Simple exploration of 4-Bromo-2-fluoropyridine

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 128071-98-7. SDS of cas: 128071-98-7.

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , SDS of cas: 128071-98-7, 128071-98-7, Name is 4-Bromo-2-fluoropyridine, molecular formula is C5H3BrFN, belongs to pyridine-derivatives compound. In a document, author is El-Mekabaty, Ahmed, introduce the new discover.

Convenient synthesis of novel sulfonamide derivatives as promising anticancer agents

Novel sulfonamide derivatives have been synthesized from the readily accessible N-(4-acetylphenyl)benzenesulfonamide (1). Condensation of 1 with phenylhydrazine in refluxing ethyl alcohol gave the corresponding phenylhydrazone 2, which was then added to the Vilsmeier-Haack reagent (POCl3/DMF) to give the 4-formylpyrazole derivative 3. Fusion of 1 with thiourea in the presence of iodine at 130 degrees C afforded the 2-aminothiazole derivative 4. Refluxing 1 with an excess of N, N-dimethylformamide dimethyl acetal furnished the enaminone 5. The chemical reactivity of enaminone 5 toward some nitrogen and carbon nucleophiles has been studied to obtain polyfunctionalized heteroaromatic systems bearing a sulfonamide moiety. Besides, the enaminone 5 undergoes the Gewald reaction and reacts with ethyl cyanoacetate and elemental sulfur in the presence of morpholine to yield the 2-aminothiophene derivative 18. Moreover, the utility of 5 for the synthesis of 4-(phenylsulfonamido)benzoic acid (19) was investigated. The synthesized sulfonamides were evaluated for their in vitro cytotoxic activities against two human cell lines, MCF-7 (breast adenocarcinoma cells) and RPE-1 (normal retina pigmented epithelium cells). The results revealed that compounds 1-3, 6-8, 10, 12b, 18, 19, and 21 have a potent cytotoxic effect on MCF-7 and less on RPE-1 cells compared to the positive control doxorubicin (R).

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 128071-98-7. SDS of cas: 128071-98-7.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem