Design, Synthesis, and Anti-Fungal Evaluation of Heterocyclic Benzoxazole Derivatives

Ruibo Wang; Ruiting Kang; Xuan Yang; Yu Cheng; Hongjin Bai; Zhenting Du

doi:10.3390/molecules27238375

. 2022 Nov 30;27(23):8375. doi: 10.3390/molecules27238375

Design, Synthesis, and Anti-Fungal Evaluation of Heterocyclic Benzoxazole Derivatives

Ruibo Wang ¹, Ruiting Kang ², Xuan Yang ², Yu Cheng ², Hongjin Bai ^1,^*, Zhenting Du ^2,^3,^*

Editor: Luana Bagnoli

PMCID: PMC9739801 PMID: 36500467

Abstract

In order to discover more promising anti-fungal agents, a series of benzoxazole family was synthesized by PPA-catalyzed condensation and a Raney nickel/hydrazine reduction. Altogether 45 compounds were obtained in good to excellent yields and characterized by FT-IR, NMR, MS, and X-ray crystal diffraction. Moreover, the biological activity against eight phytopathogenic fungi was investigated. All in all, most of these compounds bear moderate antifungal activities. Among them, three candidates show the strongest activities, compound 4ac, 4bc provided over 50% inhibition rate against five fungi. Especially, the inhibitory rate of compound 4ah on Mycosphaerella melonis reached 76.4%.

Keywords: benzoxazole, crystal structure, synthesis, anti-fungal activities

1. Introduction

In recent years, pathogenic bacteria and plant viruses targeting agricultural crops have become increasingly difficult to control, leading to enormous losses in worldwide crop production each year. As such, the development of environmentally friendly pesticides with high selectivity, high efficiency, low toxicity, and suitable degradation are important challenges to both chemists and biologists [1]. Development of drug-like heterocyclic compounds from simple and facile substrates is one of the emerging areas in modern synthetic chemistry. Heterocyclic structures are important key features in natural products or synthetic medicines and pesticides because of their high-efficiency, low toxicity, and diversity of possible substituents [2]. As shown in Figure 1, the benzoxazole is an important heteroaromatic moiety found in many pharmaceuticals and agrichemicals [3,4,5]. Benzoxazole is a structural scaffold which can be found in nonsteroidal anti-inflammatory drugs such as flunoxaprofen [6], uniprofen [7], and Prinaberel [8]. Many benzo heterocycles compounds can be found in agrichemicals, such as carbendarim [9], fubridazole [10], and thiabendazole [11]. There are also other pharmaceutical applications such as antibiotic [12,13], anticancer, [14,15,16] anti-inflammatory applications [17]. Due to their structural characteristics, they can be used in material industry such as fluorescent chemosensor for special ions [18] and mesogenic applications [19].

Benzoxazoles are important members of the family of fused heterocycles that have attracted much attention because of their diverse biological activity. In order to find new potential pesticide molecules with antifungal activities, we designed and synthesized a series of benzoxazole derivatives and evaluated their potential antifungal activities against eight kinds of plant pathogenic fungus commonly found in agriculture systematically, including Fusarium solani, Colletotrichum gloeosporioides, Mycosphaerella melonis, Alternaria brassicae, Pyricularia grisea, Curvularia lunata, Alternaria solani, and Fusarium graminearum. As Scheme 1 shows, namely the synthesis of benzoxazoles can be classified into two kinds: [20,21] one is using PPA as solvent and catalyst at the presence of acid and aniline in one step [15,17,22], the other is using condensation of aldehyde and aniline then an oxidation step using some oxidizer such as DDQ, Manganese oxide, air, etc. [23]. Our research group has been intensively studying the synthesis of heterocycles and their agricultural applications [24,25,26]. Pyridine, also known as azabenzene, has a certain aromatic structure and is widely used in sulfonamides and pesticides. Inspired by three molecules used as agrichemicals in Figure 1, we envisioned a combination of pyridine, benzoxazole, and amide might have good antifungal activities against plant pathogen (Figure 2). Prompted by the above thoughts, we wish to report the synthesis, spectroscopic, single-crystal diffraction, antifungal activity, of a series of benzoxazoles bearing a pyridine ring and amide moiety. In our devise, the two heterocyclic moiety contributes the biological activities, and the amide would tune the activities.

Scheme 1 — The syntheses of benzoxazoles.

2. Results and Discussion

2.1. Chemistry

As shown in Scheme 2, the isomers (2-, 3-, 4-, respectively) of picolinic acid condensed with 4-nitro-2-aminophenol at the presence of PPA to provide the three types of pyridyl-benzoxazole in 75–85% yield. Compared with the reported method, the PPA was preheated to 80 °C before use in order to be measured easily. Next, a mild reduction in the nitro group to amino group was adopted using hydrazine and Raney nickel in 75–80% yield. The other reduction methods proved unsuccessful, such as palladium/carbon catalytic hydrogenation, stannous chloride in common solvent (ethyl acetate and tetrahydro furan), and iron powder in acetic acid. A lot of black tar which can be solved in acidic condition was produced under these conditions. We suspected that the oxales ring was opened upon these conditions. As to the preparation of the nitro-benzoxazoles, there is another nitration method of benzoxazole, but the nitro group position is limited to the para- to the OH group. Next, we condensed three pyridyl-benzoxazole compounds with 15 different types of acyl chlorides to obtain 45 amide derivatives (4aa–4co) in fairly good to excellent yield (Table 1) and were characterized by ¹H NMR and ¹³C NMR. The stereochemistry of two compounds 4ac and 4bc with the best antifungal effect was further confirmed by the X-ray crystallographic analysis (Figure 3).

Table 1.

The syntheses of amide derivatives of benzoxazoles ^a.


Entry	2-Pyridyl	3-Pyridyl	4-Pyridyl	R^a
1	4aa	4ba	4ca
2	4ab	4bb	4cb
3	4ac	4bc	4cc
4	4ad	4bd	4cd
5	4ae	4be	4ce
6	4af	4bf	4cf
7	4ag	4bg	4cg
8	4ah	4bh	4ch
9	4ai	4bi	4ci
10	4aj	4bj	4cj
11	4ak	4bk	4ck
12	4al	4bl	4cl
13	4am	4bm	4cm
14	4an	4bn	4cn
15	4ao	4bo	4co

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^a Reaction condition: each entry was performed at 3 mmol scale, in the presence of DMAP, in THF, r.t., 6 h.

X-ray crystallographic structures of **4ac** and **4bc**.

2.2. X-ray Crystallographic Studies of 4ac, 4bc

Compound 4ac crystallizes in the monoclinic space group P2₁. There are two crystallographic independent molecules in the asymmetric unit (only one of them is shown in Figure 3). In the molecule of 4ac, bond lengths and angles are very similar to those provided in the literature for benzoxazole derivative. The benzoxazole ring was approximately planar. Compared with the 4bc, the dihedral angle between the methylphenyl plane and the oxazole ring was 55.65°. Compound 4bc crystallizes in the monoclinic space group C2/c. There are eight crystallographic independent molecules in the asymmetric unit (only one of them is shown in Figure 3). In the molecule of 4bc, bond lengths and angles are very similar to those provided in the literature for benzoxazole derivative. The whole molecule was approximately planar. The dihedral angle of the methylphenyl plane, the oxazole ring, was 8.61°. X-ray diffraction reflection data of 4ac and 4bc are shown in the Supplementary Materials.

