Synthesis of Novel α-Trifluoroanisole Derivatives Containing Phenylpyridine Moieties with Herbicidal Activity

Abstract

To find novel herbicidal compounds with high activity and broad spectrum, a series of phenylpyridine moiety-containing α-trifluoroanisole derivatives were designed, synthesized, and identified via nuclear magnetic resonance (NMR) and high-resolution mass spectrometry (HRMS). Greenhouse-based herbicidal activity assays revealed that compound 7a exhibited > 80% inhibitory activity against Abutilon theophrasti, Amaranthus retroflexus, Eclipta prostrate, Digitaria sanguinalis, and Setaria viridis at a dose of 37.5 g a.i./hm², which was better than fomesafen. Compound 7a further exhibited excellent herbicidal activity against Abutilon theophrasti and Amaranthus retroflexus in this greenhouse setting, with respective median effective dose (ED₅₀) values of 13.32 and 5.48 g a.i./hm², both of which were slightly superior to fomesafen (ED₅₀ = 36.39, 10.09 g a.i./hm²). The respective half-maximal inhibitory concentration (IC₅₀) for compound 7a and fomesafen when used to inhibit the Nicotiana tabacum protoporphyrinogen oxidase (NtPPO) enzyme, were 9.4 and 110.5 nM. The docking result of compound 7a indicated that the introduction of 3-chloro-5-trifluoromethylpyridine and the trifluoromethoxy group was beneficial to the formation of stable interactions between these compounds and NtPPO. This work demonstrated that compound 7a could be further optimized as a PPO herbicide candidate to control various weeds.

1. Introduction

Species regarded as weeds generally exhibit advantages with respect to their ability to compete for water, space, light, and nutrients as compared to crops thereby resulting in crop production losses [1,2]. The Food and Agriculture Organization of the United Nations (FAO) estimates that weeds, pests, and plant diseases result in 20–40% reductions in annual global crop yields [3]. Herbicides can effectively suppress weed growth, thereby improving crop yields. FAO data suggest that sustained herbicide use would improve global food production by a minimum of 10% per year [4]. Therefore, it is necessary to continuously develop new herbicides with high efficiency and a broad spectrum to deal with various weeds.

The presence of the trifluoromethoxy moiety yields α-trifluoroanisole compound properties, including electron-withdrawing [5], lipophilicity [6], and metabolic stability. Several pesticides containing α-trifluoroanisole structures have been successfully synthesized to date [7,8,9,10,11,12,13,14], including indoxacarb, triflumuron, metaflumizone, flufenerim, flometoquin, flucarbazone-sodium, thifluzamide, and flurprimidol (Figure 1).

Figure 1.

Reported α-trifluoroanisole structure-containing compounds.

Protoporphyrinogen oxidase (PPO) is the last shared enzyme in the plant chlorophyll and animal heme biosynthesis pathways, which catalyzes the oxidation of protoporphyrinogen IX to protoporphyrin IX. Inhibiting the activity of PPO will lead to the massive accumulation of protoporphyrinogen IX, which penetrates the cytoplasm and is oxidized to protoporphyrin IX via other non-enzymatic mechanisms or oxidases. Protoporphyrin IX can generate reactive oxygen species under light, thereby resulting in the death of the plant. Therefore, PPO has been an important target for a variety of herbicides. Commercially available PPO inhibitors with herbicidal activity can be classified into oxadiazoles, uracils, phenylpyrazoles, diphenyl ethers, thiadiazoles, triazolinones, oxazolidinediones, and N-phenylphthalimides based upon their structural characteristics [15,16,17,18,19,20,21]. These herbicides have several advantages, including rapid onset of action, prolonged efficacy, a low environmental impact, and minimal mammalian toxicity [22]. Phenylpyridine compounds, which are structurally similar to uracil and diphenyl ethers, have been studied in the context of pesticide development. Schaefer et al. demonstrated that synthesized substituted 2-phenylpyridines exhibited excellent PPO enzyme inhibitory activity and herbicidal activity [22,23]. Substituted 3-(pyridin-2-yl)benzenesulfonamide derivatives prepared by Liu et al. exhibited effective inhibition against various weeds, especially broadleaf weeds [24,25,26]. In addition, Matsuya et al. demonstrated that N-[4-(arylmethyloxy)phenyl]-4-methyl-3,4,5,6-tetrahydrophthalimide exhibited good herbicidal activity [27,28]. Theodoridis reported that 2-[(4-heterocyclic-substituted-3-halophenoxymethyl)phenoxy]alkanoates showed excellent herbicidal activities against broadleaf weeds for both pre- and postemergence [29]. Therefore, α-trifluoroanisole was introduced into the active structure of 2-phenylpyridines to discover novel broad-spectrum herbicides.

Here, 18 novel compounds were synthesized via the introduction of substituted α-trifluoroanisole moieties into 2-phenylpyridines, and the resultant compounds were found to exhibit herbicidal activity against both broadleaf and grass weeds. The synthesis strategy for these compounds is detailed in Figure 2.

Figure 2.

Design strategy of target compounds.

2. Results and Discussion

2.1. Synthesis of Target Compounds

The synthesis procedures for the target compounds used in this study are outlined in Scheme 1. Intermediates 3a–3i were synthesized via a Suzuki cross-coupling reaction from 2,3-dichloro-5-trifluoromethylpyridine 1 and substituted p-hydroxyphenylboronic acid 2a–2i, while intermediates 6j–6r were synthesized using substituted 4-trifluoromethoxybenzaldehyde as starting materials in a simple two-step reaction. These approaches yielded high levels of compounds 7a–7r using intermediates 3a–3i and intermediates 6a, 6j–6r as materials via nucleophilic substitution reactions in which N,N-Dimethylformamide DMF served as a solvent. After synthesis, compounds were characterized via HRMS and NMR, with the resultant spectral and analytical data being consistent with the expected structures. X-ray diffraction crystallography was further used to confirm the structure of compound 7a (Figure 3). The crystal data for compound 7a are shown in Tables S1–S7 in the Supplementary Material, and the NMR and HRMS spectra of compounds 7a–7r are shown in Figures S1–S81 in the Supplementary Material.

