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Article

Utility of 3-Acetyl-6-bromo-2H-chromen-2-one for the Synthesis of New Heterocycles as Potential Antiproliferative Agents

by
Sobhi M. Gomha
1,
Yasser H. Zaki
2 and
Abdou O. Abdelhamid
1,*
1
Department of Chemistry, Faculty of Science, Cairo University, Giza 12613, Egypt
2
Department of Chemistry, Faculty of Science, Beni-Suef University, Beni-Suef 62514, Egypt
*
Author to whom correspondence should be addressed.
Molecules 2015, 20(12), 21826-21839; https://doi.org/10.3390/molecules201219803
Submission received: 27 August 2015 / Revised: 25 November 2015 / Accepted: 26 November 2015 / Published: 4 December 2015
(This article belongs to the Collection Heterocyclic Compounds)
Browse Figures
Versions Notes

Abstract

:
Coumarin derivatives containing pyrazolo[1,5-a]pyrimidine, tetrazolo[1,5-a]pyrimidine, imidazo[1,2-a]pyrimidine, pyrazolo[3,4-d]pyrimidine, 1,3,4-thiadiazoles and thiazoles were synthesized from 6-bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one, methyl 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine carbodithioate, 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine carbothioamide and each of heterocyclic amine, hydrazonoyl chlorides and hydroximoyl chlorides. The structures of the newly synthesized compounds were elucidated on the basis of elemental analysis, spectral data, and alternative synthetic routes whenever possible. Moreover, selected newly synthesized products were evaluated for their antitumor activity against a liver carcinoma cancer cell line (HEPG2-1). The results revealed that pyrazolo[1,5-a]pyrimidine 7c, thiazole 23g and 1,3,4-thiadiazole 18a (IC50 = 2.70 ± 0.28, 3.50 ± 0.23 and 4.90 ± 0.69 µM, respectively) have promising antitumor activity against liver carcinoma (HEPG2-1) while most of the tested compounds showed moderate activity.

Graphical Abstract

1. Introduction

The synthesis of coumarins and their derivatives has attracted considerable attention from organic and medicinal chemists for many years as a large number of natural and synthetic products contain this heterocyclic nucleus. Coumarins possess diverse pharmacological and biological activities such as antitumor [1], analgesic and ulcerogenic [2], anti-inflammatory [3], anticoagulant [4], phototriggering [5], and fungicidal [6] properties, and can act as anticoagulants in the production of pesticides [7]. In particular, the antitumor activity of coumarin compounds has received considerable attention among researchers because of their cytotoxic activity against numerous types of cancers, including malignant melanoma, leukemia, renal cell carcinoma, prostate and breast cancer cell progression [8,9,10]. Also, certain platinum (II) complexes of aminocoumarins show very good in vitro cytotoxicity [11]. A variety of mechanisms have been proposed, such as interfering with estrogen synthesis, interfering with cell cycle progression or even acting as inhibitors of cytochrome P450 1 [12]. Despite numerous attempts to search for more effective antitumor agents, coumarins still a highly versatile class of compounds against cancer cell lines and are an important component among the molecules in drug discovery. The antitumor activities of coumarin were tested in several human tumor cell lines by Steffen et al. [13]. Both compounds inhibited cell proliferation of gastric carcinoma cell line (HSC-39), colon carcinoma cell line (Caco-2), hepatoma-derived cell line (Hep-G2) and lymphoblastic cell line (CCRF). Egan et al. [14] have synthesized, characterized and determined cytostatic and cytotoxic nature of 8-nitro-7-hydroxycoumarin using both human (including K-562 and HL-60) and animal cell lines grown in vitro. Warfarin reduces metastases from intestinal carcinomas to a great extent [15] and is also used as an adjunct to the surgical treatment of malignant tumors [16]. In addition, daphnetin inhibits tyrosine kinase, epidermal growth factor receptor, serine/threonine-specific protein kinase, and protein kinase C in vitro [17]. On the other hand, thiazole [18], 1,3,4-thiadiazole [19], azolo[1,5-a]pyrimidine [20], coumarin [21] derivatives displayed significant antitumor, cytotoxic, antiinflammatory, anticoagulant, antioxidant, antifungal, antitubercular, anticonvulsant, antimicrobial, antiviral, neuroprotective and diuretic activities. In continuation of our research program on the synthesis of novel heterocyclic compounds exhibiting antitumor activities [22,23,24,25,26], we attempted to design pyrazolo[1,5-a]pyrimidine, tetrazolo[1,5-a]-pyrimidine, imidazo[1,2-a]pyrimidine, pyrazolo[3,4-d]pyridazine, thiazoles, and thiadiazoles linked to position 3 of coumarin as a novel 3-heteroarylcoumarins, which have not been reported hitherto, to evaluate their in vitro antitumor activity against a liver carcinoma cell line (HEPG2-1).

