Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents

Liu, Chaojie; Xiang, Xiaofang; Wan, Ying; Yang, Jia; Li, Yufei; Zhang, Xinchen; Qi, Zhiqiu; He, Lu; Liu, Wei; Li, Xinghai

doi:10.3390/molecules27175468

Open AccessArticle

Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents

by

Chaojie Liu

,

Xiaofang Xiang

,

Ying Wan

,

Jia Yang

,

Yufei Li

,

Xinchen Zhang

,

Zhiqiu Qi

,

Lu He

,

Wei Liu

^*

and

Xinghai Li

^*

Department of Pesticide Science, Plant Protection College, Shenyang Agricultural University, Shenyang 110866, China

^*

Authors to whom correspondence should be addressed.

Molecules 2022, 27(17), 5468; https://doi.org/10.3390/molecules27175468

Submission received: 20 July 2022 / Revised: 17 August 2022 / Accepted: 23 August 2022 / Published: 25 August 2022

(This article belongs to the Special Issue Advances in Novel Pesticide Discovery)

Download

Browse Figures

Review Reports Versions Notes

Abstract

:

To develop new fungicides with high efficiency, 46 novel sulfonamide derivatives were designed and synthesized by introducing pinacolone fragment into chesulfamide which was used as lead compound. All compounds were characterized by ¹H NMR, ¹³C NMR, and MS spectra, and the structure of compound P-27 was also confirmed by X-ray single crystal diffraction. It was found that a variety of compounds present excellent inhibitory effect against Botrytis cinerea. The inhibition rates of P-29 on tomato and strawberry were 90.24% (200 mg/L) and 100% (400 mg/L) in vivo respectively, which were better than the lead compound chesulfamide (59.23% on tomato seedlings and 29.63% on strawberries).

Keywords:

chesulfamide; pinacolone; sulfonamide; synthesis; Botrytis cinerea

1. Introduction

Botrytis cinerea is a serious and widespread plant disease in tomato, cucumber, eggplant, pepper, grape and strawberry, especially under the condition of protected cultivation [1]. The international fungicide resistance action committee (FRAC) classified the fungi as a pathogen at high risk of fungicide resistance. The resistance of Botrytis cinerea to fungicides is very serious all over the world, which leads to a reduction or even failure of the control effect of fungicides [2,3,4,5]. The development of fungicides with novel action mechanism is the key to control the resistance of fungicides [6,7,8]. Chesulfamide is a novel candidate fungicide with excellent control effect on Botrytis cinerea without interactive resistance to multiple commercial fungicides, such as carbendazim, diethofencarb, iprodione, and procymidone, showing that it has unique mechanism of action [9,10,11]. In our previous work, several novel compounds were discovered by replacing the cyclohexanone moiety in chesulfamide with benzocyclohexanone, cyclohexanone, cyclopropyl methyl ketone, and acetophenone, respectively, which all presented superb control effect against Botrytis cinerea [12,13,14] (Figure 1).

Pinacolone is an intermediate widely used in the synthesis of pesticides [15,16,17]. At present, more than 20 kinds of pesticides containing pinacolone fragment have been developed, among which triazole fungicides such as triazole, triadimefon, and paclobutrazol are the most widely used [18,19,20] (Figure 2). Hence, the design and synthesis of novel compounds containing the structure of pinacolone still has high value and broad prospect in the development of novel pesticide. In this work, chesulfamide was used as the lead compound, and novel sulfonamide derivatives were designed and prepared by replacing the cyclohexanone moiety with pinacolone group (Figure 3). The antifungal activity against Botrytis cinerea was investigated by the mycelium growth method and living pot method.

2. Results and Discussion

2.1. Chemistry

The synthetic route of the target compounds is shown in Scheme 1. Intermediate I was prepared from pinacolone by sulfonation with a sulfur trioxide-dioxane adduct and neutralization with potassium carbonate. Then, intermediate II was prepared by chlorination with oxalyl chloride. Finally, the target compounds were obtained by an amidation reaction with amines containing various substituents [21]. According to this synthetic method, 46 novel pinacolone sulfnamide derivatives were synthesized and their structures were characterized by ¹H NMR, ¹³C NMR, and MS spectra (Supplementary Materials). Additionally, the structure of compound P-27 was also confirmed by X-ray single crystal diffraction (Figure 4).

2.2. Biological Assay

Table 1 summarizes the result of the in vitro antifungal spectrum of P-1~P-46, at a dosage of 50 mg/L against Rhizoctonia solani, Fusarium graminearum, Sclerotinia sclerotiorum, and Botrytis cinerea, which clearly shows that this series of compounds not only has good control effect on Botrytis cinerea, but also has good control effects on other pathogens. The inhibition rates of P-23 and P-30 against Botrytis cinerea were 86.44% and 93.35% (EC₅₀ were 11.57 mg/L and 4.68 mg/L, Table 2), which were better than those of the lead compound chesulfamide.

Table 1. In vitro fungicidal activity of target compounds at 50 mg/L.

