Design, synthesis, in vitro anticancer evaluation, kinase inhibitory effects, and pharmacokinetic profile of new 1,3,4-triarylpyrazole derivatives possessing terminal sulfonamide moiety

Abstract

The present work describes the design and synthesis of a novel series of 1,3-diaryl-4-sulfonamidoarylpyrazole derivatives 1a–q and 2a–q and their in vitro biological activities. The target compounds were evaluated for antiproliferative activity against NCI-60 cell line panel. Compounds 1c, 1g, 1k–m, 1o, 2g, 2h, 2k–m, 2o, and 2q showed the highest mean inhibition percentages at 10 µM single-dose testing and were selected to be tested at 5-dose mode. The ICs₅₀ of the most potent compounds were determined over the 60 cell lines. Compound 2l exhibited the strongest activity against different cell lines with IC₅₀ 0.33 µM against A498 renal cancer cell line. Compound 2l was tested over a panel of 20 kinases to determine its molecular target(s), and its IC₅₀ values over the most sensitive kinases were defined. In vitro stability and in vivo pharmacokinetic profile of compound 2l was also investigated.

Keywords:

• Anticancer
• kinase inhibitor
• pharmacokinetic
• pyrazole
• sulfonamide

Introduction

Cancer is one of the most extensively spreading diseases around the world. In 2015, one in each six global death cases occurred as a result of different cancer types¹. According to American Cancer Society, everyday there are 4750 new cancer cases and 1670 death cases². The global cancer statistics revealed that cancer is the second fatal condition after cardiovascular diseases^3,4. Despite the rapid development in the diagnostic area, development of new cancer therapy is a quite challenging mission due to the sophisticated biological pathways contributing to cancer progression.

Many compounds possessing sulfonamide moiety have been reported as highly effective antiproliferative agents^5–7. Vemurafenib (Zelboraf®, Figure 1) is the first kinase inhibitor drug possessing sulfonamide moiety to be approved by the FDA in 2011 for the treatment of late-stage melanoma. Vemurafenib acts through the inhibition of mutated B-RAF⁸. Dabrafenib (Tafinlar^®, Figure 1) is another targeted therapy, which possesses sulfonamide moiety⁹. Dabrafenib was approved in 2013 for the treatment of mutant B-RAF (V600E-B-RAF)-associated proliferative disorders¹⁰. Encorafenib (LGX 818, Figure 1) is a drug candidate that carries both sulfonamide and pyrazole backbone which has been recently approved by the FDA to be used in combination with binimetinib for the treatment of unresectable or metastatic melanoma¹¹.

Figure 1. Structures of encorafenib, vemurafenib, dabrafenib, SB203580, and the target compounds 1a–q and 2a–q.

Based on the abovementioned structures and our previous pyrazole ring anticancer investigations^7,12–21, a novel series of 1,3,4-triarylpyrazole was designed and synthesized in which the structure of both rings B and D were fixed and diverse structure modifications were performed in both rings A and C (Figure 1). The connection length between ring B and sulfonamide terminal moiety ring C was selected from two main chains, ethylene and propylene. The target compounds were tested for in vitro antiproliferative activity against the standard NCI-60 cancer cell line panel. The structure–activity relationships (SAR) are explained in details to show the effects of sulfonamide, linker length, and different substituents on the biological activity. The most promising compounds were further tested against a panel of kinases to study their molecular mechanism of action. The in vitro stability and in vivo pharmacokinetic profile were also investigated for the most potent compound. The synthetic and biological procedures, as well as relevant discussions, are presented in details.

Experimental

Chemistry

General

All solvents and reagents were commercially available and used as such with no further purification. The target compounds and intermediates were purified by column chromatography using silica gel (0.040–0.063 mm, 230–400 mesh) and technical grade solvents. Analytical thin-layer chromatography (TLC) was adopting on silica gel 60 F₂₅₄ plates from Merck. Purity percentages of the target compounds were confirmed to be more than 96% by LC-MS. ¹H NMR and ¹³C NMR spectra were recorded on a Bruker Avance 400 or 300 spectrometer using tetramethylsilane as an internal standard and signals are described as s (singlet), d (doublet), t (triplet), q (quartet), p (pentet), m (multiplet), brs (broad singlet), or dd (doublet of doublets). LC-MS analysis was carried out using the following system: Waters 2998 photodiode array detector, Waters 3100 mass detector, Waters SFO system fluidics organizer, Waters 2545 binary gradient module, Waters reagent manager, Waters 2767 sample manager, Sunfire™ C18 column (4.6 × 50 mm, 5 µm particle size); Solvent gradient = 95% A at 0 min, 1% A at 5 min; solvent A: 0.035% trifluoroacetic acid (TFA) in water; solvent B: 0.035% TFA in CH₃OH; flow rate = 3.0 mL/min; the AUC was calculated using Waters MassLynx 4.1 software. Solvents and liquid reagents were transferred using hypodermic syringes. Melting points were obtained on a Walden Precision Apparatus Electro thermal 9300 apparatus and are uncorrected.

Synthesis of N¹-(4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)ethane1,2-diamine (8) and N¹-(4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)propane-1,3-diamine (9)

They were synthesized utilizing the five-step procedure reported in the literature¹⁹. The detailed procedures are also mentioned in the supplementary file.

General procedure for synthesis of the target compounds N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)arylsulfonamides (1a-i) and N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)arylsulfonamides (2a–i)

To a solution of compound 8 or 9 (0.2 mmol) in anhydrous dichloromethane (5 mL), triethylamine (50.5 mg, 0.5 mmol) was added at 0 °C. A solution appropriate arylsulfonyl chloride (0.21 mmol) in anhydrous dichloromethane (1 mL) was added thereto dropwise. The reaction mixture was stirred at room temperature for 24 h. When the reaction completed, the solvent was removed under vacuo, and the residue was partitioned between ethyl acetate (5 mL) and water (5 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3 × 10 mL). The combined organic layer was washed with saturated saline (2 × 5 mL) and the organic solvent was evaporated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane-ethyl acetate 4:1 v/v) to give the required product.

N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1a)

White solid (65%); mp 104–6 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.93 (s, 1H, Ar-H), 7.86–7.79 (m, 4H, Ar-H), 7.51–7.40 (m, 3H, Ar-H), 7.25–7.21 (m, 5H, Ar-H), 6.92–6.88 (m, 1H, Ar-H), 6.77 (d, J = 9.0 Hz, 1H, Ar-H), 6.70 (s, 1H, Ar-H), 6.42 (d, J = 6.0 Hz, 1H, Ar-H), 6.24 (s, 1H, Ar-H), 4.98 (brs, 1H, NH), 3.65 (s, 3H, OCH₃), 3.32 (d, J = 3.0 Hz, 2H, CH₂), 3.09 (d, J = 6.0 Hz, 2H, CH₂); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.6, 147.4, 141.9, 140.1, 140.1, 139.5, 139.4, 132.4, 131.0, 130.0, 129.9, 128.9, 128.8, 127.6, 126.9, 125.1, 122.7, 120.0, 115.8, 114.7, 112.4, 105.9 (Ar-C), 55.3 (OCH₃), 43.9 (CH₂), 41.6 (CH₂).; LC-MS(m/z) calculated for C₂₉H₂₇N₅O₃S: 525.18, found: 526.0 (M + 1)⁺.

4-Bromo-N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1b)

White solid (61%); mp 136–8 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.96 (s, 1H, Ar-H), 7.89 (d, J = 6.0 Hz, 1H, Ar-H), 7.64 (d, J = 9 Hz, 2H, Ar-H), 7.58–7.55 (m, 2H, Ar-H),7.31–7.28 (m, 6H, Ar-H), 6.93 (d, J = 6.0 Hz, 1H, Ar-H), 6.81 (d, J = 9.0 Hz, 1H, Ar-H), 6.72 (s,1H, Ar-H), 6.48 (d, J = 6.0 Hz, 1H, Ar-H), 6.24 (s, 1H, Ar-H), 4.81 (brs, 1H, NH), 3.69 (s, 3H, OCH₃), 3.36 (brs, 2H, CH₂), 3.12 (brs, 2H, CH₂); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.5, 147.2, 142.2, 140.2, 139.5, 139.3, 139.2, 132.6, 132.6, 132.1, 131.0, 130.0, 128.8, 128.5, 127.6, 127.1, 125.1, 122.7, 119.8, 115.8, 114.8, 112.6, 106.1 (Ar-C), 55.3 (OCH₃), 44.4 (NH–CH₂), 41.6 (CH₂–NH); LC-MS(m/z) calculated for C₂₉H₂₆BrN₅O₃S: 603.09, found: 605.0 (M + 2)⁺.

4-Chloro-N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1c)

White solid (60%); mp 132–4 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.94 (s, 1H, Ar-H), 7.85 (d, J = 6.0 Hz, 1H, Ar-H), 7.72–7.69 (m, 2H, Ar-H), 7.54–7.51 (m, 2H, Ar-H), 7.39–7.22 (m, 6H, Ar-H), 6.91 (d, J = 9.0 Hz, 1H, Ar-H), 6.78 (d, J = 9.0 Hz, 1H, Ar-H), 6.70 (s, 1H, Ar-H), 6.43 (d, J = 3.0 Hz, 1H, Ar-H), 6.24 (s, 1H, Ar-H), 4.95 (brs, 1H, NH), 3.66 (s, 3H, OCH₃), 3.33 (d, J = 3.0 Hz, 2H, NH–CH2), 3.09 (d, J = 3.0 Hz, 2H, –CH₂–NH); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.5, 147.3, 142.0, 140.1, 139.5, 139.3, 138.6, 131.0, 129.9, 129.1, 128.8, 127.6, 125.1, 122.7, 119.9, 115.8, 114.7, 112.5, 106.9 (Ar-C), 55.2 (OCH₃), 44.1 (NH-CH₂), 41.5 (–CH₂-NH).; LC-MS(m/z) calculated for C₂₉H₂₆ClN₅O₃S: 559.14, found: 560.0 (M + 1)⁺.