2.3. In Vitro Anti-Fungal Activity

Meanwhile, the anti-fungal activities of these compounds were evaluated against eight common phytopathogenic fungi, (Fusarium solani, Colletotrichum gloeosporioides, Mycosphaerella melonis, Alternaria brassicae, Pyricularia grisea, Curvularia lunata, Alternaria solani, and Fusarium graminearum) using the inhibition zone method at the concentration of 100 μg/mL by the poisoned food technique. While thiophanate-methyl, which is a fungicide bearing similar heterocyclic structures and a commercially available agricultural fungicide, was used as a positive control at 100 μg/mL. As shown in Figure 4, the experiments revealed that most of these compounds bears moderate result to Colletotrichum gloeosporioides and Mycosphaerella melonis. Through the 3D -Bar of inhibition rate against eight fungi, we could see, compound 4ac, 4bc showed best results, providing over 50% inhibition rate against five fungi. Herein, we believe the methyl makes a rotation barrier, and to some extent enhances the combination of compound to the enzyme. Interestingly, some compounds could selectively inhibit some fungi. For example, the inhibitory rate of compound 4ah on Mycosphaerella melonis could reach 76.4%, but it had little inhibitory activity on other fungi. Another example was that compound 4bh could highly selectively inhibit the growth of Alternaria brassicae. However, 4be against Fusarium solani, 4cj and 4af against Colletotrichum gloeosporioides provided unsatisfactory results, even positive results. From the whole table, the effect of acyl ligand on antifungal activity was greater than that of pyridyl-benzoxazole skeleton. Typical examples are compounds 4ac and 4bc, and even compound 4cc, which have very good antifungal activity and all of them have the same acyl ligand.

Antifungal activities of compounds **4aa**–**4co** at 100 μg/mL.

3. Materials and Methods

3.1. Chemistry

All chemicals were purchased from Energy chemicals and Merck (used without further purification). The melting point was determined using a digital melting point meter WRS-1B. The ¹H NMR and ¹³C NMR spectra were carried out by AV 500 MHz spectrometer. X-ray analysis of the samples were recorded on a Bruker APEX II area detector diffractometer at 296(2) K with a graphite-monochromatic MoK radiation (λ = 0.71073A°).

3.1.1. General Synthesis of 3a–3c

5-Nitro-2-(pyridin-2-yl)benzo[d]oxazole (3a). To a solution of 2-picolinic acid (2.46 g 0.01 mol) condensed with 4-nitro-2-aminophenol (3.08 g, 0.01 mol) in polyphosphoric acid (30 mL) in a 100mL three-necked flask, the middle neck was installed a mechanical stirring, and the side neck was set for thermometer. The reaction mixture was heated 140 °C and the external temperature was kept at 150 °C. After 6 h, the reaction was completed through TLC. Then the reaction mixture was poured into water slowly and was adjusted to pH 6 using potassium carbonate. A quantity of solid precipitated and was collected by suction. This compound was used without further purification and drying. Because the next reduction was carried out in ethyl alcohol, the crude product 2a was used directly. The crude 2a was dissolved in 95% ethyl alcohol (40 mL), and then was added W-2 Raney nickel (ca. 0.20 g), and then hydrazine (1.96 g, 3 equiv.) was introduced drop wise. Moreover, the mixture was heated to 60 °C and monitored by TLC. After completion, the reaction mixture was filtered through a Celite pad. The filtration was condensed and purified by flash column chromatography (petroleum ether: ethyl acetate) to obtain 3a (1.94 g, 72% for two steps) as a brown solid: ¹H NMR (500 MHz, DMSO) δ 8.78 (d, J = 4.1 Hz, 1H), 8.29 (d, J = 7.9 Hz, 1H), 8.05 (dd, J = 10.9, 4.5 Hz, 1H), 7.61 (dd, J = 6.9, 5.1 Hz, 1H), 7.49 (d, J = 8.7 Hz, 1H), 6.95 (d, J = 1.6 Hz, 1H), 6.77 (dd, J = 8.7, 1.9 Hz, 1H), 5.19 (s, 2H); ¹³C NMR (126 MHz, DMSO) δ 161.53, 150.55, 147.35, 146.12, 143.46, 142.78, 138.02, 126.21, 123.63, 114.66, 111.38, 103.16.

2-(Pyridin-3-yl)benzo[d]oxazol-5-amine (3b) and 2-(pyridin-4-yl)benzo[d]oxazol-5-amine (3c) could be obtained in same procedure as a brown solid in a similar yield, respectively.

Compound 3b: ¹H NMR (500 MHz, DMSO) δ 9.31 (s, 1H), 8.79 (s, 1H), 8.48 (d, J = 6.7 Hz, 1H), 7.64 (s, 1H), 7.48 (d, J = 8.6 Hz, 1H), 6.93 (s, 1H), 6.74 (d, J = 8.6 Hz, 1H), 5.21 (s, 2H); ¹³C NMR (126 MHz, DMSO) δ 160.40, 152.31, 148.16, 147.35, 143.20, 142.75, 134.80, 124.72, 123.69, 114.18, 111.18, 103.03.

Compund 3c: ¹H NMR (500 MHz, DMSO) δ 8.83 (d, J = 5.6 Hz, 2H), 8.05 (d, J = 5.7 Hz, 2H), 7.51 (d, J = 8.7 Hz, 1H), 6.95 (d, J = 1.7 Hz, 1H), 6.79 (dd, J = 8.7, 1.9 Hz, 1H), 5.27 (s, 2H); ¹³C NMR (126 MHz, DMSO) δ 160.31, 151.26, 147.53, 143.37, 142.76, 134.33, 120.97, 115.06, 111.41, 103.07.

3.1.2. General Procedures for the Synthesis of 4aa–4co

Typical synthesis procedure of amide, taking 4aa as an example: to a vial (20 mL) was charged THF (5 mL), and then 3a (0.02 g, 1 mmol) and benzoyl chloride (0.17 mL) and catalytical amount of DMAP. Thus, the reaction mixture was stirred for 6 h. Moreover, the reaction mixture was poured into water (50 mL) and the precipitate was collected by suction. After recrystallization in ethyl acetate, the target molecules could be obtained in 75–92% yield. The detailed characterization of NMR and spectrum are attached as follows:

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4aa)

Yield 65.3%; Pink solid; mp 138.1–138.5 °C; ¹H NMR (500 MHz, DMSO) δ 10.49 (s, 1H), 8.84 (d, J = 4.2 Hz, 1H), 8.39 (d, J = 11.0 Hz, 2H), 8.10 (td, J = 7.8, 1.4 Hz, 1H), 8.01 (dd, J = 27.5, 7.2 Hz, 2H), 7.86 (s, 2H), 7.68–7.64 (m, 2H), 7.61–7.51 (m, 2H).¹³C NMR (126 MHz, DMSO) δ 166.17, 150.71, 147.41, 145.73, 141.85, 138.18, 137.08, 135.37, 132.13, 129.74, 128.92, 128.18, 126.70, 124.10, 120.13, 112.10, 111.49.

2-Phenyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)acetamide (4ab)

Yield 37.4%; Pink solid; mp 120.6–120.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.46 (s, 1H), 8.82 (d, J = 4.1 Hz, 1H), 8.35 (d, J = 7.9 Hz, 1H), 8.26 (s, 1H), 8.08 (dd, J = 11.0, 4.4 Hz, 1H), 7.80 (d, J = 8.8 Hz, 1H), 7.67–7.62 (m, 2H), 7.38 (dd, J = 13.4, 6.0 Hz, 4H), 7.29 (t, J = 7.0 Hz, 1H), 3.72 (s, 2H).¹³C NMR (126 MHz, DMSO) δ 169.70, 162.46, 150.68, 147.05, 145.70, 141.90, 138.15, 137.19, 136.42, 129.65, 128.81, 127.05, 126.67, 124.07, 118.84, 111.62, 110.70, 43.80.

2-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ac)

Yield 56.8%; Pink solid; mp 168.1–168.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.46 (s, 1H), 8.83 (d, J = 4.1 Hz, 1H), 8.38 (d, J = 10.0 Hz, 2H), 8.10 (t, J = 7.7 Hz, 1H), 7.87–7.82 (m, 4H), 7.69–7.65 (m, 1H), 7.47 (d, J = 6.6 Hz, 2H), 2.45 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 166.27, 162.47, 150.71, 147.37, 145.73, 141.83, 138.24, 138.19, 137.13, 135.36, 132.70, 128.82, 128.66, 126.70, 125.34, 124.09, 120.10, 112.05, 111.47, 21.47.