Compound	R	Inhibition rate(%)
Compound	R	R. solani	F. graminearum	S. sclerotiorum	B. cinerea
P-1	CF₃CH₂	5.33 ± 5.31	4.17 ± 8.62	9.58 ± 0	0
P-2		0	33.09 ± 1.06	0 ± 25.8	0
P-3	CH₃(CH₂)₃-	19.8 ± 2.21	33.82 ± 9.46	0	0
P-4	CH₃(CH₂)₄-	26.65 ± 1.98	21.81 ± 4.09	25.83 ± 0	42.55 ± 2.17
P-5	CH₃(CH₂)₅-	0	10.78 ± 2.76	0 ± 3.08	19.15 ± 1.59
P-6	2-F-C₆H₄-	37.31 ± 2.68	48.04 ± 0.24	36.04 ± 2.31	25.53 ± 1.06
P-7	3-F-C₆H₄-	6.09 ± 2.86	9.56 ± 6.28	0	6.38 ± 2.31
P-8	4-F-C₆H₄-	12.94 ± 0.91	0.98 ± 4.65	32.29 ± 5.84	8.51 ± 1.74
P-9	2-Cl-C₆H₄-	20.3 ± 0.91	11.76 ± 4.24	0	22.87 ± 1.74
P-10	3-Cl-C₆H₄-	39.34 ± 7.25	22.06 ± 2.20	77.92 ± 1.81	32.45 ± 1.74
P-11	4-Cl-C₆H₄-	36.29 ± 4.08	23.53 ± 0	0	25 ± 0.46
P-12	2-Br-C₆H₄-	19.8 ± 2.92	23.77 ± 0.98	19.58 ± 0.75	26.6 ± 0.46
P-13	3-Br-C₆H₄-	9.64 ± 1.83	36.76 ± 0.42	83.75 ± 0.95	34.04 ± 4.12
P-14	4-Br-C₆H₄-	25.13 ± 0.50	36.03 ± 0.73	82.5 ± 3.81	36.17 ± 0
P-15	2-OCH₃-C₆H₄-	9.14 ± 8.12	4.41 ± 2.94	10.42 ± 4.16	0 ± 1.32
P-16	2-CF₃-C₆H₄-	33.76 ± 1.01	32.6 ± 2.13	55.83 ± 2.52	41.76 ± 1.15
P-17	3-CF₃-C₆H₄-	42.89 ± 5.76	32.6 ± 0.24	36.67 ± 0	23.14 ± 0.46
P-18	4-OCF₃-C₆H₄-	49.49 ± 3.24	4.66 ± 0.24	87.71 ± 1.10	39.1 ± 0
P-19	4-Cl-2-F-C₆H₃-	47.72 ± 2.67	45.1 ± 1.06	22.5 ± 1.80	34.04 ± 4.79
P-20	4-Br-2-F-C₆H₃-	2.54 ± 1.66	2.7 ± 2.33	0 ± 1.62	47.34 ± 0.46
P-21	5-CF₃-2-F-C₆H₃-	37.31 ± 1.01	40.93 ± 2.09	90.42 ± 0.41	36.97 ± 5.31
P-22	4-Br-3-F-C₆H₃-	42.13 ± 8.64	46.57 ± 1.60	94.38 ± 0.55	75 ± 2.81
P-23	2-CF₃-4-Cl-C₆H₃-	75.13 ± 2.16	69.61 ± 1.06	94.17 ± 0.62	86.44 ± 2.31
P-24	5-CF₃-2-Cl-C₆H₃-	57.87 ± 0.43	71.57 ± 2.78	94.58 ± 1.10	64.1 ± 3.06
P-25	4-Br-2-NO₂-C₆H₃-	53.81 ± 16.5	54.66 ± 0.24	86.04 ± 9.58	78.99 ± 0.53
P-26	3-Br-4-F-C₆H₃-	19.8 ± 1.58	5.39 ± 0.42	87.5 ± 0	27.66 ± 1.61
P-27	4-Br-3-CH₃-C₆H₃-	34.77 ± 1.77	45.34 ± 2.48	80 ± 2.31	54.52 ± 5.07
P-28	2,4,5-F₃-C₆H₂-	36.8 ± 3.31	30.39 ± 2.76	36.88 ± 0.75	22.07 ± 0.53
P-29	2,4,5-Cl₃-C₆H₂-	36.8 ± 1.75	47.79 ± 0.49	80.83 ± 12.2	53.46 ± 0.79
P-30	2,4,6-Br₃-C₆H₂-	81.47 ± 2.67	62.01 ± 4.49	97.92 ± 3.47	93.35 ± 2.17
P-31	C₆H₅-CH₂CH₂-	0	16.18 ± 1.36	6.25 ± 0.41	39.63 ± 0.26
P-32	4-NO₂-C₆H₄-CH₂CH₂-	7.29 ± 3.51	37.33 ± 4.73	38.62 ± 6.43	33.33 ± 1.15
P-33	4-CH₃-C₆H₄-CH₂CH₂-	22.92 ± 17.10	22.67 ± 5.13	51.32 ± 7.09	14.18 ± 2.52
P-34	4-OCH₃-C₆H₄-CH₂CH₂-	40.63 ± 2.65	6.67 ± 4.04	42.33 ± 5.51	12.77 ± 4.36
P-35	3-OCH₃-C₆H₄-CH₂CH₂-	14.58 ± 2.08	15.33 ± 3.51	38.62 ± 6.66	19.15 ± 2.65
P-36	3,4-(OCH₃)₂-C₆H₃-CH₂CH₂-	0	4.67 ± 2.52	32.28 ± 0.58	5.67 ± 4.62
P-37	4-F-C₆H₄-CH₂CH₂-	12.50 ± 4.00	5.33 ± 4.16	40.21 ± 6.51	21.28 ± 0
P-38	3-F-C₆H₄-CH₂CH₂-	10.94 ± 2.00	7.33 ± 3.79	29.63 ± 5.77	12.77 ± 5.29
P-39	2-F-C₆H₄-CH₂CH₂-	9.38 ± 2.65	10.67 ± 2.31	40.74 ± 4.73	15.60 ± 2.08
P-40	3-Br-C₆H₄-CH₂CH₂-	44.79 ± 3.79	32.00 ± 1.73	31.75 ± 1.00	25.53 ± 0
P-41	2-Br-C₆H₄-CH₂-	46.88 ± 1.00	16.67 ± 0.58	67.20 ± 3.21	12.77 ± 3.61
P-42	4-F-C₆H₄-CH₂-	25.52 ± 2.08	15.33 ± 3.21	23.28 ± 6.43	15.60 ± 2.08
P-43	2-F-C₆H₄-CH₂-	25.52 ± 2.08	15.33 ± 3.21	23.28 ± 6.43	9.93 ± 1.53
P-44	4-Cl-C₆H₄-CH₂-	16.15 ± 1.15	27.33 ± 4.93	21.69 ± 5.03	27.66 ± 4.36
P-45	4-CN-C₆H₄-CH₂-	44.79 ± 16.86	21.33 ± 1.15	60.32 ± 6.25	17.02 ± 5.20
P-46	2,5-(OCH₃)-C₆H₄-CH₂-	54.69 ± 0	23.33 ± 5.51	31.75 ± 0	24.11 ± 4.62
Chesulfamide	/	80.18 ± 0.29	70.21 ± 1.28	80.18 ± 0.29	74.76 ± 4.61
Boscalid	/	85.28 ± 0.50	51.23 ± 2.72	98.33 ± 0.83	98.28 ± 0

In the tomato pot experiment, it was found that the control effect of various compounds on Botrytis cinerea at 200 mg/L was better than that of chesulfamide, of which compound P-13 and P-29 were slightly weaker than the positive control boscalid, which were 91.22% and 90.04%, respectively (Table 3, Figure 5). In the strawberry experiment, compounds P-18, P-29, P-30 and P-31 exhibited higher antifungal activity against Botrytis cinerea than chesulfamide, especially compound P-29, which had a 100% inhibition rate at 400 mg/L (Table 4, Figure 6).

2.3. Structure–Activity Relationship

Based on the result of antifungal activity experiments, the structure-activity relationship of target compounds can be concluded as follow. The order of substituent structures conducive to improving the activity of the compounds was phenyl (2,4,6-tribromophenyl is the best) > benzyl > phenylethyl > alkyl, which showed that phenyl can significantly improve the activity of the compound; and trisubstituted phenyl > disubstituted phenyl > monosubstituted phenyl. In the in vivo activity assay, compounds P-18, P-29 and P-31 had good antifungal activity, indicating that 4-trifluoromethoxyphenyl, 2,4,5-trichlorophenyl and phenylethyl had a positive effect on the activity of the compounds. The substituent of P-29 is 2,4,5-trichlorophenyl, which has been found to have a good control effect on Botrytis cinerea in previous studies [22,23]. Therefore, this substituent can be used as the active group for structure design in the future.

3. Materials and Methods

3.1. Instruments and Reagents

For all reactions, solvents and chemical reagents were purchased from commercial sources and used as received. All reactions were carried out under a nitrogen atmosphere unless noted. Reactions were monitored by thin layer chromatography (TLC) visualizing with ultraviolet light (UV) and phosphomolybdic acid (PMA) stain. Column chromatography purification was performed using silica gel. Proton nuclear magnetic resonance (¹H NMR) spectra and carbon nuclear magnetic resonance (¹³C NMR) were recorded on a 600 MHz spectrometer in CDCl₃ or DMSO-d₆ as the solvent and TMS as the internal standard. NMR data were presented as follows: chemical shift (δ ppm), multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, br = broad), coupling constant in Hertz (Hz), integration. High-resolution mass spectrometry (HRMS) data were obtained on an Agilent 1290-6540B Q-TOF instrument. Single crystal structure analysis was performed using X-ray diffraction on a Rigaku Oxford Diffraction Supernova Dual Source diffractometer.

3.2. General Synthetic Procedures

Synthesis of intermediate I. A mixture of pinacolone (1 mol) in DCE (300 mL) was stirred in a dry flask under nitrogen atmosphere at 0 °C. Then, the trioxide-dioxane adduct (1 mol) was slowly added into the flask, and the reaction mixture was stirred for 3 h. CaCO₃ was slowly added to adjust the pH of the reaction mixture to 7. The mixture was then filtered and the pH of the mixture was adjusted to 9 by K₂CO₃, then filtered. The aqueous layer was collected and distilled to give the intermediate I.

Synthesis of intermediate II. Under the condition of ice bath, oxalyl chloride (20.6 mmol) was slowly added into the mixture of intermediate I (13.7 mmol), CH₂Cl₂ (40 mL) and DMF (0.54 mL), and the mixture was stirred for 3 h. Finally, a yellow liquid as obtained by suction filtration.

Synthesis of target compounds. A mixture of amine (9.6 mmol), CH₂Cl₂ (40 mL), Et₃N (1.2 mL) was stirred in a dry flask in an ice-bath. Then, intermediate II (9.6 mmol) was added dropwise and the mixture was reacted for 3h. Upon completion, the mixture was filtered and extracted with DCM, washed with brine, dried over Na₂SO₄, concentrated in vacuo and purified by silica column chromatography (PE:EA = 10:1, v/v ) to give target compounds.

The spectral data of the Compound P-1~P-46 are described below.

Data for 3,3-dimethyl-2-oxo-N-(3,3,3-trifluoroethyl)butane-1-sulfonamide (P-1): Yield 38%; white solid; m.p. 121.5–123.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 8.15 (t, J = 6.7 Hz, 1H, SO₂-NH)), 4.62–4.58 (m, 2H, SO₂-CH₂), 3.79 (qd, J = 9.4, 6.5 Hz, 2H, N-CH₂), 1.11 (d, J = 0.9 Hz, 9H, CH₃).¹³C-NMR (151 MHz, DMSO-d₆) δ 204.93, 124.34 (q, ¹J_FC = 278.53 Hz, CF₃), 57.48, 44.56, 43.65 (q, ²J_FC = 34.09 Hz), 25.18. EIMS calcd. for C₈H₁₅F₃NO₃S ([M + H]⁺): 262.07, found 260.00.