4-Fluoro-N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1d)

White solid (67%); mp155-6 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.83 (s, 1H, Ar-H), 7.71–7.67 (m, 3H, Ar-H), 7.19–7.15 (m, 5H, Ar-H), 6.99 (t, J = 8.4 Hz, 2H, Ar-H), 6.80 (d, J = 8.4 Hz, 1H, Ar-H), 6.67 (d, J = 8.8 Hz, 1H, ar-H), 6.59 (s, 1H, Ar-H), 6.34 (d, J = 5.2 Hz, 1H, Ar-H), 6.13 (s, 1H, Ar-H), 4.85 (brs, NH), 3.56 (s, 3H, OCH₃), 3.23 (s, 2H, NH–CH₂), 2.98 (d, J = 4.4 Hz, 2H, –CH₂–NH); ¹³C NMR (100 MHz, CDCl₃) δ 159.7, 158.6, 147.1, 142.2, 140.1, 139.5, 139.3, 136.1, 130.9, 130.0, 129.7, 129.6, 129.5, 128.9, 128.7, 125.2, 125.0, 122.7, 119.8, 116.0, 115.0, 112.5, 105.9 (Ar-C), 55.3 (OCH₃), 44.2 (CH₂), 41.6 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆FN₅O₃S: 543.17, found: 544.0 (M + 1)⁺.

4-Methoxy-N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)benzenesulfonamide (1e)

White solid (62%); mp 144–6 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.94 (s, 1H, Ar-H),7.88 (d, J= 4.0 Hz, 1H, Ar-H), 7.74 (d, J = 8.0 Hz, 2H, Ar-H), 7.33–7.23 (m, 6H, Ar-H), 6.91 (d, J = 8.0 Hz, 3H, Ar-H), 6.79–6.77 (m, 1H, Ar-H), 6.70–6.69 (m, 1H, Ar-H), 6.43 (dd, J= 8.0, J = 4.0 Hz, 1H, Ar-H), 6.23 (s, 1H, Ar-H), 4.85 (s, NH), 3.83 (s, 3H, OCH₃), 3.67 (s, 3H, OCH₃), 3.34 (t, J = 8.0 Hz, 2H, NH–CH₂–), 3.08 (t, J = 8.0 Hz, 2H, –CH₂–NH); ¹³C NMR (100 MHz, CDCl₃) δ 162.6, 159.6, 158.6, 147.5, 141.9, 140.1, 139.5, 139.4, 131.6, 131.0, 129.9, 129.1, 128.8, 127.6, 125.1, 122.7, 120.0, 115.7, 114.7, 114.1, 112.4, 105.9 (Ar-C), 55.5 (OCH₃), 55.3 (OCH₃), 43.8 (CH₂), 41.5 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₉N5O₄S: 555.19, found: 556.0 (M + 1)⁺.

N-(2-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)-4-methylbenzenesulfonamide (1f)

White solid (69%); mp 150–2 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.97 (s, 1H, Ar-H),7.91 (d, J = 6.0 Hz, 1H), 7.71 (d, J = 9.0 Hz, 2H, Ar-H), 7.32–7.26 (m, 7H), 6.94 (d, J = 9.0 Hz, 1H, Ar-H), 6.81 (d, J= 6.0 Hz, 1H, Ar-H), 6.72 (s, 1H, Ar-H), 6.49 (d, J= 3.0 Hz, 1H, Ar-H), 6.26 (s, 1H Ar-H), 4.97 (brs, 1H, NH), 3.70 (s, 3H, OCH₃), 3.36 (brs, 2H, NH–CH₂–), 3.12 (t, J = 6.0 Hz, 2H, –CH₂–NH), 2.43 (s, 3H, CH₃); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.5, 147.4, 143.1, 142.1, 140.1, 139.6, 139.3, 137.1, 131.1, 129.9, 129.5, 128.8, 127.6, 127.0, 125.1, 122.7, 120.0, 115.7, 114.7, 112., 105.5 (Ar-C), 55.3 (OCH3), 44.0 (CH₂), 41.7 (CH₂), 21.4 (CH₃); LC-MS(m/z) calculated for C₃₀H₂₉N₅O₃S: 539.20, found: 540.0 (M + 1)⁺.

N-(2-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)-4-(trifluoromethyl)benzenesulfonamide (1g)

White solid (74%); mp 132–4 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.91 (d, J = 9.0 Hz, 4H, Ar-H), 7.71 (s, 1H, Ar-H), 7.30 (brs, 6H, Ar-H), 6.93 (s, 1H, Ar-H), 6.80 (s, 1H, Ar-H), 6.71 (s, 2H, Ar-H), 6.48 (s, 1H, Ar-H), 6.25 (s, 1H, Ar-H), 4.87 (brs, 1H, NH), 3.67 (s, 3H, OCH₃), 3.37 (s, 2H, NH–CH₂–), 3.14 (s, 2H, –CH₂–NHSO₂); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.5, 147.1, 147.0, 143.8, 142.4, 139.5, 139.4, 139.2, 134.1, 133.7, 130.9, 130.1, 129.9, 128.9, 127.4, 126.0, 125.2, 125.0, 122.7, 119.7, 115.8, 114.7, 112.8, 106.2 (Ar-C), 55.3 (OCH₃), 44.7 (CH₂), 41.7 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₆F₃N₅O₃S: 593.17, found: 594.0 (M + 1)⁺.

3-Fluoro-N-(2-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)benzenesulfonamide (1h)

White solid (66%); mp 118–20 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.94 (s, 1H, Ar-H), 7.85 (d, J = 6.0 Hz, 1H, Ar-H), 7.59 (s, 1H, Ar-H), 7.49 (s, 1H, Ar-H), 7.46–7.37 (m, 2H, Ar-H), 7.29–7.21 (m, 6 H), 6.90 (d, J = 9.0 Hz, 1H, Ar-H), 6.78 (d, J = 9.0 Hz, 1H, Ar-H), 6.71 (s, 1H), 6.43 (d, J = 6.0 Hz, 1H, Ar-H), 6.25 (s, 1H, Ar-H), 4.99 (brs, 1H, NH), 3.65 (s, 3H, OCH₃), 3.33 (brs, 2H, NH–CH₂–), 3.10 (t, J = 6.0 Hz, 2H, –CH₂–NH–SO₂); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.6, 147.3, 142.2, 142.0, 140.2, 139.5, 139.4, 130.9, 130.8, 130.7, 129.9, 128.8, 127.6, 125.1, 122.7, 119.9, 119.6, 119.3, 115.7, 114.7, 114.4, 114.1, 112.5, 106.0 (Ar-C), 55.2 (OCH₃), 44.2 (CH₂), 41.5 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆FN₅O₃S: 543.17, found: 544.0 (M + 1)⁺.

N-(2-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)naphthalene-1-sulfonamide (1i)

White solid (71%); mp 178–80 °C; ¹H NMR (400 MHz, CDCl₃) δ; 8.38 (s, 1H, Ar-H), 7.91–7.85 (m, 4H, Ar-H), 7.75 (dd, J = 8.8 Hz, J = 1.6 Hz, 1H, Ar-H), 7.64–7.55 (m, 2H, Ar-H), 7.34–7.21 (m, 6H, Ar-H), 7.02 (brs, 1H, NH), 6.89 (dd, J = 8.4 Hz, J = 2.0 Hz, 1H, Ar-H), 6.76 (d, J = 7.6 Hz, 1H, Ar-H), 6.68 (s, 1H, Ar-H), 6.42 (d, J = 4.8 Hz, 1H, Ar-H), 6.17 (s, 1H, Ar-H), 4.87 (brs, 1H, NH), 3.65 (s, 3H, OCH₃), 3.34 (d, J = 4.4 Hz, 2H, NH–CH₂–), 3.14 (t, J = 5.2 Hz, 2H, –CH₂–NH–SO₂₎; ¹³C NMR (100 MHz, CDCl₃) δ 159.6, 158.4, 147.1, 142.1, 140.1, 139.5, 139.4, 136.8, 134.6, 132.1, 130.9, 129.8, 129.3, 129.1, 128.8, 128.6, 128.2, 127.8, 127.6, 127.4, 125.1, 122.7, 122.3, 119.9, 115.7, 114.7, 112.4, 105.9 (Ar-C), 55.2 (OCH₃), 44.3 (CH₂), 41.5 (CH₂); LC-MS(m/z) calculated for C₃₃H₂₉N₅O₃S: 575.20, found: 576.0 (M + 1)⁺.

N-(3-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2a)

White solid (60%); mp 119–20 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.98 (d, J = 12.0 Hz, 2H, Ar-H), 7.83 (d, J = 9.0 Hz, 2H, Ar-H), 7.52–7.45 (m, 3H, Ar-H), 7.31–7.24 (m, 6H, Ar-H), 6.93 (d, J = 6.0 Hz, 1H, Ar-H), 6.79 (d, J = 9.0 Hz, 1H, Ar-H), 6.71 (s, 1H, Ar-H), 6.45 (d, J = 3.0 Hz, 1H, Ar-H), 6.22 (s, 1H, Ar-H), 4.73 (brs, 1H, NH), 3.68 (s, 3H, OCH₃), 3.31 (brs, 2H, NH–CH₂–), 2.97 (brs, 2H, –CH₂–NH–SO₂), 1.67–1.58 (m, 2H, –CH₂–); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.7, 147.2, 142.1, 140.4, 140.1, 139.5, 139.3, 132.2, 131.0, 129.9, 128.9, 128.8, 127.6, 126.9, 125.1, 122.7, 120.0, 115.7, 114.8, 112.1, 105.7 (Ar-C), 55.3 (OCH₃), 40.1 (CH₂), 38.3 (CH₂), 29.9 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₉N₅O₃S: 539.20, found: 540.0 (M + 1)⁺.

4-Bromo-N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2b)

White solid (62%); mp 117–19 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.98 (s, 1H, Ar-H), 7.90 (d, J = 5.6 Hz, 1H, Ar-H), 7.69 (d, J = 8.8 Hz, 2H, Ar-H), 7.60 (d, J = 8.8 Hz, 2H, Ar-H), 7.35–7.20 (m, 6H, Ar-H), 6.95 (dd, J = 8.0, J = 2.0 Hz, 1H, Ar-H), 6.72 (t, J = 2.0 Hz, 1H, Ar-H), 6.49 (dd, J = 6.0 Hz, J = 1.6 Hz, 1H, Ar-H), 6.28 (s, 1H, Ar-H), 5.21 (brs, 1H, NH), 3.70 (s, 3H, OCH₃), 3.36 (q, J = 6.4 Hz, 2H, NH-CH₂-), 2.99 (d, J = 5.6 Hz, 2H, –CH₂NHSO₂), 1.68 (p, J = 6.4 Hz, 2H, CH₂–CH₂–CH₂); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.9, 147.3, 142.1, 140.2, 139.6, 139.4, 132.2, 131.0, 130.0, 128.8, 128.5, 127.6, 127.1, 125.1, 122.8, 120.0, 115.8, 114.8, 112.1, 105.9 (Ar-C), 55.3 (OCH₃), 40.2 (CH₂), 38.3(CH₂), 29.9(CH₂); LC-MS(m/z) calculated for C₃₀H₂₈BrN₅O₃S: 617.11, found: 618.00 (M + 1)⁺.

