diverse heterocycle-containing Mannich bases have not been extensively investigated.This gap in knowledge presents a valuable avenue for future research, particularly concerning compounds that display promising activity.As the field advances, incorporating computational techniques, structural biology, and high-throughput screening accelerates the discovery of potent Mannich-based antifungal candidates.Nevertheless, challenges remain in optimizing compound selectivity, pharmacokinetic properties, and formulation for clinical or practical applications [83].Furthermore, the emergence of resistance to existing antifungal agents underscores the urgency of finding new solutions [85].In this regard, heterocycle-containing Mannich bases, with their novel structures, offer a fresh approach to combating resistant fungal strains, and it would be even better if a multitarget action could be explored.
In this context, synthesizing antifungal heterocycle-containing Mannich bases represents a dynamic and promising field with substantial potential for scientific advancement and practical applications for managing diseases, particularly fungal infections [15].The fusion of heterocyclic moieties with Mannich bases has proven to be an effective strategy, endowing these compounds with enhanced biological properties and expanding their scope in various fields, including pharmaceuticals and agriculture.As reflected in the current landscape, it becomes evident that the synthesis of these compounds has matured significantly.Much research has been devoted to investigating diverse heterocyclic scaffolds, refining synthetic methodologies, and uncovering structure-activity relationships.The efforts of researchers have yielded a multitude of insights into the intricate interplay between heterocyclic architecture and antifungal efficacy at in vitro levels.Looking ahead, several exciting directions emerge that will likely shape the future of this field.First, the continual exploration of novel heterocyclic motifs remains fundamental.The quest for hitherto unexplored heterocycles, especially those with unprecedented antifungal potential, promises to unveil compounds with superior efficacy and reduced resistance.The convergence of computational techniques and experimental synthesis can accelerate this process, enabling the targeted design of innovative structures [83].Second, the integration of sustainable and eco-friendly synthesis methodologies is gaining prominence.Green chemistry principles can guide the development of synthetic routes that minimize environmental impact and resource consumption [86].These endeavors align with the global pursuit of greener and more sustainable practices in chemical synthesis.Furthermore, the incorporation of Mannich bases into materials science can lead to the development of functional materials with antimicrobial properties, enriching fields such as coatings, textiles, and medical devices.Finally, collaboration between interdisciplinary fields is poised to play a pivotal role in advancing the synthesis and applications of these compounds.The synergy between synthetic chemists, biologists, pharmacologists, and materials scientists will accelerate the translation of novel compounds from the laboratory to real-world solutions.
Although the synthesis of heterocycle-containing Mannich bases can be achieved in a few steps and the yields were found to be moderate-to-good (>40%), employing heterocycle-containing Mannich bases as antifungal agents can present several limitations and challenges that must be considered.The studies covered demonstrated high variability in the target microorganisms, although some relevant pathogens can be shared, which limits a broad trend about several factors.Additionally, specificity and selectivity for fungal pathogens while avoiding harm to host cells are missing, and, therefore, designing compounds that effectively target fungal cells while sparing human cells should be preferred since some heterocycle-containing Mannich bases may exhibit cytotoxicity towards human cells and other non-target organisms, which restricts their therapeutic potential or agrochemical application.Balancing antifungal activity with acceptable levels of toxicity is a significant hurdle.Finally, there is a lack of comprehensible structure-activity relationships for heterocycle-containing Mannich bases, and this is very important due to the diverse range of heterocycles and substituents involved, which can hinder rational design strategies.Addressing these limitations require interdisciplinary collaboration, innovative drug-design strategies, thorough preclinical evaluations, and a deep understanding of fungal biology.
Despite these challenges, heterocycle-containing Mannich bases hold promise as potential antifungal agents, and research efforts continue to explore ways to overcome these limitations and harness their potential applications.In this context, Mannich bases as precursors or raw materials for the preparation and development of new antifungal agents and their broader relevance in the pharmaceutical and agricultural sectors demonstrate that the Mannich reaction corresponds to one of the most valuable and versatile tools of organic chemists to carry out the correct and rational design of new bioactive molecules that can contribute to the challenging endeavor of reducing the impact of various fungal pathogens that affect sustainable development.Hence, novel Mannich bases should be aimed at the search for multitarget bioactive agents, which may be more effective by reducing resistance outbreaks and generating less environmental impact since, for instance, many of the commercial antifungal agents against phytopathogens reported in the literature are associated with residuality, soil contamination, and cytotoxicity.In this context, considering Mannich bases are labile molecules under certain pH conditions and/or moisture, their use must be subject to their stability and subsequent degradation, and, thus, the least possible environmental impact will be generated.