Data for N-cyclopropyl-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-2): Yield 15%; white solid; m.p. 72.0–73.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.47 (d, J = 2.8 Hz, 1H, SO₂-NH), 4.48 (s, 2H, SO₂-CH₂), 2.52 (m, 1H, N-CH), 1.12 (d, J = 0.7 Hz, 9H, CH₃), 0.64–0.54 (m, 4H, CH₂).¹³C-NMR (151 MHz, DMSO-d₆) δ204.82, 55.34, 44.63, 25.30, 24.09, 5.37. HRMS calcd. for C₉H₁₈NO₃S ([M + H]⁺): 220.1002, found 220.1000.

Data for N-butyl-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-3): Yield 47%; white solid; m.p. 59.1–60.7 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ7.02 (t, J = 5.9 Hz, 1H, SO₂-NH), 4.41 (s, 2H, SO₂-CH₂), 2.94 (td, J = 7.2, 5.9 Hz, 2H, N-CH₂), 1.43 (m, 2H, CH₂), 1.30 (t, J = 7.3 Hz, 2H, CH₂), 1.10 (s, 9H, CH₃), 0.87 (t, J = 7.4 Hz, 3H, CH₃).¹³C-NMR (151 MHz, DMSO-d₆) δ 204.99, 55.87, 44.58, 31.47, 28.22, 25.28, 19.26, 13.52. HRMS calcd. for C₁₀H₂₂NO₃S ([M + H]⁺): 236.1315, found 236.1319.

Data for 3,3-dimethyl-2-oxo-N-pentylbutane-1-sulfonamide (P-4): Yield 51%; white solid; m.p. 52.2–54.2 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.02 (t, J = 5.9 Hz, 1H, SO₂-NH), 4.41 (s, 2H, SO₂-CH₂), 2.93 (td, J = 7.2, 6.0 Hz, 2H, N-CH₂), 1.45 (q, J = 7.2 Hz, 2H, CH₂), 1.27 (m, 4H, CH₂), 1.10 (s, 9H, CH₃), 0.86 (t, J = 6.8 Hz, 3H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 206.23, 54.27, 45.34, 43.72, 29.48, 28.68, 25.63, 22.19, 13.91. HRMS calcd. for C₁₁H₂₄NO₃S ([M + H]⁺): 250.1471, found 250.1479.

Data for N-hexyl-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-5): Yield 22%; white solid; m.p. 59.2–60.2 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.02 (t, J = 5.9 Hz, 1H, SO₂-NH), 4.41 (s, 2H, SO₂-CH₂), 2.93 (td, J = 7.2, 5.9 Hz, 2H, N-CH₂), 1.43 (q, J = 7.2 Hz, 2H, CH₂), 1.35–1.17 (m, 6H, CH₂), 1.10 (s, 9H, CH₃), 0.86 (t, J = 6.9 Hz, 3H, CH₃).¹³C-NMR (151 MHz, DMSO-d₆) δ 204.97, 55.90, 44.57, 42.59, 30.83, 29.35, 25.76, 25.28, 22.01, 13.87. HRMS calcd. for C₁₂H₂₆NO₃S ([M + H]⁺): 264.1628, found 264.1629.

Data for N-(2-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-6): Yield 79%; white solid; m.p. 126.8–128.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.75 (s, 1H, SO₂-NH), 7.61 (dd, J = 9.9, 2.1 Hz, 2H, C₆H₄-H), 7.43–7.35 (m, 2H, C₆H₄-H), 4.61 (s, 2H, SO₂-CH₂), 1.08 (s, 9H, CH³). ¹³C NMR (151 MHz, DMSO-d₆) δ 204.24, 155.39 (d, ¹J_FC = 251.79 Hz, F-Ph), 127.77 (d, ³J_FC = 3.64 Hz), 127.68, 124.53 (d, ²J_FC = 12.64 Hz), 119.38 (d, ²J_FC = 23.46 Hz), 117.84 (d, ³J_FC = 8.89 Hz), 57.05, 44.62, 25.23. HRMS calcd. for C₁₂H₁₇FNO₃S ([M + H]⁺): 274.0908, found 274.0907.

Data for N-(3-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-7): Yield 50%; white solid; m.p. 100.9–102.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.17 (s, 1H, SO₂-NH), 7.35 (m, 1H, C₆H₄-H), 7.08–7.00 (m, 2H, C₆H₄-H), 6.94–6.88 (m, 1H, C₆H₄-H), 4.59 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 205.89, 163.12 (d, ¹J_FC = 247.2 Hz, F-Ph), 138.07 (d, ²J_FC = 10.2 Hz), 130.80 (d, ³J_FC = 9.41 Hz), 117.48 (d, ³J_FC = 3.03 Hz), 112.98 (d, ²J_FC = 21.32 Hz), 109.43 (d, ²J_FC = 25.35 Hz), 53.15, 45.44, 25.52. HRMS calcd. for C₁₂H₁₇FNO₃S ([M + H]⁺): 274.0908, found 274.0907.

Data for N-(4-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-8): Yield 51%; white solid; m.p. 125.1–125.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.85 (s, 1H, SO₂-NH), 7.30- 7.23 (m, 2H, C₆H₄-H₄), 7.19 (t, J = 8.8 Hz, 2H, C₆H₄-H), 4.46 (s, 2H, SO₂-CH₂), 1.05 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 206.19, 161.10 (d, ¹J_FC = 246.23 Hz, F-Ph), 132.30 (d, ³J_FC = 3.02 Hz), 124.97 (d, ³J_FC = 8.36 Hz), 116.38 (d, ²J_FC = 22.71 Hz), 52.63, 45.45, 25.54. HRMS calcd. for C₁₂H₁₇FNO₃S ([M + H]⁺): 274.0908, found 274.0905.

Data for N-(2-chlorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-9): Yield 15%; white solid; m.p. 80.4–82.3 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.37 (s, 1H, SO₂-NH), 7.51 (m, 2H, C₆H₄-H), 7.35 (td, J = 7.7, 1.5 Hz, 1H, C₆H₄-H), 7.26 (td, J = 7.7, 1.6 Hz, 1H, C₆H₄-H), 4.63 (s, 2H, SO₂-CH₂), 1.08 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.29, 133.81, 129.84, 128.71, 127.81, 127.39, 127.22, 57.78, 44.59, 25.31. HRMS calcd. for C₁₂H₁₇ClNO₃S ([M + H]⁺): 290.0612, found 290.0614.

Data for N-(3-chlorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-10): Yield 40%; white solid; m.p. 108.7–111.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.16 (s, 1H, SO₂-NH), 7.36 (t, J = 8.1 Hz, 1H, C₆H₄-H), 7.27 (d, J = 2.1 Hz, 1H, C₆H₄-H), 7.20 (m, 1H, C₆H₄-H), 7.16 (m, 1H, C₆H₄-H), 4.59 (s, 2H, SO₂-CH₂), 1.05 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 205.94, 137.67, 135.20, 130.59, 126.34, 122.23, 120.32, 53.14, 45.46, 25.53. HRMS calcd. for C₁₂H₁₇ClNO₃S ([M + H]⁺): 290.0612, found 290.0603.

Data for N-(4-chlorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-11): Yield 45%; white solid; m.p. 112.4–114.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.03 (s, 1H, SO₂-NH), 7.41–7.36 (m, 2H, C₆H₄-H), 7.26–7.22 (m, 2H, C₆H₄-H), 4.52 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 206.03, 134.99, 131.97, 129.69, 123.89, 77.26, 77.05, 76.84, 52.81, 45.46, 25.53. HRMS calcd. for C₁₂H₁₇ClNO₃S ([M + H]⁺): 290.0612, found 290.0609.

Data for N-(2-bromophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-12): Yield 31%; white solid; m.p. 92.9–94.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.26 (s, 1H, SO₂-NH), 7.68 (dd, J = 8.0, 1.4 Hz, 1H, C₆H₄-H), 7.50 (dd, J = 8.0, 1.6 Hz, 1H, C₆H₄-H), 7.40 (td, J = 7.7, 1.5 Hz, 1H, C₆H₄-H), 7.19 (td, J = 7.7, 1.6 Hz, 1H, C₆H₄-H), 4.64 (s, 2H, SO₂-CH₂), 1.09 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.32, 135.16, 133.09, 128.43, 127.83, 127.46, 119.76, 57.98, 44.61, 25.32. EIMS calcd. for C₁₂H₁₇BrNO₃S ([M + H]⁺): 334.01, found 333.90.

