The Recycling of Substandard Rocket Fuel N,N-Dimethylhydrazine via the Involvement of Its Hydrazones Derived from Glyoxal, Acrolein, Metacrolein, Crotonaldehyde, and Formaldehyde in Organic Synthesis

“Heptil” (unsymmetrical dimethylhydrazine—UDMH) is extensively employed worldwide as a propellant for rocket engines. However, UDMH constantly loses its properties as a result of its continuous and uncontrolled absorption of moisture, which cannot be rectified. This situation threatens its long-term usability. UDMH is an exceedingly toxic compound (Hazard Class 1), which complicates its transportation and disposal. Incineration is currently the only method used for its disposal, but this process generates oxidation by-products that are even more toxic than the original UDMH. A more benign approach involves its immediate reaction with a formalin solution to form 1,1–dimethyl-2-methylene hydrazone (MDH), which is significantly less toxic by an order of magnitude. MDH can then be polymerized under acidic conditions, and the resulting product can be burned, yielding substantial amounts of nitrogen oxides. This review seeks to shift the focus of MDH from incineration towards its application in the synthesis of relatively non-toxic and readily available analogs of various pharmaceutical substances. We aim to bring the attention of the international chemical community to the distinctive properties of MDH, as well as other hydrazones (such as glyoxal, acrolein, crotonal, and meta-crolyl), wherein each structural fragment can initiate unique transformations that have potential applications in molecular design, pharmaceutical research, and medicinal chemistry.


Introduction
At normal temperature and pressure, asymmetric dimethylhydrazine (UDMH, 1,1-Dimethylhydrazine, heptil) is a hygroscopic liquid that appears colorless or slightly yellowish.It has the chemical formula (CH 3 ) 2 N 2 H 2 , a relative molecular weight of 60.08, and a density of 785 kg/m 3 .UDMH has a boiling point of +63 • C and a crystallization temperature of −57 • C.
UDMH exhibits high solubility in water, alcohols, ammonia, amines, and organic solvents while being insoluble in hydrocarbons.It is a potent reducing agent [1].When burned, UDMH produces highly toxic volatile nitro compounds [2] and releases a significant amount of energy.Due to these properties, it is widely utilized as a fuel in rocket technology.It is employed in domestic intercontinental ballistic missiles such as R36M2 "Voevoda", as well as launch vehicles like "Cosmos", "Cyclone", and "Proton".Additionally, UDMH is used in propulsion systems of manned spacecraft, automatic satellites, orbital and interplanetary stations, as well as reusable spacecraft [3,4].
However, UDMH exhibits marked toxicity [5], teratogenicity, and the capacity to absorb atmospheric moisture, leading to a loss of fuel characteristics [2][3][4].Rectification methods are unable to counteract the water absorption (up to 2% annually).Consequently, aqueous heptil must be transported over long distances while implementing special precautions to processing facilities and then returned.Any incidents during UDMH transport constitute environmental disasters, resulting in a significant increase in the cost of "restored" UDMH.Therefore, it is more economical and safer to dispose of large quantities (thousands of tons!) at designated storage locations.The current approach involves an immediate exothermic reaction with formalin [6], yielding 1,1-dimethyl-2-methylene hydrazone (MDH) with reduced toxicity on an order of magnitude.Subsequently, MDH is polymerized under acidic conditions, followed by incineration [4].However, even this relatively safe method imposes substantial harm on the environment due to the emission of significant amounts of nitrogen oxides, considering the disposal of thousands of tons of UDMH.From an ecological and economic perspective, locally processing the UDMH presents itself as the optimal and sole viable solution to the existing problem.
This review aims to show the relatively few possibilities and alternative ways of UDMH treatment [4] resulting in less toxic hydrazones (formaldehyde, glyoxal, acrolein crotonal, metacrolein) and their chemical transformations into the building blocks of UDMH-based bioactive organic compounds, using the literature from around the world up to 2022.
Currently, a notable instance of utilizing unsymmetrical dimethylhydrazine (UDMH) in the field of medicine is exemplified by the compound meldonium, which serves as an active constituent within the pharmaceutical preparation known as "Mildronate" [7].This particular substance has gained significant recognition due to its association with doping scandals in the realm of sports.Owing to the inherent toxicity and challenges associated with handling UDMH within laboratory settings (where even the mere detection of UDMH odor surpasses sixfold the maximum permissible concentration), we propose the adoption of non-toxic derivatives of UDMH, namely, dimethyldrazones, such as glyoxal, acrolein, metacrolein, and formaldehyde, for employment both within chemical laboratories and industrial contexts.

Glyoxal Monodimethylhydrazone
Mono(dimethylhydrazon) glyoxal (DMHG, monohydrazon) is a compound of significant scientific interest in the field of organic chemistry due to its potential as a versatile synthon for the synthesis of multifunctional and biologically active structures.DMHG can be readily synthesized by combining unsymmetrical dimethylhydrazine (UDMH) and glyoxal in an aqueous solution under magnetic stirring, followed by extraction of the desired product using methylene chloride and subsequent vacuum distillation [8].DMHG is characterized as a slightly yellowish liquid with a boiling point of 90 • C at 16 Torr [8].

