Solvent-free Conditions Research Articles

Malic Acid as a Green Catalyst for the N-Boc Protection under Solvent-free Condition

Abstract: A protocol for the Chemoselective N-Boc protection of various types of amines has been developed. This includes heteroaryl, aliphatic, and alicyclic amines. The process makes use of malic acid as a catalyst and operates efficiently at ambient temperature without the need for solvents. This technique has been proven to effectively protect a wide range of functionalized amines containing both electron-donating and electron-withdrawing substituents. The benefits of this method include its fast reaction rate, high selectivity, excellent yield, catalyst recyclability, and environmentally friendly conditions.

Evaluation of antibacterial, cytotoxicity, and apoptosis activity of novel chromene-sulfonamide hybrids synthesized under solvent-free conditions and 3D-QSAR modeling studies

In this study, eleven novel chromene sulfonamide hybrids were synthesized by a convenient method in accordance with green chemistry. At first, chromene derivatives (1–9a) were prepared through the multi-component reaction between aryl aldehydes, malononitrile, and 3-aminophenol. Then, synthesized chromenes were reacted with appropriate sulfonyl chlorides by grinding method to give the corresponding chromene sulfonamide hybrids (1–11b). Synthesized hybrids were obtained in good to high yield and characterized by IR, 1HNMR, 13CNMR, CHN and melting point techniques. In addition, the broth microdilution assay was used to determine the minimal inhibitory concentration of newly synthesized chromene-sulfonamide hybrids. The MTT test was used to determine the cytotoxicity and apoptotic activity of the newly synthesized compounds against fibroblast L929 cells. The 3D‑QSAR analysis confirmed the experimental assays, demonstrating that our predictive model is useful for developing new antibacterial inhibitors. Consequently, molecular docking studies were performed to validate the findings of the 3D-QSAR analysis, confirming the potential binding interactions of the synthesized chromene-sulfonamide hybrids with the target enzymes. Molecular docking studies were employed to support the 3D-QSAR predictions, providing insights into the binding interactions between the newly synthesized chromene-sulfonamide hybrids and their target bacterial enzymes, thereby reinforcing the potential efficacy of these compounds as antibacterial agents. Also, some of the experimental outcomes supported or conflicted with the pharmacokinetic prediction (especially about compound carcinogenicity). The performance of ADMET predictor results was assessed. The work presented here proposes a computationally driven strategy for designing and discovering a new sulfonamide scaffold for bacterial inhibition.

Enhanced Catalytic Activity of Binuclear Oxidovanadium(IV) Bisbenzimidazole Linked Porphyrin Dimer for the Generation of Biologically Active 3,4-Dihydropyrimidinones and Their Corresponding Thiones.

Binuclear vanadyl(IV) porphyrin (V2BP), where two vanadium(IV) porphyrin macrocycles are linked through benzimidazole units at the β-positions, has been prepared and characterized with various techniques, such as UV-vis, Fourier transform-infrared, electron paramagnetic resonance, cyclic voltammetry, density functional transform calculations, and mass spectrometry. V2BP exhibits a red shift (Δλmax = 10 nm) in the Soret band as compared with unsubstituted parent vanadyl(IV) meso-tetraphenylporphyrin (VP). The synthesized binuclear vanadyl(IV) porphyrin (V2BP) has further been studied as a catalyst to explore a single-pot multicomponent Biginelli reaction producing biologically active 3,4-dihydropyrimidin-2-(1H)-one (DHPM)-based biomolecules and the corresponding thiones under solvent-free conditions and its catalytic activity has been compared with vanadyl(IV) meso-tetraphenylporphyrin (VP). Several reaction conditions, such as the amount of catalyst, time, solvent, and temperature, have been optimized to obtain the maximum yield of DHPMs or thiones. The synthesized β-functionalized V2BP porphyrin dimer manifests much higher conversion (84-95% yield) of DHPMs or the corresponding thiones under the optimized reaction conditions with high TON (4454-5037) and TOF (1113-1259 h-1) values for the one-pot multicomponent Biginelli reaction as compared to the literature. The catalyst exhibited excellent recyclability up to 10 cycles.