Scheme 1.

Synthesis of α-trifluoroanisole derivatives containing substituted phenylpyridine moieties.

Figure 3.

The X-ray crystal structure of compound 7a.

2.2. Greenhouse Herbicidal Activity Assays

Herbicidal activity levels for compounds 7a–7r, when used for the post-emergence treatment of dicotyledonous weeds Abutilon theophrasti (A. theophrasti), Amaranthus retroflexus (A. retroflexus), Eclipta prostrate (E. prostrate), and monocotyledonous weeds Digitaria sanguinalis (D. sanguinalis), Echinochloa crusgalli (E. crusgalli), Setaria viridis (S. viridis) were next assessed (Table 1), with fomesafen serving as a control. The majority of these target compounds exhibited excellent inhibitory activity against all tested dicotyledonous weeds, with some additionally exhibiting inhibitory activity against all tested monocotyledonous weeds. Of these, compounds 7a, 7i, and 7r achieved 100% inhibitory activity when used for the post-emergence treatment of A. retroflexus, A. theophrasti, and E. prostrata at 150 g a.i./hm², compounds 7b, 7c, 7j, 7k, 7l, 7m, 7n, 7o, 7p, and 7q also exhibited > 80% activity against these broadleaf weeds. In addition, compounds 7a and 7j also effectively suppressed the growth of all tested weeds, whereas compounds 7b, 7c, 7i, 7k, and 7n exhibited > 80% inhibitory activity against all tested target weeds other than E. crusgalli. Other compounds exhibited varying levels of general herbicidal activities.

Table 1.

The structures and herbicidal activities of α-trifluoroanisole derivatives at a 150 g a.i./hm² post-emergence treatment dose in a greenhouse assay setting.

Compound	Chemical Structure				Herbicidal Activity (%)
	R1	R2	R3	R4	E. crusgalli	D. sanguinalis	S. viridis	A. theophrasti	A. retroflexus	E. prostrate
7a	H	H	H	H	90 ± 5	100 ± 0	95 ± 3	100 ± 0	100 ± 0	100 ± 0
7b	CH3	H	H	H	50 ± 4	80 ± 2	80 ± 4	100 ± 0	100 ± 0	90 ± 5
7c	H	F	H	H	40 ± 4	90 ± 2	80 ± 5	100 ± 0	100 ± 0	90 ± 2
7d	H	Cl	H	H	10 ± 2	20 ± 1	20 ± 4	100 ± 0	100 ± 0	70 ± 5
7e	H	NO2	H	H	0 ± 0	0 ± 0	0 ± 0	15 ± 1	70 ± 2	60 ± 4
7f	H	CF3	H	H	0 ± 0	0 ± 0	0 ± 0	30 ± 3	100 ± 0	30 ± 2
7g	H	CH3	H	H	0 ± 0	0 ± 0	0 ± 0	30 ± 4	20 ± 2	20 ± 5
7h	H	CN	H	H	0 ± 0	10 ± 3	10 ± 2	60 ± 7	100 ± 0	20 ± 3
7i	F	F	H	H	60 ± 2	100 ± 0	85 ± 5	100 ± 0	100 ± 0	100 ± 0
7j	H	H	H	Cl	80 ± 3	100 ± 0	100 ± 0	100 ± 0	100 ± 0	90 ± 4
7k	H	H	CH3O	H	40 ± 2	80 ± 4	80 ± 1	100 ± 0	100 ± 0	98 ± 1
7l	H	H	CH3	H	30 ± 2	75 ± 4	75 ± 6	100 ± 0	98 ± 1	100 ± 0
7m	H	H	H	F	70 ± 5	80 ± 4	40 ± 3	100 ± 0	100 ± 0	80 ± 8
7n	H	H	F	H	70 ± 6	100 ± 0	80 ± 5	100 ± 0	100 ± 0	95 ± 3
7o	H	H	H	Br	60 ± 1	60 ± 2	50 ±3	100 ± 0	90 ± 5	80 ± 1
7p	H	H	H	I	0 ± 0	30 ± 4	50 ± 2	100 ± 0	95 ± 3	98 ± 2
7q	H	H	H	cyclopropyl	40 ± 7	30 ± 2	60 ± 5	90 ± 4	100 ± 0	90 ± 5
7r	H	H	H	NO2	0 ± 0	0 ± 0	60 ± 2	100 ± 0	100 ± 0	100 ± 0
fomesafen	/				68 ± 4	76 ± 3	78 ± 5	98 ± 2	100 ± 0	76 ± 5

Further herbicidal activities revealed that at a 37.5 g a.i./hm² dose, compounds 7a, 7j, and 7k achieved 100% inhibition against the broadleaf weeds A. theophrasti and A. retroflexus in post-emergence testing, performing better than fomesafen, with compound 7a additionally exhibiting > 80% inhibitory activities against the broadleaf weed E. prostrata and the grass weeds D. sanguinalis and S. Viridis (Table 2).

Table 2.

Analysis of the herbicidal activities of the selected compounds when used for post-emergence treatment in a greenhouse setting.

Compound	Dosage/(g a.i./hm2)	E. crusgalli	D. sanguinalis	S. viridis	A. theophrasti	A. retroflexus	E. prostrate
7a	37.5	65 ± 2	80 ± 1	85 ± 0	100 ± 0	100 ± 0	80 ± 5
	75	75 ± 1	90 ± 4	90 ± 2	100 ± 0	100 ± 0	85 ± 2
7i	37.5	20 ± 2	60 ± 3	70 ± 3	90 ± 1	100 ± 0	90 ± 5
	75	50 ± 3	95 ± 1	90 ± 5	100 ± 0	100 ± 0	95 ± 3
7j	37.5	20 ± 4	90 ± 2	30 ± 6	100 ± 0	100 ± 0	80 ± 1
	75	40 ± 1	90 ± 4	50 ± 2	100 ± 0	100 ± 0	90 ± 3
7k	37.5	0 ± 0	30 ± 3	10 ± 1	100 ± 0	100 ± 0	60 ± 2
	75	0 ± 0	50 ± 1	50 ± 2	100 ± 0	100 ± 0	80 ± 5
fomesafen	37.5	47 ± 3	44 ± 2	56 ± 4	90 ± 1	87 ± 5	55 ± 2
	75	63 ± 1	69 ± 5	67 ± 3	92 ± 2	95 ± 3	67 ± 4

