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Article

A Convenient Ultrasound-Promoted Synthesis of Some New Thiazole Derivatives Bearing a Coumarin Nucleus and Their Cytotoxic Activity

by
Sobhi M. Gomha
1,* and
Khaled D. Khalil
1,2
1
Department of Chemistry, Faculty of Science, University of Cairo, Giza 12613, Egypt
2
Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat13060, Kuwait
*
Author to whom correspondence should be addressed.
Molecules 2012, 17(8), 9335-9347; https://doi.org/10.3390/molecules17089335
Submission received: 25 June 2012 / Revised: 18 July 2012 / Accepted: 24 July 2012 / Published: 3 August 2012
(This article belongs to the Section Organic Chemistry)
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Abstract

:
Successful implementation of ultrasound irradiation for the rapid synthesis of a novel series of 3-[1-(4-substituted-5-(aryldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-ones 5a–h, via reactions of 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene) thiosemicarbazide (2) and the hydrazonoyl halides 3(4), was demonstrated. Also, a new series of 5-arylidene-2-(2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl)thiazol-4(5H)-ones 10a–d were synthesized from reaction of 2 with chloroacetic acid and different aldehydes. Moreover, reaction of 2-cyano-N'-(1-(2-oxo-2H-chromen-3-yl)ethylidene)-acetohydrazide (12) with substituted benzaldehydes gave the respective arylidene derivatives 13a–c under the conditions employed. The structures of the synthesized compounds were assigned based on elemental analyses and spectral data. Also, the cytototoxic activities of the thiazole derivative 5a was evaluated against HaCaT cells (human keratinocytes). It was found that compound 5a possess potent cytotoxic 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 [1,2,3,4,5]. A number of natural and synthetic coumarin derivatives have been reported to exert notable antimicrobial [1,2], antifungal [3,4] and cytotoxic [5] activity.
Thiazole derivatives have also attracted increasing attention due to their numerous pharmacological applications and biological activities, such as anti-inflammatory, analgesic, antimicrobial, anti-HIV, antihypertensive and herbicidal activity [6,7,8,9,10].
Ultrasonic-assisted organic synthesis (UAOS) is a powerful and green approach which is being used more and more to accelerate synthesis of organic compounds [11]. Increases in reaction rate and yields occur on application of ultrasound waves [12,13,14,15,16].
In view of these observations and in continuation of our previous work on the synthesis of heterocyclic systems for biological evaluation [17,18,19], we report herein a facile route to various thiazole derivatives incorporating coumarin moieties using the ultra-sound irradiation technique. Additionally we have found that one of the synthesized compounds has shown high cytotoxic activity.