Liquid phase oxidation of cyclopentanone over metal-free carbon catalysts

AbstractOxidation of cyclopentanone (CPO) was studied over metal-free carbon catalysts in solvent-free conditions. Norit SX plus (900 m2 g−1) and Vulcan XC72 (240 m2 g−1) were used as pristine materials. Catalysts were prepared by activation in nitrogen and by treatment with urea, calcined in nitrogen at 500 °C and 950 °C. SEM, EDX, XPS, X-ray powder diffraction, nitrogen adsorption–desorption isotherms, acid–base titration, FTIR and Raman techniques were used for characterization. Catalytic tests carried out at 0.45 MPa and 80–110 °C enabled to find the best results: 30% selectivity to glutaric acid (GA) and 3% to succinic acid at 25% conversion of CPO, over Vulcan type catalysts. A low activity, selectivity and strong deactivation of Norit type catalysts can be ascribed to a higher specific surface in a disordered arrangement providing a high concentration of unselective catalytic sites. A higher extent of side reactions can yield in higher molar mass products, which stick on the surface and block catalytic sites. Optimum amount of accessible planar domains, represented by graphene and/or graphitic plates with some disorders present in Vulcan type catalysts classified them superior to Norit catalysts. A redox reaction scheme of oxidation of CPO to GA is also proposed. Graphical abstract

Mechanochemistry Drives Alkene Difunctionalization via Radical Ligand Transfer and Electron Catalysis.

A general and modular protocol is reported for olefin difunctionalization through mechanochemistry, facilitated by cooperative radical ligand transfer (RLT) and electron catalysis. Utilizing mechanochemical force and catalytic amounts of 2,2,6,6-tetramethylpiperidinyloxyl (TEMPO), ferric nitrate can leverage nitryl radicals, transfer nitrooxy-functional group via RLT, and mediate an electron catalysis cycle under room temperature. A diverse range of activated and unactivated alkenes exhibited chemo- and regioselective 1,2-nitronitrooxylation under solvent-free or solvent-less conditions, showcasing excellent functional group tolerance. Mechanistic studies indicated a significant impact of mechanochemistry and highlighted the radical nature of this nitrative difunctionalization process.

An Efficient Propylphosphonic Anhydride (T3P®)-Mediated MW-induced Solvent-free Rapid Synthesis of Enamino Esters and Ketones including 5, 5-Dimethyl-3-aminocyclohex-2-enones

Abstract: This work presents a clean and convenient synthesis of various β-enaminones including 5,5- dimethyl-3-aminocyclohex-2-enones, in satisfactory to excellent yields from the condensation reaction of primary amines with β -dicarbonyls by employing T3P® as a catalyst and performing the reaction under microwave irradiation and solvent-free conditions. These rapid reactions launched readily and stood a diversity of organic functional groups. A mixture of 1,3-dicarbonyl compound, primary amine and T3P® (50% in AcOEt) was irradiated for an appropriate time under microwave at 80°C. After completing the reaction (TLC) and cooling to r.t., ethyl acetate and saturated aqueous NaHCO3 solution were added. The aqueous phase was extracted ethyl acetate. The combined organic layer was washed with brine, dried over Na2SO4, and filtered, and the solvent was removed under reduced pressure to afford the product, which was recrystallized from diisopropyl ether. The presented results exhibit a better catalytic activity of T3P in the synthesis of enaminones. It could be concluded that T3P is the best catalyst as it took only a few minutes for the completion of the reaction with an excellent yield of product, which indicates T3P is more efficient, compared to other catalysts. A comparison of the efficiency of the present procedure with some heterogeneous solid catalysts was evaluated as well. Clearly, a higher yield was established in this procedure compared to other catalysts. Furthermore, the reaction of amines with dimedone was investigated as well, delivering excellent yields. The reaction catalyzed by T3P under microwave irradiation supplies a comprehensive method for the synthesis of enaminones. In this work, T3P is an effective, efficient and green catalyst, which forms the procedure economic, suitable, and safe with widespread application in the synthesis of enaminones. background: This work presents a clean and convenient synthesis of various β-enaminones incuding 5,5-dimethyl-3-aminocyclohex-2-enones in good to excellent yields from the reaction of different primary amines with 1,3-dicarbonyl compounds by employing T3P® as a catalyst and performing the reaction under microwave irradiation and solvent-free conditions. This one-pot rapid reaction proceeded readily and tolerated a variety of functional groups.