4-Chloro-N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2c)

White solid (62%); mp 98–100 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.95 (s, 1H, Ar-H), 7.93 (d, J = 5.2 Hz, 1H, Ar-H), 7.75 (d, J = 8.4 Hz, 2H, Ar-H), 7.42 (d, J = 8.4 Hz, 2H, Ar-H), 7.32–7.25 (m, 6H, Ar-H), 6.93 (dd, J = 8.0 Hz, J = 2.0 Hz, 1H, Ar-H), 6.79 (d, J = 7.6 Hz, 1H, Ar-H), 6.71 (s, 1H, Ar-H), 6.45 (d, J = 5.6 Hz, 1H, Ar-H), 6.25 (s, 1H, Ar-H), 4.84 (brs, 1H, NH), 3.68 (s, 3H, OCH₃), 3.34 (d, J = 5.6 Hz, 2H, NH–CH₂–), 2.90 (brs, 2H, –CH₂NHSO₂), 1.66 (t, J = 6.0 Hz, 2H, -CH₂-); ¹³C NMR (100 MHz, CDCl₃) δ 159.4, 158.4, 146.8, 142.8, 140.2, 139.3, 139.3, 138.9, 138.6, 130.9, 130.0, 129.5, 129.2, 128.8, 128.4, 127.6, 125.1, 122.7, 119.8, 115.7, 114.8, 112.0, 105.9 (Ar-C), 55.2 (OCH₃), 40.0 (CH₂), 38.2 (CH₂), 29.9 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₈ClN₅O₃S: 573.16, found: 574.0 (M + 1)⁺.

4-Fluoro-N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2d)

White solid (75%); mp 92–94 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.96 (s, 2H, Ar-H), 7.82 (d, J = 3.0 Hz, 2H, Ar-H), 7.32–7.28 (m, 6H, Ar-H), 7.14 (t, J = 9.0 Hz, 2H, Ar-H), 6.94 (d, J = 6.0 Hz, 1H, Ar-H), 6.80 (d, J = 6.0 Hz, 1H, Ar-H), 6.72 (s, 1H, ar-H), 6.46 (d, J = 6.0 Hz, 1H, Ar-H), 6.24 (s, 1H, Ar-H), 4.60 (brs, 1H, NH), 3.69 (s, 3H, OCH₃), 3.36 (s, 2H, NH–CH₂–), 2.98 (brs, 2H, –CH₂NHSO₂), 1.66 (d, J = 6.0 Hz, 2H, –CH₂–); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.7, 147.2, 140.1, 139.3, 131.0, 129.9, 129.6, 129.5, 128.8, 127.6, 125.1, 122.7, 119.9, 116.2, 115.9, 115.7, 114.8, 112.2, 106.0 (Ar-C), 55.2 (OCH₃), 40.0 (CH₂), 38.2 (CH₂), 30.0 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₈FN₅O₃S: 557.19, found: 558.0 (M + 1)⁺.

4-Methoxy-N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino) propyl)benzenesulfonamide (2e)

White solid (71%); mp 124–6 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.96 (s, 1H, Ar-H), 7.94 (d, J = 6.0 Hz, 1H, Ar-H), 7.76 (d, J = 9.0 Hz, 2H, Ar-H),7.33–7.24 (m, 6H, Ar-H), 6.93 (d, J = 9.0 Hz, 3H, Ar-H), 6.79 (d, J = 9.0 Hz, 1H, Ar-H), 6.71 (s, 1H, Ar-H), 6.54 (brs, 1H, NH), 6.45 (d, J = 3.0 Hz, 1H, Ar-H), 6.22 (s, 1H, Ar-H), 4.61 (brs, 1H, NH), 3.86 (s, 3H, OCH₃), 3.68 (s, 3H, OCH₃), 3.32 (t, J = 6.0 Hz, 2H, NH–CH₂–), 2.96 (t, J = 6.0 Hz, 2H, –CH₂NHSO₂), 1.65 (p, J = 6.0 Hz, 2H, –CH₂–); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.8, 147.5, 142.0, 140.1, 139.6, 139.4, 132.0, 131.1, 130.0, 128.8, 127.6, 125.1, 122.8, 120.1, 115.7, 114.8, 114.1, 112.2, 105.7(Ar-C), 55.6 (OCH₃), 55.3 (OCH₃), 40.2 (CH₂), 38.4(CH₂), 30.0 (CH₂); LC-MS(m/z) calculated for C₃₁H₃₁N₅O₃S: 569.21, found: 570.0 (M + 1)⁺.

N-(3-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)-4-methylbenzenesulfonamide (2f)

Buff solid (72%); mp 94–6 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.95 (s, 1H, Ar-H), 7.91 (d, J = 6.0 Hz, 1H, Ar-H), 7.71 (d, J = 9.0 Hz, 2H, Ar-H),7.30–7.24 (m, 7H, Ar-H), 6.92 (d, J = 6.0 Hz, 1H, Ar-H), 6.79 (d, J = 6.0 Hz, 1H, Ar-H), 6.71 (s, 1H, Ar-H), 6.44 (d, J = 6.0 Hz, 1H, Ar-H), 6.23 (s, 1H, Ar-H), 4.78 (brs, 1H, NH), 3.67 (s, 3H, OCH₃), 3.26 (brs, 2H, NH–CH₂–), 2.94 (d, J = 3.0 Hz, 2H, –CH₂NHSO₂), 2.60 (s, 3H, CH₃), 1.62 (d, J = 6.0 Hz, 2H, -CH₂-); ¹³C NMR (75 MHz, CDCl₃) δ 160.2, 159.3, 147.9, 143.5, 142.5, 140.6, 140.1, 139.9, 137.8, 131.5, 130.4, 130.1, 129.3, 128.1, 127.5, 125.6, 123.2, 120.6, 116.2, 115.3, 112.5, 106.1 (Ar-C), 55.8 (OCH₃), 40.7 (CH₂), 38.9 (CH₂), 30.2 (CH₂), 22.0 (CH₃); LC-MS(m/z) calculated for C₃₁H₃₁N₅O₄S: 553.21, found: 554.0 (M + 1)⁺.

N-(3-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)-4-(trifluoromethyl)benzenesulfonamide (2g)

White solid (32%); mp 150–2 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.84–7.81 (m, 4H, Ar-H), 7.61 (d, J = 6.0 Hz, 2H, Ar-H), 7.49 (brs, 1H, NH), 7.21–7.16 (m, 6H, Ar-H), 6.82 (d, J = 6.0 Hz, 1H, Ar-H), 6.68 (d, J = 5.4, 1H, Ar-H), 6.60 (s, 1H, Ar-H), 6.33 (d, J = 3.9 Hz, Ar-H), 6.14 (s, 1H, Ar-H), 4.52 (brs, 1H, NH), 3.56 (s, 3H, OCH₃), 3.26 (brs, 2H, NH–CH₂–), 2.89 (brs, 2H, CH₂NHSO₂), 1.95 (brs, 2H, -CH₂-); ¹³C NMR (75 MHz, CDCl₃) δ 159.7, 158.8, 147.1, 142.2, 140.1, 139.5, 139.3, 131.0, 129.9, 128.8, 127.6, 127.4, 126.1, 126.0, 125.1, 122.7, 119.9, 115.7, 114.8, 112.2, 106.1 (Ar-C), 55.2 (OCH₃), 40.1 (CH₂), 38.3 (CH₂), 30.1 (CH₂); LC-MS(m/z) calculated for C₃₁H₂₈ F₃N₅O₃S: 607.19, found: 608.0 (M + 1)⁺.

3-Fluoro-N-(3-((4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)benzenesulfonamide (2h)

White solid (36%); mp 120–2 °C; ¹H NMR (300 MHz, CDCl₃) δ 7.94 (s, 1H, Ar-H), 7.91 (d, J = 6.0 Hz, 1H, Ar-H), 7.30–7.22 (m, 10H, Ar-H), 6.93 (dd, J = 2.0 Hz, J = 6.0 Hz, 1H, Ar-H), 6.89 (d, J = 6.0 Hz, 1H, Ar-H), 6.70 (s, 1H, Ar-H), 6.44 (d, J = 6.0 Hz, 1H, Ar-H), 6.24 (s, 1H, Ar-H), 4.74 (s, 1H, NH) 3.67 (s, 3H, OCH₃), 3.31 (brs, 2H, NH–CH₂–), 2.98 (t, J = 6.0 Hz, 2H, CH₂NHSO₂), 1.65 (brs, 2H, –CH₂–); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.8, 147.2, 142.5, 140.1, 139.5, 139.3, 131.0, 130.8, 130.7, 129.9, 128.8, 127.6, 125.1, 122.7, 122.7, 120.0, 119.5, 119.2, 115.7, 114.8, 114.4, 114.1, 112.1, 105.9 (Ar-C), 55.2 (OCH₃), 40.1 (CH₂), 38.2(CH₂), 29.9 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₈ FN₅O₃S: 557.19, found: 558.0 (M + 1)⁺.

N-(3-((4-(3-(3-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) naphthalene-1-sulfonamide (2i)

White solid (66%); mp 134–6 °C; ¹H NMR (300 MHz, CDCl₃) δ 8.40 (s, 1H, Ar-H), 7.97–7.78 (m, 5H, Ar-H), 7.60 (d, J = 6.0 Hz, 2H, Ar-H), 730–7.22 (m, 6H, Ar-H), 6.91 (d, J = 9.0 Hz, 1H, Ar-H), 6.77 (d, J = 6.0 Hz, 1H, Ar-H), 6.70 (s, 1H, Ar-H), 6.45 (d, J = 6.0 Hz, 1H, Ar-H), 6.20 (s, 1H, Ar-H), 4.61 (s, 1H, NH) 3.65 (s, 3H, OCH₃), 3.31 (brs, 2H, NH–CH₂–), 3.00 (s, 2H, CH₂NHSO₂), 1.64 (brs, 2H, –CH₂–); ¹³C NMR (75 MHz, CDCl₃) δ 159.6, 158.8, 147.5, 142.0, 140.1, 139.6, 139.4, 137.2, 134.6, 132.1, 131.0, 129.9, 129.3, 129.1, 128.8, 128.5, 128.1, 127.8, 127.6, 127.4, 125.1, 122.7, 122.4, 120.0, 115.7, 114.8, 112.1, 105.8 (Ar-C), 55.2 (OCH₃), 40.1 (CH₂), 38.2 (CH₂), 29.9 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₈ FN₅O₃S: 589.21, found: 590.0 (M + 1)⁺.