2. Results and Discussion

2.1. Chemistry

2-(1-(2-Oxo-2H-chromen-3-yl)ethylidene)thiosemicarbazide (2) was previously prepared by refluxing 3-acetyl-2H-chromen-2-one (1) and thiosemicarbazide in absolute ethanol in the presence of catalytic amounts of HCl [20] (Scheme 1).
The target compounds 5a–h, 3-[1-(4-substituted-5-(aryldiazenyl)thiazol-2-yl)hydrazono) ethyl]-2H-chromen-2-ones, were synthesized in a one pot reaction of thiosemicarbazide 2 and hydrazonoyl halides 3(4) in the presence of TEA under ultrasonic irradiation (Scheme 1).
The structural elucidation of the compounds was based on spectral evidence and microanalyses. The mass spectra of these products 5a–c showed the molecular ion peaks at the expected m/z values. Their IR spectra showed the disappearance of the NH2 group, and revealed in each case one band at 1568–1558 cm−1, assignable to the N=N group (see Experimental).
The thiazole derivatives 8(9) were synthesized in good yields by the treatment of thiosemicarbazide derivative 2 with chloroacetone (6) or phenacyl bromide (7) in dioxane under ultrasonic irradiation following the Hantzsch thiazole synthesis [21]. Upon coupling the thiazole derivatives 8(9) with diazotized aniline, in presence of sodium acetate trihydrate, the azo derivatives 5a–h were obtained. The structures of the latter products were confirmed by the appearance of a N=N band in the IR spectra and the lack of signals due to the C-5 proton of the thiazole ring in their 1H-NMR spectra (see Experimental). The azo derivatives of similar thiazoles have found wide applications in the dyeing of synthetic fibers [22,23] and the azo derivatives described in the present work may find similar applications.
4-Thiazolidinone compound 11 was obtained by reaction of thiosemicarbazide 2 with chloroacetic acid in glacial acetic acid and in the presence of anhydrous sodium acetate. Reaction of the latter product 11 with substituted aldehydes afforded the corresponding arylidines 10a–d.
Molecules 17 09335 g002 550
Scheme 1. Synthesis of 5-arylazothiazole derivatives 5a–h.
Scheme 1. Synthesis of 5-arylazothiazole derivatives 5a–h.
Molecules 17 09335 g002
The one pot synthesis of products 10a–d has been carried out via reaction of thiosemicarbazide 2 with chloroacetic acid and aldehydes in glacial acetic acid in presence of excess anhydrous sodium acetate (Scheme 2). The 1H-NMR spectra data were also consistent with the assigned structures; thiazolidinone CH2 protons of 11 appeared at δ 3.97 ppm, arylidiene CH proton of 10a–d was observed at 8.60–8.67 ppm (see Experimental).
In addition, the hydrazide-hydrazone derivative 12 was prepared by ultrasonic irradiation of 3-acetyl-2H-chromen-2-one (1) and 2-cyanoacetohydrazide in absolute ethanol in the presence of catalytic amounts of HCl (Scheme 3). The structure of compound 12 was established on the basis of analytical and spectral data. Thus its 1H-NMR spectrum showed the presence of a singlet at δ 4.25 ppm for the CH2 group, and a singlet at δ 11.19 ppm for an NH group. Its mass spectrum revealed a molecular ion peak at m/z 269 (see Experimental).
Molecules 17 09335 g003 550
Scheme 2. Synthesis of 5-arylidenethiazolinone derivatives 10a–d.
Scheme 2. Synthesis of 5-arylidenethiazolinone derivatives 10a–d.
Molecules 17 09335 g003
Molecules 17 09335 g004 550
Scheme 3. Reaction of acetohydrazide 12 with aromatic aldehydes.
Scheme 3. Reaction of acetohydrazide 12 with aromatic aldehydes.
Molecules 17 09335 g004
Furthermore, treatment of the acetohydrazide 12 with substituted benzaldehydes, under ultrasonic irradiation, afforded the benzylidene derivatives 13a–c on the basis of their spectral data (Scheme 3) which confirmed the structures of the products by the appearance of a C=CH signal at δ 9.34 ppm and the lack of the characteristic signal due to methylene protons (see Experimental). The reaction of 12 with salicylaldehyde gave the coumarin derivative 14 (Scheme 3), in analogy with the reported literature [24,25]. The IR spectrum of compound 14 showed the lack of absorption bands corresponding to a C≡N group and presence of bands at 3,198 cm−1 due to the NH group.

2.2. In Vitro Cytotoxicity Assay

The effect of compound 5a on cellular viability was studied using the MTT Assay. The HaCaT cells are plated and cultured in 12-well cell culture plates for 24 h (four plates represent the four days incubation with 5a, each plate divided into 6 wells as control and 6 wells as a test) (Figure 1).
Molecules 17 09335 g001 550
Figure 1. Represents the MTT assay results of healthy cells HaCat cells incubated with 50 μL 0.5 mol 5a compared to control one. The used concentration of 5a does not induce significant cytotoxic effect on the healthy HaCaT cells.
Figure 1. Represents the MTT assay results of healthy cells HaCat cells incubated with 50 μL 0.5 mol 5a compared to control one. The used concentration of 5a does not induce significant cytotoxic effect on the healthy HaCaT cells.
Molecules 17 09335 g001