Synthesis of Polysubstituted Pyridines via Nitrogen-doped Graphene Catalyzed One-Pot Multicomponent Reaction under Solvent-Free Conditions

Abstract: Polysubstituted pyridine derivatives were produced with high to excellent yields in the presence of nitrogen-doped graphene (NDG) as a dual acid-based catalyst. NDG efficiently catalyzes the multicomponent reaction between arylaldehydes, diethyl-acetylene dicarboxylates, malononitrile, and ammonium acetate under solvent-free conditions at 80°C to afford the polysubstituted pyridines in short reaction times. The structures of the synthesized pyridines were established by Ft-IR, 1H, and 13C NMR spectroscopic analysis. The advantages of this method include the in-situ oxidation of prepared 1,4-dihydropyridines, one-pot procedure, solventless system, operational simplicity, and no column chromatography. Additionally, neither toxic solvents nor catalysts are needed, and the procedure can be very reliable among the reported methodologies. The yields and reaction times in the presence of four times recycled catalyst are in comparable to the fresh catalyst.

Green and Convenient Synthesis of Pharmaceutically Active Mono and Bis-dihydroquinazolines via a One-pot Multicomponent Reaction Under Sulfamic Acid Catalysis

Introduction: Multicomponent reactions (MCRs) and green chemistry are essential criteria for the development of efficient chemical syntheses for valuable organic compounds. Method: The design, synthesis, and development of sustainable procedures for the production of novel biological and pharmaceutical molecules have gained high importance. Herein, an environmentally benign synthesis of mono- and bis-2,3-dihydroquinazolin-4(1H)-ones as pharmaceutically active compounds was carried out in good to high yields of 80-99% within 45-120 minutes. Result: The desired products were synthesized via three-component and pseudo five-component condensations of isatoic anhydride, a primary amine (aniline or ammonium acetate), and an aldehyde/dialdehyde using sulfamic acid (20%) as a solid acidic catalyst under the solvent-free condition at 100°C. Conclusion: The easy work-up procedure, metal-free and environmentally benign catalyst, green reaction conditions for performing MCRs, and high yields of pure products are some advantages of the presented protocol.

Chemically engineered essential oils prepared through thiocyanation under solvent-free conditions: chemical and bioactivity alteration

The generation of chemically engineered essential oils (CEEOs) prepared from bi-heteroatomic reactions using ammonium thiocyanate as a source of bioactive compounds is described. The impact of the reaction on the chemical composition of the mixtures was qualitatively demonstrated through GC–MS, utilizing univariate and multivariate analysis. The reaction transformed most of the components in the natural mixtures, thereby expanding the chemical diversity of the mixtures. Changes in inhibition properties between natural and CEEOs were demonstrated through acetylcholinesterase TLC autography, resulting in a threefold increase in the number of positive events due to the modification process. The chemically engineered Origanum vulgare L. essential oil was subjected to bioguided fractionation, leading to the discovery of four new active compounds with similar or higher potency than eserine against the enzyme. The results suggest that the directed chemical transformation of essential oils can be a valuable strategy for discovering new acetylcholinesterase (AChE) inhibitors.Graphical

Solvent-free synthesis of composite magnetic CoO@ZIF-67 for efficient and practical use

The facile synthesis of composite material, combining magnetic CoO with ZIF-67 (CoO@ZIF-67), has been successfully developed. This innovative approach involves the growth of a crystalline (ZIF-67) derived from stable and abundant CoO, resulting in the formation of the composite magnetic CoO@ZIF-67. The synthesis method, based on a solid-state thermal approach (SST), is straightforward and efficient, conducted in a single step and under solvent-free conditions, leading to the homogeneously composite formation of CoO@ZIF-67. Importantly, the composite magnetic CoO@ZIF-67 material has demonstrated remarkable catalytic performance as a heterogeneous catalyst in various reactions while requiring a lower catalyst loading under comparable conditions to those needed for pure ZIF-67. A significant advantage of this newly developed composite catalyst, CoO@ZIF-67, is its ease of separation and recyclability. The recovery catalyst can be achieved through the use of an external magnet, making it a standout feature of the green and environmentally friendly synthetic procedure used in its production.

