Open Access

A facile access and evaluation of some novel thiazole and 1,3,4-thiadiazole derivatives incorporating thiazole moiety as potent anticancer agents

Chemistry Central Journal201711:105

Received: 16 July 2017

Accepted: 10 October 2017

Published: 16 October 2017



Many heterocyclic compounds containing thiazole or 1,3,4-thiadiazole ring in their skeletons have been reported to possess various pharmacological activities especially anticancer activities.


4-Methyl-2-phenylthiazole-5-carbohydrazide (2) was used as a synthon to prepare 2-(4-methyl-2-phenylthiazole-5-carbonyl)-N-phenylhydrazinecarbothioamide (3) and 2-(2-(4-methyl-2-phenylthiazole-5-carbonyl)hydrazono)-N′-phenylpropane hydrazonoyl chlorides 5ac. In addition, thioamide 3 was used as starting material for preparation of a new series of thiadiazole derivatives via its reaction with hydrazonoyl chlorides 5ac in dioxane using triethylamines as catalyst. In addition, a series of thiazole derivatives was synthesized by reaction of thioamide 3 with a number of α-halo compounds, namely, 3-chloropentane-2,4-dione (8) or 2-chloro-3-oxo-N-phenyl butanamide (10) phenacyl bromide 12 ethyl chloroacetate (14) in EtOH in the presence of triethylamine. The structures assigned for all the new products were elucidated based on both elemental analyses and spectral data and the mechanisms of their formation was also discussed. Moreover, the new products was evaluated in vitro by MTT assays for their anticancer activity against cell lines of Hepatocellular carcinoma cell line (HepG-2). The best result observed for compounds 7b (IC50 = 1.61 ± 1.92 (μg/mL)) and 11 (IC50 = 1.98 ± 1.22 (μg/mL)). The structure–activity relationships have been suggested based on their anticancer results.


A novel series of new pharmacophores containing thiazole moiety have been synthesized using a facile and convenient methods and evaluated as potent anticancer agents.


ThiazolesThiadiazolesHydrazonoyl chloridesPhenacyl bromideThioamideAnticancer activity


Identification of novel structure leads that may be of use in designing new, potent, selective and less toxic anticancer agents remains a major challenge for medicinal chemistry researchers. Compounds containing thiazole core have diverse biological activities as antihypertension, antifungal, antimicrobial, anti-inflammatory, antioxidant, antitubercular [17], and anticancer [812]. Also, thiazole ring present in many drugs such as Nizatidine, Abafungin, and Amiphenazole (Fig. 1).
Fig. 1

Some marketed drugs containing thiazole ring

Many biological activities were reported for the compounds containing 1,3,4-thiadiazole ring such as antituberculosis, anti-inflammatory, antidepressant and anxiolytic, antioxidant, anticonvulsants [1317] and anticancer activities [1820]. In addition, many drugs containing 1,3,4-thiadiazole ring are available in the market such as acetazolamide, methazolamide, and megazol (Fig. 2).
Fig. 2

Examples of drugs containing a 1,3,4-thiadiazole ring

In continuation of our studies dealing with the utility of hydrazonoyl halides for synthesis of various bioactive bridgehead nitrogen polyheterocycles [2130], we wish to report herein a new facile synthesis of new heterocycles containing thiazole and 1,3,4-thiadiazole or two thiazole rings in one molecular frame. We anticipated that the synthesized compounds would have potent pharmacological activities.

Results and discussion


2-(4-Methyl-2-phenylthiazole-5-carbonyl)-N-phenylhydrazinecarbothioamide (3) [31] was prepared via reaction of 4-methyl-2-phenylthiazole-5-carbohydrazide (2) with phenyl isothiocyanate in EtOH (Scheme 1).
Scheme 1