3. Experimental

3.1. Chemistry

3.1.1. General

Melting points were measured on an Electrothermal IA 9000 series digital melting point apparatus. The IR spectra were recorded in potassium bromide discs on a Pye Unicam SP 3300 or a Shimadzu FT IR 8101 PC infrared spectrophotometers. The NMR Spectra were recorded at 300 MHz on a Varian Mercury VX-300 NMR spectrometer. 1H-NMR (300 MHz) and 13C-NMR (75 MHz) were run in deuterated dimethylsulphoxide (DMSO-d6). Chemical shifts were related to that of the solvent. Mass spectra were recorded on a Shimadzu GCMS-QP1000 EX mass spectrometer at 70 eV. Elemental analyses of the products were carried out at the Microanalytical Centre of Cairo University, Giza, Egypt. All reactions were followed by TLC (Silica gel, Merck). Irradiation was done in an ultrasonicator, (Electric supply: 230 v, A.C. 50 Hz, 1phase; Ultrasonic frequency: 36 KHz; Ultrasonic power: 100 W). In vitro cytotoxicity assay was performed at Regional Center for Food & Feed, Agricultural Research Center, Giza, Egypt, using the MTT Assay. 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)thiosemicarbazide (2) [20] and hydrazonoyl halides 3 [26,27] were prepared as reported in the literature.