Stereoselectivity of DMHG
The stereoselectivity of DMHG, which is recognized as one of its significant advantages, holds great importance in the field of medicine.This is because spatial isomers of the same compound exhibit distinct properties and varying degrees of harmful effects on pathogens and the human body.Utilizing DMHG as a starting material, optically pure alpha-aminoaldehydes have been successfully synthesized [9,10].
This achievement is particularly challenging due to the racemic nature of alphaaminoaldehydes, which complicates their separation via chromatographic methods [11].Consequently, DMHG has served as a valuable precursor for diverse compounds such as interleukin-converting enzymes (an enzyme responsible for converting interleukin, a mediator of the immune system, into a protein), calpains (a calcium-dependent cysteine protease that plays a role in protein degradation and cellular mobility) [12], amino alcohol intermediates, peptide analogs [13], organometallic complexes [9,14,15] utilized in the fabrication of thin optical films, and magnesium-copper alloys [15], among other important derivatives.
Likewise, the compound based on dimethylhexahydroxyflavylium (DMHG) [16] was employed to synthesize optically pure polymetinnitrile dyes, which hold potential as photosensitizers for antimicrobial photodynamic therapy.
Furthermore, the publication [17] explores the directed synthesis of a chiral auxiliary reagent based on DMHG.The aim is to obtain an optically pure, biologically active derivative of camphor.Figures 1 and 2 in the publication outline the synthetic pathways.In their work, the authors performed condensation of DMHG with camphor 1 [17] (Figure 1).To facilitate this reaction, lithium diisopropylamide (LDA) was utilized for several reasons: other important derivatives.
Likewise, the compound based on dimethylhexahydroxyflavylium (DMHG) [16] was employed to synthesize optically pure polymetinnitrile dyes, which hold potential as photosensitizers for antimicrobial photodynamic therapy.
Furthermore, the publication [17] explores the directed synthesis of a chiral auxiliary reagent based on DMHG.The aim is to obtain an optically pure, biologically active derivative of camphor.Figures 1 and 2 in the publication outline the synthetic pathways.In their work, the authors performed condensation of DMHG with camphor 1 [17] (Figure 1).To facilitate this reaction, lithium diisopropylamide (LDA) was utilized for several reasons: LDA, being a strong base, stabilizes the lithium enolate formed during the reaction.The α-position in camphor experiences steric hindrance.The reaction was carried out at the maximum temperature acceptable for the process involving LDA in tetrahydrofuran (THF), which was 0 °C [18].It has been observed that the interaction between DMHG and enolate 2 is temperature-dependent.At −78 °C, the equilibrium shifts towards lithium alcoholates, while at +50 °C, it favors the formation of the desired isomers 3(E) and 4(Z).The racemic mixture of isomers 3/4 could be reduced to 1,4-dicarbonyl compound 5 using titanium chloride, eliminating the need for isomer separation.However, attempts to cyclize 5 with ammonium acetate resulted in the decomposition of the original compound (Figure 1).In search of an alternative cyclization method (Figure 2), the authors of [17] selectively reduced the keto group to hydroxyl using a mixture of 3/4 sodium borohydride.This facilitated the elimination of p-toluenesulfonic acid (tosylic acid) as an easily detachable leaving group [19], subsequently leading to the closure of the pyrrole ring.The results demonstrated that only one isomer, specifically the Z-isomer, participated in the cyclization process, resulting in compound 4. The N-N bond cleavage of the pyrrole ring (compound 11) was accomplished by reacting it with sodium in liquid ammonia under stirring conditions in an autoclave at room temperature.This reaction pathway ultimately yielded the desired product, compound 6 (Figure 2).LDA, being a strong base, stabilizes the lithium enolate formed during the reaction.The α-position in camphor experiences steric hindrance.The reaction was carried out at the maximum temperature acceptable for the process involving LDA in tetrahydrofuran (THF), which was 0 • C [18].It has been observed that the interaction between DMHG and enolate 2 is temperature-dependent.At −78 • C, the equilibrium shifts towards lithium alcoholates, while at +50 • C, it favors the formation of the desired isomers 3(E) and 4(Z).The racemic mixture of isomers 3/4 could be reduced to 1,4-dicarbonyl compound 5 using titanium chloride, eliminating the need for isomer separation.However, attempts to cyclize 5 with ammonium acetate resulted in the decomposition of the original compound (Figure 1).
In search of an alternative cyclization method (Figure 2), the authors of [17] selectively reduced the keto group to hydroxyl using a mixture of 3/4 sodium borohydride.This facilitated the elimination of p-toluenesulfonic acid (tosylic acid) as an easily detachable leaving group [19], subsequently leading to the closure of the pyrrole ring.The results demonstrated that only one isomer, specifically the Z-isomer, participated in the cyclization process, resulting in compound 4. The N-N bond cleavage of the pyrrole ring (compound 11) was accomplished by reacting it with sodium in liquid ammonia under stirring conditions in an autoclave at room temperature.This reaction pathway ultimately yielded the desired product, compound 6 (Figure 2).
Thus, to obtain a pyrrole ring, the authors of [40] utilized intramolecular condensation employing the Knorr method.Initially, dimethylhydrazone 13 was subjected to metallization to yield compound 14, which was subsequently converted into acetal 15.Subsequently, hydrolysis of the acetal group in the presence of trifluoroacetic acid (TFA) took place.The elimination of water from compound 17 was followed by its intramolecular cyclization, resulting in the formation of the desired compound 18.This method proved suitable for synthesizing pyrrole-pyridines II and III.However, in the case of pyrrole-pyridine I, which acts as a propyl-hydroxylase-I inhibitor, complications arose during the alkylation stage, leading to a reduction in yield.Consequently, the authors were motivated to explore an alternative pathway.A method was devised for the synthesis of α-analogues by condensing 2-acetylpyridine I with DMHG in the presence of
Thus, to obtain a pyrrole ring, the authors of [40] utilized intramolecular condensation employing the Knorr method.Initially, dimethylhydrazone 13 was subjected to metallization to yield compound 14, which was subsequently converted into acetal 15.Subsequently, hydrolysis of the acetal group in the presence of trifluoroacetic acid (TFA) took place.The elimination of water from compound 17 was followed by its intramolecular cyclization, resulting in the formation of the desired compound 18.This method proved suitable for synthesizing pyrrole-pyridines II and III.However, in the case of pyrrole-pyridine I, which acts as a propyl-hydroxylase-I inhibitor, complications arose during the alkylation stage, leading to a reduction in yield.Consequently, the authors were motivated to explore an alternative pathway.A method was devised for the synthesis of α-analogues by condensing 2-acetylpyridine I with DMHG in the presence of potassium tert-butylate [43].The latter acts as a potent base, effectively activating a "critical" terminal methyl group on ketone I.The resulting condensation product 19 was subsequently cyclized into pyrrole 21 with concurrent cleavage of the N-N bond [40], employing a safer alternative reagent, sodium dithionite, in comparison to the previously described method involving flammable sodium in an ammonia solution [17].The authors of [40] reported successful and rapid preparation of compound 19.However, during the subsequent step, a portion of the desired product 21 was lost due to its high volatility, resulting in a modest yield of only 17% (Figure 3).
Publication [38] describes the DMHG-based synthesis of the marine alkaloid Pyrido[4,3,2-mn]acridone.A monohydrazone fragment is introduced into the pyridine ring using LDA (lithium diisopropylamide).The synthesis was conducted in tetrahydrofuran (THF) at −70 • C to maintain kinetic control and prevent the decomposition of LDA, as it deprotonates the target product rapidly [18].Lithiation of pyridine 22 finally occurred at the β-position instead of γ-position.The authors of [38] explain it refering to the rearrangement of pyrazoles ("dancerearrangement") in publication [47].
The transition from intermediate 23 to 24 proceeded through multiple stages (Figure 4).Due to its high basicity, lithium derivative 23 interacted with the starting reagent 24 through an ion exchange mechanism, leading to the formation of 3-lithium-2-chloropyridine 23a and 3,4-diiodo-2-chloropyridine 23b.The interaction between these compounds resulted in the rearranged product 24 and the simultaneous regeneration of the initial compound 22, which then reentered the cyclic process until complete conversion to the intermediate compound 24.The lithiated derivatives directly interacted with the iodide ion, which exhibited higher reactivity compared to the chloride ion (Figure 4).