Synthesis of thiazoles 2,3

The reaction of compound 2 with the appropriate hydrazonoyl chlorides 4ac [32] in refluxing ethanol yielded the corresponding condensation product 5 (Scheme 2). The IR spectra of the latter products revealed a carbonyl and two NH absorption bands (see “Experimental” part). Their 1HNMR showed two D2O exchangeable signals of two NH protons in the regions δ 10.03–10.06 and δ 10.57–10.59 ppm. Also, their mass spectra confirmed the assigned structure 5 (Scheme 2). Treatment of thioamide derivative 3 with the appropriate hydrazonoyl halides of type 5ac in refluxing EtOH containing TEA gave the corresponding thiadiazole derivatives 7ac (Scheme 2). Their structures were elucidated on the basis of their spectral data and elemental analysis (see “Experimental”).
Scheme 2

Synthesis of thiadiazole derivatives 7ac

Next, refluxing of compound 3 with 3-chloropentane-2,4-dione (8) or 2-chloro-3-oxo-N-phenyl butanamide (10) in EtOH in the presence of triethylamine afforded the thiazole derivatives 9 and 11, respectively (Scheme 3).The structure of compounds 9 and 11 were elucidated based on their elemental analysis and spectral data (see “Experimental”).
Scheme 3

Synthesis of thiazole derivatives 9, 11, 13 and 15

In a similar manner, thioamide 3 reacted with phenacyl bromide 12 under the same experimental condition to afford one isolable product 13 named as N′-(3,4-diphenylthiazol- 2(3H)-ylidene)-4-methyl-2-phenyl thiazole-5-carbohydrazide (Scheme 3). The structure of thiazole 13 was established based on its elemental analysis and spectral data (see “Experimental”).

Finally, thioamide derivative 3 reacted with ethyl chloroacetate (14) to afford thiazole 15 as showed in Scheme 3. Its IR spectrum showed absorption bands at v 3331 (NH), and 1726, 1648 (2C=O) cm−1. In addition, its 1HNMR spectrum showed singlet signal at δ 4.23 ppm due to the thiazolidinone (CH2) group.

Anticancer activity

The synthesized compounds were tested as anticancer agents against human Hepatocellular carcinoma cell line (HepG-2) using colorimetric MTT assay. We also included the well-known anticancer standard drug (Cisplatin) in the same assay to compare the potency of the synthesized compounds. The IC50 (the concentration of test compounds required to kill 50% of cell population) was determined (Table 1, Fig. 3).
Table 1

The in vitro inhibitory activity of the tested compounds against tumor cell lines expressed as IC50 values (μg/mL) ± standard deviation from three replicates

Tested compounds

IC50 (μg/mL)

Tested compounds

IC50 (μg/mL)


1.43 ± 2.03


7.51 ± 0.64


22.3 ± 2.41


17.4 ± 0.73


20.3 ± 3.70


1.98 ± 1.22


57.2 ± 7.12


35.1 ± 10.8


2.14 ± 3.54


3.31 ± 2.65


1.61 ± 1.92

Fig. 3

Comparison of the IC50 of the new synthesized compounds against Cisplatin

The results of Table 1 revealed that the ascending order of the cytotoxic activity of the newly synthesized compounds towards the human Hepatocellular carcinoma cell line (HepG-2) were as follow: 5c < 13 < 5a < 5b < 9 < 7c < 15 < 7a < 11 < 7b (Fig. 4).
Fig. 4

The ascending order of the cytotoxic activity

From the data of Table 1, we concluded the following structure–activity relationships (SARs):
  • The thiazole ring is essential for the activity.

  • Less number of thiazole ring as in compounds 5ac lead to drastic drop in activity.

  • 1,3,4-Thiadiazole ring is crucial for the cytotoxic activity.

  • Presence of methyl group (electron donating group) at position 4 of the phenyl ring in compound 7b increase its activity more than compound 7a.

  • The presence of the N-phenylcarboxamide group in compound 11 leads to increasing of its cytotoxic activity.