3.1.2. Synthesis of 3-[1-(4-Substituted-5-(aryldiazenyl)thiazol-2-yl)hydrazono) ethyl]-2H-chromen-2-ones 5a–h

3.1.2.1. Method A: General Procedure

A mixture of 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene) thiosemicarbazide (2, 0.522 g, 2 mmol) and appropriate hydrazonoyl halides 3(4) (2 mmol) in dioxane (30 mL) containing triethylamine (0.2 g, 2 mmol) was irradiated by an ultrasonic generator in a water-bath at 50–60 °C for 30 min. (monitored by TLC). The formed yellow precipitate was isolated by filtration, washed with ethanol, dried and recrystallized from dioxane to give compounds 5a–h.
3-[1-(2-(4-Methyl-5-(phenyldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5a). Yield 72%; yellow solid; mp = 142 °C; IR (KBr): v 1559 (N=N), 1624 (C=N), 1724 (C=O), 3408 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.20 (s, 3H, CH3), 2.38 (s, 3H, CH3), 7.12–7.89 (m, 9H, ArH), 8.37 (s, 1H, Coumarin-H4), 10.60 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 14.61 (CH3), 9.52 (CH3), 112.15, 114.45, 120.22, 120.55, 121.85, 123.25, 124.33, 125.75, 127.16, 127.31, 129.73, 131.61, 133.73, 138.61 (Ar-C and Ar-CH), 153.13(C=N), 157.32(C=N), 167.51 (C=O); MS m/z (%):404 (M+ + 1, 7), 403 (M+, 100), 106 (75), 91 (82), 77 (27). Anal. Calcd for C21H17N5O2S (403.11): C, 62.52; H, 4.25; N, 17.36. Found C, 62.42; H, 4.18; N, 17.12%.
3-[1-(2-(4-Methyl-5-(p-tolyldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5b). Yield 74%; yellow solid; mp = 230 °C. IR (KBr): v 1558 (N=N), 1623 (C=N), 1724 (C=O), 3408 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.20 (s, 3H, CH3), 2.38 (s, 3H, CH3), 2.58 (s, 3H, CH3), 7.12–7.88 (m, 8H, ArH), 8.35 (s, 1H, coumarin-H4), 10.63 (s, 1H, D2O exchangeable, NH); MS m/z (%): 417 (M+, 4), 106 (100), 91 (82), 65 (27). Anal. Calcd for C22H19N5O2S (417.13): C, 63.29; H, 4.59; N, 16.78. Found C, 63.22; H, 4.47; N, 16.53%.
3-[1-(2-(5-((4-Chlorophenyl)diazenyl)-4-methylthiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5c). Yield 76%; yellow solid; mp = 188 °C; IR (KBr): v 1564 (N=N), 1626 (C=N), 1732 (C=O), 3410 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.20 (s, 3H, CH3), 2.38 (s, 3H, CH3), 7.10–7.98 (m, 8H, ArH), 8.38 (s, 1H, coumarin-H4), 10.66 (s, 1H, D2O exchangeable, NH); MS m/z (%): 438 (M+ + 1, 8), 437 (M+, 16), 127 (100), 73 (68). Anal. Calcd for C21H16ClN5O2S (437.07): C, 57.60; H, 3.68; N, 15.99. Found C, 57.51; H, 3.62; N, 15.71%.
3-[1-(2-(4-Methyl-5-((4-nitrophenyl)diazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5d). Yield 73%; yellow solid; mp = 195 °C; IR (KBr): v 1568 (N=N), 1629 (C=N), 1702(C=O), 3404 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.22 (s, 3H, CH3), 2.40 (s, 3H, CH3), 7.12–7.95 (m, 8H, ArH), 8.39 (s, 1H, coumarin-H4), 10.68 (s, 1H, D2O exchangeable, NH); MS m/z (%): 448 (M+, 13), 201(54), 127 (100), 82 (94), 67 (100). Anal. Calcd for C21H16N6O4S (448.10): C, 56.24; H, 3.60; N, 18.74. Found C, 56.14; H, 3.65; N, 18.42%.
3-[1-(2-(4-Phenyl-5-(phenyldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5e). Yield 72%; yellow solid; mp = 182 °C; IR (KBr): v 1558 (N=N), 1626 (C=N), 1744 (C=O), 3413 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.44 (s, 3H, CH3), 7.12–7.95 (m, 14H, ArH), 8.30 (s, 1H, coumarin-H4), 10.56 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 10.31 (CH3), 112.35, 115.35, 119.43, 119.55, 121.35, 123.29, 123.52, 124.26, 125.12, 125.65, 126.34, 127.22, 129.28, 130.29, 132.33, 132.29, 136.67, 138.34 (Ar-C and Ar-CH), 154.27 (C=N), 155.98 (C=N), 167.29 (C=O); MS m/z (%): 465 (M+, 10), 359 (100), 134 (83), 89 (60), 77 (31). Anal. Calcd for C26H19N5O2S (465.13): C, 67.08; H, 4.11; N, 15.04. Found C, 67.00; H, 4.02; N, 14.86%.
3-[1-(2-(4-Phenyl-5-(p-tolyldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5f). Yield 72%; yellow solid; mp = 178 °C; IR (KBr): v 1562 (N=N), 1628 (C=N), 1743 (C=O), 3415 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.20 (s, 3H, CH3), 2.44 (s, 3H, CH3), 7.12–7.95 (m, 13H, ArH), 8.31 (s, 1H, coumarin-H4), 10.59 (s, 1H, D2O exchangeable, NH); MS m/z (%): 480(M+ + 1, 7), 479 (M+, 100), 134 (83), 89 (82), 77 (31). Anal. Calcd for C27H21N5O2S (479.14): C, 67.62; H, 4.41; N, 14.60. Found C, 67.42; H, 4.51; N, 14.54%.
3-[1-(2-(5-((4-Chlorophenyl)diazenyl)-4-phenylthiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5g). Yield 72%; yellow solid; mp = 187 °C; IR (KBr): v 1565 (N=N), 1626 (C=N), 1742 (C=O), 3412 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.44 (s, 3H, CH3), 7.02–7.98 (m, 13H, ArH), 8.34 (s, 1H, coumarin-H4), 10.65 (s, 1H, D2O exchangeable, NH; MS m/z (%): 500 (M+ + 1, 8), 499 (M+, 28), 359 (100), 134 (64), 77 (18). Anal. Calcd for C26H18ClN5O2S (499.09): C, 62.46; H, 3.63; N, 14.01. Found C, 62.44; H, 3.56; N, 13.91%.
3-[1-(2-(5-((4-Nitrophenyl)diazenyl)-4-phenylthiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (5h). Yield 72%; brown solid; mp = 178 °C; IR (KBr): v 1566 (N=N), 1628 (C=N), 1742(C=O), 3414 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.28 (s, 3H, CH3), 7.12–7.95 (m, 13H, ArH), 8.34 (s, 1H, coumarin-H4), 10.69 (s, 1H, D2O exchangeable, NH); MS m/z (%): 511(M+ + 1, 14), 510 (M+, 46), 417 (65), 257 (24), 107 (1), 67 (100). Anal. Calcd for C26H18N6O4S (510.11): C, 61.17; H, 3.55; N, 16.46. Found C, 61.11; H, 3.48; N, 16.34%.