SAR analysis indicated that the activities of these compounds were dependent on R₁, R₂, R₃, and R₄. For R₁ and R₂ substitutions, optimal herbicidal activity was observed when both R₁ and R₂ were hydrogen or fluorine atoms. In contrast, such activity decreased markedly with R₂ substitution of bulky groups, such as CF₃ and CH₃. With respect to the R₃ and R₄ substitutions, optimal herbicidal activity was observed when R₄ was a hydrogen atom or chlorine atom, whereas other substitutions were associated with reduced activity against grass weeds. As such, the best herbicidal activity for the synthesized compounds was observed when both R₁, R₂, R₃, and R₄ were substituted with hydrogen atoms.

Compound 7a was next used in weed spectrum control and crop injury tests conducted under greenhouse conditions (Figure 4). Compound 7a exhibited good broad-spectrum inhibitory activity against the majority of tested broadleaf weeds and several grass weeds, with over 70% herbicidal activity at a dose of 18.75 g a.i./hm². In addition, compound 7a was able to fully control the growth of Medicago sativa, Portulaca oleracea, Abutilon theophrasti, Amaranthus retroflexus, Cyperus rotundus L., and Solanum nigrum. Compound 7a also exhibited slight damage to the tested crops, with 20% inhibitory effect on Zea mays (maize, Z. mays), Triticum aestivum (wheat, T. aestivum), Gossypium spp. (cotton, G. spp.), and 15% inhibitory effect on Orysa sativa (rise, O. sativa), Glycine max (soybean, G. max).

Figure 4.

The use of compound 7a at an 18.75 g a.i./hm² dose for the post-emergence treatment of broadleaf weeds, grass weeds, and crops.

To evaluate the ability of compound 7a more fully, i.e., to inhibit the growth of A. theophrasti and A. retroflexus, an ED₅₀ assay was next conducted (Table 3). Compound 7a exhibited excellent herbicidal activities against A. theophrasti and A. retroflexus, with respective ED₅₀ values of 13.32 and 5.48 g a.i./hm², performing slightly better than the control fomesafen (ED₅₀ = 36.39, 10.09 g a.i./hm²).

Table 3.

Analysis of the herbicidal activities of selected compounds when used for the postemergence treatment of A. theophrasti and A. retroflexus in a greenhouse setting.

Compound	A. theophrasti	A. retroflexus
	ED50 (g a.i./hm2)	ED50 (g a.i./hm2)
7a	13.32	5.48
fomesafen	36.39	10.09

2.3. Analysis of In Vitro PPO Inhibitory Activity

Compound 7a exhibited significant inhibitory activity against the NtPPO enzyme in vitro (IC₅₀ = 9.4 nM), with this value obviously being better than that for fomesafen (IC₅₀ = 110.5 nM) (Table 4).

Table 4.

The inhibitory activity of compound 7a against NtPPO.

Compound	IC50 (nM)
7a	9.4 ± 2.2
fomesafen	110.5 ± 1.2

2.4. Docking Analysis

To better understand the mechanism of action between the prepared compounds and PPO, molecular docking was used to predict the binding conformation of small molecule compounds and target enzymes at the active site. Specifically, compound 7a and fomesafen were selected for docking studies to predict the binding mode of all target compounds to PPO. As shown in Figure 5B, the phenyl ring-containing trifluoromethyl group of fomesafen forms a π–π stacking interaction with the amino acid residue Phe392, the fluorine atom of the trifluoromethyl group forms a hydrophobic interaction with the amino acid residue Leu356, the phenyl ring-containing nitro group forms a π–π stacking interaction with the coenzyme FAD600, the nitro group forms a hydrogen bond with the coenzyme FAD600, and the sulfonyl group forms two hydrogen bonds with the amino acid residue Arg98. As shown in Figure 5A, the phenyl ring containing trifluoromethoxy group of compound 7a forms a π–π stacking interaction with the amino acid residue Phe392 and a hydrophobic interaction with the amino acid residue Leu356, the pyridine ring forms a π–π stacking interaction with the coenzyme FAD600, the phenyl ring linked to pyridine forms a hydrophobic interaction with the amino acid residue Leu372, the fluorine atoms of the trifluoromethoxy group form a hydrophobic interaction with the amino acid residue Phe439 and Leu334, respectively. Furthermore, the difference in herbicidal activity of compound 7a and fomesafen may be attributed to the different interactions.

Figure 5.

(A) Docking model for compound 7a with the protoporphyrinogen oxidase active site; (B) docking model for fomesafen with the protoporphyrinogen oxidase active site. The carbon atoms are shown in springgreen (A) and cyan (B); the fluorine atoms are shown in aquamarine (A,B); the oxygen atoms are shown in red (A,B); the chlorine atoms are shown in green (A,B); the nitrogen atoms are shown in blue (A,B); the sulfur atom is shown in yellow (B).

3. Materials and Methods

3.1. Instrumentation

All reagents and other materials were obtained from Guangdong Guanghua Sci-tech Co., Ltd. (Guangdong, China), Bide Pharmatech Co., Ltd. (Shanghai, China), and Accela ChemBio Co., Ltd. (Shanghai, China) and used without additional purification unless otherwise noted. A B-545 melting point instrument (Buchi, Hangzhou, China) was used to quantify melting points, which were used without further correction. A Bruker AV-400 or AV-500 MHz spectrometer (Bruker, Hangzhou, China) was used to generate NMR spectra, with CDCl₃ or DMSO-d₆ serving as solvents. An Agilent 6545 Q-TOF LCMS spectrometer (Agilent, Hangzhou, China) was used for mass spectrometry. A Bruker D8 Venture diffractometer (Bruker, Hangzhou, China) was utilized to collect crystallographic data.