The transition from intermediate 23 to 24 proceeded through multiple stages (Figure 4).Due to its high basicity, lithium derivative 23 interacted with the starting reagent 24 through an ion exchange mechanism, leading to the formation of 3-lithium-2-chloropyridine 23a and 3,4-diiodo-2-chloropyridine 23b.The interaction between these compounds resulted in the rearranged product 24 and the simultaneous regeneration of the initial compound 22, which then reentered the cyclic process until complete conversion to the intermediate compound 24.The lithiated derivatives directly interacted with the iodide ion, which exhibited higher reactivity compared to the chloride ion (Figure 4).According to the authors of [38], pyridine lithiation (Figure 5) occurred at the γ-position, followed by the transformation of intermediate 23 into a more stable form, 24.According to the authors of [38], pyridine lithiation (Figure 5) occurred at the γ-position, followed by the transformation of intermediate 23 into a more stable form, 24.
The transition from intermediate 23 to 24 proceeded through multiple stages (Figure 4).Due to its high basicity, lithium derivative 23 interacted with the starting reagent 24 through an ion exchange mechanism, leading to the formation of 3-lithium-2-chloropyridine 23a and 3,4-diiodo-2-chloropyridine 23b.The interaction between these compounds resulted in the rearranged product 24 and the simultaneous regeneration of the initial compound 22, which then reentered the cyclic process until complete conversion to the intermediate compound 24.The lithiated derivatives directly interacted with the iodide ion, which exhibited higher reactivity compared to the chloride ion (Figure 4).According to the authors of [38], pyridine lithiation (Figure 5) occurred at the γ-position, followed by the transformation of intermediate 23 into a more stable form, 24.Compound 24 and DMHG, upon interaction, yielded alcohol 26.This product was subsequently oxidized to acetylpyridine 27 using either manganese dioxide or pyridinium chlorochromate (PCC), resulting in a 77% yield [38] (Figure 5).Following this, the authors of [38] employed a cross-coupling reaction.In contrast to the conventional Suzuki conditions involving potassium carbonate and diglim (bis-2-methoxyethyl ether) [48], the authors utilized barium hydroxide and dimethoxyethyl (DME) as a more basic system.This modification allowed for an increased yield of the desired product 31 (87%) obtained through the cross-coupling of acetylpyridine 27 with boronic acid 28, followed by intramolecular cyclization of amide 29 and elimination of tert-butyl carboxylic acid 30 (Figure 5).
Attempts have been made to synthesize inhibitors of p38 MAP kinases (mitogenactivated protein kinases) based on DMHG [49][50][51], aiming to reduce the production of pro-inflammatory cytokines, which contribute to tissue destruction in diseases such as rheumatoid arthritis, an inflammatory joint disease.In one method [49] (Figure 6), the authors propose a DMHG-based condensation in an alkaline medium, alcohol solution, without the use of organometallic reagents.This approach is chosen because the original aldehydes 32a,b do not hinder enolization due to the arrangement of atoms.The authors of [49,50] performed cyclization of hydrazones 33a,b followed by N-N bond cleavage using a sodium dithionite aqueous alcohol solution, similar to the method described above [40] (Figure 6).Compound 24 and DMHG, upon interaction, yielded alcohol 26.This product was subsequently oxidized to acetylpyridine 27 using either manganese dioxide or pyridinium chlorochromate (PCC), resulting in a 77% yield [38] (Figure 5).Following this, the authors of [38] employed a cross-coupling reaction.In contrast to the conventional Suzuki conditions involving potassium carbonate and diglim (bis-2-methoxyethyl ether) [48], the authors utilized barium hydroxide and dimethoxyethyl (DME) as a more basic system.This modification allowed for an increased yield of the desired product 31 (87%) obtained through the cross-coupling of acetylpyridine 27 with boronic acid 28, followed by intramolecular cyclization of amide 29 and elimination of tert-butyl carboxylic acid 30 (Figure 5).
Attempts have been made to synthesize inhibitors of p38 MAP kinases (mitogen-activated protein kinases) based on DMHG [49][50][51], aiming to reduce the production of pro-inflammatory cytokines, which contribute to tissue destruction in diseases such as rheumatoid arthritis, an inflammatory joint disease.In one method [48] (Figure 6), the authors propose a DMHG-based condensation in an alkaline medium, alcohol solution, without the use of organometallic reagents.This approach is chosen because the original aldehydes 32a,b do not hinder enolization due to the arrangement of atoms.The authors of [49,50] performed cyclization of hydrazones 33a,b followed by N-N bond cleavage using a sodium dithionite aqueous alcohol solution, similar to the method described above [39] (Figure 6).The resulting heterocycle 35a, when interacting with bromosuccinimide (NBS), underwent further chemical transformations (Figure 6) into 2-bromopyrrole 36.The halogenation was followed by lithiation providing 2-lithiumpyrrole 38.Its condensation with Nmethylpiperidone 39 led to the product 40 with a yield of 57%.However, the organometallic agent BuLi has well-defined basic properties and, therefore, interacts with an acidic heteroatom.In order to avoid adverse reactions, the authors of [49] introduced SEM-protection ((2-(chlorometoxy)ethyl)trimethylsilane) followed by pyrrole 37 lithiation and its condensation with N-methylpiperidine 39.Tretbutylammonium fluoride (TBAF) [52] when allowing mild conditions of the reaction and providing a good yield of the target product 41, was selected in order to remove SEM-protection of compound 40.
The investigated compound (DMHG) was utilized in the synthesis of lesser-known thiobazidalin antibiotic derivatives [54] (Figure 7).In the initial step, the authors of publication [54] performed the condensation of thiolactone 42, derived from tetronic acid, with DMHG in the presence of piperidine.Subsequently, hydrazone 43 reacted with diazomethane in cooled THF to prevent diazomethane ignition.Consequently, methoxy groups 44a,c were converted into amino groups 45a,c (refer to substituents in Table 1) by adding ammonia or methylamine to an EtOAc:hexane (1:1) solution at −10 • C. The desired compound 46c was obtained by hydrolyzing hydrazone 45c in a concentrated hydrochloric acid medium.Acid 45b was obtained through the hydrolysis of ester 45a in a dry acetonitrile solution under a nitrogen atmosphere.The authors likely chose DMHG as a reagent for two reasons: it possesses a protective group, and the electron saturation induced by the carbonyl nitrogen in hydrazone 45a,b,c enhances the reactivity of the aldehyde group (Figure 7).
The resulting heterocycle 35a, when interacting with bromosuccinimide (NBS), underwent further chemical transformations (Figure 6) into 2-bromopyrrole 36.The halogenation was followed by lithiation providing 2-lithiumpyrrole 38.Its condensation with N-methylpiperidone 39 led to the product 40 with a yield of 57%.However, the organometallic agent BuLi has well-defined basic properties and, therefore, interacts with an acidic heteroatom.In order to avoid adverse reactions, the authors of [49] introduced SEM-protection ((2-(chlorometoxy)ethyl)trimethylsilane) followed by pyrrole 37 lithiation and its condensation with N-methylpiperidine 39.Tretbutylammonium fluoride (TBAF) [52] when allowing mild conditions of the reaction and providing a good yield of the target product 41, was selected in order to remove SEM-protection of compound 40.
The investigated compound (DMHG) was utilized in the synthesis of lesser-known thiobazidalin antibiotic derivatives [54] (Figure 7).In the initial step, the authors of publication [54] performed the condensation of thiolactone 42, derived from tetronic acid, with DMHG in the presence of piperidine.Subsequently, hydrazone 43 reacted with diazomethane in cooled THF to prevent diazomethane ignition.Consequently, methoxy groups 44a,c were converted into amino groups 45a,c (refer to substituents in Table 1) by adding ammonia or methylamine to an EtOAc:hexane (1:1) solution at −10 °C.The desired compound 46c was obtained by hydrolyzing hydrazone 45c in a concentrated hydrochloric acid medium.Acid 45b was obtained through the hydrolysis of ester 45a in a dry acetonitrile solution under a nitrogen atmosphere.The authors likely chose DMHG as a reagent for two reasons: it possesses a protective group, and the electron saturation induced by the carbonyl nitrogen in hydrazone 45a,b,c enhances the reactivity of the aldehyde group (Figure 7).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 °C.The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 °C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).The reagents and conditions are presented in Table 1.The authors of the publication [54] tested the compounds' activity against various bacteria, such as Bacillus subtilis ("Hay bacillus", involved in microbiocenoses of soil and human and mammalian intestines and found in water and in the air) and Bacillus brevis (bacteria found in water, air, soil, and decomposing organisms), and fungi, such as Mucor miehei (a type of fungus commercially used to produce renin ("rennet enzyme") for milk production), Paecilomyces varioti (mold formed in rotting wood, soil and causing a number of infectious diseases in humans, such as ostiomyelitis-bone infection; sinusitis-mucous membranes inflammation; peritonitis-inflammation of stomach inner wall; onychomycosis-shingles; etc.), Penicillinium notatum (a genus of fungi whose representatives are found in soil, on plants in the air, indoors, in the seas), and Nematospora coryli (a genus of fungi that causes sigmatonicosis-a disease affecting cotton, soybeans, pecans, pomegranates, citrus, and pistachio families).