Concluding Remarks
The present survey led to the recognition of the importance of Mannich bases in designing drugs, particularly those containing heterocyclic systems, for possible biological activities and their applications as antifungal agents.Various modifications and improvements to the Mannich reaction to improve its efficiency have been described, including using ionic liquids and transition metal catalysts.Although these Mannich bases have shown various biological activities (e.g., antibacterial, antifungal, antiviral, and anticancer), the widespread examination of this compound class has focused on their potential as antifungal agents for agricultural and medicinal purposes.Regarding the bioactivity of heterocycle-containing Mannich bases against different fungal phytopathogens, their antifungal effect has been demonstrated against Fusarium oxysporum, F. graminearum, F. solani, Botrytis cinerea, Colletotrichum capsici, Cercospora arachidicola, Physalospora piricola, and Rhizoctonia cerealis.On the other hand, various heterocycle-containing Mannich bases have been found to be active against several human pathogens such as Aspergillus niger, A. fumigatus, Candida albicans, C. krusei.and C. parapsilosis, as well as some dermatophytic fungi species such as Microsporum gypseum, Trichophyton mentagrophytes var.erinacei, and Epidermophyton floccosum, which are of great interest due to their opportunistic and pathogenic nature.These findings highlight the use of different oxygenated and/or nitrogenated heterocyclic systems, demonstrating that various structural modifications considerably influence their effectiveness as agrochemical or medicinal agents.In this regard, the antifungal effects demonstrated by Mannich bases that are coupled with heterocycles, e.g., chromenes, 2arylchromen-4-ones (such as flavonoids), chromen-2-ones (such as coumarins), piperazines, imidazoles, benzimidazoles, triazoles, quinolines, pyrrolidines, 2-oxoindoles, 1,4-oxazines, 1,4-thioxazines, and 1,2,3-oxadiazoles, imply a promising avenue for future research.These findings suggest the potential of these compounds as synthetic candidates for developing useful antifungal agents in both medical and agricultural applications.

2 .
Heterocyclic-Based and/or Oxygenated Mannich Bases 2.1.Oxygen-Containing Heterocyclic Systems and Oxygenated Compounds 2.1.1.Coumarin Derivatives Coumarins (2H-chromen-2-one) are some of the most abundant natural products and comprise a great diversity.They have been attributed a role as part of the defense system of plants since many of these have been shown to have bactericidal, fungicidal, and/or fungistatic activity and, mainly, an efficient activity as insecticides [26].A series of coumarins based on 5H-chromeno [4,3-b]pyridin-5-one, 1, were synthesized by Patel using two methodologies involving the Mannich base derived from 4-hydroxycoumarin, 2 (Scheme 2), on the one hand, and 4-chloro-3-formylcoumarin as precursors, on the other.The Mannich base is believed to have decomposed, leading to the generation of coumarin methide.This intermediate was condensed with salt 3 under reflux and using ammonium acetate and acetic acid, yielding a coumarin intermediate.This intermediate then undergoes a Krohnke reaction, affording the desired product, 1.These Mannich base derivatives were found to be active against the fungal pathogens Aspergillus niger (MTCC 282) and Candida albicans (MTCC 227).Notably, methyl and chlorine substitutions demonstrated enhanced activity compared to other analogs, displaying MIC values of 200 and 250 µg/mL against C. albicans (MTCC 227) [27].Organics 2023, 4, FOR PEER REVIEW 3

Scheme 19 .
Scheme 19.Synthesis of Mannich bases 45 derived from isatin Scheme 19.Synthesis of Mannich bases 45 derived from isatin.2.2.7.Heterocyclic Hybrid Derivatives Numerous instances of combining diverse biologically active moieties within Mannich bases have been documented.Zhang et al. synthesized a novel set of piperazine-and triazole-based compounds, denoted 46 and 47, through Mannich reactions involving a variety of triazole Schiff bases, substituted piperazine, and HCOH.This process, carried out under moderate conditions, resulted in commendable yields, thereby underscoring its industrial potential (Scheme 20).The in vitro antifungal efficacy of Mannich bases 46 and 47 was gauged by their mycelial growth inhibitory impact on several test fungi, including F. oxysporum, Cercospora arachidicola, Phytophthora piricola, and R. cerealis.Notably, compounds 46a-c exhibited superior inhibition against F. oxysporum when compared to tridimefon, with compound 46a standing out by maintaining inhibitory rates surpassing those of the commercial controls, i.e., tridimefon and chlorothalonil.The presence of a 4-chlorophenyl group (R 1 = Cl) consistently correlated with enhanced antifungal activity against F. oxysporum, while compounds 46d and 46e, with R 1 = F, R 2 = phenyl, and dimethylpyrimidyl, demonstrated heightened efficacy against Cercospora arachidicola.Encouragingly, all the tested compounds displayed remarkable antifungal activity against Phytophthora piricola, with those containing trifluoromethyl (R 1 = CF 3 ) displaying a distinct advantage.For R. cerealis, most compounds maintained robust inhibition rates ranging from 80.2% to 97.5%.Additionally, all the compounds exhibited commendable antifungal properties against A. solani and G. sanbinetti.Applying a comparative molecular field analysis (CoMFA) based on antifungal activity data established a 3D-QSAR model, highlighting steric and electrostatic fields as pivotal contributors to compound bioactivity.This insight can potentially guide the optimization of novel structures to develop more potent agrochemicals[69].
Organics 2023, 4, FOR PEER REVIEW 13 2.2.7.Heterocyclic Hybrid Derivatives Numerous instances of combining diverse biologically active moieties within Mannich bases have been documented.Zhang et al. synthesized a novel set of piperazine-and triazole-based compounds, denoted 46 and 47, through Mannich reactions involving a variety of triazole Schiff bases, substituted piperazine, and HCOH.