3-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ad)

Yield 26.8%; Pink solid; mp 179.2–179.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.55 (s, 1H), 8.83 (d, J = 4.1 Hz, 1H), 8.44–8.31 (m, 2H), 8.09 (td, J = 7.8, 1.5 Hz, 1H), 7.83 (q, J = 8.8 Hz, 2H), 7.67 (dd, J = 6.6, 4.9 Hz, 1H), 7.54 (d, J = 7.2 Hz, 1H), 7.44 (t, J = 7.1 Hz, 1H), 7.35 (t, J = 7.5 Hz, 2H), 2.45 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 168.41, 162.49, 150.71, 147.29, 145.72, 141.89, 138.18, 137.64, 137.24, 135.78, 131.05, 130.18, 127.75, 126.69, 126.16, 124.09, 119.34, 111.57, 111.26, 19.82.

4-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ae)

Yield 43.4%; Pink solid; mp 212.2–212.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.45 (s, 1H), 8.83 (d, J = 4.1 Hz, 1H), 8.41–8.35 (m, 2H), 8.09 (t, J = 7.6 Hz, 1H), 7.96 (d, J = 7.9 Hz, 2H), 7.90–7.81 (m, 2H), 7.66 (dd, J = 6.9, 5.0 Hz, 1H), 7.38 (d, J = 7.9 Hz, 2H), 2.42 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 165.96, 162.43, 150.69, 147.32, 145.73, 142.13, 141.82, 138.16, 137.18, 132.45, 129.42, 128.24, 126.67, 124.07, 120.14, 112.07, 111.41, 21.51.

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4af)

Yield 37.8%; Pink solid; mp 182.4–182.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.83 (s, 1H), 8.84 (d, J = 4.2 Hz, 1H), 8.71 (s, 1H), 8.47 (d, J = 10.5 Hz, 1H), 8.39 (d, J = 7.8 Hz, 1H), 8.16–8.08 (m, 4H), 8.05 (d, J = 7.7 Hz, 1H), 7.95 (dd, J = 8.8, 1.5 Hz, 1H), 7.88 (d, J = 8.8 Hz, 1H), 7.72–7.61 (m, 3H).¹³C NMR (126 MHz, DMSO) δ 166.22, 162.48, 150.71, 147.41, 145.74, 141.87, 138.18, 137.24, 134.81, 132.62, 129.49, 128.60, 128.51, 128.17, 127.81, 127.33, 126.69, 126.01, 124.99, 124.09, 120.19, 112.14, 111.50.

4-Methoxy-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ag)

Yield 70.1%; Pink solid; mp 199.1–199.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.32 (s, 1H), 8.83 (d, J = 4.0 Hz, 1H), 8.38 (d, J = 3.7 Hz, 2H), 8.10 (t, J = 7.6 Hz, 1H), 8.04 (d, J = 8.6 Hz, 2H), 7.84 (s, 2H), 7.67 (dd, J = 6.9, 5.1 Hz, 1H), 7.12 (d, J = 8.7 Hz, 2H), 3.89 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 165.52, 162.47, 162.43, 150.71, 147.28, 145.75, 141.84, 138.18, 137.26, 130.12, 127.36, 126.68, 124.08, 120.13, 114.15, 112.03, 111.41, 55.95.

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4ah)

Yield 52.3%; Pink solid; mp 137.9–138.5 °C; ¹H NMR (500 MHz, DMSO) δ 10.82 (s, 1H), 8.83 (s, 1H), 8.39 (d, J = 9.9 Hz, 3H), 8.19 (s, 1H), 8.10 (t, J = 6.9 Hz, 1H), 8.01 (d, J = 6.9 Hz, 1H), 7.89–7.77 (m, 3H), 7.67–7.62 (m, 1H).¹³C NMR (126 MHz, DMSO) δ 164.66, 162.56, 150.71, 147.60, 145.69, 141.85, 138.18, 136.71, 136.22, 133.34, 132.37, 130.23, 129.22, 128.68, 126.72, 124.80, 124.11, 120.33, 112.43, 111.56.

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4ai)

Yield 42.7%; Pink solid; mp 146.0–146.6 °C; ¹H NMR (500 MHz, DMSO) δ 10.70 (s, 1H), 8.83 (d, J = 4.2 Hz, 1H), 8.43–8.35 (m, 2H), 8.22 (d, J = 8.0 Hz, 2H), 8.08 (tt, J = 12.1, 6.0 Hz, 1H), 7.96 (d, J = 8.1 Hz, 2H), 7.90–7.85 (m, 2H), 7.66 (dd, J = 6.9, 5.1 Hz, 1H).¹³C NMR (126 MHz, DMSO) δ 166.68, 164.97, 162.56, 150.69, 147.59, 145.69, 141.86, 139.15, 138.15, 136.69, 130.58, 129.12, 126.70, 125.88, 124.10, 120.16, 112.26, 111.57.

2-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4aj)

Yield 22.6%; Pink solid; mp 231.2–231.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.70 (s, 1H), 8.83 (s, 1H), 8.38 (s, 2H), 8.09 (s, 1H), 7.88–7.68 (m, 5H), 7.39 (d, J = 7.4 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 163.37, 162.57, 150.71, 147.44, 145.68, 141.90, 138.19, 136.82, 133.12, 133.06, 130.44, 126.73, 125.08, 124.11, 119.44, 116.78, 116.61, 111.70, 111.42.

3-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ak)

Yield 62.8%; Pink solid; mp 174.5–175.4 °C; ¹H NMR (500 MHz, DMSO) δ 8.83 (s, 1H), 8.38 (d, J = 11.4 Hz, 2H), 8.09 (t, J = 7.1 Hz, 1H), 7.92–7.79 (m, 4H), 7.65 (d, J = 6.2 Hz, 2H), 7.52–7.35 (m, 2H).¹³C NMR (126 MHz, DMSO) δ 164.74, 163.42, 162.52, 161.48, 150.70, 147.52, 145.69, 141.84, 138.17, 136.79, 131.06, 126.70, 124.10, 120.20, 118.93, 116.09, 114.94, 112.25, 111.53.

4-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4al)

Yield 23.7%; Pink solid; mp 168.0–168.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.56 (s, 1H), 8.83 (d, J = 4.2 Hz, 1H), 8.37 (d, J = 7.5 Hz, 2H), 8.10 (ddd, J = 9.1, 8.2, 3.5 Hz, 3H), 7.87–7.80 (m, 2H), 7.66 (dd, J = 7.1, 5.0 Hz, 1H), 7.41 (t, J = 8.8 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 165.60, 165.05, 163.62, 162.49, 150.70, 147.43, 145.71, 141.84, 138.17, 136.98, 130.90, 126.69, 124.09, 120.18, 115.76, 112.18, 111.49.

4-Chloro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4am)

Yield 32.1%; Pink solid; mp 201.9–202.3 °C; ¹H NMR (500 MHz, DMSO) δ 10.63 (s, 1H), 8.83 (d, J = 4.2 Hz, 1H), 8.37 (d, J = 9.4 Hz, 2H), 8.11–8.06 (m, 3H), 7.88–7.84 (m, 2H), 7.66 (t, J = 7.9 Hz, 3H).¹³C NMR (126 MHz, DMSO) δ 165.04, 162.50, 150.70, 147.48, 145.70, 141.83, 138.17, 136.96, 136.89, 134.03, 130.17, 128.97, 126.70, 124.09, 120.18, 112.21, 111.50.

4-Bromo-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4an)

Yield 43.2%; Pink solid; mp 284.5–285.1 °C; ¹H NMR (500 MHz, DMSO) δ 10.69 (s, 1H), 8.83 (d, J = 4.1 Hz, 1H), 8.39–8.36 (m, 1H), 8.09 (dd, J = 10.9, 4.5 Hz, 1H), 8.01 (d, J = 8.4 Hz, 2H), 7.86 (s, 2H), 7.78 (d, J = 8.4 Hz, 2H), 7.66 (dd, J = 7.1, 5.1 Hz, 1H), 7.47 (d, J = 8.2 Hz, 1H).¹³C NMR (126 MHz, DMSO) δ 165.17, 162.49, 150.70, 147.47, 145.70, 141.83, 138.17, 136.91, 134.40, 131.90, 130.37, 126.69, 125.88, 124.09, 120.20, 112.22, 111.49.