Data for N-(3-bromophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-13): Yield 26%; white solid; m.p. 114.5–115.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.13 (s, 1H, SO₂-NH), 7.40 (d, J = 2.2 Hz, 1H, C₆H₄-H), 7.32–7.25 (m, 1H, C₆H₄-H), 7.28 (s, 1H, C₆H₄-H), 7.24 (dt, J = 6.0, 2.5 Hz, 1H, C₆H₄-H), 4.58 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.20, 139.59, 131.11, 126.36, 121.83, 121.79, 118.26, 55.36, 44.72, 25.06. HRMS calcd. for C₁₂H₁₇BrNO₃S ([M + H]⁺): 334.0107, found 334.0108.

Data for N-(4-bromophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-14): Yield 38%; white solid; m.p. 112.1–113.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.04 (s, 1H, SO₂-NH), 7.54–7.48 (m, 2H, C₆H₄-H), 7.21–7.15 (m, 2H, C₆H₄-H), 4.53 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.19, 137.34, 131.95, 121.65, 115.88, 55.10, 44.70, 25.08. EIMS calcd. for C₁₂H₁₇BrNO₃S ([M + H]⁺): 334.01, found 333.90.

Data for N-(2-methoxyphenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-15): Yield 14%; white solid; m.p. 70.0–71.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 8.72 (s, 1H, SO₂-NH), 7.31 (dd, J = 7.9, 1.6 Hz, 1H, C₆H₄-H), 7.22–7.16 (m, 1H, C₆H₄-H), 7.07 (dd, J = 8.2, 1.3 Hz, 1H, C₆H₄-H), 6.94 (td, J = 7.6, 1.3 Hz, 1H, C₆H₄-H), 4.54 (s, 2H, SO₂-CH₂), 3.82 (s, 3H), 1.07 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.39, 149.67, 126.04, 125.65, 121.29, 120.82, 111.10, 56.00, 54.17, 45.13, 25.71. HRMS calcd. for C₁₃H₂₀NO₄S ([M + H]⁺): 286.1108, found 286.1109.

Data for 3,3-dimethyl-2-oxo-N-(2-(trifluoromethyl)phenyl)butane-1-sulfonamide (P-16): Yield 61%; white solid; m.p. 78.3–79.3 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.38 (s, 1H, SO₂-NH), 7.75 (dd, J = 7.9, 1.5 Hz, 1H, C₆H₄-H), 7.71 (td, J = 7.7, 1.5 Hz, 1H, C₆H₄-H), 7.65 (d, J = 8.0 Hz, 1H, C₆H₄-H), 7.50 (t, J = 7.7 Hz, 1H, C₆H₄-H), 4.70 (s, 2H, SO₂-CH₂), 1.13 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.67, 133.97, 133.19, 126.65 (d, ³J_FC = 5.03 Hz), 125.44, 123.69 (d, ¹J_FC = 273.11 Hz, CF₃), 121.83 (d, ²J_FC = 29.82 Hz), 56.57, 45.19, 25.74. HRMS calcd. for C₁₃H₁₇F₃NO₃S ([M + H]⁺): 324.0876, found 324.0866.

Data for 3,3-dimethyl-2-oxo-N-(3-(trifluoromethyl)phenyl)butane-1-sulfonamide (P-17): Yield 65%; white solid; m.p. 134.0–136.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ10.31 (s, 1H, SO₂-NH), 7.58 (t, J = 8.2 Hz, 1H, C₆H₄-H), 7.56–7.51 (m, 2H, C₆H₄-H), 7.48–7.43 (m, 1H, C₆H₄-H), 4.62 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 206.01, 137.16, 132.06 (d, ²J_FC = 32.9 Hz), 130.23, 125.43, 123.52 (d, ¹J_FC = 272,87 Hz, CF₃)122.78 (d, ³J_FC = 3.9 Hz), 118.83 (d, ³J_FC = 3.8 Hz), 53.42, 45.47, 25.50. HRMS calcd. for C₁₃H₁₇F₃NO₃S ([M + H]⁺): 324.0876, found 324.0877.

Data for 3,3-dimethyl-2-oxo-N-(4-(trifluoromethoxy)phenyl)butane-1-sulfonamide (P-18): Yield 27%; white solid; m.p. 119.3–120.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.12 (s, 1H, SO₂-NH), 7.38–7.30 (m, 4H, C₆H₄-H), 4.56 (s, 2H, SO₂-CH₂), 1.04 (s, 9H, CH₃).¹³C-NMR (151 MHz, DMSO-d₆) δ 204.27, 144.31, 137.13, 122.08, 121.12, 120.07 (q, ¹J_FC = 256.08 Hz, CF₃), 55.26, 44.69, 25.04. HRMS calcd. for C₁₃H₁₇F₃NO₄S ([M + H]⁺): 340.0825, found 340.0833.

Data for N-(4-chloro-2-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-19): Yield 71%; white solid; m.p. 115.3–117.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.75 (s, 1H, SO₂-NH), 7.51 (dd, J = 10.3, 2.4 Hz, 1H, C₆H₄-H), 7.44 (t, J = 8.6 Hz, 1H, C₆H₄-H), 7.28 (m, 1H, C₆H₄-H), 4.61 (s, 2H, SO₂-CH₂), 1.08 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.23, 155.45 (d, ¹J_FC = 251.09 Hz, F-Ph), 130.24 (d, ³J_FC = 9.60 Hz), 127.51, 124.85 (d, ³J_FC = 3.59 Hz), 124.08 (d, ²J_FC = 12.73 Hz), 116.65 (d, ²J_FC = 23.80 Hz), 57.06, 44.61, 25.23. HRMS calcd. for C₁₂H₁₆ClFNO₃S ([M + H]⁺): 308.0518, found 308.0516.

Data for N-(4-bromo-2-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-20): Yield 55%; white solid; m.p. 113.5–114.7 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.76 (s, 1H, SO₂-NH), 7.62 (dd, J = 10.0, 2.0 Hz, 1H, C₆H₄-H), 7.45–7.37 (m, 2H, C₆H₄-H), 4.60 (d, J = 27.3 Hz, 2H, SO₂-CH₂), 1.08 (d, J = 0.9 Hz, 9H, CH₃).¹³C-NMR (151 MHz, DMSO-d₆) δ 205.04, 154.12 (d, ¹J_FC = 250.99 Hz, F-Ph), 128.25 (d, ³J_FC = 3.70 Hz), 125.30, 123.85 (d, ²J_FC = 12.50 Hz), 119.52 (d, ²J_FC = 22.65 Hz), 118.83 (d, ³J_FC = 8.89 Hz), 54.60, 45.33, 25.63. HRMS calcd. for C₁₂H₁₆BrFNO₃S ([M + H]⁺):352.0013, found 352.0012.

Data for N-(2-fluoro-5-(trifluoromethyl)phenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-21): Yield 63%; white solid; m.p. 113.7–115.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.04 (s, 1H, SO₂-NH), 7.76 (dd, J = 7.2, 2.3 Hz, 1H, C₆H₄-H), 7.64 (dt, J = 7.0, 3.2 Hz, 1H, C₆H₄-H), 7.53 (t, J = 9.3 Hz, 1H, C₆H₄-H), 4.72 (s, 2H, SO₂-CH₂), 1.09 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.25, 157.02 (d, ¹J_FC = 253.Hz, F-Ph), 126.09 (d, ²J_FC = 13.74 Hz), 125.46 (dq, ²J_FC = 32.46 Hz), 123.87 (q, ³J_FC = 4.06 Hz), 123.53 (q, ¹J_FC = 272.02 Hz, CF₃), 122.40 (q, ³J_FC = 3.40 Hz) 117.32 (d, ²J_FC = 21.62 Hz), 57.46, 44.62, 25.16. HRMS calcd. for C₁₃H₁₆F₄NO₃S ([M + H]⁺): 342.0782, found 342.0780.

Data for N-(4-bromo-3-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-22): Yield 52%; white solid; m.p. 116.0–117.1 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.32 (s, 1H, SO₂-NH), 7.65 (t, J = 8.4 Hz, 1H, C₆H₄-H), 7.19 (dd, J = 10., 8 2.5 Hz, 1H, C₆H₄-H), 7.02 (dd, J = 8.7, 2.5 Hz, 1H, C₆H₄-H), 4.66 (s, 2H, SO₂-CH₂), 1.05 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.61, 158.66 (d, ¹J_FC = 243.74 Hz, F-Ph), 139.75 (d, ³J_FC = 9.93 Hz), 134.12, 117.09 (d, ³J_FC = 3.22 Hz), 107.71 (d, ²J_FC = 26.32 Hz), 101.95 (d, ²J_FC = 20.88 Hz), 55.87, 45.12, 25.41. EIMS calcd. for C₁₂H₁₆BrFNO₃S ([M + H]⁺): 352.00, found 351.90.

