(E)-3-(4-Chlorophenyl)-1-(2-fluoro-4-methoxyphenyl)-2-propen-1-one

: Natural products known as chalcones show promise as chemotherapeutic agents for the neglected tropical disease known as leishmaniasis. Our objective is to synthesize new targets of opportunity that may lead to better treatments of this debilitating disease. Claisen-Schmidt condensation of 4-chlorobenzaldehyde with 2 (cid:48) -ﬂuoro-4 (cid:48) -methoxyacetophenone using aqueous sodium hydrox-ide in ethanol yielded the novel compound ( E )-3-(4-chlorophenyl)-1-(2-ﬂuoro-4-methoxyphenyl)-2-propen-1-one. The product was obtained in good yield and purity after recrystallization from ethyl acetate/hexane. With the known antiparasitic properties of halogenated chalcones, this novel compound is suitable for antileishmanial activity study.


Introduction
Leishmaniasis is the second largest parasitic killer behind malaria. The disease is caused by the flesh-eating protozoan parasite of the genus Leishmania and is transmitted through the bites of phlebotomine sandflies. There are three main forms of leishmaniasis: cutaneous, mucocutaneous, and visceral (kala-azar). Symptoms such as severe skin disfigurement, scarring of the mouth and nose, and organ failure afflict over 1 million people annually [1-3].
The World Health Organization classifies leishmaniasis as a neglected tropical disease (NTD), meaning it occurs in tropical or subtropical regions of the Earth. The disease is endemic in Northern Africa, the Middle East, the Mediterranean, parts of Asia, and Central America; impacting those who live in poverty the most. These people typically do not have the access, finances, or ability to obtain treatments, which need intravenous delivery over multiple sessions, thus creating an unfortunate health disparity. The skin lesions and disfiguration caused by the cutaneous and mucosal forms may result in individuals becoming outcasts from their communities and could cause a significant reduction in quality of life.
The areas affected are growing due to vector habitat increase from the warming global climate; with more than 1 billion people in approximately 90 countries at risk of infection due to living in areas where leishmaniasis is endemic. There are no vaccines [4] and current drug treatments suffer from toxicity, high cost, and poor efficacy [5]. Even after treatment, the parasite is not eradicated, it remains dormant in the body to potentially strike again.
The discovery of new effective and affordable medications is imperative to improve the lives of millions worldwide. Fortunately, a group of natural products known as chalcones possess a diverse set of biological activities. These activities include antifungal [6,7], antioxidant [7], and anticancer [8] activity. Recent literature has illustrated the potential for chalcones as a new antileishmanial agent for all three forms of leishmaniasis [9][10][11]. Numerous chalcones reported in literature have exhibited inhibitory activity on promastigotes and/or amastigotes of various Leishmania species [6,7,9,12]. In a study done by Ortalli et al. 31 chalcones were synthesized. Sixteen of them were found to be active against promastigotes of L. donovani. Out of the most promising compounds, one contained a 2 of 4 fluorine as well as had low toxicity and high selectivity. Given the potential chalcones have for effectively inhibiting the disease, our objective is to discover new chalcone-based targets of opportunity that may lead to better treatments for leishmaniasis.

Results
(E)-3-(4-Chlorophenyl)-1-(2-fluoro-4-methoxyphenyl)-2-propen-1-one 3 was synthesized via a Claisen-Schmidt condensation (Scheme 1). The reaction was performed by adding 4-chlorobenzadehyde 1, 2 -fluoro-4 -methoxyacetonphenone 2, and ethanol to a round bottom flask at room temperature. Aqueous NaOH was added and allowed to stir for 40 min. Optimization of purification methods resulted in the following yields: 78% with recrystallization using ethanol and 85% mixed solvent recrystallization EtOAc/hexanes. Numerous chalcones reported in literature have exhibited inhibitory activity on promastigotes and/or amastigotes of various Leishmania species [6,7,9,12]. In a study done by Ortalli et al. 31 chalcones were synthesized. Sixteen of them were found to be active against promastigotes of L. donovani. Out of the most promising compounds, one contained a fluorine as well as had low toxicity and high selectivity. Given the potential chalcones have for effectively inhibiting the disease, our objective is to discover new chalconebased targets of opportunity that may lead to better treatments for leishmaniasis.

Discussion
The purified compound exhibited the expected spectroscopic signals ( 1 H-NMR, 13 C-NMR, IR, and ESI-MS) confirming the successful synthesis of chalcone 3. Using Figure 1 as reference, the 1 H-NMR (CDCl3) spectrum shows confirmatory assignments such as the pair of doublets integrating as two hydrogens each for H1 and H2 (J = 8.4 Hz) and the H3 and H4 J value of 15.6 Hz indicating a trans alkene geometry. In addition, both H3 and H4 have a small coupling to fluorine despite the coupling being a 6 J and 5 J, respectively. This long-range coupling is attributed to the conformation of chalcone 3. Specifically, the most stable conformation brings the fluorine in close spatial proximity to H3 and H4 resulting in the long-range coupling. Positioning of H5, H6, and H7 were corroborated by the 3 J values of H5 and H6 to each other (8.7 Hz each) and the 4 J of H6 and H7 (2.4 Hz each). All spectra can be found in the Supplementary Materials. Notable confirmatory 13 C-NMR signals include the α,β-unsaturated carbonyl peak (C7) at 186.9 ppm and the doublet of C9 with a coupling constant of 253 Hz indicative of an aryl fluoride. The vinylic carbons C5 and C6 were delineated by analyzing the shielding/deshielding effects of the various substituents. Such as the aryl chloride, which deshields C5 while also shielding C6. Furthermore, C2 and C3 were differentiated by evaluating the deshielding effects of carbonyl resonance. FT-IR exhibited the following substantiating signals: a sharp α,β unsaturated carbonyl stretch at 1658 cm −1 and a 1587 cm