The authors provide data on the inhibitory zone diameter of the compounds on a paper disk of 6 cm, inoculated (modified) by bacteria or fungi diffusion in agar of 50 micrograms per disk.Among all the tested structures, DMHG-based thiobazidalin analog 46c has all types of fungi [54] and the greatest antimicrobial activity against Bacillus brevis (see Tables S2 and S3 in the Supplementary Materials).
8-Methylthieno[2,3-g]quinoline-4,9-dione, possessing antifungal activity, was synthesized from DMHG [55].The synthesis involved two stages: the first stage comprised the Wittig reaction, followed by the second stage involving the Diels-Alder reaction (Figure 8).The Wittig reaction (Figure 8) was conducted in dichloromethane at a temperature of 40 • C. The desired product was obtained with a yield of 85.2% and subsequently purified using column chromatography with a diethyl ether:ethyl acetate mixture (5:1) as the eluent.
Tert-butylate 49 was also reacted with bromobenzothiophenedione 51 (Figure 8) at 0 • C to prevent its decomposition [56].The synthesis was conducted in anhydrous ethanol solvent, in the presence of sodium carbonate, to eliminate hydrogen bromide and dimethylamine and to reduce the carboxyl group of intermediate 52.This yielded the desired product, 5-methylthieno[3,2-g]quinoline-4,9-dione 53 (Figure 8).DMHG [57] and its derivatives [58], which are applicable in the synthesis of fluorinated pyrazoles, are of interest in the pharmaceutical and agrochemical industries [59].In the first case [57], the heterocycle was synthesized using ruthenium catalysis on a tribromofluoromethane basis (Figure 9), while in the second case [58], it was synthesized from trifluoroacetic anhydride (Figure 10).DMHG [57] and its derivatives [58], which are applicable in the synthesis of fluorinated pyrazoles, are of interest in the pharmaceutical and agrochemical industries [59].In the first case [57], the heterocycle was synthesized using ruthenium catalysis on a tribromofluoromethane basis (Figure 9), while in the second case [58], it was synthesized from trifluoroacetic anhydride (Figure 10).DMHG [57] and its derivatives [58], which are applicable in the synthesis of fluorinated pyrazoles, are of interest in the pharmaceutical and agrochemical industries [59].In the first case [57], the heterocycle was synthesized using ruthenium catalysis on a tribromofluoromethane basis (Figure 9), while in the second case [58], it was synthesized from trifluoroacetic anhydride (Figure 10).The discussed derivatives can contribute to the trend in modern organic chemistrycross-coupling reactions.Thus, in 2017 [57], a ruthenium-catalyzed synthesis of fluorinated pyrazole was proposed, as described in Figure 9.The authors suggested that the first stage of the chemical process involves the capture of the Ru(II) halide ion from CBr3F, resulting in the formation of a Ru(III) complex and a halide radical, CBr2F.The latter then interacts with DMHG, forming an aminyl radical 54.Subsequently, Ru(III) transfers the halide ion to intermediate 54, reducing to Ru(II) and forming diazene 55.The basicity of diazene 55 catalyzes the elimination of hydrobromic acid, leading to the formation of compound 56.Compound 56 then enolizes into imine ion 57, which undergoes cyclization to form pyrazoline 58.Finally, subsequent elimination of hydrogen bromide yields the desired product 59 (Figure 9).
The authors of publication [58] synthesized a fluorinated pyrazole through the reaction between a trifluoromethyl-containing DMHG derivative and trifluoroacetic anhydride in the presence of pyridine in chloroform at room temperature (Figure 10).The proposed cyclization pathway to form pyrazole 63 is as follows: Initially, trifluoroacetyl was attached to the carbonyl oxygen, resulting in the formation of salt 60.Subsequently, methylide 61 underwent cyclization to form hydropyrazole 62. Finally, the elimination of trifluoroacetic acid (TFA) led to the desired product 63 (Figure 10).
DMHG, upon reaction with hippuric acid 64, undergoes a transformation leading to the formation of an isoxazole ring 66 [60].In accordance with Lipinski's rules [61], it exhibits similarities to pharmaceutical compounds.Its logP (logarithm of partition coefficient) value is 1.996, indicating unhindered penetration of isoxazole through both aqueous and lipid barriers toward the biological target.
The synthesis of isoxazole [60] (Figure 11) was carried out in the presence of the chlorinating agent POCl3 in a mixture of acetic anhydride and a sodium acetate solution.DMHG was condensed with hippuric acid 64, resulting in the formation of chlorohydrin 65, which ultimately led to the desired isoxazole compound 66 (Figure 11).The discussed derivatives can contribute to the trend in modern organic chemistrycross-coupling reactions.Thus, in 2017 [57], a ruthenium-catalyzed synthesis of fluorinated pyrazole was proposed, as described in Figure 9.The authors suggested that the first stage of the chemical process involves the capture of the Ru(II) halide ion from CBr3F, resulting in the formation of a Ru(III) complex and a halide radical, CBr2F.The latter then interacts with DMHG, forming an aminyl radical 54.Subsequently, Ru(III) transfers the halide ion to intermediate 54, reducing to Ru(II) and forming diazene 55.The basicity of diazene 55 catalyzes the elimination of hydrobromic acid, leading to the formation of compound 56.Compound 56 then enolizes into imine ion 57, which undergoes cyclization to form pyrazoline 58.Finally, subsequent elimination of hydrogen bromide yields the desired product 59 (Figure 9).
The authors of publication [58] synthesized a fluorinated pyrazole through the reaction between a trifluoromethyl-containing DMHG derivative and trifluoroacetic anhydride in the presence of pyridine in chloroform at room temperature (Figure 10).The proposed cyclization pathway to form pyrazole 63 is as follows: Initially, trifluoroacetyl was attached to the carbonyl oxygen, resulting in the formation of salt 60.Subsequently, methylide 61 underwent cyclization to form hydropyrazole 62. Finally, the elimination of trifluoroacetic acid (TFA) led to the desired product 63 (Figure 10).
DMHG, upon reaction with hippuric acid 64, undergoes a transformation leading to the formation of an isoxazole ring 66 [60].In accordance with Lipinski's rules [61], it exhibits similarities to pharmaceutical compounds.Its logP (logarithm of partition coefficient) value is 1.996, indicating unhindered penetration of isoxazole through both aqueous and lipid barriers toward the biological target.
The synthesis of isoxazole [60] (Figure 11) was carried out in the presence of the chlorinating agent POCl3 in a mixture of acetic anhydride and a sodium acetate solution.DMHG was condensed with hippuric acid 64, resulting in the formation of chlorohydrin 65, which ultimately led to the desired isoxazole compound 66 (Figure 11).
The reactions of condensation products 68a and 68b with acetoacetic ether 67 proceed differently.In the initial stage, both compounds share a common step where the enol form 67 adds to the double C-C bond of compounds 68a and 68b.
The authors of [62] discovered that the cyclohexanone derivative 74b, when left at room temperature for 7 days, underwent conversion into N-dimethylaminopyrrole 80b.In the initial step, compound 74b likely decomposes into the starting reagents 67 and 68b through the opening of the cyclohexanone ring, followed by cleavage of the hydrazone bond 75b.Subsequently, acetoacetic ether 67 adds to the C-N bond of compound 68b, resulting in the formation of ether-ketone 76b.The latter undergoes cyclization to form dihydropyrrole 77b, while structure 78b undergoes 1,3-hydride transfer followed by water elimination.This leads to the formation of pyrrole 79b and enol compound 80b, which exist in a tautomeric equilibrium.
However, in a counter-synthesis approach, microwave radiation of the original compound 74b under conditions of 300 W and 160 °C for 30 min (equivalent to 7 days at room temperature) resulted in different outcomes.Instead of the expected product 80b, a completely new benzopyrrole 84b was formed.The transformations involved the elimination of methanol from cyclohexanone 74b, followed by enolization of ketone 81b and carbinol elimination from methyl ester 82b.Eventually, a 1-3-hydride transfer in lactone 83b led to the formation of an aromatic articulated heterocycle 84b (Figure 12).