Data for N-(4-chloro-2-(trifluoromethyl)phenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-23): Yield 63%; white solid; m.p. 127.4–128.7 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.50 (s, 1H, SO₂-NH), 7.80 (s, 1H, C₆H₄-H), 7.83–7.76 (m, 1H, C₆H₄-H), 7.66 (dd, J = 8.7, 3.2 Hz, 1H, C₆H₄-H), 4.71 (d, J = 3.0 Hz, 2H, SO₂-CH₂), 1.10 (d, J = 3.8 Hz, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.43, 133.25, 133.19, 131.46, 131.29, 127.22 (q, ²J_FC = 30.17 Hz), 126.70 (q, ³J_FC = 5.27 Hz), 122.46 (q, ¹J_FC = 274.11 Hz, CF₃), 58.52, 44.60, 25.27. HRMS calcd. for C₁₃H₁₆ClF₃NO₃S ([M + H]⁺): 358.0486, found 358.0487.

Data for N-(2-chloro-5-(trifluoromethyl)phenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-24): Yield 9%; white solid; m.p. 97.3–98.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.75 (s, 1H, SO₂-NH), 7.82 – 7.75 (m, 2H, C₆H₄-H), 7.62 (dd, J = 8.4, 2.1 Hz, 1H, C₆H₄-H), 4.77 (s, 2H, SO₂-CH₂), 1.09 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.40, 135.02, 132.39, 131.04, 128.30 (q, ²J_FC = 32.39 Hz), 123.49 (q, ³J_FC = 3.83 Hz), 123.44 (q, ¹J_FC = 272.52 Hz, CF₃), 122.89 (q, ³J_FC = 3.96 Hz), 58.36, 44.57, 25.25. HRMS calcd. for C₁₃H₁₆ClF₃NO₃S ([M + H]⁺): 358.0486, found 358.0487.

Data for N-(4-bromo-2-nitrophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-25): Yield 35%; white solid; m.p. 102.4–106.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.89 (s, 1H, SO₂-NH), 8.25 (d, J = 2.3 Hz, 1H, C₆H₄-H), 7.96 (dd, J = 8, 82.3 Hz, 1H, C₆H₄-H), 7.63 (d, J = 8.8 Hz, 1H, C₆H₄-H), 4.83 (s, 2H, SO₂-CH₂), 1.07 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.75, 142.18, 137.27, 130.61, 127.88, 126.86, 116.95, 57.53, 44.63, 25.12. HRMS calcd. for C₁₂H₁₆BrN₂O₅S([M + H]⁺ ): 378.9958, found 378.9957.

Data for N-(3-bromo-4-fluorophenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-26): Yield 68%; white solid; m.p. 146.9–148.7 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 10.06 (s, 1H, SO₂-NH), 7.50 (dd, J = 6.1, 2.6 Hz, 1H, C₆H₄-H), 7.37 (t, J = 8.8 Hz, 1H, C₆H₄-H), 7.27 (ddd, J = 8.9, 4.3, 2.7 Hz, 1H, C₆H₄-H), 4.57 (s, 2H, SO₂-CH₂), 1.06 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.37, 155.13 (d, ¹J_FC = 241.60 Hz, F-Ph), 135.25 (d, ³J_FC = 2.97 Hz), 124.57, 121.39 (d, ³J_FC = 7.49 Hz), 117.10 (d, ²J_FC = 23.24 Hz), 108.04 (d, ²J_FC = 22.11 Hz), 55.27, 44.71, 25.06. EIMS calcd. for C₁₂H₁₆BrFNO₃S ([M + H]⁺): 352.00, found 351.90.

Data for N-(4-bromo-3-methylphenyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-27): Yield 30%; white solid; m.p. 133.9–134.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.97 (s, 1H, SO₂-NH), 7.51 (d, J = 8.6 Hz, 1H, C₆H₄-H), 7.18 (d, J = 2.6 Hz, 1H, C₆H₄-H), 7.00 (dd, J = 8.6, 2.7 Hz, 1H, C₆H₄-H), 4.52 (s, 2H, SO₂-CH₂), 2.30 (s, 3H, ph-CH₃), 1.04 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 206.11, 139.85, 139.36, 134.53, 123.88, 121.06, 120.38, 57.00, 46.62, 27.00, 24.54. EIMS calcd. for C₁₃H₁₉BrNO₃S ([M + H]⁺): 348.02, found 347.90.

Data for 3,3-dimethyl-2-oxo-N-(2,4,5-trifluorophenyl)butane-1-sulfonamide (P-28): Yield 21%; white solid; m.p. 114.1–115.4°C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.84 (s, 1H, SO₂-NH), 7.65 (td, J = 10.4, 7.3 Hz, 1H, C₆H₄-H), 7.51 (dt, J = 11.5, 7.9 Hz, 1H, C₆H₄-H), 4.66 (s, 2H, SO₂-CH₂), 1.08 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 205.13, 148.28 (qd, ¹J_FC = 244.26 Hz, F-Ph), 147.69 (dq, ¹J_FC = 250,84 Hz, F-Ph) 120.63–120.51 (m), 113.34 (d, ²J_FC = 19.70 Hz), 105.79 (d, ²J_FC = 21.79 Hz), 105.70 (d, ²J_FC = 21.85), 54.81, 45.35, 25.60. HRMS calcd. for C₁₂H₁₅Cl₃NO₃S ([M + H]⁺): 310.0719, found 310.0719.

Data for 3,3-dimethyl-2-oxo-N-(2,4,5-trichlorophenyl)butane-1-sulfonamide (P-29): Yield 62%; white solid; m.p. 144.3–115.2 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.70 (s, 1H, SO₂-NH), 7.93 (s, 1H, C₆H₄-H), 7.73 (s, 1H, C₆H₄-H), 4.78 (s, 2H, SO₂-CH₂), 1.10 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 207.17, 137.04, 133.50, 132.77, 131.39, 130.59, 130.02, 61.02, 47.31, 28.00. HRMS calcd. for C₁₂H₁₅F₃NO₃S ([M + H]⁺): 357.9833, found 357.9829.

Data for 3,3-dimethyl-2-oxo-N-(2,4,6-tribromophenyl)butane-1-sulfonamide (P-30): Yield 9%; white solid; m.p. 135.6–137.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 9.61 (s, 1H, SO₂-NH), 8.02 (s, 2H, C₆H₄-H), 4.78 (s, 2H, SO₂-CH₂), 1.13 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.94, 202.64, 136.08, 135.09, 134.83, 129.43, 127.72, 122.06, 61.57, 44.89, 25.94, 25.49. HRMS calcd. for C₁₂H₁₅Br₃NO₃S ([M + H]⁺): 489.8317, found 489.8315.

Data for 3,3-dimethyl-2-oxo-N-phenethylbutane-1-sulfonamide (P-31): Yield 22%; white solid; m.p. 73.6–74.4 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.30 (t, J = 7.6 Hz, 2H, C₆H5-H), 7.26 – 7.19 (m, 3H, C₆H5-H), 7.17 (t, J = 5.8 Hz, 1H, SO₂-NH)), 4.40 (s, 2H, SO₂-CH₂), 3.23–3.18 (m, 2H, N-CH₂), 2.77 (dd, J = 8.7, 6.7 Hz, 2H, CH₂), 1.08 (s, 9H, CH₃). ¹³C-NMR (151 MHz, DMSO-d₆) δ 204.99, 138.89, 128.70, 128.30, 126.21, 56.07, 44.58, 44.13, 35.71, 25.24. HRMS calcd. for C₁₄H₂₂NO₃S ([M + H]⁺): 284.1315, found 284.1319.

Data for 3,3-dimethyl-N-(4-nitrophenethyl)-2-oxobutane-1-sulfonamide (P-32): Yield 9%; yellow solid; m.p. 92.3–98.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 8.18 (d, 2H, C₆H₄-2H), 7.55 (d,1H, 2H, C₆H₄-2H), 7.24 (s, 1H, SO₂-NH), 4.45 (s, 2H, CH₂-SO₂), 3.33 (s, 2H, NH-CH₂), 2.93 (t, 2H, C₆H₄-CH₂), 1.09 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.98, 146.90, 145.51, 129.70, 129.01, 128.10, 123.82, 54.74, 45.30, 44.00, 36.28, 26.84, 25.48. HRMS calcd. for C₁₄H₂₁N₂O₅S ([M + H]⁺): 329.1171, found 329.1166.