3.1.2.2. Method B

3.1.2.2.1. Synthesis of 3-[1-((4-Substituted thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-ones 8,9

A mixture of 2 (0.27 g, 1 mmol) and chloroacetone (6) or phenacyl bromide (7) (1 mmol) in absolute ethanol (30 mL) was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 20 min. (monitored by TLC). The product started to separate out during the course of reaction. The crystalline solid was filtered, washed with water, dried and recrystallized from DMF to give the corresponding compounds 8 and 9, respectively.
3-[1-(4-Methylthiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (8). Yield 79%; yellow solid; mp = 170 °C; IR (KBr): v 1721 (C=O), 3267 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.24 (s, 3H, CH3), 2.51 (s, 3H, CH3), 7.07–8.02 (m, 5H, ArH and thiazole-H5), 8.22 (s, 1H, coumarin-H4), 9.31 (s, 1H, D2O exchangeable, NH); MS m/z (%): 299 (M+, 6), 129 (29), 77 (12), 60 (100). Anal. Calcd for C15H13N3O2S (299.07): C, 60.18; H, 4.38; N, 14.04. Found C, 60.10; H, 4.28; N, 13.84%.
3-[1-((4-Phenylthiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-one (9). Yield 84%; yellow solid; mp = 232 °C; IR (KBr): v 1744 (C=O), 3418 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.44 (s, 3H, CH3), 7.10–8.02 (m, 10H, ArH and thiazole-H5), 8.26 (s, 1H, coumarin-H4), 9.28 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 10.11 (CH3), 112.11, 116.28, 119.42, 120.36, 122.29, 123.01, 124.33, 125.75, 127.16, 127.31, 129.73, 134.33, 135.64, 139.83 (Ar-C and Ar-CH), 154.24 (C=N), 158.12 (C=N), 167.21 (C=O); MS m/z (%): 362 (M+ + 1, 12), 361 (M+, 48), 359 (100), 133 (61), 89 (81) 77 (32). Anal. Calcd for C20H15N3O2S (361.09): C, 66.46; H, 4.18; N, 11.63. Found C, C, 66.53; H, 4.10; N, 11.43%.

3.1.2.2.2. Coupling of 8(9) with Arenediazonium Chlorides

To a solution of 8 or 9 (1 mmol) in ethanol (20 mL) was added sodium acetate trihydrate (0.138 g, 1 mmol), and the mixture was cooled to 0–5 °C in an ice bath. To the resulting cold solution was added portionwise a cold solution of arenediazonium chloride [prepared by diazotizing aniline derivatives (1 mmol) dissolved in hydrochloric acid (6 M, 1 mL) with a solution of sodium nitrite (0.07 g, 1 mmol) in water (2 mL)]. After complete addition of the diazonium salt, the reaction mixture was stirred for a further 30 min in an ice bath. The solid that separated was filtered off, washed with water and finally recrystallized from ethanol to give product proved to be identical in all respects (mp, mixed mp and IR spectra) with compounds 5a–h which obtained from method A.