Melting points were measured on an Electrothermal IA 9000 series digital melting point apparatus (Bibby Sci. Lim. Stone, Staffordshire, UK). IR spectra were measured on PyeUnicamSP 3300 and Shimadzu FTIR 8101 PC infrared spectrophotometers (Shimadzu, Tokyo, Japan) in potassium bromide discs. NMR spectra were measured on a Varian Mercury VX-300 NMR spectrometer (Varian, Inc., Karlsruhe, Germany) operating at 300 MHz (1HNMR) and run in deuterated dimethylsulfoxide (DMSO-d 6 ). Chemical shifts were related to that of the solvent. Mass spectra were recorded on a Shimadzu GCMS-QP1000 EX mass spectrometer (Tokyo, Japan) at 70 eV. Elemental analyses were measured by using a German made Elementarvario LIII CHNS analyzer. 2-(4-Methyl-2-phenylthiazole-5-carbonyl)-N-phenylhydrazinecarbothioamide (3) [31], and hydrazonoyl halides 4ac [32] were prepared as reported in the respective literature.

Synthetic procedures

Synthesis of hydrazonoyl chlorides 5a–c

A mixture of 4-methyl-2-phenylthiazole-5-carbohydrazide (2) (2.33 g, 10 mmol) and the appropriate hydrazonoyl chlorides 4ac (10 mmol) in ethanol (30 mL) was refluxed for 3–5 h (monitored through TLC).The resulting solid product was collected and recrystallized from the proper solvent to give the corresponding products 5ac.

2-(2-(4-Methyl-2-phenylthiazole-5-carbonyl)hydrazono)-N′-phenylpropane hydrazonoyl chloride (5a)

Yellow solid; yield (84%); m.p. 188–190 °C (EtOH); IR (KBr) v 3440, 3316 (2NH), 3036, 2922 (CH), 1640 (C=O), 1599 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.36 (s, 3H, CH3), 2.76 (s, 3H, CH3), 7.06–7.86 (m, 10H, ArH), 10.03 (s, br, 1H, D2O-exchangeable NH), 10.57 (s, br, 1H, D2O-exchangeable NH); MS m/z (%): 413 (M++2, 12), 411 (M+, 40), 375 (48), 202 (100), 174 (45), 71 (26). Anal. Calcd for C20H18ClN5OS (411.91): C, 58.32; H, 4.40; N, 17.00. Found: C, 58.19; H, 4.37; N, 16.88%.

2-(2-(4-Methyl-2-phenylthiazole-5-carbonyl)hydrazono)-N′-(p-tolyl)propane- hydrazonoylchloride (5b)

Yellow solid; yield (86%); m.p. 172–174 °C (EtOH); IR (KBr) v 3437, 3313 (2NH), 3041, 2917 (CH), 1679 (C=O), 1598 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.24 (s, 3H, CH3), 2.34 (s, 3H, CH3), 2.77 (s, 3H, CH3), 7.08–7.99 (m, 9H, ArH), 10.06 (s, br, 1H, D2O-exchangeable NH), 10.59 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 427 (M++2, 10), 425 (M+, 33), 389 (26), 202 (81), 106 (100), 64 (66). Anal. Calcd for C21H20ClN5OS (425.93): C, 59.22; H, 4.73; N, 16.44. Found: C, 59.18; H, 4.65; N, 16.37%.

N′-(4-Chlorophenyl)-2-(2-(4-methyl-2-phenylthiazole-5-carbonyl)hydrazono) propane hydrazonoyl chloride (5c)

Yellow solid; yield (87%); m.p. 194–196 °C (DMF); IR (KBr) v 3434, 3319 (2NH), 3044, 2926 (CH), 1682 (C=O), 1593 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.37 (s, 3H, CH3), 2.77 (s, 3H, CH3), 7.08–7.99 (m, 9H, Ar–H), 10.06 (s, br, 1H, D2O-exchangeable NH), 10.57 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 446 (M+, 8), 283 (14), 202 (39), 104 (46), 80 (100), 64 (90). Anal. Calcd for C20H17Cl2N5OS (446.35): C, 53.82; H, 3.84; N, 15.69. Found: C, 53.75; H, 3.79; N, 15.58%.

Synthesis of 1,3,4-thiadiazole derivatives 7a–c

A mixture of compound 3 (0.368 g, 1 mmol) and the appropriate hydrazonoyl chlorides 5ac (1 mmol) in ethanol (20 mL) containing triethylamine (0.1 g, 1 mmol) was refluxed for 6 h. The formed solid product was filtered, washed with methanol, dried and recrystallized from the suitable solvents to give corresponding products 7ac.