Data for 3,3-dimethyl-N-(4-methylphenethyl)-2-oxobutane-1-sulfonamide (P-33): Yield 24%; white solid; m.p. 78.6–79.8 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.13 (m, 5H, C₆H₄ + SO₂-NH), 4.37 (s, 2H, CH₂-SO₂), 3.18 (m, 2H, NH-CH₂), 2.74 (t, 2H, C₆H₄-CH₂), 2.27 (s, 3H, C₆H₄-CH₃), 1.09 (d, 9H, 3CH₃).¹³C-NMR (151 MHz, CDCl₃) δ 205.75, 136.29, 134.68, 129.33, 128.64, 54.78, 45.18, 44.87, 35.84, 25.52, 20.95. HRMS calcd. for C₁₅H₂₃NO₃NaS ([M + Na]⁺): 320.1296, found 320.1297.

Data for N-(4-methoxyphenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-34): Yield 11%; white solid; m.p. 88.9–89.8 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.14 (t, 3H, C₆H₄-3H), 6.86 (d, 2H, C₆H₄-H + SO₂-NH), 4.36 (s, 2H, CH₂-SO₂), 3.72 (s, 3H, CH₃O), 3.15 (m, 2H, NH-CH₂), 2.70 (t, 2H, C₆H₄-CH₂), 1.08 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.85, 158.51, 129.83, 129.79, 114.17, 55.28, 54.77, 45.29, 45.06, 35.48, 25.62. HRMS calcd. for C₁₅H₂₃NO₄NaS ([M + Na]⁺): 336.1245, found 336.1242.

Data for N-(3-methoxyphenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-35): Yield 5%; white solid; m.p. 52.3–53.8 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.21 (t, 1H, C₆H₄-H), 7.15 (t, 1H, C₆H₄-H), 6.81–6.77 (m, 3H, C₆H₄-2H + SO₂-NH), 4.39 (s, 2H, CH₂-SO₂), 3.74 (s, 3H, CH₃O), 3.20 (m, 2H, NH-CH₂), 2.74 (t, 2H, C₆H₄-CH₂), 1.08 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.76, 159.76, 139.34, 129.67, 120.98, 114.39, 112.23, 55.10, 54.78, 45.19, 44.65, 36.33, 25.51. HRMS calcd. for C₁₅H₂₃NO₄NaS ([M + Na]⁺): 336.1245, found 336.1248.

Data for N-(3,4-dimethoxyphenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-36): Yield 3%; yellow solid; m.p. 93.8–95.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.12 (t, 1H, C₆H₄-H), 6.85 (m, 2H, C₆H₄-2H), 6.74 (dd, 1H, C₆H₄-H), 4.36 (s, 2H, CH₂-SO₂), 3.73 (d, 6H, 2CH₃O), 3.19 (m, 2H, NH-CH₂), 2.70 (t, 2H, C₆H₄-CH₂), 1.07 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.79, 148.94, 147.77, 130.30, 120.69, 111.95, 111.34, 55.82, 55.77, 54.85, 45.17, 44.83, 35.83, 25.47. HRMS calcd. for C₁₆H₂₅NO₅NaS ([M + Na]⁺): 366.1351, found 366.1054.

Data for N-(4-fluorophenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-37): Yield 10%; yellow solid; m.p. 81.0–83.6 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.28 (dd, 2H, C₆H₄-2H), 7.17 (t, 1H, SO₂-NH), 7.13 (t, 2H, C₆H₄-2H), 4.41 (s, 2H, CH₂-SO₂), 3.20 (m, 2H, NH-CH₂), 2.77 (t, 2H, C₆H₄-CH₂), 1.09 (d, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.86, 162.51, 160.89 (s,¹J = 244.62), 133.44, 130.22, 130.21, 115.52, 115.38, 54.71, 45.23, 44.76, 35.52, 25.50. HRMS calcd. for C₁₄H₂₀FNO₃NaS ([M + Na]⁺): 324.1046, found 324.1040.

Data for N-(3-fluorophenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-38): Yield 7%; yellow solid; m.p. 47.4–52.2 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.34 (td, 1H, C₆H₄-H), 7.18 (t, 1H, C₆H₄-H), 7.09 (m, 2H, C₆H₄-2H), 7.04 (td, 1H, SO₂-NH), 4.42 (s, 2H, CH₂-SO₂), 3.23 (td, 2H, NH-CH₂), 2.80 (t, 2H, C₆H₄-CH₂), 1.09 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.85, 163.65, 162.02 (s,¹J = 246.13), 140.37, 140.32, 130.15, 130.10, 124.45, 124.43, 115.73, 115.58, 113.73, 113.59, 54.80, 45.22, 44.43, 36.06, 36.05, 28.36, 25.50. HRMS calcd. for C₁₄H₂₀FNO₃NaS ([M + Na]⁺): 324.1046, found 324.1042.

Data for N-(2-fluorophenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-39): Yield 13%; white solid; m.p. 69.8–73.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.34 (td, 1H, C₆H₄-H), 7.28 (dq, 2H, C₆H₄-2H), 7.16 (m, 2H, C₆H₄-H + SO₂-NH), 4.43 (d, 2H, CH₂-SO₂), 3.21 (d, 2H, NH-CH₂), 2.82 (t, 2H, C6H4-CH₂), 1.09 (d, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.79, 161.97, 160.34 (s,¹J = 245.54), 131.18, 131.15, 128.65, 128.60, 124.72, 124.61, 124.23, 124.21, 115.47, 115.32, 54.73, 45.21, 43.39, 43.38, 29.97, 29.96, 25.53. HRMS calcd. for C₁₄H₂₀FNO₃NaS ([M + Na]⁺): 324.1046, found 324.1043.

Data for N-(3-bromophenethyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-40): Yield 22%; yellow solid; m.p. 79.8–81.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.48 (d, 1H, C₆H₄-H), 7.42 (m, 1H, C₆H₄-H), 7.27 (m, 2H, C₆H₄-2H), 7.19 (t, 1H, SO₂-NH), 4.42 (s, 2H, CH₂-SO₂), 3.22 (td, 2H, NH-CH₂), 2.78 (t, 2H, C6H4-CH₂), 1.09 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.94, 140.21, 131.87, 130.30, 130.00, 127.54, 122.72, 54.83, 45.34, 44.55, 36.09, 25.60. HRMS calcd. for C₁₄H₂₀BrNO₃NaS ([M + Na]⁺): 384.0245, found 384.0242.

Data for N-(2-bromobenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-41): Yield 33%; yellow solid; m.p. 79.5–83.4 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.76 (t, 1H, SO₂-NH), 7.61 (dd, 1H, C₆H₄-H), 7.55 (m, 1H, C₆H₄-H), 7.42 (td, 1H, C₆H₄-H), 7.24 (td, 1H, C₆H₄-H), 4.55 (s, 2H, CH₂-SO₂), 4.28 (d, 2H, NH-CH₂), 1.10 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.73, 135.80, 133.09, 130.65, 129.84, 127.87, 123.87, 55.96, 47.78, 45.09, 25.72. HRMS calcd. for C₁₃H₁₈BrNO₃NaS ([M + Na]⁺): 370.0088, found 370.0084.

Data for N-(2- fluorobenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-42): Yield 20%; white solid; m.p. 101.1–103.4 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.74 (t, 1H, SO₂-NH), 7.54 (m, 1H, C₆H₄-H), 7.45 (dd, 1H, C₆H₄-H), 7.38 (td, 1H, C₆H₄-H), 7.32 (td, 1H, C₆H₄-H), 4.54 (s, 2H, CH₂-SO₂), 4.30 (d, 2H, NH-CH₂), 1.10 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.68, 134.01, 133.75, 130.42, 129.72, 129.54, 127.15, 55.76, 45.44, 44.99, 25.62. HRMS calcd. for C₁₃H₁₉FNO₃S ([M + H]⁺): 288.1070, found 288.1072.

Data for N-(4-fluorobenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-43): Yield 11%; white solid; m.p. 129–133.8 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.83 (t, 1H, SO₂-NH), 7.73 (d, 2H, C₆H₄-2H), 7.58 (d, 2H, C₆H₄-2H), 4.49 (s, 2H, CH₂-SO₂), 4.30 (d, 2H, NH-CH₂), 1.09 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 206.10, 140.38, 130.20, 128.26, 125.69 (q, J = 3.7 Hz), 124.72, 122.92 (s,¹J = 271.8), 55.31, 46.95, 45.22, 25.50. HRMS calcd. for C₁₃H₁₉FNO₃S ([M + H]⁺): 288.1070, found 288.1075.

Data for N-(4-chlorobenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-44): Yield 23%; white solid; m.p. 104.8–108.0 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.73 (t, 1H, SO₂-NH), 7.42 (d, 2H, C₆H₄-2H), 7.37 (d, 2H, C₆H₄-2H), 4.44 (s, 2H, CH₂-SO₂), 4.19 (d, 2H, NH-CH₂), 1.08 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 206.11, 134.83, 133.91, 129.46, 128.87, 55.37, 46.83, 45.17, 25.53. HRMS calcd. for C₁₃H₁₈ClNO₃NaS ([M + Na]⁺): 326.0594, found 326.0585.