3.1.3. Synthesis of 5-Arylidene-2-(2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl)thiazol-4(5H)-ones 10a–d

3.1.3.1. Method A

A mixture of 2 (0.261 g, 1 mmol), chloroacetic acid (0.1 g, 1 mmol) and appropriate aldehyde (1 mmol) in glacial acetic acid (20 mL) containing anhydrous sodium acetate (0.33 g, 4 mmol) was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 30 min. (monitored by TLC). The reaction mixture was left to cool and the formed solid was filtered off, washed with water, dried and recrystallized from ethanol to give 10a–d.
5-Benzylidene-2-[2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl]thiazol-4(5H)-one (10a). Yield 84%; yellow solid; mp = 176 °C; IR (KBr): v 1678, 1725 (2C=O), 3360 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.24 (s, 3H, CH3), 6.91–7.88 (m, 9H, ArH), 8.19 (s, 1H, coumarin-H4), 8.63 (s, 1H, N=CH), 10.87 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 9.97 (CH3), 112.15, 114.45, 121.23, 121.62, 121.89, 122.42, 124.19, 124.84, 126.46, 128.43, 129.87, 130.41, 134.43, 146.73 (Ar-C and Ar-CH), 154.19 (C=N), 158.12 (C=N), 167.11 (C=O), 181.56 (C=O); MS m/z (%): 302 (M+ + 1, 9), 301 (M+, 62), 218 (65), 172 (40), 130 (100), 77 (43). Anal. Calcd for C21H15N3O3S (389.08): C, 64.77; H, 3.88; N, 10.79. Found C, 64.58; H, 3.78; N, 10.48%.
5-[4-Methylbenzylidene)-2-(2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl)thiazol-4(5H)-one (10b). Yield 79%; yellow solid; mp = 172 °C; IR (KBr): v 1678, 1721 (2C=O), 3353 (NH) cm−1;1H-NMR (DMSO-d6): δ 2.24 (s, 3H, CH3), 2.51 (s, 3H, CH3), 6.91–7.88 (m, 8H, ArH), 8.19 (s, 1H, coumarin-H4), 8.60 (s, 1H, N=CH), 10.83 (s, 1H, D2O exchangeable, NH); MS m/z (%): 404 (M+ + 1, 15), 403 (M+, 46), 235 (100), 146 (64), 130 (18), 77 (39). Anal. Calcd for C22H17N3O3S (403.10): C, 65.49; H, 4.25; N, 10.42. Found C, 65.43; H, 4.11; N, 10.12%.
5-(4-Chlorobenzylidene)-2-[2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl]thiazol-4(5H)-one (10c). Yield 82%; yellow solid; mp = 186 °C; IR (KBr): v 1679, 1722 (2C=O), 3353 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H, CH3), 6.91–7.96 (m, 8H, ArH), 8.19 (s, 1H, coumarin-H4), 8.62 (s, 1H, N=CH), 10.86 (s, 1H, D2O exchangeable, NH); MS m/z (%): 424 (M+ + 1, 13), 423 (M+, 46), 235 (100), 172 (36), 130 (58), 63 (69). Anal. Calcd for C21H14ClN3O3S (423.04): C, 59.50; H, 3.33; N, 9.91. Found C, 59.37; H, 3.13; N, 9.61%.
5-(4-Nitrobenzylidene)-2-[2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl]thiazol-4(5H)-one (10d). Yield 76%; yellow solid; mp = 170 °C; IR (KBr): v 1679, 1723 (2C=O), 3366 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H, CH3), 6.91–7.96 (m, 8H, ArH), 8.16 (s, 1H, coumarin-H4), 8.67 (s, 1H, N=CH), 10.86 (s, 1H, D2O exchangeable, NH); MS m/z (%): 435 (M+ + 1, 7), 434 (M+, 44), 235 (100), 218 (66), 130 (70), 63 (58). Anal. Calcd for C21H14N4O5S (434.07): C, 58.06; H, 3.25; N, 12.90. Found C, 57.86; H, 3.26; N, 12.79%.

3.1.3.2. Method B

3.1.3.2.1. Synthesis of 2-[2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinyl]thiazol-4(5H)-one (11)

A mixture of 2 (0.261 g, 1 mmol) and chloroacetic acid (0.1 g, 1 mmol) in glacial acetic acid (30 mL) containing anhydrous sodium acetate (0.33 g, 4 mmol) was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 30 min. (monitored by TLC). The reaction mixture was cooled and the resulting precipitate was filtered off and recrystallized from ethanol to give 11. Yield 84%; yellow solid; mp = 220 °C; IR (KBr): v 1667, 1717 (2C=O), 3167 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H, CH3), 3.97 (s, 2H, CH2), 6.91–8.19 (m, 4H, ArH), 8.63 (s, 1H, coumarin-H4), 10.87 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 10.46 (CH3), 39.35 (CH2), 118.45, 120.18, 122.23, 124.33, 129.73, 131.61, 133.73, 138.61 (Ar-C and Ar-CH), 153.43 (C=N), 156.56 (C=N), 167.12 (C=O), 176.33 (C=O); MS m/z (%): 303 (M+ + 2, 3), 302 (M+ + 1, 9), 301 (M+, 36), 235 (73), 146 (36), 130 (100), 77 (59). Anal. Calcd for C14H11N3O3S (301.05): C, 55.80; H, 3.68; N, 13.95. Found C, 55.68; H, 3.60; N, 13.75%.