2. Results and Discussion

2.1. Chemistry

Treatment of 3-acetyl-6-bromo-2H-chromen-2-one (1) [27] with each of N,N-dimethylformamide-dimethylacetal in boiling xylene and methyl hydrazinecarbodithioate in 2-propanol at room temperature yielded 6-bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one (2) and methyl 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)-hydrazine-1-carbodithioate (3), respectively, in good yield (Scheme 1).
Molecules 20 19803 g001 550
Scheme 1. Synthesis of 6-bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one (2) and methyl 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine-1-carbodithioate (3).
Scheme 1. Synthesis of 6-bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one (2) and methyl 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine-1-carbodithioate (3).
Molecules 20 19803 g001
The structures of 2 and 3 were elucidated on the basis of elemental analysis, spectral data and chemical transformation. Thus, treatment of 2 with the appropriate 3-amino-1,2,4-triazole (4a), 5-amino-tetrazole (4b), 3-amino-5-phenylpyrazole (4c), 2-aminobenzimidazole (4d) or 4,6-dimethyl-1H-pyrazolo[3,4-b]pyridin-3-amine (4e) in acetic acid under reflux gave 3-([1,2,4]triazolo[1,5-a]pyrimidin-7-yl)-6-bromo-2H-chromen-2-one (8a), 6-bromo-3-(tetrazolo[1,5-a]pyrimidin-7-yl)-2H-chromen-2-one (8b), 6-bromo-3-(2-phenylpyrazolo[1,5-a]pyrimidin-7-yl)-2H-chromen-2-one (8c), 3-(benzo[4,5]imidazo[1,2-a]pyrimidin-4-yl)-6-bromo-2H-chromen-2-one (8d), and 6-bromo-3-(8,10-dimethylpyrido[2′,3′:3,4]pyrazolo[1,5-a]pyrimidin-4-yl)-2H-chromen-2-one (8e), respectively (Scheme 2). Structures 8a-e were confirmed on basis of elemental analysis and spectral data.
Analogously, compound 2 was reacted with hydrazine hydrate and phenylhydrazine in ethanol to give 6-bromo-3-(1H-pyrazol-3-yl)-2H-chromen-2-one (8a) and 6-bromo-3-(1-phenyl-1H-pyrazol-3-yl)-2H-chromen-2-one (8b), respectively (Scheme 3).
Compound 2 was also reacted with 2-oxo-N-phenyl-2-(phenylamino)acetohydrazonoyl chloride (9a) in boiling benzene containing triethylamine to afford either 5-(6-bromo-2-oxo-2H-chromene-3-carbonyl)-N,1-diphenyl-1H-pyrazole-3-carboxamide (11a) or 4-(6-bromo-2-oxo-2H-chromene-3-carbonyl)-N,1-diphenyl-1H-pyrazole-3-carboxamide (12a) (Scheme 4). The structure of the product was elucidated on the basis of elemental analysis, spectral data and chemical transformation. The 1H-NMR spectrum showed at δ = 7.13–7.73 (m, 12H, Ar-H), 8.17 (s, 1H, Ar-H5), 8.40 (s, 1H, pyrazole-H), 8.54 (1H, (s, 1H, Ar-H4), 12.05 (s, D2O-exchangeable, 1H, NH). The product was reacted with hydrazine hydrate in boiling ethanol to give 4-(6-bromo-2-oxo-2H-chromen-3-yl)-2-phenyl-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one (14). Based on the above results the product was formulated as 4-(6-bromo-2-oxo-2H-chromene-3-carbonyl)-N,1-diphenyl-1H-pyrazole-3-carboxamide (12a) and structure 11a was ruled out. Similarly, compound 2 was reacted with 9b, 10a and 10b to afford 3-(3-benzoyl-1-phenyl-1H-pyrazole-4-carbonyl)-6-bromo-2H-chromen-2-one (12b), 3-(3-benzoylisoxazole-4-carbonyl)-6-bromo-2H-chromen-2-one (13a) and 3-(3-(2-naphthoyl)isoxazole-4-carbonyl)-6-bromo-2H-chromen-2-one (13b).
Molecules 20 19803 g002 550
Scheme 2. Synthesis of azolo[1,5-a]pyrimidine and imidazo[1,2-a]pyrimidine derivatives 7a–e.
Scheme 2. Synthesis of azolo[1,5-a]pyrimidine and imidazo[1,2-a]pyrimidine derivatives 7a–e.
Molecules 20 19803 g002
Molecules 20 19803 g003 550
Scheme 3. Synthesis of pyrazoles 8a and 8b.
Scheme 3. Synthesis of pyrazoles 8a and 8b.
Molecules 20 19803 g003
Molecules 20 19803 g004 550
Scheme 4. Synthesis of pyrazoles 12a,b, isoxazoles 13a,b and pyrazolo[3,4-d]pyridazone 14.
Scheme 4. Synthesis of pyrazoles 12a,b, isoxazoles 13a,b and pyrazolo[3,4-d]pyridazone 14.
Molecules 20 19803 g004
Next, C-ethoxycarbonyl-N-phenylhydrazonoyl chloride (9c) was reacted with methyl 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazine-1-carbodithioate (3) in ethanol containing triethylamine to afford ethyl 5-((1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazono)-4-phenyl-4,5-dihydro-1,3,4-thiadiazole-2-carboxylate (18c) (Scheme 5).
Molecules 20 19803 g005 550
Scheme 5. Synthesis of 1,3,4-thiadiazoles 18a–h.
Scheme 5. Synthesis of 1,3,4-thiadiazoles 18a–h.
Molecules 20 19803 g005
Structure 18c was established by elemental analysis, spectral data, and alternative synthesis. Thus, ethyl 2-hydrazono-3-phenyl-1,3,4-thidiazoline-5-carboxylate [28] (19) reacted with 1 in ethanol to give a product identical in all aspects (m.p., mixed m.p. and spectra) with 18c. Similarly, the appropriate 9a,b,d–h was reacted with the appropriate 3 in ethanolic triethylamine to afford 2,3-dihydro-1,3,4-thiadiazoles 18a,b,d–h, respectively.
In the light of foregoing results, the mechanism outlined in Scheme 6 seems to be the most plausible pathway for the formation of 18 in the reaction of 3 with 9. The reaction involves initial formation of thiohydrazonate 16, which undergoes intramolecular cyclization as soon as it is formed to yield the intermediate 17 or undergoes 1,3-dipolar cycloaddition of nitrilimine 15 (generated in situ from 9 with triethylamine) to the C=S double bond of 3. Compound 17 was converted to 18 by elimination of methyl mercaptan.
Molecules 20 19803 g006 550
Scheme 6. Mechanism of 1,3,4-thiadiazoles 18a–h.
Scheme 6. Mechanism of 1,3,4-thiadiazoles 18a–h.
Molecules 20 19803 g006
Reaction of 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine-1-carbothioamide [29] (20) with hydrazonoyl chloride 9f–n in ethanol under reflux gave the corresponding thiazole derivatives 23a–i, respectively, in good yield (Scheme 7). The structures 23a–i were confirmed by elemental analysis and spectral data.
Molecules 20 19803 g007 550
Scheme 7. Synthesis of thiazoles 23a–i.
Scheme 7. Synthesis of thiazoles 23a–i.
Molecules 20 19803 g007

2.2. Antitumor Activity: Cytotoxicity against a Human Liver Carcinoma Cell Line (HEPG2-1)

The cytotoxic activity of 15 of the new compounds was determined against the liver carcinoma cell line HEPG2-1, using doxorubicin as a reference drug. Data generated were used to plot a dose-response curve of which the concentration (µM) of test compounds required to kill 50% of the cell population (IC50) was determined. Cytotoxic activity was expressed as the mean IC50 of three independent experiments (Table 1). The results revealed that the descending order of activity of the newly synthesized compounds was as follows: 7c > 23g > 18a > 12a > 23c > 8a > 7b > 7e > 18f > 7a > 7d > 23d > 12b > 18c > 13a.
The pyrazolo[1,5-a]pyrimidine 7c, thiazole 23g and 1,3,4-thiadiazole 18a (IC50 = 2.70, 3.50 and 4.90 µM, respectively) have promising antitumor activity against liver carcinoma (HEPG2-1) while the rest compounds have moderate activities (IC50 = 8.20 ± 1.54 − 17.4 ± 1.03 µM). On the other hand, isoxazole 13a has poor inhibitory activity against (HEPG2-1) (IC50 = 15.3 ± 1.69 µM).
Table
Table 1. Cytotoxic activities of tested compounds against liver carcinoma cell line (HEPG2-1).
Table 1. Cytotoxic activities of tested compounds against liver carcinoma cell line (HEPG2-1).
Compound No.IC50 (µM)Compound No.IC50 (µM)
Doxorubicin1.40 ± 0.2612b17.1 ± 2.28
7a14.2 ± 1.43 13a15.3 ± 1.69
7b10.0 ± 0.97 18c17.4 ± 1.03
7c2.70 ± 0.2818f13.0 ± 1.20
7d14.6 ± 0.5918a4.90 ± 0.69
7e12.8 ± 0.85 23c9.10 ± 1.29
8a9.80 ± 1.36 23d15.5 ± 1.49
12a8.20 ± 1.54 23g3.50 ± 0.23
Examination of the SAR leads to the following conclusions:
-
Among the fused pyrimidine derivatives, pyrazolo[1,5-a]pyrimidine 7c is the most active one (IC50 = 2.70 ± 0.28 µM).
-
Pyrazole derivative 12a (substituted with CONHPh group at position 3) has in vitro inhibitory activity more than pyrazole derivative 12b (substituted with Ph group at position 3)
-
For 1,3,4-thiadiazole derivatives 18a, 18c and 18f, compound 18a (IC50 = 4.90 ± 0.69 µM) (with a chlorine atom as electron-withdrawing group on the aryl moiety) has promising antitumor activity while the other 1,3,4-thiadiazole derivatives 18c and 18f have moderate activities (IC50 = 17.4 ± 1.03 and 13.0 ± 1.20 µM, respectively).
-
Among thiazole derivatives 23c, 23d and 23g, compound 23g (IC50 = 3.50 ± 0.23 µM) (with a chlorine atom as electron-withdrawing group on the aryl moiety) has promising antitumor activity, while the other thiazole derivatives 23c and 23d have moderate activities (IC50 = 9.10 ± 1.29 and 15.5 ± 1.49 µM, respectively).