Dimethylhydrazones of Acrolein and Crotonal
Methylenedimethylhydrazones of acrolein DMHA (a colorless oil [74]) and crotonal DMHC (a colorless oil, 55-58 °C/15 Torr [75]) are building blocks for various nitrogen- The reactions of condensation products 68a and 68b with acetoacetic ether 67 proceed differently.In the initial stage, both compounds share a common step where the enol form 67 adds to the double C-C bond of compounds 68a and 68b.
The authors of [62] discovered that the cyclohexanone derivative 74b, when left at room temperature for 7 days, underwent conversion into N-dimethylaminopyrrole 80b.In the initial step, compound 74b likely decomposes into the starting reagents 67 and 68b through the opening of the cyclohexanone ring, followed by cleavage of the hydrazone bond 75b.Subsequently, acetoacetic ether 67 adds to the C-N bond of compound 68b, resulting in the formation of ether-ketone 76b.The latter undergoes cyclization to form dihydropyrrole 77b, while structure 78b undergoes 1,3-hydride transfer followed by water elimination.This leads to the formation of pyrrole 79b and enol compound 80b, which exist in a tautomeric equilibrium.
However, in a counter-synthesis approach, microwave radiation of the original compound 74b under conditions of 300 W and 160 • C for 30 min (equivalent to 7 days at room temperature) resulted in different outcomes.Instead of the expected product 80b, a completely new benzopyrrole 84b was formed.The transformations involved the elimination of methanol from cyclohexanone 74b, followed by enolization of ketone 81b and carbinol elimination from methyl ester 82b.Eventually, a 1-3-hydride transfer in lactone 83b led to the formation of an aromatic articulated heterocycle 84b (Figure 12).