Discussion
The purified compound exhibited the expected spectroscopic signals ( 1 H-NMR, 13 C-NMR, IR, and ESI-MS) confirming the successful synthesis of chalcone 3. Using Figure 1 as reference, the 1 H-NMR (CDCl 3 ) spectrum shows confirmatory assignments such as the pair of doublets integrating as two hydrogens each for H1 and H2 (J = 8.4 Hz) and the H3 and H4 J value of 15.6 Hz indicating a trans alkene geometry. In addition, both H3 and H4 have a small coupling to fluorine despite the coupling being a 6 J and 5 J, respectively. This long-range coupling is attributed to the conformation of chalcone 3. Specifically, the most stable conformation brings the fluorine in close spatial proximity to H3 and H4 resulting in the long-range coupling. Positioning of H5, H6, and H7 were corroborated by the 3 J values of H5 and H6 to each other (8.7 Hz each) and the 4 J of H6 and H7 (2.4 Hz each). All spectra can be found in the Supplementary Materials.

Discussion
The purified compound exhibited the expected spectroscopic signals ( 1 H-NMR, 13 C-NMR, IR, and ESI-MS) confirming the successful synthesis of chalcone 3. Using Figure 1 as reference, the 1 H-NMR (CDCl3) spectrum shows confirmatory assignments such as the pair of doublets integrating as two hydrogens each for H1 and H2 (J = 8.4 Hz) and the H3 and H4 J value of 15.6 Hz indicating a trans alkene geometry. In addition, both H3 and H4 have a small coupling to fluorine despite the coupling being a 6 J and 5 J, respectively. This long-range coupling is attributed to the conformation of chalcone 3. Specifically, the most stable conformation brings the fluorine in close spatial proximity to H3 and H4 resulting in the long-range coupling. Positioning of H5, H6, and H7 were corroborated by the 3 J values of H5 and H6 to each other (8.7 Hz each) and the 4 J of H6 and H7 (2.4 Hz each). All spectra can be found in the Supplementary Materials. Notable confirmatory 13 C-NMR signals include the α,β-unsaturated carbonyl peak (C7) at 186.9 ppm and the doublet of C9 with a coupling constant of 253 Hz indicative of an aryl fluoride. The vinylic carbons C5 and C6 were delineated by analyzing the shielding/deshielding effects of the various substituents. Such as the aryl chloride, which deshields C5 while also shielding C6. Furthermore, C2 and C3 were differentiated by evaluating the deshielding effects of carbonyl resonance. FT-IR exhibited the following substantiating signals: a sharp α,β unsaturated carbonyl stretch at 1658 cm −1 and a 1587 cm  Notable confirmatory 13 C-NMR signals include the α,β-unsaturated carbonyl peak (C7) at 186.9 ppm and the doublet of C9 with a coupling constant of 253 Hz indicative of an aryl fluoride. The vinylic carbons C5 and C6 were delineated by analyzing the shielding/deshielding effects of the various substituents. Such as the aryl chloride, which deshields C5 while also shielding C6. Furthermore, C2 and C3 were differentiated by evaluating the deshielding effects of carbonyl resonance. FT-IR exhibited the following substantiating signals: a sharp α,β unsaturated carbonyl stretch at 1658 cm −1 and a 1587 cm

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 precoated with silica gel 60 (HF 254 , Merck, Waltham, MA, USA), and visualized with UV radiation (Fisher Scientific, Waltham, MA, USA). The product was characterized by 1 H-NMR, 13 C-NMR, IR, ESI-MS, and melting point analyses.
IR spectra were recorded on a ThermoFisher iS5 FT-IR (Waltham, MA, USA). Melting point was determined in open capillaries using a Stuart SMP3 melting point apparatus (Cole-Parmer, Vernon Hills, IL, USA). 1 H and 13 C-NMR spectra were collected using a 500 MHz Bruker AV-500 NMR spectrometer (NuMega Resonance Labs, San Diego, CA, USA). Spectra were referenced to residual CHCl 3 . Chemical shifts were quoted in ppm and coupling constants (J) were recorded in hertz (Hz). Electrospray ionization (ESI) mass spectrum was acquired using a Perkin Elmer PE-SCIEX API-150 spectrometer (NuMega Resonance Labs, San Diego, CA, USA).