3.1.3.2.2. Reaction of 8 with Aromatic Aldehydes

General procedure: To a solution of 5-thiazolidinone 11 (0.30 g, 1 mmol) and appropriate aldehyde (1 mmol) in glacial acetic acid (20 mL), anhydrous sodium acetate (0.33 g, 4 mmol) was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 30 min (monitored by TLC). The product, so separated, was filtered, washed with water, dried and recrystallized from ethanol to give compounds which proved to be identical in all respects (mp, mixed mp and IR spectra) with the hydrazonothiazolidinones 10a–d which obtained from method A.

3.1.4. Synthesis of 2-Cyano-N'-(1-(2-oxo-2H-chromen-3-yl)ethylidene)acetohydrazide (12)

To a solution of 2-cyanoacetohydrazide (1.0 g, 10 mmol) and 3-acetyl-2H-chromen-2-one (1, 1.88 g, 10 mmol) in absolute ethanol (30 mL) three drops of conc. HCl were added and the reaction mixture was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 20 min. then left to cool. The solid product formed was collected by filtration, dried and recrystallized from ethanol to give 12. Yield 86%; yellow microcrystals; mp = 172 °C; IR (KBr): v = 1690, 1724 (2C=O), 2230 (CN), 3186 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.17 (s, 3H, CH3), 4.25 (s, 2H, CH2), 7.39–8.30 (m, 4H, ArH), 8.95 (s, 1H, coumarin-H4), 11.19 (s, 1H, D2O exchangeable, NH); MS m/z (%): 270 (M+ + 1, 5), 269 (M+, 33), 229 (82), 115 (100), 89 (60), 63 (54). Anal. Calcd for C14H11N3O3 (269.08): C, 62.45; H, 4.12; N, 15.61. Found C, C, 62.41; H, 4.02; N, 15.38%.

3.1.5. Reaction of 11 with Aromatic Aldehydes

General procedure: Equimolecular mixture of 2-cyano-N'-(1-(2-oxo-2H-chromen-3-yl)ethylidene) acetohydrazide (12, 2.69 g, 0.01 mol) and appropriate aldehyde (0.01 mol), in anhydrous ethanol (20 mL) containing piperidine (0.50 mL) was irradiated with an ultrasonic generator in a water-bath at 50–60 °C for 30 min (monitored by TLC). The formed solid was collected by filtration and recrystallized from the proper solvent to give compounds 13a–d.
2-Cyano-N'-[1-(2-oxo-2H-chromen-3-yl)ethylidene]-3-phenylacrylohydrazide (13a). Yield 80%; yellow solid (from ethanol); mp = 198 °C; IR (KBr): v 1672, 1728 (2C=O), 2210 (CN), 3336 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.19 (s, 3H, CH3), 7.24–8.21(m, 9H, ArH ), 8.87 (s, 1H, coumarin-H4), 9.34 (s, 1H, C=CH), 11.22 (s, 1H, D2O exchangeable, NH); 13C-NMR (DMSO-d6): δ 10.74 (CH3), 112.36, 115.26, 117.26, 119.42, 121.65, 122.86, 123.43, 124.16, 124.86, 127.67, 127.99, 129.04, 133.43, 134.87, 139.37 (Ar-C, Ar-CH and C≡N), 154.94 (C=N), 168.13 (C=O), 174.14 (C=O); MS m/z (%): 358 (M+ + 1, 4), 357 (M+, 40), 185 (100), 129 (73), 109 (73), 55 (91). Anal. Calcd for C21H15N3O3 (357.11): C, 70.58; H, 4.23; N, 11.76. Found C, 70.49; H, 4.21; N, 11.46%.
2-Cyano-N'-[1-(2-oxo-2H-chromen-3-yl)ethylidene]-3-p-tolylacrylohydrazide (13b). Yield 82%; yellow solid (from DMF); mp = 187 °C. IR (KBr): v 1672, 1728 (2C=O), 2216 (CN), 3336 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.19 (s, 3H, CH3), 2.49 (s, 3H, CH3), 7.20–8.23 (m, 8H, ArH), 8.89 (s, 1H, coumarin-H4), 9.34 (s, 1H, C=CH), 11.26 (s, 1H, D2O exchangeable, NH); MS m/z (%): 372 (M+ + 1, 6), 371 (M+, 45), 229 (75), 186 (55), 115 (100), 63 (62). Anal. Calcd for C22H17N3O3(371.13): C, 71.15; H, 4.61; N, 11.31. Found C, C, 71.05; H, 4.36; N, 11.11%.
3-(4-Chlorophenyl)-2-cyano-N'-(1-(2-oxo-2H-chromen-3-yl)ethylidene)acrylohydrazide (13c). Yield 78%; yellow solid (from ethanol ); mp = 202 °C; IR (KBr): v 1674, 1732 (2C=O), 2218 (CN), 3334 (NH) cm−1; 1H-NMR (DMSO-d6): δ 2.19 (s, 3H, CH3), 7.21–8.23(m, 8H, ArH), 8.89 (s, 1H, coumarin-H4), 9.35 (s, 1H, C=CH), 11.34 (s, 1H, D2O exchangeable, NH); MS m/z (%): 392 (M+ + 1, 7), 391 (M+, 22), 273 (47), 219 (100), 84(94). Anal. Calcd for C21H14ClN3O3 (391.07): C, 64.37; H, 3.60; N, 10.72. Found C, C, 64.07; H, 3.62; N, 10.32%.
2-Imino-N'-[1-(2-oxo-2H-chromen-3-yl)ethylidene]-2H-chromene-3-carbohydrazide (14). Yield 78%; yellow solid (from DMF); mp = 240 °C; IR (KBr): v 1669, 1712 (2C=O), 3198, 3325 (2NH) cm−1; 1H-NMR (DMSO-d6): δ 2.19 (s, 3H, CH3), 7.10–8.36 (m, 9H, ArH ), 8.44 (s, 1H, D2O exchangeable, NH), 8.89 (s, 1H, coumarin-H4), 11.38 (s, 1H, D2O exchangeable, NH); MS m/z (%): 374 (M+ + 1, 13), 373 (M+, 13), 201 (51), 171 (100), 115 (89), 62 (58). Anal. Calcd for C21H15N3O4 (373.11): C, 67.56; H, 4.05; N, 11.25. Found C, C, 67.44; H, 4.15; N, 11.05%.