General procedure for synthesis of N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)benzenesulfonamide (1j), N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)benzenesulfonamide (1k-q), N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)benzenesulfonamide (2j) and N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) (substituted)benzenesulfonamide (2k-q)

To a mixture of compound (1a–i) or (2a–i) (0.1 mmol) in methylene chloride (5 mL), BBr₃ (0.13 g, 1.0 mmol) was added dropwise at –78 °C under nitrogen, and the reaction mixture was stirred at 0 °C for 24 h. The mixture was quenched with saturated aqueous NaHCO₃. Ethyl acetate (10 mL) was added and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (3 × 10 mL). The combined organic layer extracts were washed with brine and dried over anhydrous Na₂SO₄. The organic solvent was evaporated under reduced pressure, and the residue was purified by column chromatography.

N-(2-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1j)

Light brown solid (36%); mp 100–2 °C; ¹H NMR (400 MHz,CD₃OD) δ 8.05 (s, 1H, Ar-H), 7.83 (d, J = 7.2 Hz, 2H, Ar-H), 7.76 (d, J = 5.6 Hz, 1H, Ar-H), 7.54–7.50 (m, 3H, Ar-H), 7.37–7.34 (m, 3H, Ar-H), 7.29–7.27 (m, 2H, Ar-H), 7.18 (t, J = 8.0 Hz, 1H, Ar-H), 6.84–6.81 (m, 1H, Ar-H), 6.67–6.64 (m, 2H, Ar-H), 6.46 (dd, J = 5.2 Hz, J = 1.2 Hz, 1H, Ar-H), 6.38 (s, 1H, Ar-H), 3.26 (t, J = 6.0 Hz, 2H, NH–CH₂–), 2.99 (t, J = 6.0 Hz, 2H, –CH₂NHSO₂), ¹³C NMR (100 MHz, CD₃OD) δ 158.6, 157.6, 149.5, 141.9, 140.3, 139.3, 138.9, 132.1, 130.7, 129.7, 128.7, 128.5, 127.7, 126.5, 121.2, 119.7, 116.8, 115.9, 112.3, 105.7 (Ar-C), 42.2 (CH₂), 40.9 (CH₂); LC-MS(m/z) calculated for C₂₈H₂₅N₅O₃S: 511.17, found: 512.0 (M + 1)⁺.

4-Bromo-N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1k)

Buff solid (30%); mp 178–80 °C; ¹H NMR (400 MHz,CDCl₃) δ 7.88 (s, 1H, Ar-H), 7.56 (d, J = 6.0 Hz, 3H, Ar-H), 7.42 (d, J = 8.1 Hz, 2H, Ar-H), 7.17–7.08 (m, 6H, Ar-H), 6.80 (d, J = 7.6 Hz, 1H, Ar-H), 6.64 (s, 1H, Ar-H), 6.58 (d, J = 7.1 Hz, 1H, Ar-H), 6.37 (d, J = 4.7 Hz, 1H, Ar-H), 6.17 (s, 1H, Ar-H), 5.08 (brs, 1H, NH), 3.13 (brs, 2H, NH–CH₂–), 2.93 (brs, 2H, –CH₂NHSO₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.0, 157.3, 146.6, 146.4, 142.4, 140.6, 139.1, 138.7, 132.3, 132.1, 130.7, 129.0, 128.5, 128.3, 127.4, 125.2, 124.9, 119.6, 117.4, 117.2, 116.2, 112.2, 105.4 (Ar-C), 42.9 (CH₂), 41.5 (CH₂); LC-MS(m/z) calculated for C₂₈H₂₄BrN₅O₃S: 589.17, found: 590.0 (M + 1)⁺.

4-Chloro-N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1l)

Light brown solid (41%); mp 100–2 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.05 (s, 1H, Ar-H), 7.78–7.74 (m, 3H, Ar-H), 7.47 (d, J = 8.8 Hz, 2H, Ar-H), 7.35–7.32 (m 3H, Ar-H), 7.28–7.27 (m, 2H, Ar-H), 7.18 (t, J = 8.0 Hz, 1H, Ar-H), 6.84–6.81 (m, 1H, Ar-H), 6.67 (s, 1H, Ar-H), 6.66 (t, J = 2.0 Hz, 1H, Ar-H), 6.47 (dd, J = 5.2 Hz, J = 1.2 Hz, 1H, Ar-H), 6.34 (s, 1H, Ar-H), 3.25 (t, J = 6.0 Hz, 2H, NH–CH₂–), 3.01 (t, J = 6.0 Hz, 2H, –CH₂NHSO₂), ¹³C NMR (100 MHz, CD₃OD) δ 158.5, 157.6, 146.5, 1141.9, 14.0.9, 139.3, 139.1, 138.9, 138.2, 130.7, 129.8, 129.2, 129.0, 128.9, 128.5, 128.2, 127.7, 126.2, 121.2, 119.7, 116.9, 115.9, 111.3, 105.6 (Ar-C), 42.2 (CH₂), 40.8(CH₂); LC-MS(m/z) calculated for C₂₈H₂₄ClN₅O₃S: 545.13, found: 546.0 (M + 1)⁺.

4-Fluoro-N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl) benzenesulfonamide (1m)

Light yellow solid (40.5%); mp 106–8 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.90 (s, 1H, Ar-H), 7.78–7.75 (m, 2H, Ar-H), 7.60 (d, J = 8.0 Hz, 1H, Ar-H), 7.20 (s, 5H, Ar-H), 7.12 (t, J = 8.0 Hz, 1H, Ar-H), 7.03 (t, J = 8.0 Hz, 2H, Ar-H), 6.83 (d, J = 8.0 Hz, 1H, Ar-H), 6.67 (s, 1H, Ar-H), 6.61 (d, J = 8.0 Hz, 1H, Ar-H), 6.40 (d, J = 8.0 Hz, 1H, Ar-H), 6.22 (s, 1H, Ar-H) 3.18 (s, 2H, NH–CH₂–), 2.97 (s, 2H, –CH₂NHSO₂), ¹³C NMR (100 MHz, CDCl₃) δ 166.1, 163.6, 158.1, 157.3, 146.6, 142.4, 140.6, 139.2, 135.7, 130.7, 130.2, 129.7, 129.6, 128.8, 127.8, 125.1, 121.7, 119.6, 116.7, 116.3, 116.1, 112.3, 105.5 (Ar-C), 42.9 (CH₂), 41.6 (CH₂); LC-MS(m/z) calculated for C₂₈H₂₄FN₅O₃S: 529.59, found: 530.0 (M + 1)⁺.

N-(2-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)-4-methylbenzenesulfonamide (1n)

Yellow solid (38%); mp 114–6 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.91 (s, 1H, Ar-H), 7.69 (d, J = 8.0 Hz, 3H, Ar-H), 7.29–7.21 (m, 6H, Ar-H), 7.15 (t, J = 8.0 Hz, 1H, Ar-H), 6.87 (d, J = 8.0 Hz, 1H, Ar-H), 6.72 (s, 1H, Ar-H), 6.61 (d, J = 8.0 Hz, 1H, Ar-H), 6.44 (s, 1H, Ar-H), 6.22 (s, 1H, Ar-H), 5.32 (brs, 1H, NH), 3.20 (brs, 2H, NH–CH₂–), 3.00–2.98 (m, 2H, –CH₂NHSO₂), 2.78 (s, 3H, CH₃); ¹³C NMR (100 MHz, CDCl₃) δ 158.2, 157.1, 146.7, 143.4, 142.4, 140.4, 139.3, 139.2, 136.7, 130.8, 130.2, 129.7, 128.8, 127.6, 127.0, 125.0, 121.8, 119.7, 116.8, 112.3, 105.6 (Ar-C), 42.9 (CH₂), 41.6 (CH₂), 21.0(CH₃); LC-MS(m/z) calculated for C₂₉H₂₉N₅O₃S: 525.59, found: 526.0 (M + 1)⁺.

N-(2-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)-4-(trifluoromethyl)benzenesulfonamide (1o)

White solid (40%); mp 138–40 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.86 (d, J = 9.0 Hz, 3H, Ar-H), 7.62–7.57 (m, 3H, Ar-H), 7.17 (s, 5H, Ar-H), 7.10 (t, J = 7.6 Hz, 1H, Ar-H), 6.80 (d, J = 7.1 Hz, 1H, Ar-H), 6.64 (s, 1H, Ar-H), 6.58 (d, J = 7.0 Hz, 1H, Ar-H), 6.38 (s, 1H, Ar-H), 5.32 (brs, 1H, NH), 3.20 (brs, 2H, NH–CH₂–), 3.00–2.98 (m, 2H, –CH₂NHSO₂), 2.78 (s, 3H, CH₃); LC-MS(m/z) calculated for C₂₉H₂₄F₃N₅O₃S: 579.59, found: 580.0 (M + 1)⁺.

3-Fluoro-N-(2-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino) ethyl)benzenesulfonamide (1p)

White solid (32%); mp 146–8 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.05 (s, 1H, Ar-H), 7.87 (d, J = 5.2 Hz, 1H, Ar-H), 7.64 (d, J = 7.6 Hz, 1H, Ar-H), 7.56–7.51 (m, 2H, Ar-H), 7.37–7.28 (m, 6H, Ar-H), 7.19 (t, J = 8.0 Hz, 1H, Ar-H), 6.82 (d, J = 8.0 Hz, 1H, Ar-H), 6.68–6.65 (m, 2H, Ar-H), 6.47 (d, J = 5.6 Hz, 1H, Ar-H), 6.37 (s, 1H, Ar-H), 3.27 (t, J = 5.2 Hz, 2H, NH–CH₂–), 3.02 (t, J = 6.0 Hz, 2H, -CH₂NHSO₂); ¹³C NMR (75 MHz, CD₃OD) δ 163.6, 161.1, 158.6, 157.6, 146.6, 142.6, 141.9, 139.3, 138.9, 130.8, 130.0, 130.7, 129.7, 128.5, 127.7, 125.2, 122.5, 121.1, 119.7, 119.1, 118.8, 116.8, 113.7, 113.5, 111.3, 105.7 (Ar-C), 42.2 (CH₂), 40.8 (CH₂); LC-MS(m/z) calculated for C₂₈H₂₄ FN₅O₃S: 529.16, found: 530.0 (M + 1)⁺.