3. Experimental Protocols

3.1. General Information

Melting points were measured on an Electrothermal IA 9000 series digital melting point apparatus (Bibby Sci. Lim. Stone, Staffordshire, UK). IR spectra were recorded in potassium bromide discs on Shimadzu FTIR 8101 PC infrared spectrophotometer (Shimadzu, Tokyo, Japan). The 1H- and 13C-NMR spectra were recorded on a Varian 6 Mercury VX-300 NMR spectrometer (Varian, Inc., Karlsruhe, Germany). 1H-NMR (300 MHz) and 13C-NMR spectra were recorded on a BRUKER spectrometer (Bruker BioSpin GmbH, Rheinstetten, Germany) in DMSO-d6 and chemical shifts are expressed in ppm units using TMS as an internal reference. Mass spectra were recorded on a Shimadzu (Tokyo, Japan) GCMS-QP1000 EX mass spectrometer at 70 eV. Elemental analyses were measured by using a German made Elementar Vario EL III CHNS analyzer (GmbH & Co. KG, Hanau, Germany). Antitumor activity was evaluated at the Regional Center for Mycology and Biotechnology at Al-Azhar University, Cairo, Egypt. Hydrazonoyl halides 9a–n [30,31,32,33,34] were prepared as reported in the literature.

3.2. Chemistry

3.2.1. Synthesis of 6-Bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one (2)

A mixture of the 3-acetyl-6-bromo-2H-chromen-2-one (1, 2.67 g, 10 mmol) and N,N-dimethylformamide dimethyl acetal (DMF-DMA, 1.19 g, 10 mmol) in dry xylene (30 mL) was refluxed for 3 h, then allowed to cool. The solid product was collected by filtration, washed with petroleum ether (60/80 °C), dried and crystallized from ethanol to afford compound 3 as a pale yellow solid in 80% yield; mp 203–205 °C; IR (KBr) ν (cm−1): 3111, 3073, 3019 (=C–H), 2902 (–C–H), 1727, 1639 (2C=O), 1605 (C=N); 1H-NMR (DMSO-d6) δ: 2.86 (s, 3H, CH3), 3.14 (s, 3H, CH3), 5.83 (1H, d, J = 12.4 Hz, CH=CHCO), 7.37 (d, 1H, J = 9 Hz, Ar-H8), 7.72 (d, 1H, J = 9 Hz, Ar-H7), 7.79 (s, 1H, Ar-H5), 8.11 (d, 1H, J = 12.4 Hz, CH=CHCO), 8.38 (s, 1H, Ar-H4); MS m/z (%): 321, 323 (M+, M + 2, 37). Anal. Calcd for C14H12BrNO3 (322.15): C, 52.20; H, 3.75; N, 4.35. Found: C, 52.12; H, 3.68; N, 4.31.

3.2.2. Synthesis of Methyl 2-(1-(6-Bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazine carbodithioate (3)

To a solution of 3-acetyl-6-bromo-2H-chromen-2-one (1, 2.67 g, 10 mmol) in 2-propanol (20 mL), methyl hydrazinecarbodithioate 2 (1.22 g, 10 mmol) was added. The mixture was stirred at room temperature for 2 h. The solid product was filtered off, recrystallized from ethanol to afford 3 as a yellow solid in 72% yield; mp 187–189 °C; IR (KBr) ν (cm−1): 3337 (NH), 3092, 3066, 3041 (=C–H), 2980 (–C–H), 1735 (C=O), 1605 (C=N); 1H-NMR (DMSO-d6) δ: 2.49 (s, 3H, CH3), 2.58 (s, 3H, CH3), 3.30 (1H, s, NH), 7.40 (d, 1H, J = 9 Hz, Ar-H8), 7.85 (d, 1H, J = 9 Hz, Ar-H7), 8.18 (s, 1H, Ar-H5), 8.57 (s, 1H, Ar-H4); MS m/z (%): 370, 372 (M+, M + 2, 64). Anal. Calcd for C13H11BrN2O2S2 (371.27): C, 42.06; H, 2.99; N, 7.55; Found C, 42.01; H, 2.86; N, 7.49.