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4ao)

Yield 72.3%; Pink solid; mp 140.3–140.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.46 (s, 1H), 8.83 (s, 1H), 8.40–8.32 (m, 2H), 8.10 (s, 2H), 7.92–7.79 (m, 3H), 7.67 (s, 1H), 7.28 (s, 1H).¹³C NMR (126 MHz, DMSO) δ 162.53, 160.52, 150.70, 147.47, 145.70, 141.89, 140.37, 138.18, 136.59, 132.44, 129.73, 128.57, 126.71, 124.11, 120.15, 112.21, 111.57.

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4ba)

Yield 36.9%; Pink solid; mp 152.1–152.7 °C; ¹H NMR (500 MHz, CDCl₃) δ 10.48 (s, 1H), 9.34 (s, 1H), 8.79 (s, 1H), 8.52 (d, J = 6.9 Hz, 1H), 8.32 (s, 1H), 7.97 (d, J = 6.3 Hz, 2H), 7.79 (s, 2H), 7.65–7.52 (m, 4H).¹³C NMR (126 MHz, CDCl₃) δ 165.72, 161.05, 152.39, 147.99, 146.70, 141.37, 136.61, 134.88, 131.69, 128.45, 127.71, 124.31, 122.85, 119.28, 111.43, 111.29, 110.82.

2-Phenyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)acetamide (4bb)

Yield 47.2%; Pink solid; mp 110.9–111.6 °C; ¹H NMR (500 MHz, DMSO) δ 10.48 (s, 1H), 9.36 (s, 1H), 8.83 (s, 1H), 8.55 (d, J = 6.8 Hz, 1H), 8.23 (s, 1H), 7.79 (d, J = 8.6 Hz, 1H), 7.70–7.58 (m, 2H), 7.41–7.23 (m, 5H), 3.72 (s, 2H).¹³C NMR (126 MHz, DMSO) δ 169.71, 161.50, 152.81, 148.46, 146.82, 141.90, 137.20, 136.40, 135.23, 129.67, 128.83, 127.07, 124.82, 123.30, 118.43, 111.44, 110.41, 43.79.

2-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bc)

Yield 29.8%; Pink solid; mp 158.1–158.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.56 (s, 1H), 9.41 (s, 1H), 8.87 (s, 1H), 8.63 (d, J = 6.9 Hz, 1H), 8.37 (s, 1H), 7.85–7.73 (m, 3H), 7.54 (d, J = 6.8 Hz, 1H), 7.44 (d, J = 7.0 Hz, 1H), 7.36 (d, J = 7.3 Hz, 2H), 2.45 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 168.41, 161.29, 152.17, 147.92, 147.05, 141.86, 137.60, 137.28, 135.92, 135.76, 131.05, 130.21, 127.75, 126.17, 125.12, 123.57, 119.01, 111.42, 110.98, 19.82.

3-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bd)

Yield 36.8%; Pink solid; mp 179.1–179.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.55 (s, 1H), 9.39 (s, 1H), 8.84 (s, 1H), 8.57 (d, J = 7.2 Hz, 1H), 8.38 (s, 1H), 7.85 (s, 3H), 7.70 (d, J = 14.2 Hz, 2H), 7.45 (s, 1H), 7.17 (d, J = 20.4 Hz, 1H), 2.44 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 166.28, 161.48, 152.81, 148.47, 147.11, 141.83, 138.22, 137.17, 135.22, 132.68, 130.21, 128.80, 128.67, 125.35, 124.82, 123.33, 119.72, 111.79, 111.25, 21.47.

4-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4be)

Yield 73.5%; Pink solid; mp 186.4–186.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.45 (s, 1H), 9.39 (s, 1H), 8.84 (s, 1H), 8.57 (d, J = 7.2 Hz, 1H), 8.37 (s, 1H), 7.95 (d, J = 7.3 Hz, 2H), 7.84 (s, 2H), 7.69 (s, 1H), 7.39 (d, J = 7.4 Hz, 2H), 3.37 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 165.96, 161.47, 152.81, 148.47, 147.09, 142.15, 141.83, 137.17, 135.22, 132.44, 129.43, 128.23, 124.82, 123.33, 119.75, 111.80, 111.23, 21.52.

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4bf)

Yield 37.8%; Pink solid; mp 182.4–182.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.69 (s, 1H), 9.40 (s, 1H), 8.84 (s, 1H), 8.66 (s, 1H), 8.58 (d, J = 7.6 Hz, 1H), 8.43 (s, 1H), 8.10 (s, 4H), 7.88 (s, 2H), 7.68 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 166.20, 161.53, 152.82, 148.49, 147.18, 141.88, 137.15, 135.23, 134.80, 132.66, 132.58, 129.46, 128.55, 128.36, 128.18, 127.38, 124.94, 124.82, 123.33, 119.74, 119.64, 111.84, 111.33.

4-Methoxy-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bg)

Yield 55.3%; Pink solid; mp 204.9–205.3 °C; ¹H NMR (500 MHz, DMSO) δ 10.34 (s, 1H), 9.38 (s, 1H), 8.83 (s, 1H), 8.56 (d, J = 6.8 Hz, 1H), 8.35 (s, 1H), 8.02 (s, 2H), 7.82 (s, 2H), 7.68 (s, 1H), 7.10 (s, 2H), 3.88 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 165.50, 162.43, 161.43, 152.78, 148.46, 147.02, 141.82, 137.26, 135.19, 130.12, 127.33, 124.80, 123.33, 119.72, 114.12, 111.76, 111.18, 55.93.

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4bh)

Yield 72.6%; Pink solid; mp 127.3–127.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.73 (s, 1H), 9.39 (s, 1H), 8.85 (s, 1H), 8.59 (s, 1H), 8.36 (s, 2H), 8.02 (d, J = 7.4 Hz, 1H), 7.90–7.81 (m, 4H), 7.70 (s, 1H).¹³C NMR (126 MHz, DMSO) δ 164.65, 161.61, 152.86, 148.50, 147.36, 141.87, 138.72, 136.72, 136.24, 135.26, 132.37, 130.26, 129.82, 129.56, 128.68, 124.83, 123.29, 119.95, 112.15, 111.38.

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4bi)

Yield 42.7%; Pink solid; mp 179.8–180.4 °C; ¹H NMR (500 MHz, DMSO) δ 10.72 (s, 1H), 9.39 (s, 1H), 8.84 (s, 1H), 8.56 (s, 1H), 8.37 (s, 1H), 8.22 (d, J = 7.6 Hz, 2H), 7.97 (d, J = 7.6 Hz, 2H), 7.85 (d, J = 8.8 Hz, 2H), 7.69 (s, 1H).¹³C NMR (126 MHz, DMSO) δ 164.99, 161.61, 152.85, 148.49, 147.35, 141.86, 139.15, 136.70, 135.24, 132.03, 131.78, 129.12, 125.90, 124.82, 123.28, 119.78, 111.98, 111.39.

2-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bj)

Yield 32.6%; Pink solid; mp 208.6–209.1 °C; ¹H NMR (500 MHz, DMSO) δ 10.68 (s, 1H), 9.39 (s, 1H), 8.84 (s, 1H), 8.57 (d, J = 6.9 Hz, 1H), 8.34 (s, 1H), 7.85 (d, J = 8.5 Hz, 1H), 7.77–7.63 (m, 4H), 7.40 (dd, J = 19.0, 8.9 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 163.35, 161.62, 160.37, 152.86, 148.50, 147.20, 141.91, 136.81, 135.25, 133.07, 130.42, 125.12, 124.82, 123.28, 119.02, 116.79, 116.62, 111.51, 111.12.

3-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bk)

Yield 42.8%; Pink solid; mp 164.4–164.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.60 (s, 1H), 9.38 (s, 1H), 8.83 (s, 1H), 8.56 (d, J = 7.1 Hz, 1H), 8.36 (s, 1H), 7.90–7.82 (m, 4H), 7.65 (d, J = 24.3 Hz, 2H), 7.49 (s, 1H).¹³C NMR (126 MHz, DMSO) δ 164.73, 163.39, 161.54, 152.81, 148.47, 147.27, 141.83, 137.65, 136.78, 135.21, 131.12, 124.79, 124.42, 123.28, 119.78, 119.10, 115.11, 111.95, 111.31.