N-(2-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl)naphthalene-1-sulfonamide (1q)

White solid (33%); mp 146–8 °C; ¹H NMR (400 MHz, CDCl₃) δ 8.37 (s, 1H, Ar-H), 7.87–7.73 (m, 5H, Ar-H), 7.61–7.51 (m, 3H, Ar-H), 7.22 (d, J = 4.0 Hz, 5H, Ar-H), 7.11 (t, J = 8.0 Hz, 1H, Ar-H), 6.84 (dd, J = 8.0 Hz, J = 4.0 Hz, 1H, Ar-H), 6.69 (t, J = 4.0 Hz, 1H, Ar-H), 6.58 (d, J = 8.0 Hz, 1H, Ar-H), 6.38 (dd, J = 8.0 Hz, J = 4.0 Hz, 1H, Ar-H), 6.15 (s, 1H, Ar-H), 5.03 (brs, 1H, NH), 3.19 (brs, 2H, NH–CH₂–), 3.02 (t, J = 8.0 Hz, 2H, –CH₂NHSO₂); ¹³C NMR (75 MHz, CDCl₃) δ 158.0, 157.2, 146.5, 142.4, 140.5, 139.2, 136.4, 134.7, 132.0, 130.7, 130.2, 129.4, 129.2, 128.8, 128.3, 127.8, 127.7, 127.4, 125.0, 122.1, 121.7, 119.6, 117.3, 116.8, 112.3, 105.5 (Ar-C), 43.0 (CH₂), 41.6 (CH₂); LC-MS(m/z) calculated for C₃₂H₂₇N₅O₃S: 561.66, found: 562.0 (M + 1)⁺.

N-(3-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2j)

White solid (37%); mp 154–6 °C; ¹H NMR (400 MHz, CDCl₃) δ 7.92 (s, 1H, Ar-H), 7.81–7.74 (m, 3H, Ar-H), 7.51 (d, J = 7.2 Hz, 1H, Ar-H), 7.44 (t, J = 7.6 Hz, 2H, Ar-H), 7.26 (s, 5H, Ar-H), 7.14 (t, J = 7.9 Hz, 1H, Ar-H), 6.87 (d, J = 7.88 Hz, 1H, Ar-H), 6.74 (s, 1H, Ar-H), 6.60 (d, J = 7.4 Hz, 1H, Ar-H), 6.51 (d, J = 5.3 Hz, 1H, Ar-H), 6.11(s, 1H, Ar-H), 4.83 (brs, 1H, NH), 3.06 (brs, 2H, NH–CH₂–), 2.88 (d, J = 5.8 Hz, 2H, –CH₂NHSO₂), 1.53 (p, J = 5.8 Hz, 2H, CH₂CH₂CH₂); LC-MS(m/z) calculated for C₂₉H₂₇N₅O₃S: 525.63, found: 526.0 (M + 1)⁺.

4-Bromo-N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)benzenesulfonamide (2k)

Light yellow solid (42%); mp 184–6 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.06 (s, 1H, Ar-H), 7.79 (d, J = 5.2 Hz, 1H, Ar-H), 7.80–7.67 (m, 4H, Ar-H), 7.37–7.34 (m, 3H, Ar-H), 7.29–7.27 (m, 2H, Ar-H), 7.19 (t, J = 8.4 Hz, 1H, Ar-H), 6.84–6.81 (m, 1H, Ar-H), 6.68 (s, 1H, Ar-H), 6.66 (s, 1H, Ar-H), 6.51 (dd, J = 5.6 Hz, J = 1.2 Hz, 1H, Ar-H), 6.34 (s, 1H, Ar-H), 3.14 (t, J = 8.0 Hz, 2H, NH–CH₂–), 2.93 (t, J = 8.0 Hz, 2H, –CH₂NHSO₂); 1.61 (d, J = 6.0 Hz, 2H, CH₂CH₂CH₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.9, 157.6, 146.6, 141.9, 140.9, 139.7, 139.3, 138.9, 132.0, 130.8, 129.8, 128.5, 128.3, 127.7, 126.6, 125.2, 121.2, 119.8, 116.8, 115.9, 110.9, 105.4 (Ar-C), 40.2 (CH₂), 38.1 (CH₂), 28.8 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆BrN₅O₃S: 604.10, found: 605.0 (M + 1)⁺.

4-Chloro-N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) benzenesulfonamide (2l)

White solid (52%); mp 166–8 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.06 (s, 1H, Ar-H), 7.87–7.75 (m, 3H, Ar-H), 7.60–7.46 (m, 2H, Ar-H), 7.36 (t, J = 5.8 Hz, 3H, Ar-H), 7.32–7.26 (m, 2H, Ar-H), 7.19 (t, J = 7.9 Hz, 1H, Ar-H), 6.83 (ddd, J = 8.3 Hz, 2.3 Hz, 0.8 Hz, 1H, Ar-H), 6.67 (t, J = 5.0 Hz, 2H, Ar-H), 6.51 (dd, J = 5.5 Hz, 1.4 Hz, 1H, Ar-H), 6.34 (s, 1H, Ar-H), 3.14 (t, J = 6.6 Hz, 2H, NH–CH₂-), 2.93 (t, J = 6.8 Hz, 2H, –CH₂NHSO₂), 1.61 (p, J = 6.7 Hz, 2H, CH₂CH₂CH₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.9, 157.6, 146.7, 141.9, 140.9, 139.3, 139.2, 138.9, 138.3, 130.8, 129.8, 129.0, 128.5, 128.2, 127.7, 125.2, 121.2, 119.8, 116.8, 115.9, 110.9, 105.4 (Ar-C), 40.2 (CH₂), 38.1 (CH₂), 28.8 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆ClN₅O₃S: 560.7, found: 561.0 (M + 1)⁺.

4-Fluoro-N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)benzenesulfonamide (2m)

White solid (45%); mp 144–6 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.06 (s, 1H, Ar-H), 7.98–7.86 (m, 2H, Ar-H), 7.80 (d, J = 5.5 Hz, 1H, Ar-H), 7.37 (d, J = 6.6 Hz, 3H, Ar-H), 7.33–7.24 (m, 4H, Ar-H), 7.20 (t, J = 7.8 Hz, 1H, Ar-H), 6.83 (d, J = 8.2 Hz, 1H, Ar-H), 6.67 (d, J = 8.4 Hz, 2H, Ar-H), 6.51 (d, J = 5.5 Hz, 1H, Ar-H), 6.35 (s, 1H, Ar-H), 3.15 (t, J = 6.6 Hz, 2H, NH–CH₂–), 2.92 (t, J = 6.7 Hz, 2H, –CH₂NHSO₂), 1.74–1.53 (m, 2H, CH₂CH₂CH₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.9, 157.6, 146.7, 141.9, 139.3, 138.8, 136.7, 130.8, 129.7, 129.5, 129.4, 128.5, 127.7, 125.2, 121.2, 119.8, 116.8, 115.9, 115.8, 115.6, 110.9, 105.4 (Ar-C), 40.2 (CH₂), 38.2 (CH₂), 28.8 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆FN₅O₃S: 543.17, found: 544.0 (M + 1)⁺.

N-(3-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)-4-methylbenzenesulfonamide (2n)

White solid (33%); mp 158–60 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.06 (s, 1H, Ar-H), 7.79 (d, J = 5.5 Hz, 1H, Ar-H), 7.72 (d, J = 8.3 Hz, 2H, Ar-H), 7.41–7.25 (m, 7H, Ar-H), 7.19 (t, J = 7.9 Hz, 1H, Ar-H), 6.83 (ddd, J = 8.3 Hz, 2.3 Hz, 1.0 Hz, 1H, Ar-H), 6.71–6.61 (m, 2H, Ar-H), 6.51 (dd, J = 5.5, 1.5 Hz, 1H, Ar-H), 6.34 (s, 1H, Ar-H), 3.13 (t, J = 6.7 Hz, 2H, NH–CH₂–), 2.89 (t, J = 6.8 Hz, 2H,–CH₂NHSO₂), 2.41 (s, 3H, CH₃), 1.60 (p, J = 6.7 Hz, 2H, CH₂CH₂CH₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.9, 157.6, 146.7, 143.1, 141.9, 140.9, 139.3, 138.9, 137.4, 130.8, 129.8, 129.3, 128.5, 127.7, 126.6, 125.2, 121.2, 119.8, 116.8, 115.9, 110.9, 105.4 (Ar-C), 40.2 (CH₂), 38.2 (CH₂), 28.9 (CH₂), 20.1 (CH₃); LC-MS(m/z) calculated for C₃₀H₂₉N₅O₃S: 539.20, found: 540.0 (M + 1)⁺.

N-(3-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl)-4-(trifluoromethyl)benzenesulfonamide (2o)

White solid (39%); mp 150–2 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.09–7.99 (m, 3H, Ar-H), 7.87 (d, J = 8.3 Hz, 2H, Ar-H), 7.80 (d, J = 5.5 Hz, 1H, Ar-H), 7.41–7.34 (m, 3H, Ar-H), 7.34–7.25 (m, 2H, Ar-H), 7.20 (t, J = 7.9 Hz, 1H, Ar-H), 6.83 (ddd, J = 8.3 Hz, 2.4 Hz, 0.9 Hz, 1H, Ar-H), 6.71–6.63 (m, 2H, Ar-H), 6.52 (dd, J = 5.6 Hz, 1.5 Hz, 1H, Ar-H), 6.36 (d, J = 6.0 Hz, 1H, Ar-H), 3.16 (t, J = 6.7 Hz, 2H, NH–CH₂–), 2.96 (t, J = 6.8 Hz, 2H, –CH₂NHSO₂), 1.64 (p, J = 6.7 Hz, 2H, CH₂CH₂CH₂); ¹³C NMR (100 MHz, CD₃OD) δ 158.8, 157.6, 146.5, 142.0, 140.9, 139.3, 138.8, 130.7, 129.7, 128.5, 127.7, 127.3, 125.9, 125.2, 121.2, 119.7, 116.8, 115.9, 110.9, 105.5, (Ar-H), 40.2 (CH₂), 38.1 (CH₂), 28.9 (CH₂); LC-MS(m/z) calculated for C₃₀H₂₆F₃N₅O₃S: 593.20 found: 594.0 (M + 1)⁺.