3.2.3. Reactions of Enaminone 2 with Heterocyclic Amines 4a–e

A mixture of enaminone 2 (0.322 g, 1 mmol) and 3-amino-1,3,4-triazole (4a), 5-aminotetrazole (4b), 3-amino-5-phenylpyrazole (4c), 2-aminobenzimidazole (4d), and 4,6-dimethyl-1H-pyrazolo[3,4-b]-pyridin-3-amine (4e) (1 mmol) in acetic acid (15 mL) was refluxed for 6–8 h. The reaction mixture was cooled and diluted with MeOH and the solid product was collected by filtration and recrystallized from dioxane to give 7a–e, respectively.
3-([1,2,4]Triazolo[1,5-a]pyrimidin-7-yl)-6-bromo-2H-chromen-2-one (7a): Brown solid, 69% yield, mp 275–278 °C; IR (KBr) ν (cm−1): 3097, 3055 (=C–H), 2960 (–C–H), 1726 (C=O), 1597 (C=N); 1H-NMR (DMSO-d6) δ: 7.37 (d, 1H, J = 9 Hz, Ar-H8), 7.72 (d, 1H, J = 9 Hz, Ar-H7), 7.79 (s, 1H, Ar-H5), 8.04 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.15 (s, 1H, Ar-H4), 8.57 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.71 (1H, s, triazole-H); 13C-NMR (DMSO-d6): δ 105.2, 112.7, 117.3, 119.4, 122.0, 130.2, 134.6, 136.8, 150.2, 152.5, 153.4, 155.8, 156.7, 164.0; MS m/z (%): 342, 344 (M+, M + 2, 83). Anal. Calcd for C14H7BrN4O2 (343.13): C, 49.00; H, 2.06; N, 16.33. Found: C, 48.88; H, 2.01; N, 16.24. 1H-, 13C-NMR Spectrum is in Supplementary Materials.
6-Bromo-3-(tetrazolo[1,5-a]pyrimidin-7-yl)-2H-chromen-2-one (7b): Brown solid, 66% yield, mp 252–254 °C; IR (KBr) ν (cm−1): 3075 (=C–H), 2922 (–C–H), 1730 (C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 7.32 (d, 1H, J = 9.3 Hz, Ar-H8), 7.74 (d, 1H, J = 9.3 Hz, Ar-H7), 7.77 (s, 1H, Ar-H5), 8.06 (1H, d, J = 4.6 Hz, pyrimidine-H), 8.10 (s, 1H, Ar-H4), 8.53 (1H, d, J = 4.6 Hz, pyrimidine-H); MS m/z (%): 343, 345 (M+, M + 2, 82). Anal. Calcd for C13H6BrN5O2 (344.12): C, 45.37; H, 1.76; N, 20.35. Found: C, 45.32; H, 1.59; N, 20.28.
6-Bromo-3-(2-phenylpyrazolo[1,5-a]pyrimidin-7-yl)-2H-chromen-2-one (7c): Brown solid, 68% yield, mp 203–205 °C; IR (KBr) ν (cm−1): 3140, 3068 (=C–H), 2919 (–C–H), 1734 (C=O), 1598 (C=N); 1H-NMR (DMSO-d6) δ: 7.34–7.56 (m, 6H, Ar-H), 7.72 (d, 1H, J = 9.2 Hz, Ar-H7), 7.91 (s, 1H, Ar-H5), 8.08 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.18 (s, 1H, Ar-H4), 8.65 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.86 (s, 1H, pyrazole-H); MS m/z (%): 417, 419 (M+, M + 2, 24). Anal. Calcd for C21H12BrN3O2 (418.24): C, 60.31; H, 2.89; N, 10.05. Found: C, 60.23; H, 2.75; N, 10.01.
3-(Benzo[4,5]imidazo[1,2-a]pyrimidin-4-yl)-6-bromo-2H-chromen-2-one (7d): Yellow solid, 74% yield, mp 283–285 °C; IR (KBr) ν (cm−1): 3090, 3047 (=C–H), 2932 (–C–H), 1729 (C=O), 1607 (C=N); 1H-NMR (DMSO-d6) δ: 7.07–7.90 (m, 6H, Ar-H), 8.12 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.34 (s, 1H, Ar-H5), 8.48 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.63 (1H, (s, 1H, Ar-H4); MS m/z (%): 391, 393 (M+, M + 2, 100). Anal. Calcd for C19H10BrN3O2 (392.21): C, 58.18; H, 2.57; N, 10.71. Found: C, 58.12; H, 2.46; N, 10.53.
6-Bromo-3-(8,10-dimethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidin-4-yl)-2H-chromen-2-one (7e): Brown solid, 69% yield, mp 252–254 °C; IR (KBr) ν (cm−1): 3092, 3056 (=C–H), 2930 (–C–H), 1731 (C=O), 1601 (C=N); 1H-NMR (DMSO-d6) δ: 2.60 (s, 3H, CH3), 2.89 (s, 3H, CH3), 7.08 (s, 1H, pyridine-H), 7.54 (d, 1H, J = 9.2 Hz, Ar-H8), 7.82 (d, 1H, J = 9.2 Hz, Ar-H7), 7.94 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.17 (s, 1H, Ar-H5), 8.85 (1H, d, J = 4.5 Hz, pyrimidine-H), 8.91 (s, 1H, Ar-H4); 13C-NMR (DMSO-d6): δ 18.5, 20.5, 101.4, 110.2, 112.4, 116.8, 117.8, 118.5, 118.9, 119.4, 121.9, 128.5, 134.1, 135.2, 150.2, 150.9, 153.3, 155.3, 156.3, 165.2; MS m/z (%): 420, 422 (M+, M + 2, 96). Anal. Calcd for C20H13BrN4O2 (421.25): C, 57.02; H, 3.11; N, 13.30. Found: C, 57.14; H, 3.06; N, 13.24.

3.2.4. Reactions of Enaminone 2 with Hydrazines

To a solution of the enaminone 2 (0.322 g, 1 mmol) in EtOH (10 mL) was added hydrazine hydrate (1 mL, 99%, 20 mmol) or phenylhydrazine (1 mL, 10 mmol) and the mixture was heated under reflux for 2 h. The reaction mixture was acidified with cold HCl and the formed product was filtered and crystallized from ethanol to give the respective pyrazoles 8a and 8b.
6-Bromo-3-(1H-pyrazol-3-yl)-2H-chromen-2-one (8a): White solid, 78% yield, mp 217–219 °C; IR (KBr) ν (cm−1): 3286 (NH), 3127, 3091, 3051 (=C–H), 2928 (–C–H), 1730 (C=O), 1597 (C=N); 1H-NMR (DMSO-d6) δ: 6.74 (d, 1H, J = 7.6 Hz, pyrazole-H4), 7.34–7.43 (m, 2H, Ar-H), 7.77 (d, 1H, J = 7.5 Hz, pyrazole-H5), 7.96 (s, 1H, Ar-H5), 8.12 (s, 1H, Ar-H4), 11.42 (s, D2O-exchangeable, 1H, NH); 13C-NMR (DMSO-d6): δ 110.4, 118.3, 120.4, 123.5, 127.4, 129.1, 130.8, 134.7, 140.0, 142.5, 152.3 (Ar-C), 157.4 (C=O); MS m/z (%): 290, 292 (M+, M + 2, 100). Anal. Calcd for C12H7BrN2O2 (291.10): C, 49.51; H, 2.42; N, 9.62. Found: C, 49.48; H, 2.41; N, 9.47.
6-Bromo-3-(1-phenyl-1H-pyrazol-3-yl)-2H-chromen-2-one (8b): white solid, 69% yield, mp 246–248 °C; IR (KBr) ν (cm−1): 3043, 3058 (=C–H), 2908 (–C–H), 1728 (C=O), 1597 (C=N); 1H-NMR (DMSO-d6) δ: 6.70 (d, 1H, J = 7.6 Hz, pyrazole-H4), 7.14–7.69 (m, 7H, Ar-H), 7.95 (d, 1H, J = 7.6 Hz, pyrazole-H5), 8.16 (s, 1H, Ar-H5), 8.36 (s, 1H, Ar-H4); MS m/z (%): 366, 368 (M+, M + 2, 100). Anal. Calcd for C18H11BrN2O2 (367.20): C, 58.88; H, 3.02; N, 7.63. Found: C, 58.64; H, 3.01; N, 7.48.