3.2. Cytotoxic Activity

The method applied is similar to that reported by Skehan et al. using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. Healthy HaCaT epithelial primary cell line (human keratinocytes) was cultured on 18 mm diameter glass cover slips in a 12-well tissue culture plate in DMEM plus 5% FBS at 37–38 °C under 5% CO2. The cover slips were coated with collagen type I (Roche) in advance for optimum cell growth. The HaCaT cells are cultured in 12-well cell culture plates for 24 h, (four plates represent the four days incubation with 5a, each plate divided into 6-wells as control and 6-wells as a test). Rinsing the old medium and adding new one then 50 μL 0.5 mol 5a are added to test wells (not to the control one) and returned to incubator for 8 h washing the excess 5a by DPBS buffer and add 1 mL medium to each well then incubated for the designated periods for each plate (Figure 1).

4. Conclusions

In summary, we have developed a new green methodology and synthesized several 3-[1-(4-substituted-5-(aryldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-ones by ultrasound irradiation. The cytototoxic activity of one of them was also evaluated against healthy HaCaT cells.

Acknowledgements

The authors wish to thank Taher Salah of Nanotechnology Center, Regional Center for Food & Feed, Agricultural Research Center for his support to carry out the antimicrobial activity.

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

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MDPI and ACS Style

Gomha, S.M.; Khalil, K.D. A Convenient Ultrasound-Promoted Synthesis of Some New Thiazole Derivatives Bearing a Coumarin Nucleus and Their Cytotoxic Activity. Molecules 2012, 17, 9335-9347. https://doi.org/10.3390/molecules17089335

AMA Style

Gomha SM, Khalil KD. A Convenient Ultrasound-Promoted Synthesis of Some New Thiazole Derivatives Bearing a Coumarin Nucleus and Their Cytotoxic Activity. Molecules. 2012; 17(8):9335-9347. https://doi.org/10.3390/molecules17089335

Chicago/Turabian Style

Gomha, Sobhi M., and Khaled D. Khalil. 2012. "A Convenient Ultrasound-Promoted Synthesis of Some New Thiazole Derivatives Bearing a Coumarin Nucleus and Their Cytotoxic Activity" Molecules 17, no. 8: 9335-9347. https://doi.org/10.3390/molecules17089335

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