3-Fluoro-N-(3-((4-(3-(3-hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino) propyl) benzenesulfonamide (2p)

White solid (41%); mp 120–2 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.05 (s, 1H, Ar-H), 7.79 (d, J = 5.5 Hz, 1H, Ar-H), 7.67 (d, J = 7.9 Hz, 1H, Ar-H), 7.63–7.51 (m, 2H, Ar-H), 7.41–7.25 (m, 6H, Ar-H), 7.19 (t, J = 7.9 Hz, 1H, Ar-H), 6.87–6.79 (m, 1H, Ar-H), 6.67 (t, J = 4.2 Hz, 2H, Ar-H), 6.50 (dd, J = 5.5 Hz, 1.3 Hz, 1H, Ar-H), 6.36 (s, 1H, Ar-H), 3.15 (t, J = 6.7 Hz, 2H, NH–CH₂–), 2.93 (t, J = 6.8 Hz, 2H, –CH₂NHSO₂) , 1.63 (p, J = 6.7 Hz, 2H, CH₂CH₂CH₂), ¹³C NMR (100 MHz, CD₃OD) δ 163.7, 161.2, 158.8, 157.6, 146.5, 142.7, 141.9, 140.9, 139.3, 138.9, 130.9, 130.8, 130.8, 129.8, 128.5, 127.7, 125.2, 122.5, 122.5, 121.2, 119.8, 119.1, 118.9, 116.8, 115.9, 113.7, 113.5, 110.9, 105.5 (Ar-C), 40.2 (CH₂), 38.2 (CH₂), 28.9 (CH₂); LC-MS(m/z) calculated for C₂₉H₂₆FN₅O₃S: 543.17, found: 544.0 (M + 1)⁺.

N-(3-((4-(3-(3-Hydroxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)propyl) naphthalene-1-sulfonamide (2q)

White solid (40%); mp 168–70 °C; ¹H NMR (400 MHz, CD₃OD) δ 8.40 (s, 1H, Ar-H), 8.01 (s, 1H, Ar-H), 7.97 (d, J = 8.4 Hz, 2H, Ar-H), 7.92 (d, J = 8.0 Hz, 1H, Ar-H), 7.81 (dd, J = 8.8 Hz, 1.6 Hz, 1H, Ar-H), 7.73 (d, J = 5.2 Hz, 1H, Ar-H), 7.65–7.57 (m, 2H, Ar-H), 7.36–7.25 (m, 5H, Ar-H), 7.13 (t, J = 8.0 Hz, 1H, Ar-H), 6.79 (dd, J = 8.4 Hz, 2.0 Hz, 1H, Ar-H), 6.62 (s, 1H, Ar-H), 6.59 (d, J = 6.4 Hz, 1H, Ar-H), 6.46 (d, J = 4.8 Hz, 1H, Ar-H), 6.27 (s, 1H, Ar-H), 3.11 (t, J = 6.8 Hz, 2H), 2.94 (t, J = 6.8 Hz, 2H, Ar-H), 1.60 (t, J = 6.8 Hz, 2H, Ar-H); ¹³C NMR (100 MHz, CD₃OD) δ 158.7, 157.6, 146.4, 141.9, 140.9, 139.3, 138.9, 137.2, 134.7, 132.1, 130.7, 129.7, 129.1, 128.8, 128.5, 128.3, 127.7, 127.6, 127.5, 127.2, 125.2, 122.0, 121.2, 119.7, 116.8, 115.9, 110.9, 105.3 (Ar-C), 40.2 (CH₂), 38.2 (CH₂), 28.8 (CH₂); LC-MS(m/z) calculated for C₃₃H₂₉N₅O₃S: 575.20 found: 576.0 (M + 1)⁺.

Antiproliferative screening of the target compounds against NCI-55 cancer cell line panel

Screening against the cancer cell lines was carried out at the National Cancer Institute (NCI, Bethesda, Maryland, USA) applying the standard protocol of the NCI²².

In vitro kinase screening

To investigate the biological target of compound, Reaction Biology Corp. Kinase HotSpotSM service was used adopting standard assay protocol²³.

Plasma stability

About 10 µM of compound 2l was mixed with human plasma and rat plasma and the mixture was shaked at 37 °C for 30 min and 120 min. After each time interval, acetonitrile was added and the mixture was centrifugated (14000 rpm, 4 °C). The supernatant was injected into the LC-MS to detect the remaining amount of compound 2l.

hERG binding assay

hERG binding assay was performed using hERG Fluorescence Polarization Assay (Invitrogen: PV5365) assay kit and Synergy Neo (Biotek) and standard procedures were applied.

In vivo pharmacokinetic assay

Adult male rats (N = 3/group) were administered with compound 2l dissolved in distilled water (tween 80) at a single dose of 10 mg/kg by oral administration and 10 mg/mL by injection. Serum samples were collected each 30 min. The blood concentration of the test compounds was determined by LC-MS/MS (Agilent 1290 infinity II series equipped with on-line degasser, binary pump, thermostatted well-plate autosampler and column compartment, Waters Atlantis® HSS T3 (2.1 × 100 mm, 1.9 µm) column, and mobile phase linear gradient from 95% A (0.1% formic acid in water) /5% B (0.1% formic acid in acetonitrile) to 5% A/95% B, 6500+ QTRAP LC-MS/MS/MS system, Turbo Spray Ion Drive as ion source, and Carbamazepine as internal standard. Pharmacokinetic parameters were obtained by non-compartmental analysis of the plasma concentration–time profiles using KineticaTM 4.4.1 (Thermo Fisher Scientific, Inc., Woburn, MA, USA).

Result and discussion

Chemistry

Synthesis of the final compounds was achieved using the pathway illustrated in Scheme 1. Esterification of 3-methoxybenzoic acid (3) using methanol and Conc. sulphuric acid produced methyl 3-methoxybenzoate (4). Reaction of 4 with 2-bromo-4-methylpyridine in the presence of LiHMDS led to formation of 2-(2-bromopyridin-4-yl)-1-(3-methoxyphenyl)ethan-1-one (5). Compound 5 was refluxed with DMF-DMA to give (Z)-2-(2-bromopyridin-4-yl)-3-(dimethylamino)-1-(3-methoxyphenyl)prop-2-en-1-one (6), which further reacts with phenylhydrazine produced 2-bromo-4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridine (7). Compound 7 reacted with ethylenediamine or 1,3-propylenediamine to produce N¹-(4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)ethane-1,2-diamine (8) and N¹-(4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)propane-1,3-diamine (9). Reaction of compound 8 or 9 with the appropriate arylsulfonyl chloride in the presence of Et₃N afforded the first group of final compounds 1a–i and 2a–i which bears the m-methoxyphenyl group at position 3 of the pyrazole ring. Demethylation of compounds 1a–i and 2a–i using boron tribromide produced corresponding hydroxyl derivatives 1j–q and 2j–q. An alternative pathway was investigated to synthesize the final compounds starting from compound 7. Arylation of N-(2-aminoethyl)benzenesulfonamide (10) or N-(3-aminopropyl)benzenesulfonamide (11) with compound 7 in the presence of pyridine at 110 °C led to formation of compounds 1a–i and 2a–i (Scheme 2).

Scheme 1. Synthetic pathway for final target compounds 1a–q and 2a–q. Reagents and conditions: (i) H₂SO₄, CH₃OH, reflux, 8 h; (ii) 2-bromo-4-methylpyridine, LiHMDS, THF, –25 °C to rt, overnight; (iii) DMF-DMA, reflux, 18 h; (iv) phenylhydrazine, C₂H₅OH, rt, overnight; (v) 1,2-ethylenediamine or 1,3-propylenediamine, reflux, 8 h.; (vi) appropriate sulfonyl chloride, Et₃N, CH₂Cl₂, 0 °C, overnight; (vii) BBr₃, CH₂Cl₂, –78 °C; 0 °C, overnight.

Scheme 2. Alternative pathway for synthesis of compounds 1a–i and 2a–i. Reagents and conditions: (i) pyridine, 110 °C, overnight.

Biology

Antiproliferative activity of the target compounds

Single-dose testing

The final target compounds were submitted to the National Cancer Institute (NCI), Maryland, USA²³. Thirty-one compounds were selected to be tested over 60 cell lines at single dose 10 µM. The mean per cent inhibition of the tested compounds are presented in Tables 1 and 2.

Table 1. Structures of compounds 1a–i and 2a–i and their mean inhibition percentages in single-dose (10 μM) 60-cancer cell line screening.

Compound	n	Ar	Mean % inhibition

Table 2. Structures of compounds 1j–q and 2j–q and their mean inhibition percentages in single-dose (10 μM) 60-cancer cell line screening.

Compound	n	Ar	Mean % inhibition

The results in Table 1 represent the activity of methoxy compounds 1a–i and 2a–i. In general, the methoxy compounds have moderate activity over the cell line panel with the highest activity for compound bearing p-trifluoromethyl group and ethylene bridge 1g with per cent inhibition 92.80% followed by compound 2h with m-fluorobenzensulfonamide moiety and propylene linker and compound 2g having p-trifluoromethyl group and propylene spacer and mean inhibition percentages 76.81% and 76.53%, respectively. Compounds with ethylene bridge and electron-withdrawing group and moderate size such as the chloro derivative 1c possess mean per cent inhibition higher compared to one with electron-donating group (1e and 1f) and large electron-withdrawing group such as bromo derivative 1b. Regarding compounds with propylene bridge, compound without any substituents 2a was more active than corresponding one with both elctron withdrawing groups and electron donating one with exception of p-trifluoromethyl and m-fluoro (compounds 2g and 2h).

On the other side, all demethylated compounds 1j–p and 2j–p showed more than 50% per cent inhibition (Table 2). Compounds containing electron-withdrawing group at para position such as bromo (1k and 2k), chloro (1l and 2l), and fluoro (1 m and 2m) showed the highest per cent inhibition. Compounds with propylene bridge are more potent compared to compounds having ethylene bridge. The propylene bridge might be suitable for optimum fitting at the receptor site. The most potent compounds in this series were 2 l with mean per cent inhibition 97.80%, and 2k with mean per cent inhibition 90.64%. Target compounds with ethylene bridge and electron-withdrawing groups (1k–m) were equipotent to 2m with propylene bridge and p-fluoro electron-withdrawing group. The meta substitution at sulfonamide moiety was less active than para substitution, but more active than methoxy series (1a–i and 2a–1).

