Extracurricular laboratory:new discovery of Thiazolidin-2-one

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While the job of a research scientist varies, most chemistry careers in research are based in laboratories, where research is conducted by teams following scientific methods and standards. An article , which mentions Quality Control of Thiazolidin-2-one, molecular formula is C3H5NOS. The compound – Thiazolidin-2-one played an important role in people’s production and life., Quality Control of Thiazolidin-2-one

A new series of benzimidazole bearing pyridine derivatives were synthesized by condensation of 1,2-phenylenediamine with 2-oxo-1,2-dihydro-pyridine-3-carboxylic acid derivative 2 in phosphoric acid to give 3-(1Hbenzo[ d]imidazol-2-yl)-pyridin-2(1H)-one derivative 3. Compound 3 on further reaction with a mixture of phosphorus oxychloride and phosphorus pentachloride gave 2-(2-chloro-) pyridin-3-yl)-1H-benzo[d] imidazole derivative 4. Moreover, 4 were reacted with different amines to give 3-(1H-benzo[d]imidazol-2-yl)-N-(substituted) pyridin-2-amine derivatives 5a-c. Meanwhile, N-(N-(substituted) sulfamoyl) pyridin-3-yl)-1H-benzo[d]imidazole-1-carboxamide derivatives 7a,b were synthesized by reaction of 5c with chlorosulfonyl isocyanate to give 2-(pyridin-3-yl)-1H-benzo [d]imidazole-1-carbonyl) sulfamoyl chloride derivative followed by reaction of the latter with different amines. On the other hand, upon treatment compound 4 with hydrazine hydrate gave the hydrazide derivative 8. The reaction of compound 8 with different alkyl/arylisothiocyanates gave the corresponding thiosemicarbazide derivatives 9a-d, while their cyclo condensation reaction with ethyl chloro acetate gave the corresponding thiazolidin-4-one derivatives 10a-c. Moreover, condensation of 10a,c with aromatic aldehydes afforded the corresponding 5-arylidine-thiazolidin-4-one derivatives 11a,b. Cytotoxic evaluation of some of the newly synthesized compounds against human breast carcinoma cell line MCF-7 revealed that, these compounds showed promising activity compared with Doxorubicin as positive control.

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Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H274N | ChemSpider