3.2. Synthesis

The synthesis approach for α-trifluoroanisole derivatives in this study is outlined in Scheme 1. Among these, compounds 6a, 6j, and 6k were obtained from commercial sources and used without additional purification.

3.2.1. General Approach to the Synthesis of Compounds 3a–3i

To prepare these compounds, 2,3-dichloro-5-trifluoromethylpyridine 1 (5 mmol), potassium carbonate (10 mmol), triphenylphosphorus (0.5 mmol), substituted p-hydroxybenzeneboronic acid 2a–2i (5.5 mmol), and palladium(II) acetate (0.25 mmol) were mixed for 6 h with 5 mL of CH₃OH and 10 mL of CH₃CN at 50 °C under N₂. Following the completion of this reaction as determined via TLC, the mixture was extracted thrice using ethyl acetate. Organic layers from these three extraction steps were then combined, rinsed with brine, and dried over MgSO₄. Vacuum filtration was used to remove solid residues, and the solvent was removed. The remaining residue was then recrystallized with ethanol and water at 70 °C to obtain compounds 3a–3i [30].

3.2.2. General Approach to the Synthesis of Compounds 5l–5r, 6l–6r

Sodium borohydride (10 mmol) was slowly added to a solution of substituted p-trifluoromethoxy benzaldehyde (5 mmol) in methanol (20 mL) with constant magnetic stirring at −10 °C over a 10 min period, followed by further stirring for an 8 h period. Following the completion of this reaction as determined via TLC, the mixture was evaporated until dry at which time HCl (3 N) was added to the remaining residue to yield an acidic solution that was subsequently extracted thrice using ethyl acetate. The combined ethyl acetate layers were then rinsed using brine, after which the organic layer was evaporated to yield compounds 5l–5r for subsequent use without additional purification [31].

Phosphorus tribromide (5.4 mmol) in CH₂Cl₂ (2 mL) was added in a dropwise manner to a substituted 4-trifluoromethoxybenzyl alcohol 5l–5r (3 mmol) in CH₂Cl₂ (10 mL) solution at −5 °C with stirring for 5 h. Following the completion of this reaction as determined via TLC, the mixture was extracted thrice with CH₂Cl₂. The combined dichloromethane layers were then rinsed using NaHCO₃ and brine, dried over MgSO₄, and concentrated to yield the substituted 4-trifluoromethoxybenzyl bromide 6l–6r for subsequent use without additional purification [31].

3.2.3. General Approach to Synthesis of Compounds 7a–7r

Substituted phenylpyridines 3a–3i (2 mmol), N,N-dimethylformamide (10 mL), and NaH (3 mmol, 0.12 g) were mixed and stirred in a three-necked reaction flask at 20 °C for 30 min under N₂. Next, the substituted 4-trifluoromethoxybenzyl bromide 6a, 6j–6r (2.4 mmol) was added followed by stirring for 8 h at 60 °C. Following the completion of this reaction as determined via TLC, the mixture was extracted thrice using ethyl acetate (30 mL × 3). The pooled ethyl acetate layers were then rinsed thrice using brine and concentrated. Residues were then purified via silica gel column chromatography using ethyl acetate (EA) and petroleum ether (PE) (V_EA:V_PE=1:15) to yield compounds 7a–7r [30].

3-Chloro-2-(4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7a): White solid, yield 79.3%, m.p. 59.1-60.5 °C, ¹H NMR (500 MHz, DMSO-d₆) δ: 8.99 (d, J = 1.1 Hz, 1H), 8.51 (s, 1H), 7.78 − 7.75 (m, 2H), 7.65 − 7.61 (m, 2H), 7.41 (d, J = 8.0 Hz, 2H), 7.19 − 7.16 (m, 2H), 5.24 (s, 2H). ¹³C NMR (126 MHz, DMSO-d₆) δ: 159.27, 158.81, 147.92 (q, J = 1.4 Hz), 144.26 (q, J = 3.9 Hz), 136.26, 135.68 (q, J = 3.5 Hz), 131.01, 129.56, 129.30, 129.16, 124.39 (q, J = 33.04 Hz), 122.87 (q, J = 271.67 Hz), 120.99, 120.05(q, J = 256.86 Hz), 114.35, 68.42. HRMS (ESI): calculated for C₂₀H₁₃ClF₆NO₂ [M+H]⁺ 448.0534, found 448.0534.

3-Chloro-2-(2-methyl-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7b): White solid, yield 93.5%, m.p. 67.8-69.4 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.01 (s, 1H), 8.58 (s, 1H), 7.62 (d, J = 8.5 Hz, 2H), 7.41 (d, J = 8.3 Hz, 2H), 7.22 (d, J = 8.4 Hz, 1H), 7.03 (d, J = 2.0 Hz, 1H), 6.96 (dd, J = 8.5, 2.3 Hz, 1H), 5.19 (s, 2H), 2.07 (s, 3H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 161.04, 158.60, 147.93 (q, J = 1.8 Hz), 144.19 (q, J = 4.0 Hz), 137.32, 136.54, 135.03 (q, J = 3.4 Hz), 131.11, 130.25, 129.95, 129.66, 125.11 (q, J = 33.0 Hz), 122.94 (q, J = 274.0 Hz), 121.13, 120.12 (q, J = 256.9 Hz), 116.27, 111.91, 68.29, 19.27. HRMS (ESI): calculated for C₂₁H₁₄ClF₆NO₂Na [M+Na]⁺ 484.0509, found 484.0505.