The detailed inhibitory effects of the most potent hydroxyl compounds 2k and 2l and their corresponding methoxy analogues 2b and 2c, and the most potent methoxy compound 2g against NCI-60 cell line panel are depicted in Figure 2. Compound 2g exhibited more than 100% inhibition over 13 cell lines and showed lethal effect on two cell lines belonging to colon cancer (Colo 205 and HT29) and melanoma (SK-MEL-5). Regarding compounds 2 b and 2k, the cellular activity of compound 2k is much greater than 2b. The maximum inhibition percentage of compound 2b was 83.30% over T-47D cell line, while compound 2k showed per cent inhibition over 100% against 13 cell lines and maximum inhibitions against Colo 205 (168%), HCC-116 (140%) [colon cancer cell lines], and SF-295 (147%) [CNS cancer cell line]. Compound 2c showed maximum activity 92.74% against SR leukaemia cell line and 88.66% against HT29 colon cancer cell line. Finally, compound 2l exhibited more than 100% against 24 cell lines and maximum activity against Colo 205, HCC-2998 [colon cancer cell lines], SF-295 [CNS cancer cell line], LOX IMVI, SK-MEL-28, and SK-MEL-5 [melanoma cell lines] with per cent inhibition 170.28%, 162.39%, 155.19%, 129.50%, 136.19%, and 156.35, respectively.

Figure 2. (A) Per cent inhibition of compound 2g over all cancer cell lines of the NCI panel; (B) per cent inhibition of compound 2c and 2l over all cancer cell lines of the NCI panel; (C) mean per cent inhibition of compound 2b and 2k over all cancer cell lines of the NCI panel. The compounds were tested at 10 µM concentration.

Five-dose results

Compounds 1c, 1g, 1k–m, 1o, 2g, 2 h, 2k–m, 2o, and 2q with the highest activity in single-dose tests were selected to be tested in a five-dose testing mode to determine their IC₅₀, TGI, and LD₅₀. The mean IC₅₀ of the selected compounds over different cancer subtypes are shown in Table 3. Compounds 1k, 2k, 2l, 2o, and 2q were more potent against leukaemia cell lines than sorafenib with mean IC₅₀ ranging from 1.44 µM to 2.11 µM. Regarding non-small cell lung cancer, compound 2k was the most potent compound with IC₅₀ 1.96 µM. Compounds 1k, 1m, 2k, 2l and 2o were more potent against colon cancer and CNS cancer cell line with IC₅₀ 1.48 µM for 2k against colon cancer and IC₅₀ 1.65 µM against CNS cell lines for 2l. All tested compounds were more active than sorafenib with IC₅₀ 1.62 µM for compound 2k. Compound 2l was the most potent compound against ovarian cancer with mean IC₅₀ of 2.09 µM. Compound 2k was the most potent compound against renal cancer cell lines, prostate cancer cell lines, and breast cancer cell lines with mean IC₅₀ 1.89, 2.03, and 1.11 µM, respectively.

Table 3. Mean ICs₅₀ of the most potent compounds and sorafenib over different cancer subtypes.

		Subpanel cancer cell lines^a
		I	II	III	IV	V	VI	VII	VIII	IX
Compound No.	1c	2.89	6.02	4.08	6.33	4.58	5.23	4.79	4.99	3.79
	1g	3.35	6.36	4.91	5.28	4.94	6.10	5.32	13.03	4.05
	1k	2.11	2.69	2.29	2.18	2.03	2.87	2.48	2.54	2.34
	1l	2.44	3.16	2.46	2.85	2.38	3.29	3.18	3.03	2.48
	1m	2.29	2.65	2.34	2.51	2.06	2.68	2.88	2.88	2.16
	1o	2.34	3.03	2.38	2.67	2.37	3.12	2.45	3.45	2.11
	2g	3.35	6.36	4.91	5.28	4.94	6.10	5.32	13.03	4.05
	2h	3.18	5.01	4.69	4.49	4.14	3.88	4.25	4.65	3.49
	2k	1.55	1.96	1.48	1.70	1.62	2.11	1.89	2.03	1.11
	2l	1.44	2.32	1.51	1.65	1.68	2.09	2.06	2.28	1.58
	2m	2.25	3.91	2.68	3.28	2.89	3.79	3.81	3.62	2.69
	2o	1.90	2.12	1.64	1.71	1.72	2.32	2.03	2.79	1.87
	2q	1.96	3.05	2.62	2.33	2.27	5.28	2.99	3.44	1.95
Sorafenib		2.23	2.11	2.35	2.51	8.57	2.77	2.89	3.16	2.15

Mean IC₅₀ values were calculated by dividing the summation of IC₅₀ values of the compound over cell lines of the same cancer type by the number of cell lines in the subpanel.

The bold values indicate more potent compared to the reference standard compound.

^a I: Leukaemia; II: non-small cell lung cancer; III: colon cancer; IV: CNS cancer; V: melanoma; VI: ovarian cancer; VII: renal cancer; VIII: prostate cancer; IX: breast cancer.

The activity of the most potent compounds 1c, 1g, 1k–m, 1o, 2g, 2h, 2k–m, 2o, and 2q against the most sensitive cell lines is represented in Table 4. Compounds 2k, 2l, 2o, and 2q were the most potent compounds against K-562 leukaemia cell line with IC₅₀ 0.44, 0.43, 0.61, and 0.92 µM, respectively. Compound 2o was the most potent compound against HOP-92 non-small cell lung cancer cell line with IC₅₀ 1.41 µM followed by compound 2l with IC₅₀ 1.52 µM and compound 2k with IC₅₀ 1.83μM. Compounds 2l, 2o, and 2k were most potent against HT-29 cell line. Compound 2k was the most potent compound against U251 CNS cancer cell line and OVCAR-4 ovarian cancer cell line with IC₅₀ 1.21 µM and 1.66 µM, respectively. On the other hand, compound 2l was the most potent compound against SK-Mel-5 [melanoma], A498 [renal], PC-3 [prostate], and MDA-MB-468 [breast] with an IC₅₀ values of 1.23, 0.33, 1.74, and 1.16 µM, respectively. In general, compounds having 3-hydroxyphenyl and propylene bridge were more potent than the corresponding derivatives with 3-methoxyphenyl and ethylene bridge. Also, compounds with electron-withdrawing group showed high potency than compounds with electron-donating group. Both chloro and bromo substituents were more potent than fluoro compounds.

Table 4. IC₅₀ values of the most potent compounds over the most sensitive cell lines from each cancer subpanel.

		Cancer cell lines^a
		K-562	HOP-92^b	HT-29^c	U251^d	SK-MEL-5^e	OVCAR-4^f	A498^g	PC-3^h	MDA-MB-468^i
Compound No.	1c	3.73	2.46	3.37	5.89	1.95	4.15	4.56	2.44	3.90
	1g	2.87	2.12	2.32	3.54	1.72	2.94	3.40	2.86	3.31
	1k	1.98	2.00	2.17	2.21	1.64	2.32	3.33	2.07	2.70
	1l	1.98	2.34	2.24	3.21	2.02	4.37	2.63	2.45	2.78
	1m	1.98	2.03	1.99	2.62	1.73	3.05	2.32	2.29	1.88
	1o	2.48	1.97	2.04	2.65	1.78	2.85	1.71	2.47	2.05
	2g	3.06	3.68	3.21	5.63	2.18	4.36	3.80	3.36	3.11
	2h	3.31	2.42	2.87	4.83	1.86	3.28	3.52	2.97	3.49
	2k	0.44	1.83	0.63	1.21	1.27	1.66	0.38	2.11	1.54
	2l	0.43	1.52	0.47	1.35	1.23	1.67	0.33	1.74	1.16
	2m	2.40	2.66	2.26	2.97	3.06	3.82	3.52	3.11	2.55
	2o	0.617	1.41	0.50	1.78	1.57	3.06	1.09	2.87	1.85
	2q	0.92	1.56	1.23	1.28	1.53	1.92	1.1	1.93	1.8
Sorafenib		3.16	1.85	2.51	2.51	1.25	3.16	2.51	2.51	1.99

^aLeukaemia cell line; ^bnon-small cell lung cancer cell line; ^ccolon cancer cell line; ^dCNS cancer cell line; ^emelanoma cell line; ^fovarian cancer cell line; ^grenal cancer cell line; ^hprostate cancer cell line; ⁱbreast cancer cell line.

The bold values indicate more potent compared to the reference standard compound.

In addition to IC₅₀, total growth inhibition (TGI) concentration and lethal dose 50 (LD₅₀) for the most potent compounds were determined (Table 5). The total growth inhibition in case of K-562 leukaemia cell line was ranging from 2.5 µM for compound 2l to 19 µM for compound 1g. For non-small cell lung cancer cell line HOP-92, compound 2o exerted the lowest TGI (3.6 µM) and LD₅₀ (9.7 µM). Compounds 2l and 2k exhibited TGI 4.7 and 7.5 µM, respectively. Compounds 2q and 2l were the most efficacious among this new series against HT-29 colon cancer cell line with TGI 1.7 µM for each of them and LD₅₀ 4.5 and 4.7 µM, respectively. Compounds 2o and 2l showed the highest efficacy against U251 CNS cancer cell line with TGI 3.2 and 3.4 µM, respectively, and LD₅₀ 8.1 and 8.8 µM, respectively. All the tested compounds except 2g and 2m exhibited significant one-digit micromolar TGI and LD₅₀ values against SK-MEL-5 melanoma cell line. Both compounds 2k and 2 l showed lethal dose 50 5.3 µM. Compound 2k had TGI of 2.6 µM, while compound 2l had TGI equal to 2.5 µM. Compound 2l was the most potent against OVCAR-4, A498, PC-3 and MDA-MB-468 with TGI 5.9, 2.2, 6.1, and 4.6 µM and LD₅₀ 6.9 µM for A498 cell line. Compound 2k was the second most potent compound against the same cell lines with TGI 8.6, 2.8, 7.8, and 5.6 µM and LD₅₀ 11.9 µM against A498 cell line.

Table 5. TGI and LD₅₀ values of the most potent compounds over the most sensitive cell lines from each cancer subpanel.