3.2.5. Reactions of Enaminone 2 with Hydrazonoyl Chlorides 9a, 9b and Hydroximoyl Chlorides 10a, 10b

To a stirred solution of enaminone 2 (0.322 g, 1 mmol) and the appropriate hydrazonoyl chloride 9a or 9b or hydroximoyl chlorides 10a or 10b (1 mmol) in dry benzene (15 mL), an equivalent amount of triethylamine (0.15 mL 1 mmol) was added. The reaction mixture was heated under reflux for 4–6 h. The precipitated triethylamine hydrochloride was filtered off, and the filtrate was evaporated under reduced pressure. The residue was triturated with MeOH. The solid product, so formed in each case, was collected by filtration, washed with water, dried, and crystallized from EtOH to afford the corresponding pyrazole 12a, 12b and isoxazole derivatives 13a, 13b, respectively. The synthesized products together with their physical and spectral data are listed below.
4-(6-Bromo-2-oxo-2H-chromene-3-carbonyl)-N,1-diphenyl-1H-pyrazole-3-carboxamide (12a): Brown solid, 67% yield, mp 223–225 °C; IR (KBr) ν (cm−1): 3412 (NH), 3111, 3073, 3018 (=C–H), 2903 (–C–H), 1728, 1682, 1640 (3 C=O), 1601 (C=N); 1H-NMR (DMSO-d6) δ: 7.13–7.73 (m, 12H, Ar-H), 8.17 (s, 1H, Ar-H5), 8.40 (s, 1H, pyrazole-H), 8.54 (s, 1H, Ar-H4), 12.05 (s, D2O-exchangeable, 1H, NH); 13C-NMR (DMSO-d6): δ 117.2, 117.6, 118.2, 123.8, 124.7, 129.3, 130.5, 131.1, 134.4, 135.9, 139.5, 140.2, 142.3, 145.7, 154.2, 156.1, 157.4, 175.6; MS m/z (%): 513, 515 (M+, M + 2, 60). Anal. Calcd for C26H16BrN3O4 (514.33): C, 60.72; H, 3.14; N, 8.17. Found: C, 60.59; H, 3.11; N, 8.04.
6-Bromo-3-(1,3-diphenyl-1H-pyrazole-4-carbonyl)-2H-chromen-2-one (12b): Yellow solid, 69% yield, mp 192–194 °C; IR (KBr) ν (cm−1): 3111, 3073, 3018 (=C–H), 2902 (–C–H), 1727, 1640 (2 C=O), 1601 (C=N); 1H-NMR (DMSO-d6) δ: 7.18–7.69 (m, 12H, Ar-H), 8.15 (s, 1H, Ar-H5), 8.36 (s,1H, pyrazole-H), 8.47 (s, 1H, Ar-H4); MS m/z (%): 470, 472 (M+, M + 2, 83). Anal. Calcd for C25H15BrN2O3 (471.30): C, 63.71; H, 3.21; N, 5.94. Found: C, 63.64; H, 3.18; N, 5.79.
3-(3-Benzoylisoxazole-4-carbonyl)-6-bromo-2H-chromen-2-one (13a): Yellow solid, 66% yield, mp 262–264 °C; IR (KBr) ν (cm−1): 3111, 3072, 3018 (=C–H), 2902 (–C–H), 1729, 1640 (2 C=O), 1601 (C=N); 1H-NMR (DMSO-d6) δ: 7.14–7.64 (m, 7H, Ar-H), 8.17 (s, 1H, Ar-H5), 8.38 (s, 1H, Ar-H4), 8.61 (s,1H, isoxazole-H); MS m/z (%): 423, 425 (M+, M+2, 100). Anal. Calcd for C20H10BrNO5 (424.20): C, 56.63; H, 2.38; N, 3.30. Found: C, 56.69; H, 2.24; N, 3.16.
3-(3-(2-Naphthoyl)isoxazole-4-carbonyl)-6-bromo-2H-chromen-2-one (13b): Yellow solid, 74% yield, mp 186–188 °C; IR (KBr) ν (cm−1): 3110, 3073, 3020 (=C–H), 2915 (–C–H), 1728, 1673, 1639 (3 C=O), 1601 (C=N); 1H-NMR (DMSO-d6) δ: 7.27–8.18 (m, 10H, Ar-H), 8.42 (s, 1H, Ar-H4), 8.63 (s,1H, isoxazole-H); 13C-NMR (DMSO-d6): δ 116.5, 117.2, 118.4, 119.3, 119.8, 126.4, 127.8, 129.2, 129.7, 131.2, 132.5, 133.6, 134.2, 134.4, 134.7, 145.7, 153.2, 154.7, 158.6, 177.6, 187.4, 188.5; MS m/z (%): 473, 475 (M+, M + 2, 37). Anal. Calcd for C24H12BrNO5 (474.26): C, 60.78; H, 2.55; N, 2.95. Found: C, 60.49; H, 2.52; N, 2.76.

3.2.6. Reaction of pyrazole 12a with hydrazine hydrate

Hydrazine hydrate (80%, 2 mL) was added to a solution of the compound 12a (1 mmol) in EtOH (10 mL). The reaction mixture was heated under reflux for 2 h, concentrated under vacuum, and diluted with water. The precipitate obtained was filtered off, washed with ice-cold water, dried and crystallized from EtOH to afford the pyrazolo[3,4-d]pyridazine 14 as yellow crystals in 70% yield; mp 280–282 °C; IR (KBr) ν (cm−1): 3346 (NH), 3110, 3054, 3020 (=C–H), 2921 (–C–H), 1728, 1653 (2C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 7.06–7.69 (m, 7H, Ar-H), 8.15 (s, 1H, Ar-H5), 8.38 (s, 1H, pyrazole-H), 8.59 (1H, (s, 1H, Ar-H4), 11.08 (s, 1H, D2O-exchangeable, NH); MS m/z (%): 434, 436 (M+, M + 2, 100). Anal. Calcd for C20H11BrN4O3 (435.23): C, 55.19; H, 2.55; N, 12.87. Found: C, 55.19; H, 2.55; N, 12.87.

