SYNTHESIS AND ANTICANCER ACTIVITY OF ARYLAZOTHIAZOLES AND 1,3,4-THIADIAZOLES USING CHITOSAN-GRAFTED-POLY(4-VINYLPYRIDINE) AS A NOVEL COPOLYMER BASIC CATALYST

Авторы

  • Sobhi M. Gomha Chemistry Department, Faculty of Science, Cairo University
  • Sayed M. Riyadh Chemistry Department, Faculty of Science, Cairo University Department of Chemistry, Faculty of Science, Taibah University, Almadinah Almunawrah, 30002, Saudi Arabia
  • Elmahdi M. Mahmmoud Department of Chemistry, Faculty of Science, Taibah University, Almadinah Almunawrah, 30002, Saudi Arabia
  • Mahmoud M. Elaasser Regional Center for Mycology and Biotechnology, Al-Azhar University, Cairo, Egypt

DOI:

https://doi.org/10.1007/2544

Ключевые слова:

arylazothiazole, 1, 3, 4-thiadiazole, anticancer activity, cyclocondensation

Аннотация

A novel series of 4-substituted 5-arylazo-2-[1-(pyrrol-3-yl)ethylidenehydrazinyl]thiazoles and 5-arylazo-2-[1-(pyrrol-3-yl)ethylidenehydrazinyl]-2,3-dihydrothiazol-3-amines was prepared by cyclocondensation of α-oxohydrazonoyl halides with 1-(pyrrol-3-yl)ethylidenethiosemicarbazide and 1-(pyrrol-3-yl)ethylidenethiocarbohydrazide, respectively. These cyclocondensation reactions were achieved by using chitosan-grafted-poly(4-vinylpyridine) as a novel basic catalyst under microwave irradiation. Furthermore, the reaction of the above mentioned thiosemicarbazide and thiocarbohydrazide with N-phenylbenzenecarbohydrazonyl chlorides (bereft of the α-oxo group) using chitosan-grafted catalyst proceeded via a similar mechanism and afforded the same 2-hydrazono-1,3,4-thiadiazoles. The structures of the newly synthesized compounds were established on the basis of spectroscopic evidences as well as by their synthesis via alternative methods. Finally, the appraisal of the newly synthesized products for their anticancer activity against a colon carcinoma cell line (HCT-116) and liver carcinoma cell line (HEPG2-1) revealed promising activity, especially 4-phenyl- and 4-(thiophen-2-yl)-substituted 1,3-thiazole derivatives.

How to Cite
Gomha, S. M.; Riyadh, S. M.; Mahmmoud, E. A.; Elaasser, M. M. Chem. Heterocycl. Compd. 2015, 51, 1030. [Khim. Geterotsikl. Soedin. 2015, 51, 1030.]

For this article in the English edition see DOI 10.1007/s10593-016-1815-9

Опубликован

2015-12-24

Выпуск

Раздел

Оригинальные статьи