Search

Reactions of indole-2,3-diones with biuret afforded 1,3-dihydro-3-ureidoformimido-2H-indol-2-ones and spiro[3H-indole-3,2′(1′H)-(1,3,5)triazine]-2,4′,6′(1H,3′H,5′H)-triones indicated these to be solvent dependent. The chemical structures of the products were elucidated by their comprehensive spectroscopic (IR, 1H-NMR, 13C-NMR, 19F-NMR, and Mass) as well as analytical analysis.

One pot green synthesis of 1-(1,2,4-triazol-4-yl)spiro[azetidine-2,3′-(3H)-indole]-2′,4′(1′H)-diones was carried out by the reaction of indole-2,3-diones,4-amino-4H-1,2,4-triazole and acetyl chloride/chloroacetyl chloride in ionic liquid [bmim]PF6 with/without using a catalyst. It was also prepared by conventional method via Schiff's bases, 3-[4H-1,2,4-triazol-4-yl]imino-indol-2-one. Further, the corresponding phenoxy derivatives were obtained by the reaction of chloro group attached to azetidine ring with phenols. The synthesized compounds were characterized by analytical and spectral (IR, 1H NMR, 13C NMR, and FAB mass) data. Evaluation for insecticidal activity against Periplaneta americana exhibited promising results.

1-Trifluoroacetyl-3-dialkylaminomethyl-5-monosubstituted benzimidazoline-2-thiones have been synthesized from p-substituted anilines which were acetylated with trifluoroacetic acid. The trifluoroacetanilides were nitrated, reduced and cyclised with carbon disulphide in the presence of alcoholic potassium hydroxide and finally treated with formaldehyde and suitable secondary amines to afford the Mannich bases. The compounds were characterised by their analytical and spectral (ir, pmr, 19F and mass) data. The synthesized compounds have been screened for anti-inflammatory and analgesic activity and found to be active.

Reaction of 2-hydrazinobenzimidazoles with β-diketones in neutral and acidic media revealed that 2-(3,5-disubstituted-1H-pyrazol-1-yi)benzimidazoles are formed in the former case, whereas hydrazones are obtained in acidic medium. Further the alkylation of > NH of the title compound was investigated. Characterisation of these products have been done by elemental analysis, ir, pmr, 19F nmr, 13C nmr and mass spectral studies.