Yellow solid; yield (74%); m.p. 162–164 °C (EtOH); IR (KBr) v 3421, 3307 (2NH), 3031, 2951 (CH), 1649 (C=O), 1596 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.34 (s, 3H, CH3), 2.66 (s, 3H, CH3), 2.76(s, 3H, CH3), 6.97-8.14 (m, 15H, ArH), 10.18 (s, br, 1H, D2O-exchangeable NH), 11.17 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 650 (M+, 34), 526 (30), 416 (60), 358 (28), 104 (55), 64 (100). Anal. Calcd for C32H26N8O2S3 (650.80): C, 59.06; H, 4.03; N, 17.22. Found C, 58.94; H, 4.01; N, 17.07%.

4-Methyl-N′-(1-(5-(2-(4-methyl-2-phenylthiazole-5-carbonyl)hydrazono)-4-(p-tolyl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)ethylidene)-2-phenylthiazole-5-carbohydrazide (7b)

Yellow solid; yield (72%); m.p. 149–151 °C (EtOH); IR (KBr) v 3422, 3328 (2NH), 3053, 2929 (CH), 1647 (C=O), 1597 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.26 (s, 3H, CH3),2.35 (s, 3H, CH3), 2.65 (s, 3H, CH3), 2.76(s, 3H, CH3), 6.91–8.03 (m, 14H, ArH), 10.18 (s, br, 1H, D2O-exchangeable NH), 11.14 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 664 (M+, 35), 553 (60), 334 (19), 202 (65), 104 (85), 64 (100). Anal. Calcd for C33H28N8O2S3 (664.82): C, 59.62; H, 4.25; N, 16.85. Found C, 59.47; H, 4.17; N, 16.79%.

N′-(3-(4-Chlorophenyl)-5-(1-(2-(4-methyl-2-phenylthiazole-5-carbonyl)hydrazono)eth-yl)-1,3,4-thiadiazol-2(3H)-ylidene)-4-methyl-2-phenylthiazole-5-carbohydrazide (7c)

Yellow solid; yield (76%); m.p. 191–193 °C (Dioxane); IR (KBr) v 3424, 3312 (2NH), 3047, 2932 (CH), 1649 (C=O), 1599 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.33 (s, 3H, CH3), 2.66 (s, 3H, CH3), 2.77(s, 3H, CH3), 6.90–8.11 (m, 14H, ArH), 10.13 (s, br, 1H, D2O-exchangeable NH), 11.19 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 686 (M++2, 8), 684 (M+, 26), 513 (53), 368 (39), 257 (17), 104 (25), 64 (100). Anal.Calcd for C32H25ClN8O2S3 (685.24): C, 56.09; H, 3.68; N, 16.35. Found C, 56.02; H, 3.58; N, 16.22%.

General procedure for the synthesis of thiazole derivatives 9, 11, 13, and 15

A mixture of compound 3 (0.368 g, 1 mmol) and the appropriate α-halo-compounds namely, 3-chloropentane-2,4-dione (8), 2-chloro-3-oxo-N-phenylbutanamide (10), 2-bromo-1-phenyl ethanone (12) and ethyl 2-chloroacetate (14) (1 mmol for each) in ethanol (20 mL) containing triethylamine (0.1 g, 1 mmol) was refluxed for 4–6 h. (monitored by TLC The solid product was filtered, washed with water, dried and recrystallized from the proper solvent to give the corresponding thiazole derivatives 9, 11, 13, and 15, respectively.

N′-(5-Acetyl-4-methyl-3-phenylthiazol-2(3H)-ylidene)-4-methyl-2-phenylthiazole-5-carbohydrazide (9)

Yellow solid; yield (78%); m.p. 155–157 °C (EtOH); IR (KBr) v 3432 (NH), 3036, 2993 (CH), 1695, 1648 (2C=O), 1590 (C=N) cm−1; 1H NMR(DMSO-d 6 ) δ 2.32 (s, 3H, CH3),2.46 (s, 3H, CH3), 2.77 (s, 3H, CH3), 6.91–7.86 (m, 10H, ArH), 10.61 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 448 (M+, 57), 246 (60), 176 (35), 104 (80), 77 (100). Anal.Calcd for C23H20N4O2S2 (448.56): C, 61.59; H, 4.49; N, 12.49. Found C, 61.48; H, 4.36; N, 12.37%.