3-Chloro-2-(3-fluoro-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7c): White solid, yield 71.6%, m.p. 48.5-51.8 °C, ¹H NMR (500 MHz, CDCl₃) δ: 8.74 (s, 1H), 7.94 (d, J = 1.3 Hz, 1H), 7.56 (dd, J = 12.0, 2.0 Hz, 1H), 7.49 (d, J = 8.6 Hz, 1H), 7.42 (d, J = 8.5 Hz, 2H), 7.18 (s, 1H), 7.17 (s, 1H), 7.01 (t, J = 8.4 Hz, 1H), 5.13 (s, 2H). ¹³C NMR (126 MHz, CDCl₃) δ: 158.07, 152.35 (d, J = 247.4 Hz), 149.30 (q, J = 1.7 Hz), 147.96 (d, J = 10.8 Hz), 144.40 (q, J = 3.8 Hz), 135.70 (q, J = 3.5 Hz), 134.99, 130.66 (d, J = 6.7 Hz), 130.06, 129.02, 126.20 (q, J = 33.8 Hz), 126.13 (d, J = 3.6 Hz), 122.84 (q, J = 273.3 Hz), 121.34, 120.63 (q, J = 257.8 Hz), 118.04 (d, J = 20.4 Hz), 115.02 (d, J = 1.6 Hz), 70.63. HRMS (ESI): calculated for C₂₀H₁₁ClF₇NO₂Na [M+Na]⁺ 488.0259, found 488.0255.

3-Chloro-2-(3-chloro-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7d): White solid, yield 99.1%, m.p. 60.2-62.0 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.01 (s, 1H), 8.56 (s, 1H), 7.86 (d, J = 1.9 Hz, 1H), 7.75 (dd, J = 8.6, 1.9 Hz, 1H), 7.64 (d, J = 8.5 Hz, 2H), 7.43 (d, J = 8.2 Hz, 2H), 7.39 (d, J = 8.7 Hz, 1H), 5.34 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 157.56, 154.48, 148.04 (q, J = 1.4 Hz), 144.45 (q, J = 3.9 Hz), 135.97 (q, J = 3.4 Hz), 135.85, 130.98, 130.20, 129.75, 129.50, 129.48, 124.91 (q, J = 33.1 Hz), 122.87 (q, J = 274.0 Hz), 121.23, 120.11 (q, J = 257.3 Hz), 113.63, 69.29. HRMS (ESI): calculated for C₂₀H₁₂Cl2F₆NO₂ [M+H]⁺ 482.0144, found 482.0144.

3-Chloro-2-(3-nitro-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7e): White solid, yield 71.8%, m.p. 122.1-124.8 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.06 (s, 1H), 8.63 (s, 1H), 8.34 (d, J = 2.2 Hz, 1H), 8.11 (dd, J = 8.8, 2.2 Hz, 1H), 7.63 (m, 3H), 7.45 (d, J = 8.4 Hz, 2H), 5.45 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 156.78, 151.74, 148.12 (q, J = 1.2 Hz), 144.63 (q, J = 4.0 Hz), 139.04, 136.12 (q, J = 3.5 Hz), 135.44, 135.31, 129.73, 129.46, 129.20, 126.36, 125.32 (q, J = 33.1 Hz), 122.84 (q, J = 274.2 Hz), 121.29, 120.11 (q, J = 257.5 Hz), 115.28, 69.86. HRMS (ESI): calculated for C₂₀H₁₂ClF₆N₂O₄ [M+H]⁺ 493.0384, found 493.0378.

3-Chloro-2-(4-((4-(trifluoromethoxy)benzyl)oxy)-3-(trifluoromethyl)phenyl)-5-(trifluoromethyl)pyridine (7f): White solid, yield 40.8%, m.p. 73.3-75.1 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.02 (s, 1H), 8.58 (s, 1H), 8.08 (d, J = 8.7 Hz, 1H), 8.04 (s, 1H), 7.60 (d, J = 8.5 Hz, 2H), 7.51 (d, J = 8.8 Hz, 1H), 7.43 (d, J = 8.2 Hz, 2H), 5.41 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 157.47, 156.75, 148.02 (q, J = 1.4 Hz), 144.54 (q, J = 4.0 Hz), 136.01 (q, J = 3.4 Hz), 135.66, 135.41, 129.56, 129.13, 129.01, 128.20 (q, J = 5.3 Hz), 125.05 (q, J = 33.2 Hz), 123.50 (q, J = 273.6 Hz), 122.86 (q, J = 274.0 Hz), 121.24, 120.11 (q, J = 257.2 Hz), 117.06 (q, J = 30.6 Hz), 113.79, 69.20. HRMS (ESI): calculated for C₂₁H₁₁Cl₂F₉NO₂ [M+Cl]⁻ 550.0029, found 550.0036.

3-Chloro-2-(3-methyl-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7g): White solid, yield 54.3%, m.p. 58.8-61.2 °C, ¹H NMR (500 MHz, CDCl₃) δ: 8.81 (d, J = 0.9 Hz, 1H), 8.00 (d, J = 1.6 Hz, 1H), 7.66 − 7.60 (m, 2H), 7.49 (d, J = 8.6 Hz, 2H), 7.26 (s, 1H), 7.24 (s, 1H), 6.96 (d, J = 9.1 Hz, 1H), 5.15 (s, 2H), 2.36 (s, 3H). ¹³C NMR (126 MHz, CDCl₃) δ: 159.59, 157.92, 148.92 (q, J = 1.7 Hz), 144.13 (q, J = 3.9 Hz), 135.76, 135.34 (q, J = 3.4 Hz), 132.10, 129.91, 129.50, 128.53, 128.51, 127.14, 125.51 (q, J = 33.7 Hz), 122.87 (q, J = 273.2 Hz), 121.15, 120.54 (q, J = 257.7 Hz), 110.73, 69.13, 16.48. HRMS (ESI): calculated for C₂₁H₁₅ClF₆NO₂ [M+H]⁺ 462.0690, found 462.0690.

5-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-2-((4-(trifluoromethoxy)benzyl)oxy)benzonitrile (7h): White solid, yield 45.2%, m.p. 130.0-132.5 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.03 (s, 1H), 8.61 (s, 1H), 8.16 (d, J = 2.1 Hz, 1H), 8.08 (dd, J = 8.9, 2.2 Hz, 1H), 7.65 (d, J = 8.5 Hz, 2H), 7.51 (d, J = 9.0 Hz, 1H), 7.45 (d, J = 8.2 Hz, 2H), 5.42 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 160.49, 157.11, 148.18 (q, J = 1.4 Hz), 144.55 (q, J = 4.0 Hz), 136.25, 136.00 (q, J = 3.4 Hz), 135.31, 134.80, 129.91, 129.69, 129.64, 125.23 (q, J = 33.2 Hz), 122.84 (q, J = 273.8 Hz), 121.29, 120.10 (q, J = 257.5 Hz), 115.83, 113.37, 100.76, 69.58. HRMS (ESI): calculated for C₂₁H₁₂ClF₆N₂O₂ [M+H]⁺ 473.0487, found 473.0486.