			Cancer cell lines^a
			K-562^a	HOP-92^b	HT-29^c	U251^d	SK-MEL-5^e	OVCAR-4^f	A498^g	PC-3^h	MDA-MB-468^i
Compound No.	1c	TGI	>100	9.4	11.3	>100	3.8	>100	>100	>100	>100
		LD50	>100	>100	>100	>100	7.7	>100	>100	>100	>100
	1g	TGI	19	6.8	5.7	13.9	3.1	>100	6.5	26.7	>100
		LD50	>100	>100	37.7	63.4	5.6	>100	>100	>100	>100
	1k	TGI	5.4	5.0	5.0	5.6	3.0	13.7	5.4	6.4	7.7
		LD50	>100	34.6	17.3	25.6	5.6	>100	34.3	>100	>100
	1l	TGI	5.4	8.3	5.2	11.4	4.0	>100	9.5	12.0	7.66
		LD50	>100	70.5	61.8	45.9	7.9	>100	57.1	>100	>100
	1m	TGI	>100	8.4	47.9	6.8	3.2	>100	9.2	10.2	5.3
		LD50	>100	68.8	54.3	50.9	6.0	>100	45.7	>100	>100
	1o	TGI	6.5	6.2	5.4	7.2	3.3	16.9	14.5	10.9	5.02
		LD50	>100	52.0	35.1	44.1	6.3	81.2	41.4	93.4	>100
	2g	TGI	>100	>100	10	>100	5.0	>100	>100	>100	>100
		LD50	>100	>100	>100	>100	23.1	>100	>100	>100	>100
	2h	TGI	>100	>100	18.8	>100	3.7	>100	>100	>100	30.4
		LD50	>100	>100	>100	>100	7.6	>100	>100	>100	>100
	2k	TGI	2.8	7.55	2.3	4.4	2.6	8.6	2.8	7.8	5.6
		LD50	>100	>100	7.1	19.9	5.3	>100	11.9	>100	>100
	2l	TGI	2.5	4.7	1.7	3.4	2.5	5.9	2.2	6.1	4.6
		LD50	>100	93.2	4.7	8.8	5.3	>100	6.9	>100	>100
	2m	TGI	6.3	7.6	6.4	10.3	10.1	4.8	9.8	8.5	6.7
		LD50	>100	84.2	47.8	69.5	33.0	>100	52.3	80.7	>100
	2o	TGI	5.3	3.6	3.1	3.2	2.9	5.1	2.6	4.5	5.5
		LD50	>100	9.7	8.1	8.1	5.6	>100	6.3	18.9	>100
	2q	TGI	4.4	7.2	1.7	13.2	3.4	>100	6.6	44.9	6.0
		LD50	>100	>100	4.5	41.3	7.4	>100	>100	>100	>100

^aLeukaemia cell line; ^bnon-small cell lung cancer cell line; ^ccolon cancer cell line; ^dCNS cancer cell line; ^emelanoma cell line; ^fovarian cancer cell line; ^grenal cancer cell line; ^hprostate cancer cell line; ⁱbreast cancer cell line.

Kinase profiling

In order to determine the molecular target(s) of the newly synthesized compounds, a panel of 20 kinases of different families was used. The inhibitory effects of compounds 1l, 2c, and 2l, which showed the strongest potencies against the NCI-60 cancer cell line panel, on different kinases are depicted in Table 6. It can be concluded that compound 2l had a strong activity against JNK1, JNK2, JNK3, P38a/MAPK14, and BRAF (V600E) with mean per cent inhibitions 99.02%, 98.47%, 89.50%, 86.54%, and 93.67%, respectively. Also, compound 2l showed a moderate activity against GSK3b and BRAF with mean per cent inhibitions 75.26% and 72.56%, respectively. On the other hand, compounds 1l and 2c showed moderate activity against JNK1, JNK2, and BRAF(V600E). The stronger kinase inhibitory effects of the hydroxyl compound 2l compared to the corresponding methoxy derivative 2c can be rationalized that the presence of hydrogen bond donor and the lower bulkiness of OH group may contribute to stronger affinity with the enzymes. Furthermore, the propylene linker of 2l seems to be more appropriate for activity than ethylene.

Table 6. Inhibitory effect of compounds 1l, 2c, and 2 l on different kinases activity at a single dose of 10 µM.

Kinase	Inhibition %
	1l	2c	2l
ABL1 (T315I)	6.39 ± 0.35%	4.53 ± 0.45%	–10.98 ± 0.40%
BRAF	21.28 ± 0.21%	20.87 ± 0.30%	72.56 ± 0.27%
BRAF (V599E)	48.09 ± 0.45%	44.20 ± 0.40%	93.67 ± 0.47%
CDK2/cyclin E	8.36 ± 0.95%	9.80 ± 1.01%	22.92 ± 1.14%
EGFR	10.33 ± 3.40%	9.20 ± 4.45%	11.74 ± 4.78%
ERK1	ND	ND	13.07 ± 0.93%
ERK2/MAPK1	ND	ND	22.21 ± 0.41%
FMS	ND	ND	24.24 ± 1.14%
GSK3b	15.88 ± 0.21%	49.31 ± 0.30%	75.45 ± 0.28%
IKKb/IKBKB	7.80 ± 0.10%	7.79 ± 0.15%	−2.94 ± 0.17%
JNK1	53.79 ± 0.04%	69.19 ± 0.02%	99.05 ± 0.03%
JNK2	44.68 ± 0.01%	59.68 ± 0.01%	98.49 ± 0.02%
JNK3	35.70 ± 0.04%	24.23 ± 0.03%	89.50 ± 0.03%
KDR/VEGFR2	ND	ND	10.05 ± 0.10%
MEK1	ND	ND	0.56 ± 1.08%
MEK2	ND	ND	11.73 ± 1.60%
MKK6	ND	ND	16.65 ± 0.11%
mTOR/FRAP1	ND	ND	0.72 ± 0.32%
P38a/MAPK14	68.43 ± 0.59%	65.73 ± 0.66%	86.54 ± 0.61%
ROS/ROS1	ND	3.40 ± 0.39%	24.03 ± 0.51%

ND: not determined.

ICs₅₀ of compound 2l against its target enzymes are tabulated in Table 7. Compound 2l exhibited an IC₅₀ 0.35 µM over JNK1 and 0.36 µM over JNK2. JNK kinases are hyperactivated in different types of cancer such as leukaemia, lung cancer, skin cancer, glioblastoma and other brain tumours, and breast cancer. JNK kinases induce tumorigenesis through induction of cell proliferation and survival, and their inhibition is a potential avenue for cancer therapy²⁴. So inhibition of JNK1 and JNK2 kinases could be, at least partially, a possible mechanism of antiproliferative activity of compound 2l.

Table 7. IC₅₀ of compound 2l against BRAF, BRAF(V600E), JNK1, JNK2, P38a/MAPK14 and RAF1.

Compound	BRAF	BRAF(V600E)	JNK1	JNK2	MAPK14	RAF1
2l	4.87 ± 0.07	1.16 ± 0.04	0.35 ± 0.04	0.36 ± 0.07	1.13 ± 0.09	3.52 ± 0.01

Plasma stability

The plasma stability test for compound 2l revealed that compound 2l has high stability profile in both human and rat plasma. After 30 min, 100% of compound 2 l remained unchanged which decreased to 95.3% after 2 h, while that of procaine was 1.2% after 30 min and 0.2% after 2 h and the percentage for diltiazem was 91.5% after 30 min and 89.3% after 2 h (Table 8).

Table 8. Plasma stability of compound 2l.

Compound	Human		Rat
	30 min	120 min	30 min	120 min
2l	100%	95.3%	100%	100%
Procaine	1.2%	0.2%	89.9%	42.7%
Diltiazem	91.5%	89.3%	86.3%	45.4%

hERG binding assay.

One of the most important features to be investigated during drug development is the ability of the compound to bind to the human ether-a-go-go related gene (hERG). The inhibition of hERG can lead to sudden death and should be avoided during drug discovery²⁵. Compound 2l was tested for its ability to inhibit hERG and the IC₅₀ was 8.28 µM which is fifteen times greater than its IC₅₀ against the most sensitive cell line. So the compound has high safety and selectivity index, and low risk of sudden death induction.

In vivo pharmacokinetic

Compound 2 l was the most potent compound against both in vitro cell line assay and enzyme activity. The human plasma stability is excellent compared to standard reference compounds. The in vivo pharmacokinetic profile following oral or intravenous administration, and oral bioavilability of 2 l are represented in Table 9 and Figure 3.

Figure 3. Plasma concentration-time curves of 2l in rats following iv (10 mg/kg) or oral (10 mg/kg) administration.

Table 9. PK Parameters of 2l in SD Rats (N = 3).

PK parameter	2l (IV, 10 mg /kg)			2l (PO, 10 mg /kg)
	Mean	SD	N	Mean	SD	N
Dose (mg/kg)	10		3	10		3
Tmax (hr)	NA			0.5	0.0	3
Cmax (ng/ml)	NA			36.6	4.9	3
AUClast (ng.hr/ml)	1471.6	156.2	3	136.0	46.7	3
AUCinf (ng.hr/ml)	1478.2	157.3	3	142.1	44.8	3
CL (L/hr/kg)	6.8	0.8	3	NA
t1/2 (hr)	5.8	1.0	3	6.1	2.2	3
F (%)	NA			9.2	3.2	3

Conclusion

In the current work, design and synthesis of a new N-(2-((4-(3-(3-methoxy and/or hydroxyl)phenyl)-1-phenyl-1H-pyrazol-4-yl)pyridin-2-yl)amino)ethyl and/or propyl) substituted benzene sulfonamides 1a–q and 2a–q were accomplished. The antiprolifertave activity of the new synthesized compounds revealed that compounds having propyl bridge between the pyridine ring and sulfonamide moiety 2a–q were more potent compared to compounds having ethylene bridge 1a–q. In addition, compounds possessing m-hydroxyl group at ring A were more potent than their methoxy analogues with an exception of compounds 2g and 2h which carry out terminal p-triflouromethyl sulfonamide and m-fluoro sulfonamide moieties which showed excellent activity compared to other methoxy compounds. Compounds with electron-withdrawing groups such as chloro 2l and bromo 2k presented the highest per cent inhibition among the newly synthesized compounds and lowest IC₅₀ 0.33 µM against A498 renal cancer cell line for compound 2l. Compound 2l significantly inhibited the activity of JNK1, JNK2, JNK3, V600E BRAF, and P38 alpha with IC₅₀ 0.35 and 0.36 µM against JNK1 and JNK2. Moreover, compound 2l exhibited high plasma stability in both human and rat. Compound 2l had 9.2% oral bioavailability with t_1/2 ranging from 5.8 h for intravenously administrated to 6.1 h for orally administrated doses.

Acknowledgements

The authors are thankful to Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea, for financially supporting this work (KIST Project 2E26900). We would like to thank the National Cancer Institute (NCI), Bethesda, Maryland, USA, for performing the in vitro anticancer testing over the cell lines.

Disclosure statement

No potential conflict of interest was reported by the authors.