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(E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one

Mathematics, Natural, and Health Sciences Division, University of Hawai‘i West O‘ahu, 91-1001 Farrington Hwy, Kapolei, HI 96707, USA
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Author to whom correspondence should be addressed.
Academic Editor: Oleg A. Rakitin
Molbank 2021, 2021(3), M1269; https://doi.org/10.3390/M1269
Received: 29 April 2021 / Revised: 22 July 2021 / Accepted: 27 July 2021 / Published: 10 August 2021
(This article belongs to the Section Organic Synthesis)

Abstract

Imidazole-containing chalcones have been shown to be strongly effective against Aspergillusfumigatus, the causative agent for the disease pulmonary aspergillosis. Claisen–Schmidt condensation of 4-(1H-imidazol-1-yl)benzaldehyde with 4′-methylacetophenone using aqueous sodium hydroxide in methanol yielded the novel compound (E)-3-[4-(1H-imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one in good yield and purity after recrystallization from hot methanol. With the known antifungal properties of these combined pharmacophores, this novel compound is suitable for anti-aspergillus activity study.
Keywords: chalcone; synthesis; aldol; pulmonary aspergillosis; imidazole chalcone; synthesis; aldol; pulmonary aspergillosis; imidazole

1. Introduction

Pulmonary aspergillosis (PA) is a spectrum of respiratory diseases that can range from mild to fatal depending on the state of an individual’s immune system [1]. Milder manifestations of PA include allergic bronchopulmonary aspergillosis (ABPA), and chronic pulmonary aspergillosis (CPA). These milder forms tend to cause fatigue, difficulty breathing, and hemoptysis [2], while its most lethal diagnosis, invasive aspergillosis (IA), can cause respiratory failure, neurological conditions, and multiorgan failure, depending on where the infection spreads [2]. Named after its infectious agent, the disease stems from the inhalation of conidia of the fungus genus Aspergillus.
Aspergillus species are ubiquitous saprophytes and typically inhabit the soil where they recycle essential nutrients from the soil. Aspergillus’ omnipresence is attributed to its asexual spores called conidia. The conidia are easily propagated, so much so that Aspergillus DNA is often found in the lungs of healthy adults [3]. Pulmonary aspergillosis only manifests if the individual who inhales the conidia is immunocompromised [1].
Typically, in the non-immunocompromised host, invasion of Aspergillus conidia into the bronchioles and alveoli is eliminated by macrophages and neutrophils [1,2,3,4]. Individuals with conditions that compromise these components of the immune system are the most at risk for developing pulmonary aspergillosis. The mortality rate for these individuals ranges from 20% to 90% [1,2,3,4,5,6], and Bongomin et al. has postulated that there are roughly 3 million cases of CPA worldwide every year. These numbers will only continue to grow if factors such as limited drug therapies, antifungal resistant strains [7,8], and the influx of individuals with compromised immune systems continue. In addition, recent literature illustrates respiratory viruses such as influenza and coronavirus disease 2019 (COVID-19) have led to new classifications of pulmonary aspergillosis, making matters more urgent [9,10,11,12].
These classifications are especially disconcerting because they expand the current demographic beyond the immunocompromised. Furthermore, influenza associated aspergillosis (IAA) and COVID-19 associated pulmonary aspergillosis (CAPA) are associated with higher mortality rates and more complications than their counterparts without these co-infections [9,10]. There seems to be an appreciable prevalence of CAPA (20–30%), especially in mechanically ventilated or severely ill individuals [11]. In particular, one study discovered co-infections of Aspergillus in 26% of those with severe ammonia and 40% in those with acute respiratory distress syndrome engendered by COVID-19 [12]. These factors demonstrate that it is imperative to discover new treatments for the evolving disease pulmonary aspergillosis.
Fortunately, pharmacophores like chalcone and imidazoles have shown a wide range of biological activities. These pharmacophores share many pharmacological effects such as anti-inflammatory, antibacterial, anticancer, and antimicrobial activity [13,14,15,16]. Recent literature has illustrated that these two pharmacophores in conjunction show potential as an antifungal agent [17,18]. We seek to synthesize similar novel imidazole chalcones as potential treatments for pulmonary aspergillosis.

2. Results

(E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one 3 was synthesized via a Claisen–Schmidt condensation (Scheme 1). The reaction was performed by adding 4-(1H-Imidazol-1-yl)benzaldehyde 1, 4′-methylacetophenone 2, and methanol to a round bottom flask at room temperature. Aqueous NaOH was added and allowed to stir for 2 h. The crude product was recrystallized in hot methanol resulting in a yield of 75%.

3. Discussion

The purified compound exhibited spectroscopic signals that confirmed the successful synthesis of chalcone 3. Using Figure 1 as reference, the 1H-NMR spectrum shows notable confirmatory assignments such as the trans vinylic hydrogens H6 and H7, which were the only two doublets with an integration of one hydrogen. The J value of 15.7 Hz represents the trans alkene geometry. A noteworthy substantiating 13C-NMR signal is the α,β-unsaturated carbonyl peak (C10) at 189.7 ppm being more upfield than a non-conjugated ketone carbonyl. HSQC was then used to assign all carbons bearing protons.
Assignments from the 1H-NMR and 13C-NMR that were validated by the HSQC were utilized in the HMBC to corroborate other assignments by analyzing the 2J/3J cross peaks. For example, C14 (144.1 ppm) and C13 (129.6 ppm) were verified by their 2J/3J cross peaks with the methyl hydrogens (H10). Additionally, from the carbonyl carbon (C10), cross peaks to H8 (7.98 ppm), H7 (7.54 ppm), and H6 (7.79 ppm) assignments were further established. Chemical shifts of the protons and carbons also were in agreement with predicted anisotropic and resonance effects. The aforementioned signals could then be used to substantiate other signals until all assignments were verified. FT-IR exhibited a sharp carbonyl stretch at 1660 cm−1, which is indicative of an α,β-unsaturated carbonyl. High resolution mass spectrometry analysis found an M+ ion at 288.12531 m/z compared to a calculated mass of 288.12626.