Data for N-(4-cyanobenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-45): Yield 13%; white solid; m.p. 118.8–120.5 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.84 (dd, 3H, SO₂-NH+ C₆H₄-2H), 7.55 (d, 2H, C₆H₄-2H), 4.52 (s, 2H, CH₂-SO₂), 4.30 (d, 2H, NH-CH₂), 1.10 (s, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 206.09, 141.99, 132.47, 128.43, 118.39, 111.81, 55.43, 46.84, 45.29, 25.51. HRMS calcd. for C₁₄H₁₉N₂O₃S ([M + H]⁺): 295.1116, found 295.1111.

Data for N-(2,5-dimethoxybenzyl)-3,3-dimethyl-2-oxobutane-1-sulfonamide (P-46): Yield 29%; white solid; m.p. 58.6–60.8 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 7.39 (t, 1H, SO₂-NH), 6.96 (d, 1H, C6H4-H), 6.90 (d, 1H, C₆H₄-H), 6.81 (dd, 1H, C₆H₄-H), 4.40 (s, 2H, CH₂-SO₂), 4.18 (d, 2H, NH-CH₂), 3.72 (d, 6H, 3OCH₃), 1.06 (d, 9H, 3CH₃). ¹³C-NMR (151 MHz, CDCl₃) δ 205.45, 153.27, 151.60, 125.11, 116.01, 113.71, 111.09, 55.77 (d, J = 6.6 Hz), 55.53, 44.67, 44.39, 25.63. HRMS calcd. for C₁₅H₂₃NO₅NaS ([M + Na]⁺): 352.1195, found 352.1193.

3.3. Fungicidal Activity Bioassays

The antifungal activity of the compounds was evaluated by a mycelial growth experiment, a tomato pot experiment, and a strawberry experiment.

Mycelium Growth Experiments. The method is given in reference [24]. The culture media was potato dextrose agar (PDA). The final concentrations of compounds was 50 mg/L on PDA, and each treatment was repeated three times. Boscalid was used as positive control while acetone was used as blank control. The pathogen cake (5.00mm) was inoculated in the center of PDA culture dish for 5 days. The inhibition rate I (%) was calculated according to following formula:

I (%) = [(C − T)/(C − 5)] × 100%

(1)

C is the average fungal mycelium diameters of the blank control (mm);

T is the average fungal mycelium diameters of the treatment (mm).

Tomato Pot Experiment. The method is given in reference [25]. The compound tested (200 mg/L) was evenly sprinkled on the tomato seedlings, and a spore suspension was inoculated 24 h later. Each treatment was repeated three times. When the rate of diseased leaves in the blank control reached more than 50%, the classification investigation was carried out. The inhibition rate I (%) was calculated according to the following formula:

X = [∑(Ni × i)/(N × 9)] × 100%

(2)

where X is the disease index, Ni the number of diseased leaves, i the disease grade and N the total leaves investigated.

I (%) = [(CX − TX)/(CX − 5)] × 100%

(3)

CX is the average disease index of the blank control;

TX is the average disease index of the treatment.

Strawberry Experiment. The method is given in reference [25]. The compound to be tested (400 mg/L) was evenly sprinkled on the strawberries, and the spore suspension was inoculated 24 h later. Each treatment was repeated three times. When the disease spot diameter of the blank control was greater than 30 mm, the investigation wase carried out. The inhibition rate I (%) was calculated according to the following formula:

I (%) = [(CM − TM)/CM] × 100%

(4)

CM is the average lesion diameters of the blank control (mm);

TM is the average lesion of the treatment (mm).

4. Conclusions

In summary, 46 pinacolone sulfonamides were designed and synthesized, and presented excellent antifungal activity against a variety of plant pathogenic fungi, especially Botrytis cinerea. The high activity compound P-29 was screened by biological activity evaluation and presented superb inhibition efficacy. Compound P-29 has high research value and great potential to be developed as the novel lead compound in the design of a new pesticide.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27175468/s1, Section S1: NMR spectra of P-1~P-46; Section S2: MS of P-1~P-46; Section S3: HPLC spectra of P-18, P-23, P-29, P-30, P-31; Section S4: X-ray single crystal diffraction of P-27.

Author Contributions

X.L. and W.L. conceived and designed the experiments; C.L., X.X., Y.W., J.Y. and Y.L. performed the experiments; C.L., X.X., J.Y., Y.L. and X.Z. analyzed the data; Z.Q., L.H. and W.L. contributed reagents, materials and strains; C.L., X.X., X.L. and W.L. collaborated in the discussion and interpretation of results; C.L. and W.L. wrote the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported in part by the Scientific Research Project of Liaoning Education Department (LJKZ0645), National Natural Science Foundation of China (32172454), Hightech R&D Program of Liaoning (Project 2019JH2/10200012).

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors confirm that this article content has no conflict of interest.

Sample Availability

Samples of the compounds P-1~P-46 are available from the authors.