3.2.7. General Procedure for Synthesis of 1,3,4-Thiadiazole Derivatives 18a–h

To a mixture of alkyl carbodithioate 3 (0.371 g, 1 mmol) and the appropriate hydrazonoyl halides 9a–h (1 mmol) in ethanol (20 mL), triethylamine (0.5 mL) was added, the mixture was stirred at room temperature for 3 h. The resulting solid was collected and recrystallized from N,N-dimethylformamide to give the corresponding 1,3,4-thiadiazolines 18a–h. The products 18a–h together with their physical constants are listed below.
5-((1-(6-Bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazono)-N,4-diphenyl-4,5-dihydro-1,3,4-thiadiazole-2-carboxamide (18a). Pale yellow solid, 75% yield, mp 173–175 °C; IR (KBr) ν (cm−1): 3427 (NH), 3041 (=C–H), 2921 (–C–H), 1735, 1674 (2C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 3.27 (s, 3H, CH3), 7.35 (d, 1H, J = 9.2 Hz, Ar-H8), 7.40–7.80 (m, 10H, Ar-H), 7.85 (d, 1H, J = 9.2 Hz, Ar-H7), 8.19 (s, 1H, Ar-H5), 8.58 (s, 1H, Ar-H4), 11.84 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 559, 561 (M+, M + 2, 64). Anal. calcd for C26H18BrN5O3S (560.42): C, 55.72; H, 3.24; N, 12.50; found: C, 55.72; H, 3.24; N, 12.50.
6-Bromo-3-(1-((3,5-diphenyl-1,3,4-thiadiazol-2(3H)-ylidene)hydrazono)ethyl)-2H-chromen-2-one (18b). Yellow solid, 73% yield, mp 273–275 °C; IR (KBr) ν (cm−1): 3092, 3065, 3041 (=C–H), 2979, 2921 (–C–H), 1735, 1674 (2C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 3.27 (s, 3H, CH3), 7.08–7.83 (m, 12H, Ar-H), 8.19 (s, 1H, Ar-H5), 8.58 (s, 1H, Ar-H4); MS, m/z (%) 516, 518 (M+, M + 2, 52). Anal. calcd for C25H17BrN4O2S (517.40): C, 58.03; H, 3.31; 10.83; found: C, 58.01; H, 3.26; 10.67.
Ethyl 5-((1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazono)-4-phenyl-4,5-dihydro-1,3,4-thiadiazole-2-carboxylate (18c). Yellow solid, 69% yield, mp 176–178 °C; IR (KBr) ν (cm−1): 3092, 3066, 3041 (=C–H), 2979, 2921 (–C–H), 1734, 1674 (C=O), 1505 (C=N); 1H-NMR (DMSO-d6) δ: 1.31 (t, 3H, J = 6.9 Hz, CH2CH3), 3.29 (s, 3H, CH3), 4.30 (q, 2H, J = 6.9Hz, CH2CH3), 7.40 (d, 1H, J = 9.1 Hz, Ar-H8), 7.43–7.67 (m, 5H, Ar-H), 7.84 (d, 1H, J = 9.1 Hz, Ar-H7), 8.18 (s, 1H, Ar-H5), 8.57 (s, 1H, Ar-H4); 13C-NMR (DMSO-d6): δ 13.5, 15.1, 61.8, 118.6, 119.4, 120.6, 122.6, 125.7, 127.2, 127.6, 128.4, 132.5, 135.4, 144.7, 146.3, 152.1, 153.7, 154.5, 160.2, 161.7; MS, m/z (%) 512, 514 (M+, M + 2, 73). Anal. calcd for C22H18BrN4O4S (513.36): C, 51.47; H, 3.34; N, 10.91; found: C, 51.47; H, 3.34; N, 10.91.
Ethyl 5-((1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazono)-4-(p-tolyl)-4,5-dihydro-1,3,4-thiadiazole-2-carboxylate (18d). Yellow solid, 69% yield, mp 192–194 °C; IR (KBr) ν (cm−1): 3039 (=C–H), 2918 (–C–H), 1735, 1673 (2C=O), 1603 (C=N); 1H-NMR (DMSO-d6) δ: 1.29 (t, 3H, J = 6.9Hz, CH2CH3), 2.34 (s, 3H, CH3), 3.28 (s, 3H, CH3), 4.33 (q, 2H, J = 6.9Hz, CH2CH3), 7.41 (d, 1H, J = 9.1 Hz, Ar-H8), 7.46–7.66 (m, 4H, Ar-H), 7.83 (d, 1H, J = 9.1 Hz, Ar-H7), 8.18 (s, 1H, Ar-H5), 8.59 (s, 1H, Ar-H4); MS, m/z (%) 526, 528 (M+, M + 2, 20). Anal. calcd for C23H19BrN4O4S (527.39): C, 52.38; H, 3.63; N, 10.62; found: C, 52.26; H, 3.60; N, 10.51.
Ethyl 5-((1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene)hydrazono)-4-(4-chlorophenyl)-4,5-dihydro-1,3,4-thiadiazole-2-carboxylate (18e). Yellow solid, 73% yield, mp 216–218 °C; IR (KBr) ν (cm−1): 3074 (=C–H), 2932 (–C–H), 1734, 1673 (2C=O), 1605 (C=N); 1H-NMR (DMSO-d6) δ: 1.33 (t, 3H, J = 6.9Hz, CH2CH3), 3.22 (s, 3H, CH3), 4.34 (q, 2H, J = 6.9Hz, CH2CH3), 7.41 (d, 1H, J = 9.1 Hz, Ar-H8), 7.43–7.66 (m, 4H, Ar-H), 7.85 (d, 1H, J = 9.1 Hz, Ar-H7), 8.20 (s, 1H, Ar-H5), 8.59 (s, 1H, Ar-H4); MS, m/z (%) 546, 548 (M+, M + 2, 20). Anal. calcd for C22H16BrClN4O4S (547.81): C, 48.23; H, 2.94; N, 10.23; found: C, 48.15; H, 2.84; N, 10.17.
3-(1-((5-Acetyl-3-phenyl-1,3,4-thiadiazol-2(3H)-ylidene)hydrazono)ethyl)-6-bromo-2H-chromen-2-one (18f). Yellow solid, 73% yield, mp 228–230 °C; IR (KBr) ν (cm−1): 3092, 3066, 3041 (=C–H), 2979, 2921 (–C–H), 1734, 1674 (2C=O), 1505 (C=N); 1H-NMR (DMSO-d6) δ: 2.49 (s, 3H, CH3), 3.29 (s, 3H, CH3), 7.39 (d, 1H, J = 9.1 Hz, Ar-H8), 7.43–7.74 (m, 5H, Ar-H), 7.83 (d, 1H, J = 9.1 Hz, Ar-H7), 8.17 (s, 1H, Ar-H5), 8.56 (s, 1H, Ar-H4); MS, m/z (%) 482, 484 (M+, M+2, 63). Anal. calcd for C21H15BrN4O3S (483.34): C, 52.18; H, 3.13; N, 11.59; found: C, 52.12; H, 3.11; N, 11.46.
3-(1-((5-Acetyl-3-(p-tolyl)-1,3,4-thiadiazol-2(3H)-ylidene)hydrazono)ethyl)-6-bromo-2H-chromen-2-one (18g). Yellow solid, 69% yield, mp 182–184 °C; IR (KBr) ν (cm−1): 3093, 3068, 3041 (=C–H), 2979, 2921 (–C–H), 1734, 1674 (2C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 2.28 (s, 3H, CH3), 2.49 (s, 3H, CH3), 3.26 (s, 3H, CH3), 7.39 (d, 1H, J = 9.1 Hz, Ar-H8), 7.42–7.68 (m, 4H, Ar-H), 7.84 (d, 1H, J = 9.1 Hz, Ar-H7), 8.19 (s, 1H, Ar-H5), 8.56 (s, 1H, Ar-H4); MS, m/z (%) 496 , 498 (M+, M + 2, 100). Anal. calcd for C22H17BrN4O3S (497.36): C, 53.13; H, 3.45; N, 11.26; found: C, 53.05; H, 3.42; N, 11.18.
3-(1-((5-Acetyl-3-(4-chlorophenyl)-1,3,4-thiadiazol-2(3H)-ylidene)hydrazono)ethyl)-6-bromo-2H-chromen-2-one (18h). Yellow solid, 69% yield, mp 182–184 °C; IR (KBr) ν (cm−1): 3093, 3067, 3041 (=C–H), 2978, 2921 (–C–H), 1734, 1674 (2C=O), 1606 (C=N); 1H-NMR (DMSO-d6) δ: 2.49 (s, 3H, CH3), 3.26 (s, 3H, CH3), 7.41 (d, 1H, J = 9.1 Hz, Ar-H8), 7.47–7.68 (m, 4H, Ar-H), 7.85 (d, 1H, J = 9.1 Hz, Ar-H7), 8.20 (s, 1H, Ar-H5), 8.56 (s, 1H, Ar-H4); MS, m/z (%) 517, 519 (M+, M + 2, 100). Anal. calcd for C21H14BrClN4O3S (517.78): C, 48.71; H, 2.73; N, 10.82; found: C, 48.68; H, 2.59; N, 10.69.