DMHA and DMHC in Cycloaddition Reactions
DMHA was utilized in the synthesis of dihydro- [75] and tetrahydropyrane structures [78], which constitute components of diverse natural products [75,79].These include cyclic saccharides obtained from coconut [79], irciniastatins (cytotoxins that induce necrosis within malignant neoplasm cells) isolated from sea sponges, exhibiting potential as anticancer agents [80], as well as a variety of marine products possessing a broad spectrum of biological activities such as antitumor, immunostimulatory, and analgesic properties [81].
In the contemporary scientific literature, the hydrazone methylene derivative (DMHA) has gained significant prominence as a fundamental component for constructing heterocyclic structures.In publication [75], this reagent was employed as a dienophile in the Diels-Alder reaction.The classical version of this reaction presents two primary challenges concerning α,β-unsaturated carbonyl compounds: (1) a substantial energy barrier between the diene and dienophile; (2) a lack of regioselectivity in the chemical process.
The former is explained by the energy sublevel discrepancy at the boundaries of molecular orbitals, which complicates the reaction between the reagents.The latter is caused by the fact that the highest occupied molecular orbital (HOMO) is occupied by electrons at the α and β positions.The electron arrangement facilitates cycloaddition simultaneously in two directions, leading to by-products.
The authors of [75] proposed an enhancement to the Diels-Alder reaction technique by employing dimethylhydrazone of acrolein (DMHA) (Figure 13) as a dienophile.The DMHA imine's electron-donating effect contributes to system saturation, thereby reducing the energy barrier between the reagents.To activate diene 74, rare-earth metal salts were utilized as catalysts.The most favorable outcome was observed with heptafluorobutanol europium campherate (condition a), which is a widely employed catalyst in enantioselective simultaneously in two directions, leading to by-products.
The authors of [75] proposed an enhancement to the Diels-Alder reaction technique by employing dimethylhydrazone of acrolein (DMHA) (Figure 13) as a dienophile.The DMHA imine's electron-donating effect contributes to system saturation, thereby reducing the energy barrier between the reagents.To activate diene 74, rare-earth metal salts were utilized as catalysts.The most favorable outcome was observed with heptafluorobutanol europium campherate (condition a), which is a widely employed catalyst in enantioselective Diels-Alder reactions.The reaction was carried out in toluene at room temperature for 15 h, resulting in the target product 77 with a quantitative yield (Figure 13).A method has been developed for the one-step synthesis of piperidino-indoloquinolines, which are challenging to access.These compounds are key components of marine alkaloid discorhabdin C analogs, specifically hydrogenated Diels-Alder adducts 79 and 80 [78] (Figure 14).In this method, the DMHA-based Diels-Alder reaction with indoloquinone 78 was accompanied by a simultaneous selective reduction catalyzed by palladium under a hydrogen atmosphere in an alcoholic solution at a pressure of 10 bar overnight.The resulting reaction mixture was purified using chromatography with aluminum oxide as the sorbent.The desired products of this reaction were obtained as blue crystals, with yields of 64% for compound 79 and 3% for compound 80 (Figure 14).A method has been developed for the one-step synthesis of piperidino-indoloquinolines, which are challenging to access.These compounds are key components of marine alkaloid discorhabdin C analogs, specifically hydrogenated Diels-Alder adducts 79 and 80 [78] (Figure 14).In this method, the DMHA-based Diels-Alder reaction with indoloquinone 78 was accompanied by a simultaneous selective reduction catalyzed by palladium under a hydrogen atmosphere in an alcoholic solution at a pressure of 10 bar overnight.The resulting reaction mixture was purified using chromatography with aluminum oxide as the sorbent.The desired products of this reaction were obtained as blue crystals, with yields of 64% for compound 79 and 3% for compound 80 (Figure 14).The Diels-Alder reaction with DMHA as a diene was previously investigated ([82], 1992).It has been observed that acrylonitrile 81 participates in the DMHA-based diene synthesis not only through [4+2] cycloaddition but also through [2+2] cycloaddition.Consequently, bicyclooctane 83 was obtained in acetonitrile at a temperature of 140 °C with a yield of 11%.A similar reaction was conducted in benzene in the presence of hydroquinone at 120 °C, resulting in the formation of a six-membered product of diene synthesis 82 with a yield of 67% (Figure 15).The Diels-Alder reaction with DMHA as a diene was previously investigated ([82], 1992).It has been observed that acrylonitrile 81 participates in the DMHA-based diene synthesis not only through [4+2] cycloaddition but also through [2+2] cycloaddition.Consequently, bicyclooctane 83 was obtained in acetonitrile at a temperature of 140 • C with a yield of 11%.A similar reaction was conducted in benzene in the presence of hydroquinone at 120 • C, resulting in the formation of a six-membered product of diene synthesis 82 with a yield of 67% (Figure 15).
The Diels-Alder reaction with DMHA as a diene was previously investigated ( [82], 1992).It has been observed that acrylonitrile 81 participates in the DMHA-based diene synthesis not only through [4+2] cycloaddition but also through [2+2] cycloaddition.Consequently, bicyclooctane 83 was obtained in acetonitrile at a temperature of 140 °C with a yield of 11%.A similar reaction was conducted in benzene in the presence of hydroquinone at 120 °C, resulting in the formation of a six-membered product of diene synthesis 82 with a yield of 67% (Figure 15).However, the diene and dienophile cycloaddition reactions may exhibit different reaction pathways.Therefore, the authors of publication [76] investigated the interaction between quinonmonoimide 84 and dimethylhydrazadiene DMHC in ethanol at 0 °C.It was discovered that the reaction proceeded in two directions (Figure 16).One direction involved a [2+3]-cycloaddition, resulting in the formation of adduct 87.The other direction involved a [2+4]-cycloaddition, yielding compound 88.Upon reacting with a second molecule of quinon-imine 84, the Diels-Alder adduct 88 produced a tetracyclic product 89.The latter underwent slow isomerization to form aromatic aminophenol 90 in a deuterated chloroform solvent and was even slower in polar solvents such as acetone and ethyl acetate [76] (Figure 16).However, the diene and dienophile cycloaddition reactions may exhibit different reaction pathways.Therefore, the authors of publication [76] investigated the interaction between quinonmonoimide 84 and dimethylhydrazadiene DMHC in ethanol at 0 • C. It was discovered that the reaction proceeded in two directions (Figure 16).One direction involved a [2+3]-cycloaddition, resulting in the formation of adduct 87.The other direction involved a [2+4]-cycloaddition, yielding compound 88.Upon reacting with a second molecule of quinon-imine 84, the Diels-Alder adduct 88 produced a tetracyclic product 89.The latter underwent slow isomerization to form aromatic aminophenol 90 in a deuterated chloroform solvent and was even slower in polar solvents such as acetone and ethyl acetate [76] (Figure 16).
The synthesis of the latter compound 102 is described in publication [84] (Figure 17).The authors of [84] achieved the synthesis of compound 102 by reducing the nitro group
The synthesis of the latter compound 102 is described in publication [84] (Figure 17).The authors of [84] achieved the synthesis of compound 102 by reducing the nitro group of the initial ketone 91 to the corresponding amine 92 with a yield of 99% in the presence of iron in acetic acid and catalytic amounts of hydrogen chloride.Subsequently, amine 92 underwent halogenation in a mixture of ethyl ether and chloroform with a slight excess of bromine (1:0.9),resulting in the formation of target compound 93 with a yield of 62%.Brominated adduct 93 was then subjected to Friedlander's reaction [86] with cyclohexanone 94, leading to the formation of tricyclic product 95 with a yield of 100%.Compound 95 was further oxidized to quinone 97 using cerium ammonium nitrate (CAN) due to its ability to selectively affect ether functional groups, specifically the methoxy group, in this case [87].The oxidation reaction was carried out in an aqueous acetonitrile medium, and compound 97 was obtained with a yield of 98%.Dienophile 97 was also employed in a hetero-Diels-Alder reaction with DMHA, yielding adduct 98 with a yield of 79%.Adduct 98 served as a methylene-active linker in the subsequent Mannich reaction, leading to the formation of the target compound 101 with a yield of 14% (Figure 17).The article [84] presents data on the antitumor activity of synthesized derivatives 98 and 101 in comparison to the known alkaloid ascididemine [84] against four cell lines (Table S5).The compounds exhibited an inhibitory concentration of 50% in cell lines at approximately 10 −6 M [84] (see Table S4 in the Supplementary Materials).
Moreover, Ascididemine derivatives with enhanced efficacy against oncology were synthesized [85] (Figure 18).In the initial step, a [4+2]-cycloaddition reaction was per- The article [84] presents data on the antitumor activity of synthesized derivatives 98 and 101 in comparison to the known alkaloid ascididemine [84] against four cell lines (Table S5).The compounds exhibited an inhibitory concentration of 50% in cell lines at approximately 10−6 M [84] (see Table S4 in the Supplementary Materials).