Soft-templating synthesis of mesoporous MnSiOx composites as catalytic supports for Pd nanoparticles towards solvent-free oxidation of benzyl alcohol under atmospheric pressure O2

Solvent-free and liquid-phase selective oxidation of aromatic alcohols using O2 as an oxidant is a green strategy for the synthesis of aromatic aldehydes and other carbonyl compounds. Wherein, the design and preparation of heterogeneous catalysts with high activity and selectivity is a hot topic in this process. Herein, a series of manganese oxide-silica (MnSiOx) composites were synthesized using cetyltrimethylammonium bromide as a soft template. During the preparation process, the amounts of tetraethyl orthosilicate and ammonia and the calcination temperature significantly affected the textural properties and Mn cation distributions of MnSiOx. The MnSiOx composites were then employed as catalysts for Pd nanoparticles. In the solvent-free and atmospheric conditions, Pd/MnSiOx materials showed high catalytic conversions of benzyl alcohol (BZA), and the catalytic activity thereof is related to the fractions of Pd0 and Mn3+. As the reaction time and temperature are 4 h and 90 °C, the conversion of BZA (feeding dosage: 4 mL) and the selectivity of benzaldehyde are 64.8 % and 94.9 %, respectively. The catalyst can be reused at least five times without any significant loss of activity. Furthermore, the correlation between physiochemical properties and catalytic activity of Pd/MnSiOx was analyzed.

Two-Dimensional Cu(II)-MOF with Lewis Acid-Base Bifunctional Sites for Chemical Fixation of CO2 and Bioactive 1,4-DHP Synthesis via Hantzsch Condensation.

Five- and six-membered heterocycles containing nitrogen or oxygen have been considered as privileged scaffolds in organic chemistry and the chemical industry because of their usage in high-value commodities. Herein, we report a two-dimensional (2D) Cu(II)-based MOF catalyst, IITKGP-40, via the strategic employment of ample Lewis acid-base bifunctional sites (open metal nodes and free pyrazine moieties) along the pore wall. IITKGP-40 could convert toxic CO2 to cyclic carbonates in an atom-economical manner under solvent-free conditions and aromatic aldehyde to bioactive 1,4-DHPs via Hantzsch condensation. Exceptional catalytic performance (99%) and turnover number under mild reaction conditions for CO2 fixation using sterically hindered styrene oxide, and good-to-excellent yields for a wide range of aromatic aldehydes toward 1,4-dihydropyridines (1,4-DHPs) make IITKGP-40 promising as a multipurpose heterogeneous catalyst. Moreover, to demonstrate the practical utility of the catalyst, two biologically important drug molecules, diludine and nitrendipine analogue, have also been synthesized. IITKGP-40 is recyclable for at least three consecutive runs without significant loss of activity, making it promising for real-time applications.

Metal-acid synergistic catalysis accelerates the hydrogen borrowing amination of alcohols by confining Ru sites in Beta zeolite

Direct hydrogen transfer amination of alcohols with amines is an environmentally friendly and atom-economical route for the synthesis of N-alkylamines. Noble metal species are highly catalytic active sites, but the exorbitant price makes the urgency to boost the atom efficiency with stable recyclability. Herein, we demonstrated that encapsulation of Ru nanoparticles (NPs) within BEA zeolite through direct hydrothermal approach greatly promoted the catalytic efficiency in the N-alkylation of aromatic alcohols and amines under additive- and solvent-free conditions, resulting in the high yield (∼93 %), maximum turnover number (TON) of 12,822 and turnover frequency (TOF) of 9012 h−1, with stable recyclability and extendable substrate scope. The kinetic studies and in-situ characterizations revealed that the synergy of confined Ru NPs and adjacent acid sites of BEA zeolite significantly promoted the C–H bond activation in the rate-determining step of alcohol dehydrogenation into aldehydes. Besides, the acid sites also accelerated the condensation of aldehyde intermediates and anilines to promote the kinetic equilibrium, while the moderate strength of the Ru–H bond resulting from the confined Ru NPs is advantageous to balance the dehydrogenation and hydrogenation steps to reach the fascinating H-transfer process.

One-Pot Synthesis of Ce-SSZ-39 Zeolite with Performance in the NH3-SCR Reaction.