3-Chloro-2-(2,3-difluoro-4-((4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7i): White solid, yield 49.7%, m.p. 62.0-64.0 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.07 (s, 1H), 8.66 (s, 1H), 7.65 (d, J = 8.5 Hz, 2H), 7.43 (d, J = 8.1 Hz, 2H), 7.38 − 7.28 (m, 2H), 5.35 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 154.70, 148.71 (dd, J = 7.6, 3.2 Hz), 148.23 (q, J = 1.5 Hz), 148.02 (dd, J = 249.4, 11.2 Hz), 144.71 (q, J = 3.6 Hz), 140.21 (dd, J = 247.2, 14.3 Hz), 135.46, 135.44 (q, J = 3.5 Hz), 131.44, 129.99, 125.96 (q, J = 33.3 Hz), 125.50 (t, J = 3.6 Hz), 122.76 (q, J = 274.4 Hz), 121.25, 120.10 (q, J = 256.8 Hz), 118.90 (d, J = 12.8 Hz), 110.60, 69.93. HRMS (ESI): calculated for C₂₀H₁₀Cl₂F₈NO₂ [M+Cl]⁻ 517.9966, found 517.9976.

3-Chloro-2-(4-((3-chloro-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7j): White solid, yield 91.5%, m.p. 62.3-63.8 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 8.98 (s, 1H), 8.52 (s, 1H), 7.81 (s, 1H), 7.75 (d, J = 8.5 Hz, 2H), 7.63 − 7.56 (m, 2H), 7.17 (d, J = 8.5 Hz, 2H), 5.24 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 159.09, 158.84, 144.37 (q, J = 4.0 Hz), 143.50 (q, J = 1.2 Hz), 138.40, 135.82 (q, J = 3.4 Hz), 131.13, 129.97, 129.50, 129.26, 128.13, 126.10, 124.46 (q, J = 33.4 Hz), 123.29, 122.94 (q, J = 274.2 Hz), 120.08 (q, J = 259.3 Hz), 114.40, 67.73. HRMS (ESI): calculated for C₂₀H₁₂Cl₂F₆NO₂ [M+H]⁺ 482.0144, found 482.0145.

3-Chloro-2-(4-((2-methoxy-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7k): White solid, yield 92%, m.p. 99.6-101.4 °C, ¹H NMR (500 MHz, DMSO-d₆) δ: 9.00 − 8.99 (m, 1H), 8.53 − 8.50 (m, 1H), 7.78 − 7.75 (m, 2H), 7.56 (d, J = 8.3 Hz, 1H), 7.17 − 7.14 (m, 2H), 7.08 (d, J = 1.9 Hz, 1H), 7.00 − 6.97 (m, 1H), 5.15 (s, 2H), 3.89 (s, 3H). ¹³C NMR (126 MHz, DMSO-d₆) δ: 159.44, 158.82, 158.08, 149.18 (q, J = 1.4 Hz), 144.26 (q, J = 3.9 Hz), 135.70 (q, J = 3.4 Hz), 131.02, 130.24, 129.20, 129.14, 124.36 (q, J = 33.1 Hz), 122.87 (q, J = 273.4 Hz), 123.82, 120.05 (q, J = 256.9 Hz), 114.21, 112.09, 104.69, 64.19, 56.07. HRMS (ESI): calculated for C₂₁H₁₅ClF₆NO₃ [M+H]⁺ 478.0639, found 478.0639.

3-Chloro-2-(4-((2-methyl-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7l): White solid, yield 65%, m.p. 77.6-78.6 °C, ¹H NMR (500 MHz, DMSO-d₆) δ: 9.02 − 8.98 (m, 1H), 8.52 (d, J = 1.5 Hz, 1H), 7.79 − 7.76 (m, 2H), 7.58 (d, J = 8.4 Hz, 1H), 7.27 (s, 1H), 7.23 − 7.19 (m, 3H), 5.21 (s, 2H), 2.40 (s, 3H). ¹³C NMR (126 MHz, DMSO-d₆) δ: 159.37, 158.82, 147.96 (q, J = 1.5 Hz), 144.26 (q, J = 3.8 Hz), 139.44, 135.69 (q, J = 3.5 Hz), 134.21, 131.00, 130.08, 129.32, 129.16, 124.37 (q, J = 33.1 Hz), 122.87 (q, J = 273.3 Hz), 122.34, 120.05 (q, J = 256.6 Hz), 117.98, 114.32, 67.20, 18.29. HRMS (ESI): calculated for C₂₁H₁₅ClF₆NO₂ [M+H]⁺ 462.0690, found 462.0693.

3-Chloro-2-(4-((3-fluoro-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine (7m): White solid, yield 57.4%, m.p. 73.9-75.1 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 8.99 (s, 1H), 8.53 (s, 1H), 7.75 (d, J = 8.7 Hz, 2H), 7.66 − 7.58 (m, 2H), 7.44 (d, J = 8.4 Hz, 1H), 7.17 (d, J = 8.8 Hz, 2H), 5.24 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 159.09, 158.86, 153.58 (d, J = 251.1 Hz), 144.39 (q, J = 4.0 Hz), 139.06 (d, J = 6.9 Hz), 135.84 (q, J = 3.4 Hz), 134.66 (dq, J = 11.5, 1.7 Hz), 131.13, 129.51, 129.27, 124.57 (d, J = 3.5 Hz), 124.39 (q, J = 33.5 Hz), 124.22, 122.95 (q, J = 274.2 Hz), 120.09 (q, J = 259.0 Hz), 116.60 (d, J = 19.1 Hz), 114.42, 67.88. HRMS (ESI): calculated for C₂₀H₁₂ClF₇NO₂ [M+H]⁺ 466.0439, found 466.0439.