4-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bl)

Yield 23.7%; Pink solid; mp 174.5–175.1 °C; ¹H NMR (500 MHz, DMSO) δ 10.54 (s, 1H), 9.38 (s, 1H), 8.83 (s, 1H), 8.56 (d, J = 7.0 Hz, 1H), 8.35 (s, 1H), 8.12 (s, 2H), 7.83 (s, 2H), 7.68 (s, 1H), 7.42 (s, 2H).¹³C NMR (126 MHz, DMSO) δ 165.02, 163.60, 161.50, 152.78, 148.45, 147.18, 141.82, 136.97, 135.23, 131.72, 130.91, 124.81, 123.31, 119.78, 115.93, 111.91, 111.26.

4-Chloro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bm)

Yield 62.5%; Pink solid; mp 211.9–211.3 °C; ¹H NMR (500 MHz, DMSO) δ 10.62 (s, 1H), 9.39 (d, J = 1.4 Hz, 1H), 8.86–8.83 (m, 1H), 8.58–8.56 (m, 1H), 8.36 (s, 1H), 8.07 (d, J = 8.5 Hz, 2H), 7.91 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.70–7.66 (m, 2H), 7.41 (d, J = 8.3 Hz, 1H).¹³C NMR (126 MHz, DMSO) δ 165.07, 161.57, 152.84, 148.50, 147.28, 141.87, 135.24, 134.05, 131.39, 130.18, 128.99, 128.05, 124.82, 123.33, 119.84, 111.99, 111.31.

4-Bromo-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bn)

Yield 27.6%; Pink solid; mp 263.0–263.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.57 (s, 1H), 9.38 (s, 1H), 8.84 (s, 1H), 8.56 (d, J = 7.0 Hz, 1H), 8.35 (s, 1H), 7.98 (d, J = 7.3 Hz, 2H), 7.82 (d, J = 13.6 Hz, 4H), 7.68 (s, 1H).¹³C NMR (126 MHz, DMSO) δ 165.13, 161.54, 152.82, 148.48, 147.23, 141.84, 136.86, 135.22, 134.38, 131.92, 130.32, 125.90, 124.80, 123.29, 119.76, 111.91, 111.31.

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4bo)

Yield 42.3%; Pink solid; mp 161.2–161.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.49 (s, 1H), 9.39 (s, 1H), 8.84 (s, 1H), 8.56 (s, 1H), 8.30 (s, 1H), 8.10 (s, 1H), 7.92 (s, 1H), 7.85 (d, J = 8.6 Hz, 1H), 7.78 (d, J = 8.7 Hz, 1H), 7.69 (s, 1H), 7.28 (s, 1H); ¹³C NMR (126 MHz, DMSO) δ 161.56, 160.50, 152.83, 148.49, 147.22, 141.88, 140.34, 136.59, 135.24, 132.46, 129.73, 128.58, 124.81, 123.30, 119.77, 111.94, 111.36.

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ca)

Yield 56.2%; Pink solid; mp 132.1–132.6 °C; ¹H NMR (500 MHz, DMSO) δ 10.50 (s, 1H), 8.88 (d, J = 5.8 Hz, 2H), 8.40 (s, 1H), 8.17–8.10 (m, 2H), 8.03 (d, J = 7.2 Hz, 2H), 7.87 (s, 2H), 7.61 (dt, J = 12.2, 5.9 Hz, 3H).¹³C NMR (126 MHz, DMSO) δ 166.21, 161.42, 151.37, 147.29, 141.80, 137.26, 135.33, 133.97, 132.16, 128.93, 128.18, 121.28, 120.44, 112.05, 111.51.

2-Phenyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)acetamide (4cb)

Yield 67.7%; Pink solid; mp 120.5–120.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.52 (s, 1H), 8.86 (d, J = 6.1 Hz, 2H), 8.27 (s, 1H), 8.11 (d, J = 6.1 Hz, 2H), 7.82 (d, J = 8.9 Hz, 1H), 7.65 (d, J = 10.9 Hz, 1H), 7.42–7.34 (m, 4H), 7.29 (d, J = 7.0 Hz, 1H), 3.72 (s, 2H).¹³C NMR (126 MHz, DMSO) δ 169.76, 161.39, 151.37, 146.93, 141.85, 137.39, 136.38, 133.94, 129.67, 128.82, 127.06, 121.26, 119.15, 111.68, 110.62, 43.78.

2-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cc)

Yield 22.3%; Pink solid; mp 151.6–152.0 °C; ¹H NMR (500 MHz, DMSO) δ 10.57 (s, 1H), 8.87 (s, 2H), 8.40 (s, 1H), 8.13 (d, J = 5.9 Hz, 2H), 7.84 (dd, J = 20.2, 8.8 Hz, 2H), 7.54 (d, J = 7.4 Hz, 1H), 7.44 (t, J = 7.2 Hz, 1H), 7.36 (t, J = 7.7 Hz, 2H), 1.94 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 172.49, 168.44, 161.43, 151.40, 147.16, 141.84, 137.41, 135.78, 133.95, 131.07, 130.23, 127.75, 126.18, 121.27, 119.63, 111.64, 111.18, 21.55.

3-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cd)

Yield 26.9%; Pink solid; mp 189.1–189.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.47 (s, 1H), 8.88 (d, J = 6.0 Hz, 2H), 8.40 (s, 1H), 8.13 (d, J = 6.0 Hz, 2H), 7.87–7.79 (m, 4H), 7.50–7.41 (m, 2H), 2.45 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 166.31, 161.41, 151.39, 147.24, 141.79, 138.26, 137.30, 135.34, 133.96, 132.74, 128.84, 128.66, 125.34, 121.27, 120.38, 111.98, 111.52, 21.47.

4-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ce)

Yield 73.2%; Pink solid; mp 193.6–194.0 °C; ¹H NMR (500 MHz, DMSO) δ 10.44 (s, 1H), 8.87 (d, J = 6.0 Hz, 2H), 8.40 (s, 1H), 8.13 (d, J = 6.0 Hz, 2H), 7.95 (d, J = 8.1 Hz, 2H), 7.86 (s, 2H), 7.39 (d, J = 7.9 Hz, 2H), 2.43 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 166.00, 161.38, 151.38, 147.21, 142.19, 141.78, 137.34, 133.97, 132.41, 129.45, 128.23, 121.27, 120.42, 111.99, 111.48, 21.52.

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4cf)

Yield 37.8%; Pink solid; mp 178.6–178.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.69 (s, 1H), 8.88 (d, J = 5.9 Hz, 2H), 8.65 (s, 1H), 8.46 (d, J = 1.3 Hz, 1H), 8.16–8.03 (m, 6H), 7.91 (dt, J = 18.0, 5.3 Hz, 2H), 7.71–7.64 (m, 2H).¹³C NMR (126 MHz, DMSO) δ 166.24, 161.43, 151.35, 147.32, 141.84, 137.33, 134.83, 134.00, 132.63, 132.60, 129.46, 128.80, 128.56, 128.37, 128.19, 127.38, 124.93, 121.29, 120.46, 112.08, 111.55.

4-Methoxy-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cg)

Yield 35.3%; Pink solid; mp 194.9–195.4 °C; ¹H NMR (500 MHz, DMSO) δ 10.34 (s, 1H), 8.88 (d, J = 5.7 Hz, 2H), 8.39 (s, 1H), 8.17–8.11 (m, 2H), 8.03 (d, J = 8.8 Hz, 2H), 7.86 (s, 2H), 7.12 (d, J = 8.8 Hz, 2H), 3.88 (s, 3H).¹³C NMR (126 MHz, DMSO) δ 165.55, 162.49, 161.37, 151.38, 147.17, 141.79, 137.45, 133.99, 130.13, 127.31, 121.27, 120.44, 114.15, 111.99, 111.44, 55.95.

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4ch)

Yield 65.6%; Pink solid; mp 138.3–138.9 °C; ¹H NMR (500 MHz, DMSO) δ 10.75 (s, 1H), 8.88 (d, J = 5.9 Hz, 2H), 8.36 (dd, J = 21.3, 13.1 Hz, 3H), 8.14 (d, J = 5.9 Hz, 2H), 8.03 (d, J = 7.7 Hz, 1H), 7.86 (dd, J = 20.6, 12.0 Hz, 3H).¹³C NMR (126 MHz, DMSO) δ 164.70, 161.53, 154.77, 151.40, 147.49, 141.81, 136.84, 136.15, 133.93, 132.38, 130.29, 129.84, 128.80, 124.81, 121.30, 120.63, 112.37, 111.65.