Cu-SSZ-39 zeolite with 8-membered rings is regarded as a very promising catalyst in the NH3-SCR reaction, but its hydrothermal stability still remains to be improved. One of the solutions to promote hydrothermal stability is the insertion of rare earth elements in the product. Nevertheless, normal ion exchange of rare earth elements limits their contents in the zeolite product due to their large hydrated ionic radius and alkaline environment under hydrothermal conditions. Herein, we for the first time present a new method for the one-pot synthesis of Ce-SSZ-39 zeolite under solvent-free conditions. The key to success is the use of Ce-FAU zeolite as a precursor. The obtained product shows good crystallinity, sheet-like morphology, large BET surface area, and 4-coordinated Al species. Detailed investigations illustrate that Ce species in the Cu/Ce-SSZ-39 zeolite micropore can prevent the dealumination and thus formation of CuAlOx species during hydrothermal aging at 850 °C for 16 h, giving the excellent hydrothermal stability and thus showing the excellent catalytic performance in the NH3-SCR reaction. One-pot synthesis of Ce-SSZ-39 zeolite with excellent catalytic performance might open a new door for developing very efficient selective catalytic reduction (SCR) catalysts in near future.

Green Synthesis of Zinc Oxide NPs as a New Catalyst for the Synthesis of Imidazo[2,1-b]quinazoline Derivatives with Docking Validation as Aurora Kinase (AKI-001) Inhibitors

Abstract: As natural capping reagents, flaxseed gel, caprylic/capric triglyceride, aloe vera, and propylene glycol were utilized in the synthesis of ZnO-NPs in the current study. The synthesized ZnO NPs structure was characterized by Transmission Electron Microscopy (TEM), Fourier Transform Infrared (FT-IR), and X-Ray Diffraction (XRD). The prepared ZnO-NPs were used as an efficient catalyst for the production of a new series of fused polynuclear heterocyclic system-based imidazoquinazoline by multicomponent reaction. The reaction was initiated by mixing 2-aminobenzimidazole, aryl/hetaryl aldehydes, and betanaphthol under solvent-free conditions at 60-70 °C in the presence of a catalytic amount of the synthesized ZnO-NPs. As demonstrated by molecular docking, the prepared ligands (4, 7, 8, 9, and 11) exhibited outstanding validation as aurora kinase inhibitors in comparison to AKI-001, the prototype pentacyclic inhibitor. result: synthesis of some new imidazo[2,1-b]quinazoline derivatives by green method with docking validation as aurora kinase (AKI-001) inhibitor other: no

One-Pot and Three-Component Coupling Synthesis of Novel p-[(Benzothiazolylamino)(aryl/heteroaryl)methyl]phenols and Its Corresponding O-Tosylates under Catalyst- and Solvent-Free Conditions

AbstractA catalyst- and solvent-free procedure has been developed for the synthesis of p-[( benzothiazolylamino)(aryl/heteroaryl)methyl]-functionalized phenols and its O-tosylates via one-pot three-component coupling reaction of thymol or carvacrol, aryl/heteroaryl aldehydes, and 2-aminobenzothiazoles with high selectivity. The present amino methylation process is convenient to perform even on large scale with a broad scope. The products were likely formed through the initial para attack of thymol on aldehydes to generate p-quinone methide intermediate and subsequent 1,6-aza-Michael addition of 2-aminobenzothiazoles on in-situ generated p-quinone methide intermediate.

Variation in Catalytic Efficacies of a 2D pH-Stable MOF by Altering Activation Methods.

Although it is well-known that the Lewis acidity of Metal-Organic Frameworks (MOFs) can effectively enhance their catalytic activity in organic transformations, access to these Lewis-acidic sites remains a key hurdle to widespread applications of Lewis-acidic catalysis by MOFs. Easy accessibility of strong Lewis acidic sites onto 2D MOFs by using proper activation methods can be a cornerstone in attaining desired catalytic performance. Herein, we report a new 2D chemically stable MOF, IITKGP-60, which displayed excellent framework robustness over a wide pH range (2-12). Benefiting from the abundant open metal sites (OMSs) and framework robustness, the catalytic activity of the developed material was explored in one-pot three-component Strecker reaction and Knoevenagel condensation reaction. Moreover, the developed catalyst is superior in catalyzing the reactions involving sterically hindered substrate (1-naphthaldehyde) with high turnover number. A comparative catalytic study was conducted using different activation methods (chloroform and methanol exchanged activated samples), highlighting the significant effect of activation methods on its catalytic performances. The sustainable synthetic pathway under solvent-free conditions for a broad scope of substrates using low catalyst loading and excellent recyclability made the developed pH-stable framework a promising heterogeneous catalyst.