4-Methyl-2-(2-(4-methyl-2-phenylthiazole-5-carbonyl)hydrazono)-N-3-diphenyl-2,3-dihydrothiazole-5-carboxamide (11)

Yellow solid; yield (79%); m.p. 182–84 °C (DMF); IR (KBr): v 3435, 3176 (2NH), 3030, 2928(CH), 1671, 1649 (2C=O), 1594 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.36 (s, 3H, CH3),2.76(s, 3H, CH3), 6.97–7.73 (m, 15H, ArH), 10.46 (s, br, 1H, D2O-exchangeable NH), 11.72 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 525 (M+, 7), 447 (16), 334 (100), 200 (59), 77 (89). Anal.Calcd for C28H23N5O2S2 (525.64): C, 63.98; H, 4.41; N, 13.32. Found C, 63.84; H, 4.30; N, 13.28%.

N′-(3,4-Diphenylthiazol-2(3H)-ylidene)-4-methyl-2-phenylthiazole-5-carbohydrazide (13)

Yellow solid; yield (70%); m.p. 174–178 °C (EtOH); IR (KBr) v 3369 (NH), 3047, 2926(CH), 1648 (C=O), 1594 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.75 (s, 3H, CH3), 7.03 (s, 1H, thiazole-H5), 7.35–8.02 (m, 15H, ArH), 10.73 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 468 (M+, 25), 334 (100), 200 (40), 104 (69), 64(65). Anal.Calcd for C26H20N4OS2 (468.59): C, 66.64; H, 4.30; N, 11.96. Found C, 66.55; H, 4.21; N, 11.79%.

4-Methyl-N′-(4-oxo-3-phenylthiazolidin-2-ylidene)-2-phenylthiazole-5-carbo- hydrazide (15)

Yellowish-white solid; yield (72%); m.p. 192–194 °C (Dioxane); IR (KBr) v 3331(NH), 3036, 2926 (CH), 1726, 1648 (2C=O), 1596 (C=N) cm−1; 1H NMR (DMSO-d 6 ) δ 2.65 (s, 3H, CH3), 4.23 (s, 2H, thiazolone-CH2), 7.40–7.88 (m, 10H, ArH), 10.82 (s, br, 1H, D2O-exchangeable NH); MS m/z (%) 408 (M+, 65), 334 (18), 202 (100), 104 (86), 64 (69). Anal.Calcd for C20H16N4O2S2 (408.50): C, 58.80; H, 3.95; N, 13.72. Found C, 58.68; H, 3.84; N, 13.64%.

Anticancer activity

The cytotoxic evaluation of the synthesized compounds was carried out at the Regional Center for Mycology and Biotechnology at Al-Azhar University, Cairo, Egypt according to the reported method [33].


We successfully synthesized a series of novel heterocycles containing thiazole and 1,3,4-thiadiazole rings by a facile and convenient method. The structure of the newly prepared compounds was established based on both elemental analysis and spectroscopic data. The anticancer activity of the synthesized compounds was measured and showed promising activity.



human hepatocellular carcinoma




melting point






American Type Culture Collection


thin layer chromatography


Authors’ contributions

SMG, NAK and YNM carried the literature study and designed synthetic schemes, MRA and SA contributed in the synthesis and purification of the compounds. All authors read and approved the final manuscript.


The authors extend their sincere appreciation to the Deanship of Scientific Research at the King Saud University for its funding this Prolific Research group (PRG-1437-29).

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, MIU University, Cairo, Egypt
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, King Khalid University, Abha, Saudi Arabia
Department of Chemistry, Faculty of Science, University of Beni Suef, Beni Suef, Egypt
Department of Chemistry, College of Science, King Saud University, Riyadh, Saudi Arabia


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