3.2.8. Alternative Synthesis of 18c

To a solution of 3-acetyl-6-bromo-2H-chromen-2-one (1, 0.265 g, l mmol) in 2-propanol (10 mL), ethyl 5-hydrazono-4-phenyl-4,5-dihydro-1,3,4-thiadiazole-2-carboxylate (19, 0.264 g, 1 mmol) was added. The mixture was refluxed for 2 h then cooled to room temperature. The solid precipitated was filtered off, washed with water, dried and recrystallized from dimethylformamide to give the corresponding product, 18c which were identical in all aspects (m.p., mixed m.p. and IR spectra) with those obtained from reaction of 3 with 9c but in 69% yield.

3.2.9. General Procedure for the Synthesis of 1,3-Thiazole Derivatives 23a–i

A mixture of thiosemicarbazone 20 (0.338 g, 1 mmol) and the appropriate hydrazonoyl halides 9n–f (1 mmol) in dioxane (20 mL) containing TEA (0.07 mL) was refluxed for 6 h, allowed to cool and the solid formed was filtered off, washed with EtOH, dried and recrystallized from DMF to give the corresponding thiazoles 23a–i. The products 23a–i together with their physical constants are listed below.
6-Bromo-3-(1-(2-(4-methyl-5-(phenyldiazenyl)thiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23a). Red solid, 69% yield, mp 164–166 °C; IR (KBr) ν (cm−1): 3431 (NH), 3041 (=C–H), 2922 (–C–H), 1734 (C=O), 1600 (C=N); 1H-NMR (DMSO-d6) δ: 2.12 (s, 3H, CH3), 2.74 (s, 3H, CH3), 6.73–7.83 (m, 7H, Ar-H), 8.11 (s, 1H, Ar-H5), 8.33 (1H, (s, 1H, Ar-H4), 10.63 (s, 1H, D2O-exchangeable, NH); 13C-NMR (75 MHz, DMSO-d6): δ =10.3, 13.6 (CH3), 114.4, 116.2, 118.3, 119.9, 125.3, 127.4, 132.4, 136.5, 136.8, 138.7, 139.3, 142.2, 144.1, 144.5, 153.5, 157.6 (Ar-C), 163.4 (C=O); MS, m/z (%) 481, 483 (M+, M + 2, 46). Anal. calcd for C21H16BrN5O2S (482.35): C, 52.29; H, 3.34; N, 14.52. Found: C, 52.16; H, 3.21; N, 14.45%.
6-Bromo-3-(1-(2-(4-methyl-5-(p-tolyldiazenyl)thiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23b). Red solid, 68% yield, mp 180–182 °C; IR (KBr) ν (cm−1): 3423 (NH), 3025 (=C–H), 2917 (–C–H), 1732 (C=O), 1599 (C=N); 1H-NMR (DMSO-d6) δ: 2.21 (s, 3H, CH3), 2.38 (s, 3H, CH3), 2.73 (s, 3H, CH3), 6.73–7.84 (m, 6H, Ar-H), 8.13 (s, 1H, Ar-H5), 8.33 (1H, (s, 1H, Ar-H4), 10.59 (s, 1H, D2O-exchangeable, NH); 13C-NMR (DMSO-d6): δ 11.6, 12.7, 20.5, 114.2, 118.3, 118.7, 120.6, 122.2, 127.4, 129.2, 129.7, 135.3, 137.1, 146.3, 149.5, 150.4, 151.8, 163.7, 164.8; MS, m/z (%) 495, 597 (M+, M + 2, 100). Anal. calcd for C22H18BrN5O2S (496.38): C, 53.23; H, 3.66; N, 14.11. Found: C, 53.09; H, 3.21; N, 14.03.
6-Bromo-3-(1-(2-(5-((4-chlorophenyl)diazenyl)-4-methylthiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23c). Red solid, 74% yield, mp 214–216 °C; IR (KBr) ν (cm−1): 3416 (NH), 3089 (=C–H), 2920 (–C–H), 1732 (C=O), 1595 (C=N); 1H-NMR (DMSO-d6) δ: 2.20 (s, 3H, CH3), 2.72 (s, 3H, CH3), 6.76–7.83 (m, 6H, Ar-H), 8.16 (s, 1H, Ar-H5), 8.34 (1H, (s, 1H, Ar-H4), 10.62 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 515, 517 (M+, M + 2, 100). Anal. calcd for C21H15BrClN5O2S (516.80): C, 48.81; H, 2.93; N, 13.55. Found: C, 48.79; H, 2.86; N, 13.50.
6-Bromo-3-(1-(2-(4-methyl-5-(2-tolyldiazenyl)thiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23d). Red solid, 69% yield, mp 189–191 °C; IR (KBr) ν (cm−1): 3411 (NH), 3064 (=C–H), 2920 (–C–H), 1732 (C=O), 1597 (C=N); 1H-NMR (DMSO-d6) δ: 2.20 (3H, s, CH3), 2.34 (s, 3H, CH3), 2.74 (s, 3H, CH3), 6.73–7.84 (m, 6H, Ar-H), 8.13 (s, 1H, Ar-H5), 8.33 (1H, (s, 1H, Ar-H4), 10.60 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 495, 497 (M+, M + 2, 70). Anal. calcd for C22H18BrN5O2S (496.38): C, 53.23; H, 3.66; N, 14.11. Found: C, 53.03; H, 3.27; N, 14.23.
6-Bromo-3-(1-(2-(4-methyl-5-(m-tolyldiazenyl)thiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23e). Red solid, 68% yield, mp 168–170 °C; IR (KBr) ν (cm−1): 3427 (NH), 3052 (=C–H), 2918 (–C–H), 1733 (C=O), 1598 (C=N); 1H-NMR (DMSO-d6) δ: 2.21 (s, 3H, CH3), 2.36 (s, 3H, CH3), 2.74 (s, 3H, CH3), 6.70–7.83 (m, 6H, Ar-H), 8.15 (s, 1H, Ar-H5), 8.34 (1H, (s, 1H, Ar-H4), 10.62 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 495, 597 (M+, M + 2, 34). Anal. calcd for C22H18BrN5O2S (496.38): C, 53.23; H, 3.66; N, 14.11. Found: C, 53.07; H, 3.17; N, 14.12.
6-Bromo-3-(1-(2-(5-((4-methoxyphenyl)diazenyl)-4-methylthiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23f). Red solid, 69% yield, mp 194–196 °C; IR (KBr) ν (cm−1): 3427 (NH), 3028 (=C–H), 2923 (–C–H), 1730 (C=O), 1596 (C=N); 1H-NMR (DMSO-d6) δ: 2.20 (s, 3H, CH3), 2.72 (s, 3H, CH3), 3.85 (s, 3H, OCH3), 6.76–7.79 (m, 6H, Ar-H), 8.13 (s, 1H, Ar-H5), 8.33 (1H, (s, 1H, Ar-H4), 10.63 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 511, 513 (M+, M + 2, 41). Anal. calcd for C22H18BrN5O3S (512.38): C, 51.57; H, 3.54; N, 13.67. Found: C, 51.52; H, 3.48; N, 13.49.
6-Bromo-3-(1-(2-(5-((3-chlorophenyl)diazenyl)-4-methylthiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23g). Red solid, 67% yield, mp 178–180 °C; IR (KBr) ν (cm−1): 3421 (NH), 3021 (=C–H), 2920 (–C–H), 1729 (C=O), 1593 (C=N); 1H-NMR (DMSO-d6) δ: 2.22 (s, 3H, CH3), 2.73 (s, 3H, CH3), 6.73–7.79 (m, 6H, Ar-H), 8.13 (s, 1H, Ar-H5), 8.34 (1H, (s, 1H, Ar-H4), 10.60 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 515, 517 (M+, M + 2, 35). Anal. calcd for C21H15BrClN5O2S (516.80): C, 48.81; H, 2.93; N, 13.55. Found: C, 48.81; H, 2.93; N, 13.55.
6-Bromo-3-(1-(2-(5-((4-bromophenyl)diazenyl)-4-methylthiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23h). Orange solid, 74% yield, mp 193–195°C; IR (KBr) ν (cm−1): 3430 (NH), 3053 (=C–H), 2921 (–C–H), 1731 (C=O), 1600 (C=N); 1H-NMR (DMSO-d6) δ: 2.20 (s, 3H, CH3), 2.72 (s, 3H, CH3), 6.76–7.84 (m, 6H, Ar-H), 8.13 (s, 1H, Ar-H5), 8.34 (1H, (s, 1H, Ar-H4), 10.61 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 560, 562 (M+, M + 2, 84). Anal. calcd for C21H15Br2N5O2S (561.25): C, 44.94; H, 2.69; N, 12.48. Found: C, 44.83; H, 2.62; N, 12.30.
6-Bromo-3-(1-(2-(4-methyl-5-((4-nitrophenyl)diazenyl)thiazol-2-yl)hydrazono)ethyl)-2H-chromen-2-one (23i). Orange solid, 68% yield, mp 177–179 °C; IR (KBr) ν (cm−1): 3416 (NH), 3073 (=C–H), 2920 (–C–H), 1731 (C=O), 1596 (C=N); 1H-NMR (DMSO-d6) δ: 2.20 (s, 3H, CH3), 2.73 (s, 3H, CH3), 6.74–7.85 (m, 6H, Ar-H), 8.16 (s, 1H, Ar-H5), 8.34 (1H, (s, 1H, Ar-H4), 10.62 (s, 1H, D2O-exchangeable, NH); MS, m/z (%) 526, 528 (M+, M+, 73). Anal. calcd for C21H15BrN6O4S (527.35): C, 47.83; H, 2.87; N, 15.94. Found: C, 47.72; H, 2.80; N, 15.79.