4. Materials and Methods

All chemicals, reagents, and solvents used were obtained from commercial sources (Sigma Aldrich, St. Louis, MO, USA and Fisher Scientific, Waltham, MA, USA) and used without further purification. Thin layer chromatography (TLC) was used to monitor reactions and performed using aluminum sheets pre-coated silica gel 60 (HF254, Merck, Waltham, MA, USA), and visualized with UV radiation (Fisher Scientific, Waltham, MA, USA). The product was characterized by 1H-NMR, 13C-NMR, HSQC and HMBC NMR, IR, HRMS, and melting point analysis. Spectra can be found in the supplementary information.
IR spectra were recorded on a ThermoFisher iS5 FT-IR. Melting point was determined in open capillaries using a Stuart SMP3 melting point apparatus. 1H and 13C-NMR spectra were collected using a 500 MHz Bruker AV-500 NMR spectrometer. HSQC and HMBC were collected using a 600 MHz Agilent DD2 600 MHz NMR spectrometer. Spectra were referenced to residual CHCl3. Chemical shifts were quoted in ppm and coupling constants (J) were recorded in hertz (Hz). High resolution mass spectrum was acquired using an Agilent Technologies Series 6200 TOF spectrometer.
A solution of aqueous NaOH (0.25 mL, 3.75 mmol, 15 M) was added to a round bottom flask containing 4-(1H-imidazol-1-yl)benzaldehyde 1 (0.430 g, 2.50 mmol), 4′-methylacetophenone 2 (0.335 g, 2.50 mmol), and methanol (7.5 mL). The mixture was stirred at room temperature for 2 h (monitored by TLC in 5% dichloromethane/hexanes and visualized with UV radiation) during which a yellow-white precipitate formed. The mixture was diluted with water (10 mL) then cooled to 0 °C, and collected in vacuo, washed twice with an ice-cold solution of 10% methanol/H2O (5 mL portions). The crude product was purified by recrystallization from hot methanol to yield pure chalcone 3 as light yellow crystals (0.543 g, 1.88 mmol, 75%).
(E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one (3): mp 171–172 °C; 1H-NMR (CDCl3, 500 MHz): 7.93 ppm (2H, d, J = 8.2 Hz, H8), 7.90 ppm (1H, s, H1), 7.79 ppm (1H, d, J = 15.7 Hz, H6), 7.73 ppm (2H, d, J = 8.5 Hz, H5), 7.54 ppm (1H, d, J = 15.7 Hz, H7), 7.43 ppm (2H, d, J = 8.6 Hz, H4), 7.30 ppm (2H, d, J = 8.4 Hz, H9), 7.30 ppm (1H, s, H2), 7.22 ppm (1H, s, H3), 2.42 ppm (3H, s, H10); 13C-NMR (CDCl3, 125 MHz): 186.7 ppm (C10), 144.1 ppm (C14), 142.7 ppm (C8), 138.7 ppm (C4), 135.6 ppm (C11), 135.5 ppm (C1), 134.4 ppm (C7), 131.0 ppm (C3), 130.1 ppm (C6), 129.6 ppm (C13), 128.8 ppm (C12), 122.9 ppm (C9), 121.6 ppm (C5), 118.0 ppm (C2), 21.8 ppm (C15); FT-IR (KBr) 3167 cm−1 (C-HAr), 3117 cm−1 (C-HAr), 3041 cm−1 (C-HAr), 1660 cm−1 (C=O), 1597 cm−1 (C=C), 1518 cm−1 (C=C); HRMS m/z calc for C19H16N2O is 288.12626; found 288.12531.

Supplementary Materials

The following are available online: Copies of the 1H, 13C-NMR, HSQC, HMBC, IR, and HRMS spectra.

Author Contributions

Conceptualization, B.O.A.; methodology, B.O.A.; investigation, B.O.A. and N.B.; writing—original draft preparation, B.O.A. and N.B.; writing—review and editing, B.O.A. and N.B.; All authors have read and agreed to the published version of the manuscript.

Funding

This project was supported by grants from the National Institutes of Health (NIH), National Institute of General Medical Sciences (NIGMS), IDeA Networks of Biomedical Research Excellence (INBRE), Award number: P20GM103466. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the Supplemental Materials.

Conflicts of Interest

The authors declare no conflict of interest.

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Scheme 1. Claisen-Schmidt condensation to form chalcone 3.
Scheme 1. Claisen-Schmidt condensation to form chalcone 3.
Molbank 2021 m1269 sch001
Figure 1. NMR assignment of chalcone 3.
Figure 1. NMR assignment of chalcone 3.
Molbank 2021 m1269 g001
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