3-Chloro-2-(4-((2-fluoro-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine(7n): White solid, yield 86.0%, m.p. 74.5-76.7 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.00 (s, 1H), 8.54 (s, 1H), 7.77 − 7.73 (m J = 3H), 7.48 (d, J = 10.4 Hz, 1H), 7.31 (d, J = 8.5 Hz, 1H), 7.19 (d, J = 8.8 Hz, 2H), 5.25 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 161.65, 159.15, 158.88, 148.80 (dq, J = 11.6, 1.3 Hz), 144.42 (q, J = 3.8 Hz), 135.87 (q, J = 3.4 Hz), 132.03, 131.16, 130.83 (d, J = 254.2 Hz), 129.30, 124.49 (q, J = 33.5 Hz), 123.34 (d, J = 14.7 Hz), 122.97 (q, J = 274.0 Hz), 119.96 (q, J = 258.5 Hz), 117.22 (d, J = 3.3 Hz), 114.34, 109.51 (d, J = 25.5 Hz), 63.16. HRMS (ESI): calculated for C₂₀H₁₂ClF₇NO₂ [M+H]⁺ 466.0439, found 466.0439.

2-(4-((3-Bromo-4-(trifluoromethoxy)benzyl)oxy)phenyl)-3-chloro-5-(trifluoromethyl)pyridine(7o): White solid, yield 64.5%, m.p. 79.0-80.8 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.03 (s, 1H), 8.57 (s, 1H), 7.99 (s, 1H), 7.79 (d, J = 8.4 Hz, 2H), 7.64 (q, J = 8.3 Hz, 2H), 7.21 (d, J = 8.4 Hz, 2H), 5.28 (s, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 159.11, 158.85, 144.88 (q, J = 1.3 Hz), 144.39 (q, J = 4.1 Hz), 138.53, 135.84 (q, J = 3.4 Hz), 133.03, 131.15, 129.50, 129.27, 128.80, 124.47 (q, J = 33.0 Hz), 122.95 (q, J = 273.7 Hz), 122.94, 120.07 (q, J = 259.3 Hz), 115.39, 114.41, 67.65. HRMS (ESI): calculated for C₂₀H₁₂BrClF₆NO₂ [M+H]⁺ 525.9639, found 525.9639.

3-Chloro-2-(4-((3-iodo-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine(7p): White solid, yield 61.1%, m.p. 75.8-77.5 °C, ¹H NMR (500 MHz, DMSO-d₆) δ: 9.00 (s, 1H), 8.52 (s, 1H), 8.11 (d, J = 1.5 Hz, 1H), 7.77 (d, J = 8.7 Hz, 2H), 7.63 (dd, J = 8.4, 1.6 Hz, 1H), 7.48 (d, J = 8.3 Hz, 1H), 7.18 (d, J = 8.7 Hz, 2H), 5.22 (s, 2H). ¹³C NMR (126 MHz, DMSO-d₆) δ: 159.10, 158.80, 148.12 (q, J = 1.5 Hz), 144.28 (q, J = 3.8 Hz), 138.98, 138.21, 135.72 (q, J = 3.3 Hz), 131.03, 129.42, 129.18, 124.40 (q, J = 33.1 Hz), 122.87 (q, J = 273.6 Hz), 121.41, 120.07 (q, J = 258.7 Hz), 114.36, 90.77, 67.52. HRMS (ESI): calculated for C₂₀H₁₂ClF₆INO₂ [M+H]⁺ 573.9500, found 573.9500.

3-Chloro-2-(4-((3-cyclopropyl-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine(7q): White solid, yield 47.2%, m.p. 99.8-102.6 °C, ¹H NMR (400 MHz, DMSO-d₆) δ: 9.04 (s, 1H), 8.58 (s, 1H), 7.80 (d, J = 8.7 Hz, 2H), 7.45 − 7.37 (m, 2H), 7.21 (s, 2H), 7.19 (s, 1H), 5.21 (s, 2H), 2.18 − 2.09 (m, 1H), 1.10 − 1.04 (m, 2H), 0.79 (q, J = 5.1 Hz, 2H). ¹³C NMR (101 MHz, DMSO-d₆) δ: 159.34, 158.90, 146.93 (q, J = 1.3 Hz), 144.39 (q, J = 4.0 Hz), 136.47, 136.43, 135.84 (q, J = 3.4 Hz), 131.09, 129.29, 129.25, 126.23, 125.17, 124.43 (q, J = 33.1 Hz), 122.96 (q, J = 273.7 Hz), 121.17, 120.41 (q, J = 257.1 Hz), 114.38, 68.63, 9.25, 8.62. HRMS (ESI): calculated for C₂₃H₁₇ClF₆NO₂ [M+H]⁺ 488.0847, found 488.0847.

3-Chloro-2-(4-((3-nitro-4-(trifluoromethoxy)benzyl)oxy)phenyl)-5-(trifluoromethyl)pyridine(7r): White solid, yield 20.3%, m.p. 86.6-88.1 °C, ¹H NMR (500 MHz, DMSO-d₆) δ: 9.00 (d, J = 1.1 Hz, 1H), 8.54 (s, 1H), 8.33 (d, J = 2.1 Hz, 1H), 8.00 (dd, J = 8.5, 2.1 Hz, 1H), 7.81 (dd, J = 8.5, 1.1 Hz, 1H), 7.80 − 7.76 (m, 2H), 7.23 − 7.19 (m, 2H), 5.36 (s, 2H). ¹³C NMR (126 MHz, DMSO-d₆) δ: 158.95, 158.82, 144.37 (q, J = 3.7 Hz), 142.14, 139.12 (q, J = 1.8 Hz), 138.37, 135.81 (q, J = 3.4 Hz), 134.12, 131.17, 129.66, 129.27, 124.99, 124.50 (q, J = 33.1 Hz), 123.86, 122.93 (q, J = 273.3 Hz), 119.82 (q, J = 259.8 Hz), 114.44, 67.44. HRMS (ESI): calculated for C₂₀H₁₂ClF₆N₂O₄ [M+H]⁺ 493.0384, found 493.0383.