Moreover, Ascididemine derivatives with enhanced efficacy against oncology were synthesized [85] (Figure 18).In the initial step, a [4+2]-cycloaddition reaction was performed using dienes DMHA and DMHC as well as dienophiles 102a, 102b, and 102c.Subsequent elimination reactions via acetic anhydrid and manganese dioxide [88] yielded adducts 103a, 103b, and 103c.Among these, adduct 103a was specifically chosen for the synthesis of its dimethylamino derivative 104a'.This was achieved by employing dimethylamine in hydrochloride form (due to the gaseous nature of the amine), followed by an alkali treatment to neutralize the reaction medium.A solvent mixture of water and tetrahydrofuran was utilized, where water facilitated the dissolution of hydrochloride and alkali, while nonpolar tetrahydrofuran prevented undesired side reactions such as pyridinium salt formation.Compounds 104a', 103a, 103b, and 103c were subsequently employed in further chemical transformations [85].The subsequent stage involved elements of the Bracher method [85,89].A combination of polar and basic solvents, namely dimethylformamide (DMF) and diethanolamine (DEA), was used to promote the condensation of compounds 103a, 103b, 103c, and 104a' with DMF under an inert nitrogen atmosphere.This led to the formation of intermediates 104a, 104b, 104c, and 105a'.These intermediates then underwent cyclization to yield the desired products 105a, 105c, 106a', and 106b (Figure 18).The bromine atom of phenanthroline-7-one derivative 106b [85] was substituted with various amino groups (Figure 18).Dimethylamino and N-piperidino groups were introduced in an aqueous THF solution under basic conditions, resulting in the formation of compounds 107b and 109b, respectively.Amine 108b was obtained from sodium azide.Subsequent chemical transformations of compound 108b were carried out using aldehydes and acetals in the presence of sodium boron anhydride and TFA, yielding compounds 110, 111, and 112.Chlorine (compound 108) was incorporated into structure 105c through the use of phosphoric acid chlorohydride.Hydroxyl and butyl groups (structures 106 and 108, respectively) were introduced by reacting with butyl alcohol in the presence of ammonium chloride [85] (Figure 18).
The synthesized marine alkaloid analogs were tested on 12 cancer cell lines [87].The IC 50 value of these compounds on 12 cell lines made 10 −6 M. (see Table S5 in the Supplementary Materials).
tions, resulting in the formation of compounds 107b and 109b, respectively.Amine 108b was obtained from sodium azide.Subsequent chemical transformations of compound 108b were carried out using aldehydes and acetals in the presence of sodium boron anhydride and TFA, yielding compounds 110, 111, and 112.Chlorine (compound 108) was incorporated into structure 105c through the use of phosphoric acid chlorohydride.Hydroxyl and butyl groups (structures 106 and 108, respectively) were introduced by reacting with butyl alcohol in the presence of ammonium chloride [85] (Figure 18).The DMHA chain lengthening described in publication [90] (Figure 19) is also of interest in organic synthesis.N,N-dimethylformiminium hydrochloride 114 in absolute dimethylformamide (DMF) was used as the electrophile.The authors of [90] proposed that DMHA adds to N,N-dimethylformiminium 114 (Figure 19) through its tautomeric form 113, with the hydrogen being replaced by the methylene group of intermediate 115 located at the dimethylamino group.When one equivalent of N,N-dimethylformiminium 116 was added to DMHA, salt 117 was formed.Crystallization of salt 117 was achieved by adding DMF*HCl, resulting in the formation of dihydrochloride product 117.However, when twice the amount of the same reagent 114a was added, compound 118 crystallized independently without salting out (Figure 19).
The DMHA chain lengthening described in publication [90] (Figure 19) is also of interest in organic synthesis.N,N-dimethylformiminium hydrochloride 114 in absolute dimethylformamide (DMF) was used as the electrophile.The authors of [90] proposed that DMHA adds to N,N-dimethylformiminium 114 (Figure 19) through its tautomeric form 113, with the hydrogen being replaced by the methylene group of intermediate 115 located at the dimethylamino group.When one equivalent of N,N-dimethylformiminium 116 was added to DMHA, salt 117 was formed.Crystallization of salt 117 was achieved by adding DMF*HCl, resulting in the formation of dihydrochloride product 117.However, when twice the amount of the same reagent 114a was added, compound 118 crystallized independently without salting out (Figure 19).  ) is also applicable in the synthesis of the tetrahydroquinoline ring [92,93], which is a part of various natural products.These include benzostatins that prevent lipid peroxidation, thereby reducing the likelihood of patagenesis [94] and reducing the toxicity of glutamate [95], of cusparin and allocusparin having anti-tuberculosis activity [96], and martellinic acid activity against conjunctivitis [97].  ) is also applicable in the synthesis of the tetrahydroquinoline ring [92,93], which is a part of various natural products.These include benzostatins that prevent lipid peroxidation, thereby reducing the likelihood of patagenesis [94] and reducing the toxicity of glutamate [95], of cusparin and allocusparin having anti-tuberculosis activity [96], and martellinic acid activity against conjunctivitis [97].
In 2021, the authors of publication [92] reported the potential enhancement of benzostatin derivatives 119 yield (90%) through the utilization of a 20 Hz vibrating ball mill and appropriate catalyst selection in the Povarov reaction (Figure 20).Initially, Schiff base 121 was synthesized by reacting p-anisidine 119 with phenylglyoxal 120.Subsequently, the reaction with methylacrolein DMHM was catalyzed by tosylic acid (p-TsOH).The catalytic process likely proceeded as follows: firstly, the proton p-TsOH was localized at the imine 121, resulting in the formation of tosylate 122.Secondly, the addition of DMHM led to electron density and proton migration from the phenyl ring 123.Consequently, tosylic acid was regenerated, followed by the cyclization of aryl 123 to tetrahydroquinoline 124 (Figure 20).
base 121 was synthesized by reacting p-anisidine 119 with phenylglyoxal 120.Subsequently, the reaction with methylacrolein DMHM was catalyzed by tosylic acid (p-TsOH).The catalytic process likely proceeded as follows: firstly, the proton p-TsOH was localized at the imine 121, resulting in the formation of tosylate 122.Secondly, the addition of DMHM led to electron density and proton migration from the phenyl ring 123.Consequently, tosylic acid was regenerated, followed by the cyclization of aryl 123 to tetrahydroquinoline 124 (Figure 20).The synthetic capabilities of DMHM (dimethylhydrazone methacrolein) in the Povarov reaction were previously described in 2012.In their publication [93], the authors investigated the pathways for two-component and three-component syntheses (Figure 21).In the first case, tetrahydroquinoline 128 was synthesized through the indium (III) chloride-catalyzed reaction of DMHM with Schiff base 125 in acetonitrile at room temperature.In the second case, the authors of [90] elucidated the formation of a tricyclic structure 132 from arylamine 135.This was explained by a cascade process involving several steps.Firstly, compound 129 was added to the double C-C and C-N bonds of compound 127.Subsequently, an intramolecular cyclization of the amino group occurred via the double bond of hydrazone 130, leading to simultaneous catalyst regeneration.Following this, product 131 underwent cyclization with the elimination of asymmetric dimethylhydrazine (UDMH).The UDMH then underwent transamination with the original compound 133, resulting in the formation of dimethylhydrazon 134 (Figure 21).The synthetic capabilities of DMHM (dimethylhydrazone methacrolein) in the Povarov reaction were previously described in 2012.In their publication [93], the authors investigated the pathways for two-component and three-component syntheses (Figure 21).In the first case, tetrahydroquinoline 128 was synthesized through the indium (III) chloridecatalyzed reaction of DMHM with Schiff base 125 in acetonitrile at room temperature.In the second case, the authors of [90] elucidated the formation of a tricyclic structure 132 from arylamine 135.This was explained by a cascade process involving several steps.Firstly, compound 129 was added to the double C-C and C-N bonds of compound 127.Subsequently, an intramolecular cyclization of the amino group occurred via the double bond of hydrazone 130, leading to simultaneous catalyst regeneration.Following this, product 131 underwent cyclization with the elimination of asymmetric dimethylhydrazine (UDMH).The UDMH then underwent transamination with the original compound 133, resulting in the formation of dimethylhydrazon 134 (Figure 21).
To enhance the yield of the tricyclic derivative 132, the researchers of [93] utilized the BF3*Et2O/CHCl3 catalyst/solvent system, resulting in a 93% yield of the desired compound.In certain instances, minor quantities of transamination products and tetrahydroquinoline were also obtained (Figure 22).Conducting the synthesis in a concentrated solution of the same system, as anticipated, increased the yield of condensate 132 but led to the formation of diastereomers.The excess arylamine contributed to transamination reactions rather than cyclization towards the desired compound 132 [93] (Figure 22).
The synthesis of the hard-to-reach azetidine cycle [101] (Figure 23) was accomplished via hydrochloric acid elimination, followed by MDH addition to the ketene 136 C=O bond.The electron density in intermediate 137 facilitated intramolecular cyclization to form azetidine 138 (Figure 23).TCNE (tetracyanoethylene) undergoes a reaction with the mobile hydrogen of the MDH (methylene active link) moiety, as depicted in Figure 24.Simultaneously, tricyanohydrazone derivatives are formed, which are recognized as promising antimicrobial dyes and photosensitizers [15] (Figure 24).
The synthesis of the hard-to-reach azetidine cycle [101] (Figure 23) was accomplished via hydrochloric acid elimination, followed by MDH addition to the ketene 136 C=O bond.The electron density in intermediate 137 facilitated intramolecular cyclization to form azetidine 138 (Figure 23).TCNE (tetracyanoethylene) undergoes a reaction with the mobile hydrogen of the MDH (methylene active link) moiety, as depicted in Figure 24.Simultaneously, tricyanohydrazone derivatives are formed, which are recognized as promising antimicrobial dyes and photosensitizers [15] (Figure 24).MDH is capable of undergoing [4+2]-cycloaddition reactions, specifically Alder-Rickett-type reactions (Figure 25), with a tetrazene derivative 140.This reaction leads to the formation of a bicyclic structure 141, which can be cleaved to release nitrogen and subsequently form triazinamine 142 [112] (Figure 25).MDH is capable of undergoing [4+2]-cycloaddition reactions, specifically Alder-Rickett-type reactions (Figure 25), with a tetrazene derivative 140.This reaction leads to the formation of a bicyclic structure 141, which can be cleaved to release nitrogen and subsequently form triazinamine 142 [112] (Figure 25).MDH is capable of undergoing [4+2]-cycloaddition reactions, specifically Alder-Rickett-type reactions (Figure 25), with a tetrazene derivative 140.This reaction leads to the formation of a bicyclic structure 141, which can be cleaved to release nitrogen and subsequently form triazinamine 142 [112] (Figure 25).