Solvent-free synthesis, anticancer activity and in-silico studies of 7-hydroxy-4-methylquinolin-2(1H)-one analogues

Several analogues (4a–f) of 7-hydroxy-4-methylquinolin-2(1H)-one were synthesized with high efficiency in a solvent-free condition. The new analogues were characterization using infrared (IR), nuclear magnetic resonance (1H- and 13C NMR), and mass spectral data. Subsequently, they were tested for anticancer activity following the protocol established by the National Cancer Institute (NCI US). 7-Hydroxy-4-methyl-N-(naphthalen-1-yl)-2-oxoquinoline-1(2H)-carboxamide (4d) demonstrated significant anticancer activity against a few cancer cell lines including UO-31 (renal cancer) SNB-75 (CNS cancer) and PC-3 (prostate cancer) cell lines with PGI of 50.40, 45.37 and 35.36 respectively. Similarly, 1-((2,4-Dinitrophenyl)amino)-7-hydroxy-4-methylquinolin-2(1H)-one (4b) demonstrated significant anticancer activity against non-small cell lung cancer, HOP-92 with PGI of 43.79 percent. The correlation between the HOMO-LUMO energy gap (∆E) and bioactivity was investigated using density functional theory (DFT). A significant relationship was observed between ∆E and anticancer activity, particularly in compounds 4b and 4d. Furthermore, a molecular docking and dynamics studies against EGFR were carried out to analyze the binding mode of the compounds (4a–f) and dynamic states and binding stability of the most active compound (4d) respectively. The compound 4d had a docking score of −9.962 kcal/mol, indicating H-bond interactions with the residues Thr854 and Met793. In general evaluation of structural parameters over time reveals compound 4d forms a more stable complex with EGFR as compared to gefitinib. All of the compounds adhered to the Lipinski's rule of five, that was a set of parameters used in ADME studies. Additionally, these compounds were predicted to belong to class IV in terms of toxicity, with LD50 values ranging from 1000 to 1200 mg/Kg.

Antimicrobial polymeric coatings synthesized by solvent-free initiated Chemical Vapor Deposition: A review

Microbial adhesion on surfaces may cause infectious diseases that seriously threaten human health, which can be controlled by antimicrobial surfaces. Antimicrobial polymeric coatings can endow surfaces with biocidal properties to address infectious diseases. Initiated Chemical Vapor Deposition (iCVD) is a novel technique to synthesize high-quality polymeric antimicrobial coatings on various surfaces. Owing to the solvent-free and mild deposition conditions, iCVD facilitates solvent-susceptible, delicate, or fragile substrates. Herein, we provided a comprehensive review of antimicrobial coatings fabricated by iCVD. First, iCVD was introduced. Then, antimicrobial iCVD coatings were discussed based on killing and antifouling strategies. The microbe-killing coatings were discussed according to release-killing and contact-killing approaches. Next, hydrophilic, hydrophobic, and amphiphilic antifouling coatings were reviewed. Finally, micro/nano-structured antimicrobial surfaces fabricated via iCVD were also discussed, followed by the future directions of iCVD coatings in the antimicrobial field.

Alkylaluminium complexes supported by Schiff base as pre-catalysts in hydroboration of alkynes and nitriles

Dinuclear Schiff base aluminium complexes (C1, C2) were synthesized from salicylaldehyde derivatives and 2-aminopyridine. Complexes C1 and C2 were characterized by NMR and single-crystal X-ray diffraction. Subsequently, the catalytic activity of C1 as a pre-catalyst for the hydroboration of alkynes and nitriles was investigated. It exhibited good functional group tolerance towards both terminal alkynes and nitriles under solvent-free and low-load conditions. The potential mechanism for the C1-catalyzed reaction of alkynes and nitriles with HBpin are proposed by the NMR spectroscopy of the intermediates.