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4ci)

Yield 42.7%; Pink solid; mp 189.8–190.4 °C; ¹H NMR (500 MHz, DMSO) δ 10.71 (s, 1H), 8.86 (d, J = 6.0 Hz, 2H), 8.39 (s, 1H), 8.21 (d, J = 8.1 Hz, 2H), 8.11 (d, J = 6.0 Hz, 2H), 7.95 (d, J = 8.3 Hz, 2H), 7.86 (s, 2H).¹³C NMR (126 MHz, DMSO) δ 164.99, 161.48, 151.35, 147.44, 141.78, 139.09, 136.86, 133.89, 132.06, 129.12, 125.89, 123.32, 121.25, 120.43, 112.17, 111.60.

2-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cj)

Yield 47.8%; Pink solid; mp 221.2–221.5 °C; ¹H NMR (500 MHz, DMSO) δ 10.69 (s, 1H), 8.88 (d, J = 5.5 Hz, 2H), 8.38 (s, 1H), 8.14 (d, J = 5.6 Hz, 2H), 7.88 (d, J = 8.8 Hz, 1H), 7.82–7.73 (m, 2H), 7.64 (d, J = 6.6 Hz, 1H), 7.40 (dd, J = 19.6, 8.8 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 163.39, 161.54, 151.41, 147.33, 141.86, 136.98, 133.92, 133.18, 130.45, 125.42, 125.11, 121.29, 119.72, 116.81, 116.63, 111.77, 111.35.

3-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ck)

Yield 32.8%; Pink solid; mp 163.3–163.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.67 (s, 1H), 8.88 (d, J = 4.1 Hz, 2H), 8.38 (s, 1H), 8.14 (d, J = 4.2 Hz, 2H), 7.88 (d, J = 8.7 Hz, 1H), 7.81–7.73 (m, 2H), 7.64 (d, J = 5.8 Hz, 1H), 7.40 (dd, J = 17.4, 9.2 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 163.39, 161.54, 151.40, 147.35, 141.87, 136.98, 133.93, 133.17, 133.10, 130.43, 125.12, 121.29, 119.75, 116.80, 116.62, 111.75, 111.39.

4-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cl)

Yield 23.7%; Pink solid; mp 154.6–155.1 °C; ¹H NMR (500 MHz, DMSO) δ 10.54 (s, 1H), 8.88 (d, J = 5.9 Hz, 2H), 8.39 (s, 1H), 8.15–8.09 (m, 4H), 7.87 (d, J = 7.4 Hz, 2H), 7.43 (t, J = 8.8 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 165.08, 161.44, 151.39, 147.31, 141.79, 137.13, 133.94, 131.73, 130.90, 121.27, 120.47, 115.97, 115.79, 112.11, 111.55.

4-Chloro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cm)

Yield 34.5%; Pink solid; mp 216.5–217.0 °C; ¹H NMR (500 MHz, DMSO) δ 10.60 (s, 1H), 8.87 (d, J = 4.5 Hz, 2H), 8.38 (s, 1H), 8.12 (d, J = 5.8 Hz, 2H), 8.05 (d, J = 8.5 Hz, 2H), 7.86 (s, 2H), 7.66 (d, J = 8.5 Hz, 2H).¹³C NMR (126 MHz, DMSO) δ 165.07, 161.45, 151.37, 147.37, 141.80, 137.08, 136.99, 134.02, 133.94, 130.16, 128.99, 121.27, 120.50, 112.18, 111.53.

4-Bromo-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cn)

Yield 17.6%; Pink solid; mp 268.1–268.7 °C; ¹H NMR (500 MHz, DMSO) δ 10.55 (s, 1H), 8.86 (s, 2H), 8.37 (s, 1H), 8.11 (d, J = 5.7 Hz, 2H), 7.97 (d, J = 8.4 Hz, 2H), 7.86–7.77 (m, 4H).¹³C NMR (126 MHz, DMSO) δ 165.17, 161.43, 151.36, 147.34, 141.78, 137.01, 134.33, 133.91, 131.93, 130.32, 125.95, 121.26, 120.42, 112.11, 111.54.

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4co)

Yield 62.8%; Pink solid; mp 162.4–162.8 °C; ¹H NMR (500 MHz, DMSO) δ 10.48 (s, 1H), 8.88 (d, J = 6.0 Hz, 2H), 8.34 (s, 1H), 8.14 (d, J = 4.5 Hz, 2H), 8.09 (d, J = 3.6 Hz, 1H), 7.90 (dd, J = 18.6, 7.3 Hz, 2H), 7.81 (d, J = 8.9 Hz, 1H), 7.31–7.27 (m, 1H).¹³C NMR (126 MHz, DMSO) δ 161.49, 160.54, 151.40, 147.36, 141.84, 140.29, 136.76, 133.95, 132.53, 129.77, 128.60, 121.30, 120.47, 112.17, 111.63.

3.1.3. Structure Determination

The crystal structures of 4ac–4bc were determined by single-crystal X-ray diffraction [27]. A total of 100 mg of the compound 4ac–4bc was dissolved in 3 mL of ethyl acetate, and the solution was placed in a 25 mL micro-reaction bottle. The reaction bottle was placed in a dryer containing petroleum ether and the dryer was sealed. After 3 days, the reaction bottle was taken out, and the single-crystal culture was completed. Reflection data were collected at room temperature on a Bruker APEX II area detector diffractometer equipped with graphite-monochromatic MoK radiation (λ = 0.71073A°) at 296(2)K with ω–2θ scan mode. Empirical adsorption corrections were applied to all data using SADABS. The structures were solved by direct methods and refined by full matrix least squares on F₂ using SHELXTL 97 software. All non-hydrogen atoms were located by direct methods and subsequent difference Fourier syntheses. The hydrogen atoms bound to carbon were located by geometrical calculations, and their positions and thermal parameters were fixed during the structure refinement in 4ac–4bc. Crystallographic data and pertinent information are provided in Supplementary Materials.

3.2. Anti-Fungal Activity

Herein, the antifungal activities of these compounds were evaluated against 8 common phytopathogenic fungi, (Fusarium solani, Colletotrichum gloeosporioides, Mycosphaerella melonis melonis, Alternaria brassicae, Pyricularia grisea, Curvularia lunata, Alternaria solani, and Fusarium graminearum) using inhibition zone method [28] at the concentration of 100 μg/mL by poisoned food technique. Inoculate the potato dextrose agar (PDA) plate: the potato dextrose agar (PDA) culture solution without compounds to be tested (blank controls) was poured in the petri dish evenly, until it became cold and solidified. In the same way, the potato dextrose agar (PDA) culture solution of different concentrations with the compound to be tested was poured into the petri dish evenly until it became cold and solidified. Then colonies from 24-h-old potato dextrose agar (PDA) petri dishes were inoculated on each cold petri dish by sterile drill to drill holes (5 mm). Among them, the concentration of the stock solutions for in vitro studies was 400 μg/mL and the amount of DMSO must be less than 2% of the overall solution volume. As a positive control, thiophanate-methyl (a commercially available agricultural fungicide) was used, the solution without the test compound was used as a blank control. Moreover, then petri dishes were incubated for 5–7 days under suitable cultivation conditions in the light incubator. All experiments were independently repeated three times.

4. Conclusions

In conclusion, a series of benzoxazoles were synthesized efficiently using a combination of PPA and Raney nickel reduction. On the basis of syntheses, their anti-phytopathogenic activities were investigated as well. All the synthesized coumarin derivatives were characterized by NMR and MS. The single crystal of 4ac, 4bc were obtained and characterized by X-ray. These compounds showed moderate to good excellent inhibition rate using linear growth rate method. These results will not only be helpful in the synthesis of similar heterocycles, but also will enlighten the discovery of a new kind of agrochemicals in the future.

Acknowledgments

Financial support from the National Natural Science Foundation of China (20802058) is greatly appreciated.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27238375/s1, supplementary data associated with this article can be found in the online version at doi.