Conclusions
Thus, hydrazones of dimethylhydrazine carbonyl derivatives hold promise in the creation of various natural structure analogs (alkaloids, enzymes, antibacterial, antitumor drugs), as well as serving as a tool for molecular design in organic synthesis.
The treatment of substandard rocket fuel through the formation of hydrazones of carbonyl compounds offers several advantages: 1. Negative cost of the original unsymmetrical dimethylhydrazine (UDMH); 2. Reduced toxicity and less pungent odor of carbonyl derivatives (compared to UDMH itself), facilitating their use in large-scale and multi-stage synthesis; 3. The possibility of conducting stereoselective reactions and obtaining optically pure compounds; 4. The electron-rich nitrogen-carbon double bond enables various cycloaddition reactions (4+2, 3+2, 2+2) and the synthesis of heterocyclic derivatives with high yields.5.Many heterocyclic compounds based on dimethylhydrazone have demonstrated high antitumor activity (phenanthroline-7-ones), antifungal activity, and antibacterial activity (thiobazidalin derivatives); 6.In numerous reactions, target products with quantitative yields have been obtained.
For example, dihydropyran, a component of irciniastatins (marine products), can be synthesized via the Diels-Alder reaction with a 100% yield (Eu(hfc)3, room temperature, 15 h).The Povarov reaction can provide a tetrahydroquinoline ring, which is a constituent of benzostatins.However, one of the main drawbacks of using DMH carbonyl derivatives in organic synthesis is the requirement for hard-to-access reagents (LDA, Bu-Li, t-BuOK, InCl2, AcOAc, Eu(hfc)3) for the transformation into target compounds.

Figure 1 .
Figure 1.Annealing of camphor with pyrrole heterocycle (method 1).The red cross indicates that ammonium acetate is an incorrect reagent for the cyclization of compound 5 into pyrrole 6.

Figure 1 .
Figure 1.Annealing of camphor with pyrrole heterocycle (method 1).The red cross indicates that ammonium acetate is an incorrect reagent for the cyclization of compound 5 into pyrrole 6.

Figure 5 .
Figure 5. Preparation of acetylpyridine is followed by cross-coupling.

Figure 6 .
Figure 6.Intramolecular cyclization into a pyrrole ring and further chemical transformations of compound 35a.

Figure 6 .
Figure 6.Intramolecular cyclization into a pyrrole ring and further chemical transformations of compound 35a.

Figure 21 .
Figure 21.Directions of reaction according to Povarov type.

Figure 21 .
Figure 21.Directions of reaction according to Povarov type.

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a

Table 1 .
Reagents and conditions for synthesis of compounds 45a