References

Richards, J.; Xiao, C.L.; Jurick, I.W. Botrytis spp.: A contemporary perspective and synthesis of recent scientific developments of a widespread genus that threatens global food security. Phytopathology 2021, 111, 432–436. [Google Scholar] [CrossRef] [PubMed]
Fred, G.; Zachary, S.B.; Jennifer, K. Wicked evolution: Can we address the sociobiological dilemma of pesticide resistance? Science 2018, 360, 728–732. [Google Scholar]
Shao, W.Y.; Zhao, Y.F.; Ma, Z.H. Advances in understanding fungicide resistance in Botrytis cinerea in China. Phytopathology 2021, 111, 455–463. [Google Scholar] [CrossRef] [PubMed]
Cui, K.D.; He, L.M.; Li, T.T.; Mu, W.; Liu, F. Development of boscalid resistance in Botrytis cinerea and an efficient strategy for resistance management. Plant Dis. 2021, 105, 1042–4047. [Google Scholar] [CrossRef]
Alzohairy, S.A.; Gillett, J.; Saito, S.; Naegele, R.P.; Xiao, C.L.; Miles, T.D. Fungicide resistance profiles of Botrytis cinerea isolates from Michigan vineyards and development of a TaqMan assay for detection of fenhexamid resistance. Plant Dis. 2021, 105, 285–294. [Google Scholar] [CrossRef]
Gressel, J. Perspective: Present pesticide discovery paradigms promote the evolution of resistance—Learn from nature and prioritize multi-target site inhibitor design. Pest. Manag Sci. 2020, 76, 421–425. [Google Scholar] [CrossRef]
Liu, C.L.; Guan, A.Y.; Xie, Y.; Li, M.; Yang, J.C. Intermediate derivatization and creation of new pesticides. J. Pest. Sci. 2020, 22, 121. [Google Scholar]
Zhang, Y.B. Overview of new pesticide creation methods. Pesticide 2006, 6, 364–367. [Google Scholar]
Yan, X.J.; Liang, X.M.; Wang, D.Q. Primary mode of action of novel fungicide chesulfamide against Botrytis cinerea. Abstr. Pap. Am. Chem. Soc. 2014, 248, 248. [Google Scholar]
Li, X.H.; Rui, P.; Pan, Q.; Chen, X.Y.; Qiu, Z.Q.; Ji, M.S. Combinatorial synthesis and bactericidal activity of 2-oxo-2-phenylethanesulfonamide compounds. J. Pest. Sci. 2016, 18, 28–36. [Google Scholar]
China, A.U. Novel fungicide-Chesulfamide. World Pestic. 2012, 34, 56. [Google Scholar]
Wang, M.L.; Rui, P.; Liu, C.X.; Du, Y.; Qin, P.; Qi, Z.; Ji, M.; Li, X.; Cui, Z. Design, Synthesis and Fungicidal Activity of 2-Substituted Phenyl-2-oxo-2-Hydroxy-and 2-Acyloxyethylsulfonamides. Molecules 2017, 22, 738. [Google Scholar] [CrossRef]
Li, X.H.; Ji, M.S.; Qi, Z.Q.; Li, X.W.; Shen, Y.X.; Gu, Z.M.; Zhang, Y.; Wei, S.H.; Wang, Y.Z.; Wang, D.Q. Synthesis of 2-amino-6-oxocyclohexenylsulfonamides and their activity against Botrytis cinerea. Pest. Manag. Sci. 2011, 67, 986–992. [Google Scholar] [CrossRef]
Li, X.H.; Yang, X.L.; Liang, X.M.; Kai, Z.; Yuan, H.; Yuan, D.; Zhang, J.; Wang, R.; Ran, F.; Qi, S.; et al. Synthesis and biological activities of 2-oxocycloalkylsulfonamides. Bioorg. Med. Chem. 2008, 16, 4538–4544. [Google Scholar] [CrossRef]
Zeng, D.Q.; Zhang, Y.M.; Chen, J. N-substituted benzene sulfonyl group-α-Synthesis and bactericidal activity of nadone hydrazone on triazole substrate. G. Agric. Bios. 2004, 4, 313–315. [Google Scholar]
Vavrina, C.S.; Phatak, S.C.; Smith, A.E. Uptake translocationand metabolite partitioning of 14 C-labeled metribuzin in plant growth-regulated soybean(Glycine max). J. Plant Grow Reg. 1988, 7, 77–84. [Google Scholar] [CrossRef]
Chernyad, I.I. Photosynthesis in sugar beet plants treated with benzyladenine and Metribuzin during leaf ontogeny. Rus. J. Plant Phys. 2000, 47, 161–167. [Google Scholar]
Prinsloo, G.C.; Villiers, D. Activity of triadimenol and flusilazol against Thielaviopsis basicola in tobacco. Phytophylactica 1989, 14, 78–82. [Google Scholar]
Shi, J. Mechanisms of Controlling Wheat Sharp Eyespot by Triazoles—Effects of Triadimefor and Triadimenol Seed Treatment on Wheat Seedling Growth and Rhizoctonia cerealis Vander Hoven Adhering to Wheat Sheaths. Jian J. Agric. Sci. 1992, 1, 35–42. [Google Scholar]
Lu, Y.C.; Hua, Y.L.; Li, X.L.; Jin, G.Y.; Fang, J.X. Synthesis and herbicidal activity of α-Aryloxypropionate. Chin. J. Pestic. Sci. 2006, 8, 218–221. [Google Scholar]
Li, X.H.; Wu, D.C.; Qi, Z.Q.; Li, X.W.; Gu, Z.M.; Wei, S.H.; Zhang, Y.; Wang, Y.Z.; Ji, M.S. Synthesis, fungicidal activity, and structure-activity relationship of 2-oxo- and 2-hydroxycycloalkylsulfonamides. J. Agric. Food Chem. 2010, 58, 11384–11389. [Google Scholar] [CrossRef]
Li, X.H.; Pan, Q.; Cui, Z.N.; Ji, M.S.; Qi, Z.Q. Synthesis and Fungicidal Activity of N-(2,4,5-trichlorophenyl)-2-Oxo-and 2-Hydroxycycloalkylsulfonamides. Lett. Drug Des. Discov. 2013, 10, 353–359. [Google Scholar] [CrossRef]
Qi, Z.Q.; Sun, Q.B.; Li, X.H.; Gu, Z.M.; Li, X.W.; Ji, M.S. Inhibitory effect of N- (2,4,5-trichlorophenyl)—2-oxo cyclohexyl sulfonamide on Botrytis cinerea. Chin. J. Pestic. Sci. 2014, 16, 523–528. [Google Scholar]
Liu, W.; Zhang, S.; Xiao, L.F.; Wan, Y.; He, L.; Wang, K.; Qi, Z.; Li, X. Synthesis and Biological Activity of Novel Hydantoin Cyclohexyl Sulfonamide Derivatives as Potential Antimicrobial Agents in Agriculture. Pest. Manag. Sci. 2022, 78, 1438–1447. [Google Scholar] [CrossRef]
Zhang, Y.M.; Wang, M.L.; Ahmed, M.; He, L.; Ji, M.; Qi, Z.; Li, X. Synthesis, fungicidal activity and SAR of 3,4-dichloroisothiazole-based cycloalkylsulfonamides. Bioorg. Med. Chem. Lett. 2019, 29, 1345–1349. [Google Scholar] [CrossRef]

Figure 1. Structures of active compounds in previous work.

Figure 2. Agricultural active compounds containing pinacolone fragment.

Figure 3. Design strategy of the target compounds.

Scheme 1. Synthetic route of the target compounds (Table 1).

Figure 4. X-ray single crystal diffraction of compound P-27.

Figure 5. Tomato pot experiment.

Figure 6. Strawberry experiment.

Table 2. EC₅₀ of compounds against Botrytis cinerea.

Compound	EC₅₀(95 Confidence Interval) (mg/L)	Regression Equation	R
P-22	>50	Y = 3.4148 + 0.6774X	0.9650
P-23	11.57(7.45–17.98)	Y = 3.9031 + 1.0316X	0.9810
P-25	39.00(27.22–55.88)	Y = 2.2268 + 1.7430X	0.9346
P-30	4.68(3.26–6.71)	Y = 4.2520 + 1.1166X	0.9648
Chesulfamide	38.47(15.35–96.62)	Y = 4.3874 + 0.4032X	0.9179
Boscalid	<0.2	Y = 5.25981 + 0.2237X	0.9514

Table 3. Control efficacy of target compounds in tomato pot tests at 200 mg/L.

Compound	Control Efficacy % (Tomato Leaves)	Compound	Control Efficacy % (Tomato Leaves)
P-1	26.83 ^abc	P-25	41.46 ^abc
P-2	70.73 ^ab	P-26	0
P-3	12.20 ^d	P-27	0
P-4	0	P-28	41.82 ^abc
P-5	34.15 ^abc	P-29	90.24 ^a
P-6	0	P-30	41.46 ^abc
P-7	0	P-31	85.37 ^a
P-8	0	P-32	0
P-9	12.20 ^d	P-33	74.35 ^ab
P-10	41.12 ^abc	P-34	3.21 ^d
P-11	56.10 ^abc	P-35	58.78 ^abc
P-12	70.73 ^ab	P-36	25.19 ^d
P-13	70.73 ^ab	P-37	64.12 ^abc
P-14	76.59 ^ab	P-38	67.48 ^abc
P-15	26.83 ^abc	P-39	0
P-16	34.15 ^abc	P-40	8.71 ^d
P-17	26.83 ^abc	P-41	60.00 ^abc
P-18	91.22 ^a	P-42	14.35 ^d
P-19	0	P-43	70.84 ^ab
P-20	48.78 ^abc	P-44	0
P-21	78.05 ^ab	P-45	0
P-22	70.73 ^ab	P-46	66.11 ^abc
P-23	26.83 ^abc	chesulfamide	59.23 ^abc
P-24	26.83 ^abc	boscalid	92.20 ^a

The letters ^a–d denote results with significant differences.

Table 4. Control efficacy of some compounds in strawberry test at 400 mg/L.

Compound	Control Efficacy % (Strawberry)
P-18	73.33 ^a,b
P-23	0
P-29	100 ^a
P-30	66.67 ^a,b
P-31	88.89 ^a
Chesulfamide	29.63 ^b,c
Boscalid	94.07 ^a

The letters ^a–c denote results with significant differences.

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

© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

Share and Cite

MDPI and ACS Style

Liu, C.; Xiang, X.; Wan, Y.; Yang, J.; Li, Y.; Zhang, X.; Qi, Z.; He, L.; Liu, W.; Li, X. Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents. Molecules 2022, 27, 5468. https://doi.org/10.3390/molecules27175468

AMA Style

Liu C, Xiang X, Wan Y, Yang J, Li Y, Zhang X, Qi Z, He L, Liu W, Li X. Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents. Molecules. 2022; 27(17):5468. https://doi.org/10.3390/molecules27175468

Chicago/Turabian Style

Liu, Chaojie, Xiaofang Xiang, Ying Wan, Jia Yang, Yufei Li, Xinchen Zhang, Zhiqiu Qi, Lu He, Wei Liu, and Xinghai Li. 2022. "Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents" Molecules 27, no. 17: 5468. https://doi.org/10.3390/molecules27175468

APA Style

Liu, C., Xiang, X., Wan, Y., Yang, J., Li, Y., Zhang, X., Qi, Z., He, L., Liu, W., & Li, X. (2022). Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents. Molecules, 27(17), 5468. https://doi.org/10.3390/molecules27175468

Article Menu

Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents

Abstract

1. Introduction

2. Results and Discussion

2.1. Chemistry

2.2. Biological Assay

2.3. Structure–Activity Relationship

3. Materials and Methods

3.1. Instruments and Reagents

3.2. General Synthetic Procedures

3.3. Fungicidal Activity Bioassays

4. Conclusions

Supplementary Materials

Author Contributions

Funding

Data Availability Statement

Conflicts of Interest

Sample Availability

References

Share and Cite

Article Metrics

Article Access Statistics

Further Information

Guidelines

MDPI Initiatives

Follow MDPI