Click here for additional data file.^{(15.6MB, zip)}

Author Contributions

R.W.: Writing original draft. R.K.: NMR data collection. X.Y.: Single Crystal Diffraction Data collection, Y.C., Methodology. H.B.: Methodology and Supervision. Z.D.: Supervision. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the all the tested compounds 4aa–4co are available from the authors.

Funding Statement

This research received no external funding.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

1.Ruan X., Zhang C., Jiang S., Guo T., Xia R., Chen Y., Tang X., Xue W. Design, Synthesis, and Biological Activity of Novel Myricetin Derivatives Containing Amide, Thioether, and 1,3,4-Thiadiazole Moieties. Molecules. 2018;23:3132. doi: 10.3390/molecules23123132. [DOI] [PMC free article] [PubMed] [Google Scholar]
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6.Lampa E., Romano A.R., Berrino L., Tortora G., Di Guglielmo R., Filippelli A., Marmo E. Pharmacological properties of a new non-steroidal anti-inflammatory drug: Flunoxaprofen. Drugs Under Exp. Clin. Res. 1985;11:501–509. [PubMed] [Google Scholar]
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19.Xu Y., Hu K., Chen P., Gao A., Du W., Chen X., An Z. Synthesis and properties of mesogenic laterally fluorinated compounds containing benzoxazole unit. Liq. Cryst. 2014;41:1042–1056. doi: 10.1080/02678292.2014.898344. [DOI] [Google Scholar]
20.Bansal S. Recent advances in synthesis of benzoxazole. Mini-Rev. Org. Chem. 2021;18:383–397. doi: 10.2174/1570193X17999200706010457. [DOI] [Google Scholar]
21.Xing R.G., Li Y.N. Progress in synthesis of 2-substituted benzoxazoles. Chin. J. Org. Chem. 2014;36:131–135. [Google Scholar]
22.Arisoy M., Temiz-Arpaci O., Yildiz I., Kaynak-Onurdag F., Aki E., Yalcin I., Abbasoglu U. Synthesis, antimicrobial activity and QSAR studies of 2,5-disubstituted benzoxazoles. SAR QSAR Environ. Res. 2008;19:589–612. doi: 10.1080/10629360802348738. [DOI] [PubMed] [Google Scholar]
23.Rida S.M., Ashour F.A., El-Hawash S.A.M., ElSemary M.M., Badr M.H., Shalaby M.A. Synthesis of some novel benzoxazole derivatives as anticancer, anti-HIV-1 and antimicrobial agents. Eur. J. Med. Chem. 2005;40:949–959. doi: 10.1016/j.ejmech.2005.03.023. [DOI] [PubMed] [Google Scholar]
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26.Zhou J., Huang L.Z., Li Y.-Q., Du Z.T. Synthesis of substituted 6H-benzo[c]chromenes: A palladium promoted ring closure of diazonium tetrafluoroborates. Tetrahedron Lett. 2012;53:7036–7070. doi: 10.1016/j.tetlet.2012.10.038. [DOI] [Google Scholar]
27.Li C., Zhong J., Liu B., Yang T., Lv B., Luo Y. Study on Typical Diarylurea Drugs or Derivatives in Cocrystallizing with Strong H-Bond Acceptor DMSO. ACS Omega. 2021;6:5532–5547. doi: 10.1021/acsomega.0c05908. [DOI] [PMC free article] [PubMed] [Google Scholar]
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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Click here for additional data file.^{(15.6MB, zip)}

Data Availability Statement

Not applicable.

[B1-molecules-27-08375] 1.Ruan X., Zhang C., Jiang S., Guo T., Xia R., Chen Y., Tang X., Xue W. Design, Synthesis, and Biological Activity of Novel Myricetin Derivatives Containing Amide, Thioether, and 1,3,4-Thiadiazole Moieties. Molecules. 2018;23:3132. doi: 10.3390/molecules23123132. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B2-molecules-27-08375] 2.Mu J.X., Shi Y.X., Yang M.Y., Sun Z.H., Liu X.H., Li B.J., Sun N.B. Design, Synthesis, DFT Study and Antifungal Activity of Pyrazolecarboxamide Derivatives. Molecules. 2016;21:68. doi: 10.3390/molecules21010068. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B3-molecules-27-08375] 3.Wong X.K., Yeong K.Y. A patent review on the current developments of benzoxazoles in drug discovery. Chem. Med. Chem. 2021;16:3237–3262. doi: 10.1002/cmdc.202100370. [DOI] [PubMed] [Google Scholar]

[B4-molecules-27-08375] 4.Kakkar S., Kumar S., Narasimhan B., Lim S.M., Ramasamy K., Mani V., Shah S.A.A. Design, synthesis and biological potential of heterocyclic benzoxazole scaffolds as promising antimicrobial and anticancer agents. Chem. Cent. J. 2018;12:96. doi: 10.1186/s13065-018-0464-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B5-molecules-27-08375] 5.Jabbar S.S. Most common benzoxazole derivatives as antimicrobial agent (1990–2018) Int. J. Pharm. Technol. 2018;10:6695–6712. [Google Scholar]

[B6-molecules-27-08375] 6.Lampa E., Romano A.R., Berrino L., Tortora G., Di Guglielmo R., Filippelli A., Marmo E. Pharmacological properties of a new non-steroidal anti-inflammatory drug: Flunoxaprofen. Drugs Under Exp. Clin. Res. 1985;11:501–509. [PubMed] [Google Scholar]

[B7-molecules-27-08375] 7.Taylor E.C., Katz A.H., Alvarado S.I., McKillop A. Thallium in Organic Synthesis. 65. A Novel Synthesis of Benzoxazoles from Anilides. J. Org. Chem. 1986;51:1607–1609. doi: 10.1021/jo00359a045. [DOI] [Google Scholar]

[B8-molecules-27-08375] 8.Malamas M.S., Manas E.S., McDevitt R.E., Gunawan I., Xu Z.B., Collini M.D., Miller C.P., Dinh T., Henderson R.A., Keith J.C., et al. Design and Synthesis of Aryl Diphenolic Azoles as Potent and Selective Estrogen Receptor-β Ligands. J. Med. Chem. 2004;47:5021–5040. doi: 10.1021/jm049719y. [DOI] [PubMed] [Google Scholar]

[B9-molecules-27-08375] 9.Chen Q., Tian W., Han G., Qi J., Zheng C., Zhou Y., Ding L., Zhao J., Zhu J., Lv J., et al. Design and synthesis of novel benzoheterocyclic derivatives as human acrosin inhibitors by scaffold hopping. Eur. J. Med. Chem. 2013;59:176–182. doi: 10.1016/j.ejmech.2012.11.005. [DOI] [PubMed] [Google Scholar]

[B10-molecules-27-08375] 10.Das S., Mallick S., De Sarkar S. Cobalt-Catalyzed Sustainable Synthesis of Benzimidazoles by Redox-Economical Coupling of o-Nitroanilines and Alcohols. J. Org. Chem. 2019;84:12111–12119. doi: 10.1021/acs.joc.9b02090. [DOI] [PubMed] [Google Scholar]

[B11-molecules-27-08375] 11.Zhang C., Zhong B., Yang S., Pan L., Yu S., Li Z., Li S., Su B., Meng X. Synthesis and biological evaluation of thiabendazole derivatives as anti-angiogenesis and vascular disrupting agents. Bioorg. Med. Chem. 2015;23:3774–3780. doi: 10.1016/j.bmc.2015.03.085. [DOI] [PubMed] [Google Scholar]

[B12-molecules-27-08375] 12.Zeyrek C.T., Arpacı Ö.T., Arısoy M., Onurdağ F.K. Synthesis, antimicrobial activity, density functional modelling and molecular docking with COVID-19 main protease studies of benzoxazole derivative: 2-(p-chloro-benzyl)-5-[3-(4-ethly-1-piperazynl) propionamido]-benzoxazole. J. Mol. Struct. 2021;1237:130413. doi: 10.1016/j.molstruc.2021.130413. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B13-molecules-27-08375] 13.Temiz-Arpaci O., Eylem Cifcioglu Goztepe B., Kaynak-Onurdag F., Ozgen S., Senol F., Erdogan Orhan I. Synthesis and different biological activities of novel benzoxazoles. Acta Biol. Hung. 2013;64:249–261. doi: 10.1556/ABiol.64.2013.2.10. [DOI] [PubMed] [Google Scholar]