Note: Due to the existence of the symmetrical structure and the multiplet caused by the fluorine atom, the number of signals in the NMR carbon spectrum of all the above compounds does not correspond to the number of carbons in the molecule.

3.3. Herbicidal Activities Assay

3.3.1. Herbicidal Activities Glasshouse Assay

All weeds were obtained from the Pesticide Creation Center of the Zhejiang Research Institute of Chemical Industry. Levels of herbicidal activity for compounds 7a–7r against the monocotyledonous weeds Digitaria sanguinalis (D. sanguinalis), Echinochloa crusgalli (E. crusgalli), and Setaria viridis (S. viridis), and the dicotyledonous weeds Abutilon theophrasti (A. theophrasti), Amaranthus retroflexus (A. retroflexus), and Eclipta prostrate (E. prostrate) were assessed as in prior reports [30,32,33,34].

DMF was used to dissolve all test compounds, followed by their dilution with distilled water containing 0.1% Tween-80 to an appropriate dose. The application rates for post-emergence treatment were 150, 75, and 37.5 g a.i./ha. Seedlings were treated with test compounds at the three-leaf stage with three replicates, treated without test compound seedlings serving as blank controls, and fomesafen-treated seedlings serving as positive controls. The herbicidal activity was assessed after a 20-day period, with the results being compiled in Table 1 and Table 2.

Growth inhibition rates (0–100%) were assessed based on/evaluated by a visual inspection, with 0% and 100%, respectively, corresponding to no damage and the total destruction of aboveground plant structures.

3.3.2. Weed Spectrum and Crop Injury Tests

Weed spectrum and crop injury tests were conducted for compound 7a using the same procedures as above in a greenhouse, with an estimated post-emergence application rate of 18.75 g a.i./hm². The utilized species included dicotyledonous weeds Pharbitis nil (P. nil), Aeschynomene indica (A. indica), Veronica didyma (V. didyma), Eclipta prostrate (E. prostrate), Orychophragmus violaceus (O. violaceus), Chenopodium serotinum (C. serotinum), Galium spurium L. (G. spurium L.), Medicago sativa (M. sativa), Portulaca oleracea (P. oleracea), Abutilon theophrasti (A. theophrasti), Amaranthus retroflexus (A. retroflexus), Solanum nigrum (S. nigrum); monocotyledonous weeds Polypogon fugax (P. fugax), Setaria viridis (S. viridis), Eleusine indica (E. indica), Digitaria sanguinalis (D. sanguinalis), Pseudosorghum zollingeri (P. zollingeri), Poa annua (P. annua), Alopecurus aequalis (A. aequalis), Leptochloa panacea (L. panacea), Lolium perenne (L. perenne), Echinochloa crusgalli (E. crusgalli); Cyperaceae weeds Cyperus rotundus L. (C. rotundus L.), and crop species Orysa sativa (rise, O. sativa), Glycine max (soybean, G. max), Zea mays (maize, Z. mays), Triticum aestivum (wheat, T. aestivum), Gossypium spp. (cotton, G. spp.). The results are summarized in Figure 4.

3.3.3. Herbicidal Activities Glasshouse Assay against Abutilon theophrasti and Amaranthus retroflexus

To study the control effect of 7a with the highest herbicidal activities against Abutilon theophrasti and Amaranthus retroflexus, its herbicidal activities were tested using the same procedures as above in a greenhouse, with fomesafen serving as a control. The application rates for post-emergence treatment were 450, 225, 150, 75, 45, 30, 15, 7.5, 3.75, and 1.875 g a.i./hm². Seedlings were treated with test compounds at the three-leaf stage with three replicates, treated without test compound seedlings serving as blank controls, and fomesafen-treated seedlings serving as positive controls. The herbicidal activity was assessed after a 14-day period, with the results being compiled in Table 3.

Then fresh weight inhibition rates were established by measuring fresh weight values for the aboveground parts of target weeds, and the ED₅₀ values were calculated.

3.4. In Vitro Analysis of NtPPO Inhibitory Activity

To explore the mode of action more fully, i.e., for the prepared compounds, compound 7a was selected as a representative target in effort to confirm its ability to inhibit PPO, with fomesafen serving as a control compound. NtPPO was prepared as reported previously [35]. The inhibitory activities of the NtPPO enzyme were determined using a previously reported method [36]. The NtPPO catalytic rate was calculated by measuring changes in the concentrations of the NtPPO catalytic product protoporphyrin IX over a given time period by measuring the absorbance at 410 nm via a UV–Vis spectrophotometer.

3.5. Molecular Docking Analysis

The NtPPO (PDB ID: 1SEZ) structure was obtained from the Protein Data Bank, with molecular docking analysis being performed using chain A of the NtPPO structure [37]. The crystal structures of NtPPO and the small molecule 7a were obtained via a standard approach using Dock 6.9 (University of California, San Francisco, California 94158, USA) [38], with fomesafen serving as a control compound. The optimal binding conformation was then selected in light of the results of the docking score (Figure 5).

4. Conclusions

In conclusion, a series of new α-trifluoroanisole derivatives containing phenylpyridine moieties were herein developed and synthesized. Among these, compound 7a exhibited optimal structural characteristics and good herbicidal activity when utilized for the post-emergence treatment of a wide spectrum of dicotyledonous weeds (at a dosage of 18.75 g a.i./hm²) in greenhouse testing. In addition, the excellent inhibitory activity against PPO and the docking result of compound 7a will provide directions for further optimization as a candidate PPO herbicide.

Supplementary Materials

The supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms231911083/s1.

Author Contributions

Z.C. and Y.C. carried out experimental work; Z.C. prepared the manuscript; X.D. designed the material, supervised the project, and revised the paper. All authors have read and agreed to the published version of the manuscript.

Data Availability Statement

Samples of the compounds are not available from the authors.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This research received no external funding.