2-((4-Amino-5-((2,4-dichlorophenoxy)methyl)-4H-1,2,4-triazol-3-yl)thio)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one

Abstract

The reaction of 2-bromo-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (1) with 4-amino-5-((2,4-dichlorophenoxy)methyl)-4H-1,2,4-triazole-3-thiol (2) in absolute ethanol in the presence of triethyl amine as catalyst gave 2-((4-amino-5-((2,4-dichlorophenoxy)methyl)-4H-1,2,4-triazol-3-yl)thio)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (3) in 73% yield. The structure of the title heterocycle (3) was confirmed by X-ray single crystal diffraction and spectral analyses (NMR and IR).

1. Introduction

Heterocycles containing the 1,2,3-triazole fragment are active ingredients in a variety of drugs, including antibiotics (e.g., cefatrizine and tazobactam). 1,2,3-triazole derivatives exhibit a variety of promising biological properties, including antibacterial, antituberculosis, antiviral, and anticancer properties [1,2,3,4,5].

The diverse pharmacological activities of 1,2,4-triazoles as fungicides, antivirals, herbicides, and catalase inhibitors have led to deep interest in discovering new entities for their broader applications. There are many drugs based on 1,2,4-triazole in clinical use for the treatment of various diseases, such as antifungals (fluconazole, itraconazole, and voriconazole) and antivirals (rifavirin) [6,7,8,9].

Therefore, the current work reports the synthesis and crystal structure of a new heterocycle containing both 1,2,3-triazole and 1,2,4-triazole moieties using a simple procedure. Recently, the synthesis and structure elucidation of new heterocycles have been reported [10,11].

2. Results and Discussion

2.1. Synthesis

The heating under reflux conditions of 2-bromo-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (1) with 4-amino-5-((2,4-dichlorophenoxy)methyl)-4H-1,2,4-triazole-3-thiol (2) in absolute ethanol in the presence of triethyl amine as catalyst gave 2-((4-amino-5-((2,4-dichlorophenoxy)methyl)-4H-1,2,4-triazol-3-yl)thio)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (3) in 73% yield (Scheme 1). Crystallization of the solid obtained from dimethylformamide (DMF) gave 3 in crystal form.

2.2. NMR Spectroscopy

The ¹H NMR spectrum of 3 showed both the methylene protons (CH₂) as a singlet signal at 4.95 and 6.10 ppm and the presence of a singlet signal that appeared at 5.30 ppm due to the NH₂ protons. We cannot perform the ¹³C NMR due to the poor solubility of product 3.

2.3. Crystal Structure Analysis

An ortep view of the geometry of the title structure can be seen in Figure 1. The structure typically comprises two formulae in the unit cell and a monoclinic crystal system with the P2₁/c space group. The molecule geometry is in good agreement with the reported standard bond distance [12].

The constituents of the structure showed a planar appearance for each component separately. However, torsion angles between the consisting moieties give a non-planar appearance to the compound, such as C6/O6/C7/C8 (178.6°), N13/N14/C15/C20 (25.50°), and N9/C9/S9/C10 (5.76°). Also, the angle between the planes of the rings (C9 N9 N8 C8 N10) and (C5 C4 C3 C2 C1 C6) is 85°.

Figure 2 shows that the structure is stabilized by hydrogen bonds between the carbon atom and the nitrogen, oxygen, and chlorine atoms, as follows: C7—H7B---N9, C7—H7A---O11, C10—H10B---O11 and C20—H20---Cl3 together. Beautiful parallel networks with a wavy pattern could be seen in the crystal packing (Figure 3).

3. Materials and Methods

3.1. General

Chemicals and solvents were obtained from Merck. The IR was recorded on Bruker Tensor 27 FTIR spectroscope. The NMR spectra (600 MHz) of 3 were performed on a Bruker NMR spectrometer. The chemical shift (δ) was reported in ppm. The NMR spectra were recorded in DMSO-d₆. The literature procedures were used to prepare 1 [13] and 2 [14].

3.2. Synthesis of 3

A mixture of 1 (0.65 g, 2.0 mmol), 2 (0.58 g, 2.0 mmol), and triethyl amine (0.2 mL) in absolute ethanol (15 mL) was heated under reflux conditions for 3 h and left to cool to at room temperature. Then, the colorless solid produced was collected by filtration. The product was washed with EtOH, dried, and recrystallized from DMF to give 3 in 73% yield, mp 230–231 °C. IR: 3345 (NH₂), 3171-2915 (CH), 1681 (C=O),1613-1596(C=N) cm⁻¹. ¹H NMR: 2.55 (s, 3H, Me), 4.95 (s, 2H, CH₂), 5.30 (s, 2H, NH₂), 6.10 (s, 2H, CH₂), 7.40 (s, 2H, Ar), 7.69 (s, 1H, Ar), 8.04 (d, 2H, J= 9 MHz, Ar), 8.50 (d, J= 9 MHz, 2H, Ar). Anal. Calcd. for C₂₀H₁₆Cl₂N₈O₄S (535.36): C, 44.87; H, 3.01; N, 20.93. Found: C, 44.93; H, 3.19; N, 20.99%.

3.3. X-ray Crystallography

A Bruker APEX-II CCD X-ray diffractometer (Mo X-ray tube) was used to collect data from a colorless plate crystal that had approximate dimensions of 0.286 × 0.274 × 0.046 mm³ [15]. The structure was solved and refined using SHELXT [16] and SHELXL [17]. The structure was analyzed and graphically demonstrated using the crystallographic computer programs PLATON [18], Mercury [19], and ORTEP-3 for Windows [20].

The full crystallographic details are Ided in the Supplementary Materials (CIF and Tables S1–S3). The data have been deposited in the Cambridge Crystallographic Data Centre (CSD) with the number CCDC 2288217.

4. Conclusions

A new heterocycle containing both 1,2,3-triazole and 1,2,4-triazole moieties has been synthesized with good yield using a simple procedure. The structure of the title heterocycle was established using X-ray single crystal diffraction and nuclear magnetic resonance spectroscopy.