[B14-molecules-27-08375] 14.Karatas E., Foto E., Ertan-Bolelli T., Yalcin-Ozkat G., Yilmaz S., Ataei S., Zilifdar F., Yildiz I. Discovery of 5-(or 6)-benzoxazoles and oxazolo[4,5-b]pyridines as novel candidate antitumor agents targeting hTopo IIα. Bioorg. Chem. 2021;112:104913. doi: 10.1016/j.bioorg.2021.104913. [DOI] [PubMed] [Google Scholar]

[B15-molecules-27-08375] 15.Huang S.T., Hsei I.J., Chen C. Synthesis and anticancer evaluation of bis (benzimidazoles), bis (benzoxazoles), and benzothiazoles. Biorg. Med. Chem. 2006;14:6106–6119. doi: 10.1016/j.bmc.2006.05.007. [DOI] [PubMed] [Google Scholar]

[B16-molecules-27-08375] 16.Kumar D., Jacob M.R., Reynolds M.B., Kerwin S.M. Synthesis and evaluation of anticancer benzoxazoles and benzimidazoles related to UK-1. Biorg. Med. Chem. 2002;10:3997–4004. doi: 10.1016/S0968-0896(02)00327-9. [DOI] [PubMed] [Google Scholar]

[B17-molecules-27-08375] 17.Sondhi S.M., Singh N., Kumar A., Lozach O., Meijer L. Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases. Biorg. Med. Chem. 2006;14:3758–3765. doi: 10.1016/j.bmc.2006.01.054. [DOI] [PubMed] [Google Scholar]

[B18-molecules-27-08375] 18.Paderni D., Giorgi L., Voccia M., Formica M., Caporaso L., Macedi E., Fusi V. A new benzoxazole-based fluorescent macrocyclic chemosensor for optical detection of Zn2+ and Cd2+ Chemosensors. 2022;10:188. doi: 10.3390/chemosensors10050188. [DOI] [Google Scholar]

[B19-molecules-27-08375] 19.Xu Y., Hu K., Chen P., Gao A., Du W., Chen X., An Z. Synthesis and properties of mesogenic laterally fluorinated compounds containing benzoxazole unit. Liq. Cryst. 2014;41:1042–1056. doi: 10.1080/02678292.2014.898344. [DOI] [Google Scholar]

[B20-molecules-27-08375] 20.Bansal S. Recent advances in synthesis of benzoxazole. Mini-Rev. Org. Chem. 2021;18:383–397. doi: 10.2174/1570193X17999200706010457. [DOI] [Google Scholar]

[B21-molecules-27-08375] 21.Xing R.G., Li Y.N. Progress in synthesis of 2-substituted benzoxazoles. Chin. J. Org. Chem. 2014;36:131–135. [Google Scholar]

[B22-molecules-27-08375] 22.Arisoy M., Temiz-Arpaci O., Yildiz I., Kaynak-Onurdag F., Aki E., Yalcin I., Abbasoglu U. Synthesis, antimicrobial activity and QSAR studies of 2,5-disubstituted benzoxazoles. SAR QSAR Environ. Res. 2008;19:589–612. doi: 10.1080/10629360802348738. [DOI] [PubMed] [Google Scholar]

[B23-molecules-27-08375] 23.Rida S.M., Ashour F.A., El-Hawash S.A.M., ElSemary M.M., Badr M.H., Shalaby M.A. Synthesis of some novel benzoxazole derivatives as anticancer, anti-HIV-1 and antimicrobial agents. Eur. J. Med. Chem. 2005;40:949–959. doi: 10.1016/j.ejmech.2005.03.023. [DOI] [PubMed] [Google Scholar]

[B24-molecules-27-08375] 24.Du Z., Si C., Li Y., Wang Y., Lu J. Improved synthesis of 5-substituted 1H-tetrazoles via the 3+2 cycloaddition of nitriles and sodium azide catalyzed by silica sulfuric acid. Int. J. Mol. Sci. 2012;13:4696–4703. doi: 10.3390/ijms13044696. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B25-molecules-27-08375] 25.Zhang T., Huang L.Z., Wu J., Lu D., Ma B.L., Du Z.T. Microwave-assisted synthesis of 2-substituted 1h-benzo[d]imidazoles and their antifungal activities in vitro. Heterocycles. 2013;87:1545–1550. doi: 10.1002/chin.201344126. [DOI] [Google Scholar]

[B26-molecules-27-08375] 26.Zhou J., Huang L.Z., Li Y.-Q., Du Z.T. Synthesis of substituted 6H-benzo[c]chromenes: A palladium promoted ring closure of diazonium tetrafluoroborates. Tetrahedron Lett. 2012;53:7036–7070. doi: 10.1016/j.tetlet.2012.10.038. [DOI] [Google Scholar]

[B27-molecules-27-08375] 27.Li C., Zhong J., Liu B., Yang T., Lv B., Luo Y. Study on Typical Diarylurea Drugs or Derivatives in Cocrystallizing with Strong H-Bond Acceptor DMSO. ACS Omega. 2021;6:5532–5547. doi: 10.1021/acsomega.0c05908. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B28-molecules-27-08375] 28.Zhou K., Chen D., Li B., Zhang B., Miao F., Zhou L. Bioactivity and structure-activity relationship of cinnamic acid esters and their derivatives as potential antifungal agents for plant protection. PLoS ONE. 2017;12:e0176189. doi: 10.1371/journal.pone.0176189. [DOI] [PMC free article] [PubMed] [Google Scholar]

PERMALINK

Design, Synthesis, and Anti-Fungal Evaluation of Heterocyclic Benzoxazole Derivatives

Ruibo Wang

Ruiting Kang

Xuan Yang

Yu Cheng

Hongjin Bai

Zhenting Du

Roles

Abstract

1. Introduction

Figure 1.

Scheme 1.

Figure 2.

2. Results and Discussion

2.1. Chemistry

Scheme 2.

Table 1.

Figure 3.

2.2. X-ray Crystallographic Studies of 4ac, 4bc

2.3. In Vitro Anti-Fungal Activity

Figure 4.

3. Materials and Methods

3.1. Chemistry

3.1.1. General Synthesis of 3a–3c

3.1.2. General Procedures for the Synthesis of 4aa–4co

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4aa)

2-Phenyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)acetamide (4ab)

2-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ac)

3-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ad)

4-Methyl-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ae)

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4af)

4-Methoxy-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ag)

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4ah)

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4ai)

2-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4aj)

3-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4ak)

4-Fluoro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4al)

4-Chloro-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4am)

4-Bromo-N-(2-(pyridin-2-yl)benzo[d]oxazol-5-yl)benzamide (4an)

N-(2-(Pyridin-2-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4ao)

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4ba)

2-Phenyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)acetamide (4bb)

2-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bc)

3-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bd)

4-Methyl-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4be)

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4bf)

4-Methoxy-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bg)

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4bh)

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4bi)

2-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bj)

3-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bk)

4-Fluoro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bl)

4-Chloro-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bm)

4-Bromo-N-(2-(pyridin-3-yl)benzo[d]oxazol-5-yl)benzamide (4bn)

N-(2-(Pyridin-3-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4bo)

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ca)

2-Phenyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)acetamide (4cb)

2-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cc)

3-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cd)

4-Methyl-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ce)

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-2-naphthamide (4cf)

4-Methoxy-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cg)

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-3-(trifluoromethyl)benzamide (4ch)

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)-4-(trifluoromethyl)benzamide (4ci)

2-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cj)

3-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4ck)

4-Fluoro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cl)

4-Chloro-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cm)

4-Bromo-N-(2-(pyridin-4-yl)benzo[d]oxazol-5-yl)benzamide (4cn)

N-(2-(Pyridin-4-yl)benzo[d]oxazol-5-yl)thiophene-2-carboxamide (4co)

3.1.3. Structure Determination

3.2. Anti-Fungal Activity

4. Conclusions

Acknowledgments

Supplementary Materials

Author Contributions

Institutional Review Board Statement

Informed Consent Statement

Data Availability Statement