3.3. Evaluation of the Antitumor Activity Using Viability Assay

Human hepatocellular carcinoma cell line (HEPG2) was obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA). The cells were grown on RPMI-1640 medium supplemented with 10% inactivated fetal calf serum and 50 µg/mL gentamycin. The cells were maintained at 37 °C in a humidified atmosphere with 5% CO2 and were subcultured two to three times a week. Potential cytotoxicity of the compounds was evaluated on tumor cells using the method of Gangadevi and Muthumary [35]. The cells were grown as monolayers in growth RPMI-1640. The monolayers of 104 cells adhered at the bottom of the wells in a 96-well microtiter plate incubated for 24 h at 37 °C in a humidified incubator with 5% CO2. The monolayers were then washed with sterile phosphate buffered saline (0.01 M pH 7.2) and simultaneously the cells were treated with 100 µL from different dilutions of tested sample in fresh maintenance medium and incubated at 37 °C. A control of untreated cells was made in the absence of tested sample. Positive controls containing doxorubicin drug was also tested as reference drug for comparison. Six wells were used for each concentration of the test sample. Every 24 h the observation under the inverted microscope was made. The number of the surviving cells was determined by staining the cells with crystal violet [36,37] followed by cell lysing using 33% glacial acetic acid and read the absorbance at 590 nm using microplate reader (SunRise, TECAN, Inc., San Diego, CA, USA) after well mixing. The absorbance values from untreated cells were considered as 100% proliferation. The number of viable cells was determined using microplate reader as previously mentioned before and the percentage of viability was calculated as [1 − (ODt/ODc)] × 100% where ODt is the mean optical density of wells treated with the tested sample and ODc is the mean optical density of untreated cells. The relation between surviving cells and drug concentration is plotted to get the survival curve of each tumor cell line after treatment with the specified compound. The 50% inhibitory concentration (IC50), the concentration required to cause toxic effects in 50% of intact cells, was estimated from graphic plots.

4. Conclusions

In the investigation described above, the 3-acetyl-6-bromo-2H-chromen-2-one moiety was introduced as a new class of antitumor agent against liver carcinoma. The scaffold has the advantage of facile synthetic protocol access. Briefly, target compounds were prepared via reactions of 6-bromo-3-(3-(dimethylamino)acryloyl)-2H-chromen-2-one, methyl 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)-ethylidene)hydrazine carbodithioate, 2-(1-(6-bromo-2-oxo-2H-chromen-3-yl)ethylidene) hydrazine-carbothioamide with C- and N-nucleophiles. The newly synthesized products were found to exhibit antitumor activities against liver carcinoma cell line (HEPG2-1) compared to doxorubicin as reference drug. Among all the test compounds, the most reactive compounds were the pyrazolo[1,5-a]pyrimidine 7c, thiazole 23g and 1,3,4-thiadiazole 18c (IC50 = 2.70 ± 0.28, 3.50 ± 0.23 and 4.90 ± 0.69 µM, respectively).

Supplementary Materials

Supplementary materials can be accessed at: https://www.mdpi.com /1420-3049/20/12/19803/s1.

Author Contributions

A.O.A., S.M.G. and Y.H.Z. designed research; A.O.A., S.M.G. and Y.H.Z. performed research, analyzed the data, wrote and read the paper. A.O.A., S.M.G. approved the final manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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  • Sample Availability: Samples of the synthesized compounds are available from the authors.

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Gomha, S.M.; Zaki, Y.H.; Abdelhamid, A.O. Utility of 3-Acetyl-6-bromo-2H-chromen-2-one for the Synthesis of New Heterocycles as Potential Antiproliferative Agents. Molecules 2015, 20, 21826-21839. https://doi.org/10.3390/molecules201219803

AMA Style

Gomha SM, Zaki YH, Abdelhamid AO. Utility of 3-Acetyl-6-bromo-2H-chromen-2-one for the Synthesis of New Heterocycles as Potential Antiproliferative Agents. Molecules. 2015; 20(12):21826-21839. https://doi.org/10.3390/molecules201219803

Chicago/Turabian Style

Gomha, Sobhi M., Yasser H. Zaki, and Abdou O. Abdelhamid. 2015. "Utility of 3-Acetyl-6-bromo-2H-chromen-2-one for the Synthesis of New Heterocycles as Potential Antiproliferative Agents" Molecules 20, no. 12: 21826-21839. https://doi.org/10.3390/molecules201219803

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